Showing posts with label nutrition. Show all posts
Showing posts with label nutrition. Show all posts

Tuesday, April 17, 2018

MIND diet

While the Mediterranean diet focuses more on heart health benefits and the prevention of coronary heart disease, or CVD, and the DASH diet has been shown to prevent and reverse hypertension, or high blood pressure, studies show that when combined, these diets provide brain health benefits to those who are recovering from stroke. Cardiovascular disease (CVD) is a class of diseases that involve the heart or blood vessels. Cardiovascular disease includes coronary artery diseases (CAD) such as angina and myocardial infarction (commonly known as a heart attack).

Dietary Approaches to Stop Hypertension (DASH)

One of the steps your doctor may recommend to lower your high blood pressure is to start using the DASH diet. DASH stands for Dietary Approaches to Stop Hypertension. The diet is simple: Eat more fruits, vegetables, and low-fat dairy foods. Cut back on foods that are high in saturated fat, cholesterol, and trans fats.
 
Stroke survivors suffer damage to the brain tissue due to a lack of oxygen to the brain during a stroke. Because of this trauma, they have a higher risk of cognitive decline and twice the risk of dementia. An initial study that was funded by the U.S. National Institute on Aging suggests that stroke survivors who eat a diet primarily consisting of leafy greens, fish and a variety of healthy and natural whole foods can potentially preserve brain functionality over time.
 
In this initial study, both the Mediterranean diet and the DASH diet were combined to create the MIND diet which stands for Mediterranean-DASH Intervention for Neurodegenerative Delay diet. Researchers looked at the link between 106 stroke survivors, their dietary intakes and their cognitive decline over a 5-year period.
 
The study showed that the stroke survivors who ate the largest amounts of green leafy vegetables, berries, nuts, olive oil, whole grain and beans had the highest cognitive ratings. The researchers went on to state that when an individual’s diet included dark green leafy vegetables and berries as the major sources of vegetable and fruit intake, that individual suffered less problems with memory and other markers of cognitive decline. They concluded that there likely is an association and that more research is needed to prove this theory.
 
The MIND diet is rich in nutrients that can help strengthen our brain tissues and brain functions. Such nutrients discussed in this study included vitamin K, folate, beta carotene and lutein which can be found in dark green leafy vegetables such as spinach, kale, arugula, mustard greens and collard greens.
 
This heart-healthy and brain health-promoting diet is a positive treatment option for stroke survivors who tend to be put on many medications after their strokes. A dietary change requires no prescription, and it tastes great! It’s a simple and enjoyable way to maintain high cognitive function post-stroke.
 
This research leads us to think about stroke prevention, as well. Perhaps we should all MIND our diets for a host of reasons. Now let’s go have a large kale salad with almonds, blueberries and roasted red pepper and olive oil dressing!
 

MIND diet slows

cognitive decline

with aging

Martha Clare Morris, S.D., Christy C. Tangney, Ph.D., Yamin Wang, Ph.D.,  Frank M. Sacks, M.D., Lisa L Barnes, Ph.D., David A Bennett, M.D.,and Neelum T. Aggarwal, M.D.
 

Abstract


Background

The Mediterranean and DASH diets have been shown to slow cognitive decline, however, neither diet is specific to the nutrition literature on dementia prevention.

Methods

We devised the MIND diet score that specifically captures dietary components shown to be neuro-protective and related it to change in cognition over an average 4.7 years among 960 participants of the Memory and Aging Project.

Results

In adjusted mixed models, the MIND score was positively associated with slower decline in global cognitive score (β=0.0092; p<.0001) and with each of 5 cognitive domains. The difference in decline rates for being in the top tertile of MIND diet scores versus the lowest was equivalent to being 7.5 years younger in age.

Conclusion

The study findings suggest that the MIND diet substantially slows cognitive decline with age. Replication of these findings in a dietary intervention trial would be required to verify its relevance to brain health.
 
Keywords: cognition, cognitive decline, nutrition, diet, epidemiological study, aging
 

INTRODUCTION

Dementia is now the 6th leading cause of death in the U.S. and the prevention of cognitive decline, the hallmark feature of dementia, is a public health priority. It is estimated that delaying disease onset by just 5 years will reduce the cost and prevalence by half. Diet interventions have the potential to be effective preventive strategies. Two randomized trials of the cultural-based Mediterranean diet and of the blood pressure lowering DASH diet (Dietary Approach to Systolic Hypertension) observed protective effects on cognitive decline.; We devised a new diet that is tailored to protection of the brain, called MIND (Mediterranean-DASH Diet Intervention for Neurodegenerative Delay). The diet is styled after the Mediterranean and DASH diets but with modifications based on the most compelling findings in the diet-dementia field. For example, a number of prospective studies observed slower decline in cognitive abilities with high consumption of vegetables, and in the two U.S. studies, the greatest protection was from green leafy vegetables.; Further, all of these studies found no association of overall fruit consumption with cognitive decline. However, animal models and one large prospective cohort study indicate that at least one particular type of fruit – berries - may protect the brain against cognitive loss. Thus, among the unique components of the MIND diet score are that it specifies consumption of green leafy vegetables and berries but does not score other types of fruit. In this study, we related the MIND diet score to cognitive decline in the Memory and Aging Project (MAP) and compared the estimated effects to those of the Mediterranean and DASH diets, dietary patterns that we previously reported were protective against cognitive decline among the MAP study participants.
 

METHODS

Study Population

The analytic sample is drawn from the Rush Memory and Aging Project (MAP), a study of residents of more than 40 retirement communities and senior public housing units in the Chicago area. Details of the MAP study were published previously. Briefly, the ongoing open cohort study began in 1997 and includes annual clinical neurological examinations. At enrollment, participants are free of known dementia; and agree to annual clinical evaluation and organ donation after death. We excluded persons with dementia based on accepted clinical criteria as previously described., Participants meeting criteria for mild cognitive impairment (n=220) were not excluded except in secondary analyses. From February 2004- 2013, the MAP study participants were invited to complete food frequency questionnaires at the time of their annual clinical evaluations. During that period, a total of 1,545 older persons had enrolled in the MAP study, 90 died and 149 withdrew before the diet study began, leaving 1306 participants eligible for these analyses. Of these, 1068 completed the dietary questionnaires of which 960 survived and had at least two cognitive assessments for the analyses of change. The analytic sample was 95% white and 98.5% non-Hispanic. The Institutional Review Board of Rush University Medical Center approved the study, and all participants gave written informed consent.

Cognitive Assessments

Each participant underwent annual structured clinical evaluations including cognitive testing. Technicians, trained and certified according to standardized neuropsychological testing methods, administered 21 tests, 19 of which summarized cognition in five cognitive domains (episodic memory, working memory, semantic memory, visuospatial ability, and perceptual speed) as described previously. Composite scores were computed for each cognitive domain and for a global measure of all 19 tests. Raw scores for each test were standardized using the mean and standard deviation from the baseline population scores, and the standardized scores averaged. The number of annual cognitive assessments analyzed for participants ranged from 2 to 10 with 52% of sample participants having 5 or more cognitive assessments.

Diet Assessment

FFQs were collected at each annual clinical evaluation. For these prospective analyses of the estimated dietary effects on cognitive change, we used the first obtained FFQ to relate dietary scores to cognitive change from that point forward. Longitudinal analyses of change in MIND diet score using all available FFQs in a linear mixed model indicated a very small but statistically significant decrease in MIND score of −0.026 (p=0.02) compared to the intercept MIND diet score of 7.37.
 
Diet scores were computed from responses to a modified Harvard semi-quantitative food frequency questionnaire (FFQ) that was validated for use in older Chicago community residents. The FFQ ascertains usual frequency of intake over the previous 12 months of 144 food items. For some food items, natural portion sizes (e.g. 1 banana) were used to determine serving sizes and calorie and nutrient levels. Serving sizes for other food items were based on sex-specific mean portion sizes reported by the oldest men and women of national surveys.

MIND Diet Score

The MIND diet score was developed in three stages: 1) determination of dietary components of the Mediterranean and DASH diets including the foods and nutrients shown to be important to incident dementia and cognitive decline through detailed reviews of the literature, 2) selection of FFQ items that were relevant to each MIND diet component, and 3) determination of daily servings to be assigned to component scores guided by published studies on diet and dementia. Among the MIND diet components are 10 brain healthy food groups (green leafy vegetables, other vegetables, nuts, berries, beans, whole grains, seafood, poultry, olive oil and wine) and 5 unhealthy food groups (red meats, butter and stick margarine, cheese, pastries and sweets, and fried/fast food). Olive oil consumption was scored 1 if identified by the participant as the primary oil usually used at home and 0 otherwise. For all other diet score components we summed the frequency of consumption of each food item portion associated with that component and then assigned a concordance score of 0, 0.5, or 1. (Table 1) The total MIND diet score was computed by summing over all 15 of the component scores.

Table 1


MIND diet component servings and scoring









00.51
Green Leafy Vegetablesa≤2 servings/wk> 2 to <6 td="" wk="">
≥6 servings/wk
Other Vegetablesb<5 serving="" td="" wk="">
5 – <7 td="" wk="">
≥1 serving/day
Berriesc<1 serving="" td="" wk="">
1 /wk≥2 servings/wk
Nuts<1 mo="" td="">
1/mo – <5 td="" wk="">
≥5 servings/wk
Olive OilNot primary oilPrimary oil used
Butter, Margarine>2 T/d1–2 /d<1 d="" t="" td="">
Cheese7+ servings/wk1–6 /wk< 1 serving/wk
Whole Grains<1 d="" serving="" td="">
1–2 /d≥3 servings/d
Fish (not fried)dRarely1–3 /mo≥1 meals/wk
Beanse<1 meal="" td="" wk="">
1–3/wk>3 meals/wk
Poultry (not fried)f<1 meal="" td="" wk="">
1 /wk≥2 meals/wk
Red Meat and productsg7+ meals/wk4–6 /wk< 4 meals/wk
Fast Fried Foodsh4+ times/wk1–3 /wk<1 td="" time="" wk="">
Pastries & Sweetsi7+ servings/wk5 −6 /wk<5 servings="" td="" wk="">
Wine>1 glass/d or never1/mo – 6/wk1 glass/d

TOTAL SCORE15
akale, collards, greens; spinach; lettuce/tossed salad
 
bgreen/red peppers, squash, cooked carrots, raw carrots, broccoli, celery, potatoes, peas or lima beans, potatoes, tomatoes, tomato sauce, string beans, beets, corn, zucchini/summer squash/eggplant, coleslaw, potato salad
 
cstrawberries
 
ebeans, lentils, soybeans)
 
dtuna sandwich, fresh fish as main dish; not fried fish cakes, sticks, or sandwiches
 
fchicken or turkey sandwich, chicken or turkey as main dish and never eat fried at home or away from home
 
gcheeseburger, hamburger, beef tacos/burritos, hot dogs/sausages, roast beef or ham sandwich, salami, bologna, or other deli meat sandwich, beef (steak, roast) or lamb as main dish, pork or ham as main dish, meatballs or meatloaf
 
hHow often do you eat fried food away from home (like French fries, chicken nuggets)?
 
ibiscuit/roll, poptarts, cake, snack cakes/twinkies, Danish/sweetrolls/pastry, donuts, cookies, brownies, pie, candy bars, other candy, ice cream, pudding, milkshakes/frappes

DASH and Mediterranean Diet Scores

We used the DASH diet scoring of the ENCORE trial in which 10 dietary components were each scored 0, 0.5, or 1 and summed for a total score ranging from 0 (lowest) to 10 (highest) diet concordance. The Mediterranean Diet Score was that described by Panagiotakos et al. that includes 11 dietary components each scored 0 to 5 that are summed for a total score ranging from 0 to 55 (highest dietary concordance). We used serving quantities specific to the traditional Greek Mediterranean diet to score concordance in contrast to the use of sex-specific within population median servings employed by other studies so that the scoring metric aligned with the actual Mediterranean diet.

Covariates

Total energy intake was computed based on responses of frequency of consumption of the FFQ food items. Non-dietary variables were obtained from structured interview questions and measurements at the participants’ annual clinical evaluations. Age (in years) was computed from self-reported birth date and date of the first cognitive assessment in this analysis. Education was based on self-reported years of regular schooling. Apolipoprotein E genotyping was performed using high throughput sequencing as previously described. Smoking history was categorized as never, past and current smoker. All other covariates were based on data collected at the time of each cognitive assessment and were modeled as time-varying covariates to represent updated information from participants’ previous evaluations. A variable for frequency of participation in cognitively stimulating activities was computed as the average frequency rating, based on a 5-point scale, of different activities (e.g. reading, playing games, writing letters, visiting the library). Hours per week of physical activity was computed based on the sum of self-reported minutes spent over the previous two weeks on five activities (walking for exercise, yard work, calisthenics, biking, and water exercise). Number of depressive symptoms was assessed by a modified 10-item version of the Center for Epidemiological Studies-Depression scale that has been related to incident dementia. Body mass index (weight in kg/height in m2) was computed from measured weight and height and modeled as two indicator variables, BMI≤20 and BMI ≥30.
Hypertension history was determined by self-reported medical diagnosis, measured blood pressure (average of 2 measurements ≥160 mmHg systolic or ≥90 mmHg diastolic) or current use of hypertensive medications. Myocardial infarction history was based on self-reported medical diagnosis or interviewer recorded use of cardiac glycosides (e.g. lanoxin, digitoxin). Diabetes history was determined by self-reported medical diagnosis or current use of medications. Medication use was based on interviewer inspection. Clinical diagnosis of stroke was based on clinician review of self-reported history, neurological examination and cognitive testing history.

Statistical Methods

We used separate linear mixed models with random effects in SAS© to examine the relations of the MIND diet score to change in the global cognitive score and in each cognitive domain score. The basic-adjusted model included terms for age, sex, education, APOE-ε4, smoking history, physical activity, participation in cognitive activities, total energy intake, MIND diet score, a variable for time, and multiplicative terms between time and each model covariate, the latter providing the covariate effect on cognitive decline. For all analyses, we investigated both linear (MIND diet score modeled as a continuous term) and non-linear associations (MIND diet score modeled in tertiles) with the cognitive scores. Because the study results were identical for the two sets of models, we report the effect estimates for the continuous linear term in tables and text and the tertile estimates in Figure 1. Non-static covariates (e.g. cognitive and physical activities, BMI, depressive symptoms and cardiovascular conditions) were modeled as time-varying except when they were analyzed as potential effect modifiers in which case only the baseline measure for that covariate was modeled. Tests for statistical interaction by potential effect modifiers were computed in the basic-adjusted model by modeling 2-way and 3-way multiplicative terms between MIND diet score, time, and the effect modifier, with the 3-way multiplicative term test for interaction set at p≤0.05. We compared the relative effects of the MIND, Mediterranean and DASH diet scores on cognitive decline by computing standardized β coefficients ( β to 4 decimal places /standard error) for each diet score based on the parameter estimates of the basic model. We then performed formal statistical tests using Meng et al.’s revision of Hotelling’s procedure for comparing two non-independent correlation coefficients, in this case, the correlations between the diet scores and cognitive change from the basic model. To provide an estimate of the equivalent age difference in years to the difference in decline rates for tertiles 3 and 1 of the MIND diet score, we computed the ratio of the beta coefficients [β (time*age) / β (time*tertile 3 MIND score) in the basic-adjusted model.



Rates of change in global cognitive score over 10 years for MAP participants with MIND diet scores in the highest tertile of scores (- - -; median 9.5, range 8.5–12.5), the second tertile of scores (…; median 7.5, range 7.0–8.0), and the lowest tertile of scores (An external file that holds a picture, illustration, etc.
Object name is nihms693732ig1.jpg; median 6, range 2.5–6.5). The rates of change were based on the mixed model with MIND diet score modeled as two indicator variables for tertile 2 and tertile 3 (tertile 1, the referent) and adjusted for age, sex, education, smoking, physical activity, participation in cognitively stimulating activities, and total energy intake. For tertile 3: β=0.0366, standard error=0.0101, p=0.003 and for tertile 2: β=0.0243, standard error=0.0099, p=0.01.
 

RESULTS

The analytic sample was on average 81.4 (± 7.2) years of age, primarily female (75%) and with a mean educational level of 14.9 (±2.9) years, and was demographically comparable to the entire MAP cohort of 1,545 participants (mean age, 80.1 years; 73% female; mean education, 14.4 years). Computed MIND scores from food frequency data on MAP study participants averaged 7.4 (range: 2.5–12.5). MIND diet scores were positively correlated with both the Mediterranean (r=0.62) and the DASH (r=0.50) diet scores. MAP participants with the highest MIND diet scores tended to have a more favorable risk profile for preserving cognitive abilities including higher education, greater participation in cognitive and physical activities and lower prevalence of cardiovascular conditions. (Table 2)

Table 2


Baseline characteristics * of analyzed MAP participants according to tertile of MIND diet score
CharacteristicMIND Diet Score Tertile
NTertile 1Tertile 2Tertile 3
Age, mean years96081.981.780.5
Male, percent960282623
APOE-ε4, percent823222621
Education, mean years96014.315.115.6
Cognitive Activities, mean9593.13.23.4
Total Energy Intake, mean kcal960166517881794
Smoking, percent never960403842
Physical Activity, mean hours/week9582.53.44.3
Depressive Symptoms, mean number9591.40.90.9
BMI, mean92727.527.126.7
Hypertension, percent954797672
Diabetes, percent960242017
Heart Disease History, percent959181218
Clinical Stroke History, percent8701179
 
 
Characteristics were standardized by age in 5-year categories
The overall rate of change in cognitive score was a decline of 0.08 standardized score units (SU) per year. In mixed models adjusted for age, sex, education, total energy intake APOE-ε4, smoking history, physical activity and participation in cognitive activities, the MIND diet score was positively and statistically significantly associated with slower rate of cognitive decline. (Table 3) Compared to the decline rate of participants in the lowest tertile of scores, the rate for participants in the highest tertile was substantially slower. (Figure 1) The difference in rates was the equivalent of being 7.5 years younger in age. The MIND diet score was statistically significantly associated with each cognitive domain, particularly for episodic memory, semantic memory and perceptual speed. (Table 3)

Table 3


Estimated effects (β)* of the MIND diet score on the rate of change in global cognitive score and change in five cognitive domains among MAP participants over an average 4.7 years of follow-up in adjusted* mixed models




GlobalEpisodicaSemanticbPerceptualcPerceptualdWorkinge
CognitionMemoryMemoryOrganizationSpeedMemory
Age-Adjustedn**960949945932934957
β0.00900.00790.00690.00570.00880.0049
Standard Error(0.0023)(0.0027)(0.0026)(0.0025)(0.0024)(0.0024)
P-Value0.00010.0030.0070.020.00020.04
Basicn**818808804793794816
β0.00950.00800.01050.00770.00840.0050
Standard Error(0.0023)(0.0028)(0.0027)(0.0025)(0.0024)(0.0024)
P-Value<0 .0001="" td="">
0.0040.00010.0020.00030.04
Basic +
Cardiovascular
Conditions ±n**860850846835836858
β0.01060.00900.01130.00770.00970.0060
Standard Error(0.0023)(0.0028)(0.0027)(0.0025)(0.0023)(0.0024)
P-Value<0 .0001="" td="">
0.001<0 .0001="" td="">
0.002<0 .0001="" td="">
0.01
*β=beta coefficient from the model for the interaction term between MIND diet score and time
 
**n=total number of participants with complete data for model
Basic model includes age at the first cognitive assessment, Mind diet score, sex, education, participation in cognitive activities, APOE-ε4 (any ε4 allele), smoking history (current, past, never), physical activity hours per week, total energy intake, time and interaction terms between time and each model covariate
 
±Basic model plus history of stroke, myocardial infarction, diabetes, hypertension and interaction terms between each covariate and time
 
aComposite score of the following 7 instruments: Immediate memory test and delayed memory test from Story A Logical Memory subset of the Wechsler Memory Scale-Revised; immediate word recall and delayed word recall of the CERAD Word List Recall; CERAD Word list Recognition; and immediate memory test and delayed memory test of the East Boston Story.
 
bComposite score of the following 3 instruments: Verbal fluency from CERAD; 15 item version of the Boston Naming Test; and 15-item reading test
 
cComposite score of the 15-item version of Judgment of Line Orientation and the 16-item version of Standard Progressive Matrice
 
dComposite score of the following 4 measure: Oral version of the Symbol Digit Modalities Test; Number Comparison; and, 2 indices from a modified version of the Stroop Neuropsychological Screening test
 
eComposite score of the following 3 instruments: Digit Span subtests-forward of the Wechsler Memory Scale-Revised; Digit Span subtests-backward of the Wechsler Memory Scale-Revised; and Digit Ordering
 
The Mediterranean and DASH diets have demonstrated effects on the reduction of cardiovascular conditions and risk factors which raises the possibility that the MIND diet association with cognitive decline may be through its effects on cardiovascular disease. To investigate potential mediation by these factors we reanalyzed the basic model for the global cognitive score and each cognitive domain score with the inclusion of terms for hypertension, stroke, myocardial infarction, and diabetes, however, the effect estimates did not change. (Table 3)

Depression and weight have complex relations with dementia; they are known both as risk factors (depression, obesity) and as outcomes of the disease (depressive symptoms, weight loss). Both factors are also affected by diet quality. Therefore, we examined in the basic model what impact additional control for these variables might have on the observed association between the MIND diet score and cognitive decline but these adjustments also did not change the results for any of the cognitive measures (e.g. for global cognitive function β=0.00922, SE=0.0022, p<0 .0001="" p="">
We also investigated potential modifications in the estimated effect of the MIND diet score on cognitive decline by age, sex, APOE-ε4, education, physical activity, low weight (BMI≤20), obese (BMI≥30), and each of the cardiovascular-related conditions (hypertension, myocardial infarction, stroke, diabetes). However, there was no statistical evidence that the diet effect on the global or individual domain cognitive scores differed by level or presence of any of these risk factors. (Data not shown)

To examine whether the observed MIND diet –cognitive decline relation may be due to dementia effects on dietary behaviors or on reporting accuracy, we reanalyzed the data after eliminating 220 participants who had mild cognitive impairment at the baseline; the resulting decline rate for higher MIND diet score (β=0.0104, p<.00001) was even more protective, by 9.5%, compared to that of the entire sample (β=0.0095).

We also investigated the potential effects of dietary changes over time on the observed associations of baseline MIND diet score with cognitive change. We reanalyzed the data after excluding 144 participants whose MIND diet scores either improved (top 10%) or decreased (bottom 10%) over the study period. The protective estimates of effect of the MIND diet score on change in global cognitive score increased considerably (β=0.0120, p<0 .00001="" 30="" ability="" also="" basic-adjusted="" by="" change="" cognitive="" diet="" domains="" effects="" estimated="" exception="" had="" in="" increased="" individual="" little="" mind="" model.="" of="" on="" p="0.02).</p" the="" visuospatial="" which="" with="">
In a previous study of the MAP participants, we observed protective relations of both the MedDiet and DASH diet scores to cognitive decline. A comparison of these diet components and scores is provided in eTable 1. We analyzed the data for these two diet scores in separate basic-adjusted models of the global cognitive scores and compared the standardized regression coefficients for all three diet scores. The MIND diet score was more predictive of cognitive decline than either of the other diet scores; the standardized β coefficients of the estimated diet effects were 4.39 for MIND, 2.46 for the MedDiet and 2.60 for DASH. The correlation between the MIND score with cognitive change was statistically significantly higher compared with that for either the MedDiet (p=0.02) or the DASH (p=0.03).


 

DISCUSSION

In this community-based study of older persons, we investigated the relation of diet to change in cognitive function using an á priori-defined diet composition score (MIND) based on the foods and nutrients shown to be protective for dementia. Higher MIND diet score was associated with slower decline in cognitive abilities. The rate reduction for persons in the highest tertile of diet scores compared with the lowest tertile was the equivalent of being 7.5 years younger in age. Strong associations of the MIND diet were observed with the global cognitive measure as well as with each of five cognitive domains. The strength of the estimated effect was virtually unchanged after statistical control for many of the important confounders, including physical activity and education as well as with the exclusion of individuals with the lowest baseline cognitive scores.
 
The MIND diet was based on the dietary components of the Mediterranean and DASH diets, including emphasis on natural plant-based foods and limited intake of animal and high saturated fat foods. However, the MIND diet uniquely specifies consumption of berries and green leafy vegetables, and does not specify high fruit consumption (both DASH and Mediterranean), high dairy (DASH), high potato consumption or greater than 1 fish meal per week (Mediterranean). The MIND modifications highlight the foods and nutrients shown through the scientific literature to be associated with dementia prevention.;; A number of prospective cohort studies found that higher consumption of vegetables was associated with slower cognitive decline with the strongest relations observed for green leafy vegetables.; Green leafy vegetables are sources of folate, vitamin E, carotenoids and flavonoids, nutrients that have been related to lower risk of dementia and cognitive decline. There is a vast literature demonstrating neuroprotection of the brain by vitamin E, rich sources of which are vegetable oils, nuts, and whole grains. Dietary intakes of berries were demonstrated to improve memory and learning in animal models and to slow cognitive decline in the Nurses’ Health Study. However, the prospective epidemiological studies of cognitive decline or dementia do not observe protective benefit from the consumption of fruits in general. These dietary components have been demonstrated to protect the brain through their antioxidant and anti-inflammatory properties (vitamin E),; and inhibition of β-amyloid deposition (vitamin E, folate, flavonoids, carotenoids) and neurotoxic death (vitamin E, flavonoids). Studies of fish consumption observed lower risk of dementia with just 1 fish meal a week with no additional benefit evident for higher servings per week. Thus, the highest possible score for this component of the MIND diet score is attributed to one or more servings per week. Mediterranean diet interventions supplemented with either nuts or extra-virgin olive oil were effective in maintaining higher cognitive scores compared to a low-fat diet in a sub-study of PREDIMED, a randomized trial designed to test diet effects on cardiovascular outcomes among Spaniards at high cardiovascular risk. The MIND diet components directed to limiting intake of unhealthy foods for the brain target foods that contribute to saturated and trans fat intakes, such as red meat and meat products, butter and stick margarine, whole fat cheese, pastries and sweets and fried/fast foods. Fat composition that is higher in saturated and trans fats and lower in polyunsaturated and monounsaturated fats lead to blood brain barrier dysfunction and increased Aβ aggregation. Fish are a rich source of long-chain n-3 fatty acids which have been shown to reduce Aβ formation and oxidative damage, and to increase synaptic proteins and dendritic spine density.;

The study findings are supported by a number of strengths including the prospective study design with up to 10 years of follow-up, annual assessment of cognitive function using a battery of standardized tests, comprehensive assessment of diet using a validated questionnaire, and statistical control of the important confounding factors. Another important strength is that the MIND diet score was devised based on expansive reviews of studies relating diet to brain function.; None of the studies included in these reviews were conducted in the MAP study cohort. The fact that the food components were selected independently of the best statistical prediction of the outcome in the MAP study population lends validity to the MIND diet as a preventive measure for cognitive decline with aging.

A limitation of the study is that the dietary questionnaire had few questions to measure some of the dietary components and limited information on frequency of consumption. For example, a single item each provided information on consumption of nuts, berries (strawberries), beans, and olive oil. However, this imprecision in the measurement of the MIND score would tend to underestimate the diet effect on cognitive decline. Another limitation is the self-report of diet which some studies suggest can lead to biased reporting in overweight and cognitively impaired adults. Concern that biased diet reporting could explain the findings is mitigated by the fact that statistical control for factors like obesity, education, age, and physical activity had no impact on the estimated MIND diet effect and the association remained strong in analyses that omitted the participants with MCI and whose diet scores changed over the study period. Further we observed no modification in the effect by level of these potential confounders.

The primary limitation of the study is that it is observational and thus the findings cannot be interpreted as a cause and effect relation. Replication of the findings in other cohort studies is important for confirmation of the association, however, a diet intervention trial is required to establish a causal relation between diet and prevention of cognitive decline. Further, the findings were based on an old, largely non-Hispanic white study population and cannot be generalized to younger populations or different racial/ethnic groups.

The MIND diet is a refinement of the extensively studied cardiovascular diets, the Mediterranean and DASH diets, with modifications based on the scientific literature relevant to nutrition and the brain. This literature is underdeveloped and therefore, modifications to the MIND diet score would be expected as new scientific advances are made.

Systematic Review

We performed extensive reviews of the literature on nutrition and neurodegenerative diseases and cognitive decline to devise a brain healthy diet called MIND. The reviews included animal models, prospective epidemiological studies and randomized trials of nutrients, individual foods, and whole diets.

Interpretation

The MIND diet builds on previously tested diets, particularly the Mediterranean and DASH diets, for prevention of dementia outcomes by incorporating specific foods and intake levels that reflect the current state of knowledge in the field.

Future Directions

In the current study, the MIND diet was strongly associated with slower cognitive decline and had greater estimated effects than either the Mediterranean diet or the DASH diet. Future studies should evaluate and confirm the preventive relation of the MIND diet to cognitive change in other populations. As the field develops, the MIND dietary components should be modified to reflect new knowledge on nutrition and the brain.


 



Wednesday, August 16, 2017

Are We Hollow?

We are used to thinking of our human bodies as solid, and that everything that lies beneath our skin belongs to an inside world. It would be more correct to say that we are hollow. The design of the human body is much more interesting, and artistic than you may or dare think.

Running through the middle of the body is a log tunnel, the digestive tract. The space inside this tunnel (the lumen, from the Latin for light or opening inside a tubular structure), bordered by the inner layers of the mucosa, carries substances that don't belong to you. This strange exterior world flows inside you, transporting foods, liquids, substances, chemicals, and bacteria ー everything that you have swallowed and consumed. The digestive tract controls the passage of all these foreign substances, as they pass through your body from the mouth to the anus during digestion. En route, the foods you eat are assimilated and become the building blocks that make up your body, they become you. 

The digestive mucosa is the human body's customs service: a "high-intelligence service of the state." You depend on its work for your health and your life. The digestion and absorption of nutrients that it undertakes are vital functions, as essential as breathing and the beating of the heart. A bad digestion should be given equal importance to poor respiration or a cadiac condition.

Looked at in a certain way, you really are hollow. Your essence and continuity to interrupted by the lumen of this tube that runs through you carrying foreign substances; this tube is in charge of the vital functions of defence, strength, nutrition, energy, growth, construction of new tissues, and detoxification. 

Sunday, August 6, 2017

Laugh with Health

Laugh With Health



Adult Section Loan Call Number  613.2 KOC-[HEA]

Laugh with Health is the complete ‘body system’ 
guide to health and healing. Now completely 
revised and updated, this practical, easy-to-use 
book includes:
Unique food charts and vital health hints for 
everyday use. 
A detailed explanation of 36 essential vitamins 
and minerals.
Food combination charts for improved digestion 
and health.
Simple recipe ideas based on a full range of 
natural foods.
Specific natural food diets for various common 
health conditions.
Recommended by medical doctors and 
naturopaths, Laugh with Health is everyone’s 
essential reference for living a life of health and 
well-being.

In print for over 25 years, it has been the top-selling Australian health book for the last 10 years. Over 130,000 copies have been sold. This new edition with Exisle has been fully revised, updated and redesigned to give the book a fresh look and a new lease on life! Your complete guide to health, diet, nutrition and natural foods.

Manfred Urs Koch has had a lifelong passion for natural health, and after years of intense research, he has completed the most comprehensive guide to natural health available 
in this country, ‘Laugh With Health’. Every home needs a copy of this book — it’s like having your very own naturopath on your bookshelf!

“This book, ‘Laugh with Health’, gives us the opportunity of understanding the benefits of eating well, eating naturally.” — Dr John Tickell.

“‘Laugh with Health’ is beautifully illustrated, with information set out in an easily readable format. I can highly recommend it to all those who seek a better way of life.” — Peggy Zindler, naturopath.

“I will continue to recommend your book to all I know.” — Steven Ward.


“I have found it an incredibly helpful resource book.” — Roselyn Bowen.

MINERALS INTRODUCTION

Minerals perform a multitude of vital functions throughout the human body. There are 14 essential main minerals and five essential trace minerals.

Minerals are required for the construction of new cells. Every day the human body bilds new cells : blood cells, bone cells, connective cells, epithelium cells, muscular cells, nerve cells, skin cells, and skeletal cells.

Minerals are the major building blocks for cells in addition to amino acids and fatty acids. Throughout, there are over 200 specific functions of the individual minerals.

  Minerals are the conveyer of vital electrical stimuli along nerves to activate the human body. Minerals are converted into organic salts via digestion. These organic salts are dissolved into body fluids such as water and blood.

  Minerals have either positive ions or negative ions. Similar ions will repel and opposite charged ions will attract. This is essential for all human body movements, such as relaxation and contraction of muscles, triggered by stimulus from the brain and nervous system. 

  Minerals are vital for the acid-alkaline blood and body balance. Ideally, the diet should provide 75% alkaline-forming foods and 25% acid-forming foods.

  The main alkaline-forming foods are fruits, vegetables, almonds, millet and brown rice. Most other foods are acid forming. Every food has both acid and alkaline minerals. A food is termed acid when the end product, after digestion, provides an acid ash or residue.

  Various common ailments can be attributed to a prolonged deficiency of a particular mineral. Processed foods are often depleted in their supply of minerals, especially the trace minerals.

  Balance your life and body with the right foods that give life, not the wrong foods that take away life! Any substance that causes cells dehydration is a wrong food.

See that you are obtaining at least a few of those foods each mineral group regularly. Following is a guide to the approx. percentage of minerals compared to body weight and also the various essential nutrients and their proportion with the human body composition.

ELEMENTS & MINERALS BODY WEIGHT

CARBON 18 % + NITROGEN 3 % + HYDROGEN 10 % + OXYGEN 65 % = 96 %
WATER H2O 75 %.
CALCIUM 2 % 
PHOSPHORUS 1 %
POTASSIUM 0.4 %
SULPHUR 0.25 %
CHLORINE 0.25 %
SODIUM 0.25 %
FLUORIDE 0.20 %
MAGNESIUM 0.05 %
IRON 0.008 %
MANGANESE 0.003 %
SILICON 0.002 %
COPPER 0.002 %
IODINE 0.00004 %
TOTAL OF MINERALS: 4 %
ELEMENTS & MINERALS

TOTAL BODY WEIGHT : 96 % + 4 % = 100 %

NUTRIENT COMPOSITION OF THE HUMAN BODY
CARBOHYDRATES 2 %
PROTEIN 20 %
LIPIDS 15 %
WATER 55 %
MINERALS 7 %
VITAMINS 1 %
TOTAL NUTRIENT COMPOSITION 100 %

CALCIUM (CA) - ALKALINE MINERAL

1. CIRCULATORY SYSTEM
Calcium regulates the heartbeat and, in combination with the mineral magnesium, it is vital for the nourishment of the cardiovascular system: heart, arteries, veins and capillaries.

2. DIGESTIVE SYSTEM
Calcium is essential for the involuntary muscular movements of the digestive system (peristaltic action) and thereby protects against constipation.

3. GLANDULAR SYSTEM
The parathyroid glands regulate the storage of calcium throughout the human body in combination with sunlight, vitamin D. Regular moderate sunlight is vital for healthy glands and for calcium metabolism.

5. MUSULAR SYSTEM
Muscle need calcium to contract and relax. Cramps are often due to a calcium deficiency, as muscle fibres cannot contract or slide and mesh properly without a steady flow of calcium ions. Eating yoghurt the night before a big race can prevent cramps.

6. NERVOUS SYSTEM
CALCIUM COMBINED WITH MAGNESIUM IS REQUIRED FOR THE TRANSMISSION OF NERVE IMPULSES TO MUSCLES. 

20. REPAIR SYSTEM
Calcium foods are essential for the repair of bone fractures, and in combination with a regular daily supply of vitamin D (sunlight) plus such foods such as almonds, tahini and fresh vegetables, for the nutrients phosphorus, magnesium, zinc, silicon, fluorine, copper and vitamins A and C. Try a salad sandwich with Cheddar cheese and a spread of tahini on rye bread for a great bone repair lunch, while sitting outside in moderate sunlight, 10 A.M to 2 P.M.

8. SKELETAL SYSTEM
Calcium is the most important bone mineral, and with 200 bones in the adult skeleton it is vital to ensure a regular supply of calcium, with most emphasis for growing children and for women during pregnancy and lactation, plus the elderly.
  Various factors are important with regard to proper calcium absorption for a strong-skeletal system. 

Tuesday, June 6, 2017

Your Water requirements for daily life

How much should people drink? Official recommendations give guidelines for daily requirements.

The most recent official recommendation about water requirement has been published by the European Food Safety Authority in 2010.1 This extensive scientific review has enabled the definition of adequate water intakes, based on European fluid intakes, desirable urine osmolarity and energy intake. The reference values assumed a moderate climate and moderate level of physical activity.

Table: Dietary Reference Values for water1

A table showing dietary reference values for water
 
These values include water that originates from both consumed fluids and food. The European Scientific Authority has also stated that the contribution of food to total water intake represents about 20% in adults. On this basis, it means that male adults should drink 2 L per day, and female adults 1.6 L.

No maximal tolerable intake level has been set by EFSA. This is justified by the great ability of healthy individuals to excrete excess water intakes within a large range of observed intakes. In healthy subjects the kidneys have the ability to excrete up to 0.7 to 1L/hour.1

Reference

EFSA Panel on Dietetic Products, Nutrition, and Allergies (NDA); Scientific Opinion on Dietary reference values for water. EFSA Journal 2010; 8(3):1459. doi:10.2903/j.efsa.2010.1459. Available online:www.efsa.europa.eu.

Tuesday, May 30, 2017

Nutrition Response Testing

Nutrition Response Testing
By the time a person has a diagnosable disease or condition, the body has been suffering
from an imbalance or imbalances for a long time—perhaps decades. During this time, the
body may be compensating so there are no symptoms experienced, or there may be
symptoms that aren't identifiable as a "named condition".

Wouldn't it be great if there were a way to identify these roadblocks to healthy functioning
and to correct them before they become bigger problems? There is. Nutrition Response
Testing TM allows the trained practitioner to locate organs and tissues in the body where
there are imbalances. This is done through a non-invasive testing method involving muscle
testing. This technique is also extremely effective even if a disease or condition has been
diagnosed.

In muscle testing, a muscle that is normally strong will weaken in response to stress
applied to some other part of the body. In Nutrition Response Testing [TM] this stress is
created by the practitioner applying light pressure to the skin over various organs of the
body.

If the area being touched is over (connects to) an organ that is stressed due to an
imbalance, the indicator muscle (usually an arm) will become weak. This is because the
body withdraws resources from the arm to go the aid of the organ. When the correct
nutrition is applied to the body, the arm will "go strong". In this way we can design a precise
nutrition program to address what your body needs. We retest regularly over time to assess
how well the body is responding and to change the nutrition program as needed.
Nutrition Response Testing is one of many tools we use to assess your health and
nutritional needs.


 Nutritional Assessment Questionnaire 1.5
Name: ________________________________________________ Date: _____/____/_____
Birth Date: __________________________ Gender: ___________
Please list your five major health concerns in order of importance:
1. 
2.
3.
4.
5.
Notes:

PART I. Read the following questions and circle the number that applies:
KEY: 0 = Do not consume or use
1 = Consume or use 2 to 3 times monthly
2 = Consume or use weekly
3 = Consume or use daily

DIET (58)
1. 0 1 2 3 Alcohol
2. 0 1 2 3 Artificial sweeteners
3. 0 1 2 3 Candy, desserts, refined sugar
4. 0 1 2 3 Carbonated beverages
5. 0 1 2 3 Chewing tobacco
6. 0 1 2 3 Cigarettes
7. 0 1 2 3 Cigars/pipes
8. 0 1 2 3 Caffeinated beverages
9. 0 1 2 3 Fast foods
10. 0 1 2 3 Fried foods
11. 0 1 2 3 Luncheon meats
12. 0 1 2 3 Margarine
13. 0 1 2 3 Milk products
14. 0 1 Radiation exposure (0=no, 1=yes)
15. 0 1 2 3 Refined flour/baked goods
16. 0 1 2 3 Vitamins and minerals
17. 0 1 2 3 Water, distilled
18. 0 1 2 3 Water, tap
19. 0 1 2 3 Water, well
20. 0 1 2 3 Diet often for weight control

LIFESTYLE (12)
21. 0 1 2 3 Exercise per week (0 = 2 or more times a week, 1 = 1 time a week, 2 = 1 or 2 times a month, 3 = never, less than once a
month)

22. 0 1 2 3 Changed jobs (0 = over 12 months ago, 1 = within last 12 months, 2 = within last 6 months, 3 = within last 2 months)

23. 0 1 2 3 Divorced (0 = never, over 2 years ago, 1 = within last 2 years, 2 = within last year, 3 = within last 6 months)

24. 0 1 2 3 Work over 60 hours/week (0 = never, 1 = occasionally, 2 = usually, 3 = always)

MEDICATIONS Indicate any medications you’re currently taking or have taken in the last month (0=no, 1=yes): (54)
25. 0 1 Antacids
26. 0 1 Antianxiety medications
27. 0 1 Antibiotics
28. 0 1 Anticonvulsants
29. 0 1 Antidepressants
30. 0 1 Antifungals
31. 0 1 Aspirin/Ibuprofen
32. 0 1 Asthma inhalers
33. 0 1 Beta blockers
34. 0 1 Birth control pills/implant contraceptives
35. 0 1 Chemotherapy
36. 0 1 Cholesterol lowering medications
37. 0 1 Cortisone/steroids
38. 0 1 Diabetic medications/insulin
39. 0 1 Diuretics
40. 0 1 Estrogen or progesterone (pharmaceutical,
prescription)
41. 0 1 Estrogen or progesterone (natural)
42. 0 1 Heart medications
43. 0 1 High blood pressure medications
44. 0 1 Laxatives
45. 0 1 Recreational drugs
46. 0 1 Relaxants/Sleeping pills
47. 0 1 Testosterone (natural or prescription)
48. 0 1 Thyroid medication
49. 0 1 Acetaminophen (Tylenol)
50. 0 1 Ulcer medications
51. 0 1 Sildenafal citrate (Viagra)

PART II (See key at bottom of page)
Section 1 – Upper Gastrointestinal System (55)
52. 0 1 2 3 Belching or gas within one hour after eating
53. 0 1 2 3 Heartburn or acid reflux
54. 0 1 2 3 Bloating within one hour after eating
55. 0 1 Vegan diet (no dairy, meat, fish or eggs) (0=no,
1=yes)
56. 0 1 2 3 Bad breath (halitosis)
57. 0 1 2 3 Loss of taste for meat
58. 0 1 2 3 Sweat has a strong odor
59. 0 1 2 3 Stomach upset by taking vitamins
60. 0 1 2 3 Sense of excess fullness after meals
61. 0 1 2 3 Feel like skipping breakfast
62. 0 1 2 3 Feel better if you don’t eat
63. 0 1 2 3 Sleepy after meals
64. 0 1 2 3 Fingernails chip, peel or break easily
65. 0 1 2 3 Anemia unresponsive to iron
66. 0 1 2 3 Stomach pains or cramps
67. 0 1 2 3 Diarrhea, chronic
68. 0 1 2 3 Diarrhea shortly after meals
69. 0 1 2 3 Black or tarry colored stools
70. 0 1 2 3 Undigested food in stool 

KEY: 0=No, symptom does not occur
1=Yes, minor or mild symptom, rarely occurs (monthly)
2=Moderate symptom, occurs occasionally (weekly)

3=Severe symptom, occurs frequently (daily) 

Section 2 – Liver and Gallbladder (68)
71. 0 1 2 3 Pain between shoulder blades
72. 0 1 2 3 Stomach upset by greasy foods
73. 0 1 2 3 Greasy or shiny stools
74. 0 1 2 3 Nausea
75. 0 1 2 3 Sea, car, airplane or motion sickness
76. 0 1 History of morning sickness (0 = no, 1 = yes)
77. 0 1 2 3 Light or clay colored stools
78. 0 1 2 3 Dry skin, itchy feet or skin peels on feet
79. 0 1 2 3 Headache over eyes
80. 0 1 2 3 Gallbladder attacks (0=never, 1=years ago,
2=within last year, 3=within past 3 months)
81. 0 1 Gallbladder removed (0=no, 1=yes)
82. 0 1 2 3 Bitter taste in mouth, especially after meals
83. 0 1 Become sick if you were to drink wine (0=no,
1=yes)
84. 0 1 Easily intoxicated if you were to drink wine
(0=no, 1=yes)
85. 0 1 Easily hung over if you were to drink wine (0=no,
1=yes)
86. 0 1 2 3 Alcohol per week (0=<3 1="<7," 2="<14," 3="">14)
87. 0 1 Recovering alcoholic (0=no, 1=yes)
88. 0 1 History of drug or alcohol abuse (0=no, 1=yes)
89. 0 1 History of hepatitis (0=no, 1=yes)
90. 0 1 Long term use of prescription/recreational drugs
(0=no, 1=yes)
91. 0 1 2 3 Sensitive to chemicals (perfume, cleaning
agents, etc.)
92. 0 1 2 3 Sensitive to tobacco smoke
93. 0 1 2 3 Exposure to diesel fumes
94. 0 1 2 3 Pain under right side of rib cage
95. 0 1 2 3 Hemorrhoids or varicose veins
96. 0 1 2 3 Nutrasweet (aspartame) consumption
97. 0 1 2 3 Sensitive to Nutrasweet (aspartame)
98. 0 1 2 3 Chronic fatigue or Fibromyalgia

Section 3 – Small Intestine (47)
99. 0 1 2 3 Food allergies
100. 0 1 2 3 Abdominal bloating 1 to 2 hours after eating
101. 0 1 Specific foods make you tired or bloated (0=no,
1=yes)
102. 0 1 2 3 Pulse speeds after eating
103. 0 1 2 3 Airborne allergies
104. 0 1 2 3 Experience hives
105. 0 1 2 3 Sinus congestion, "stuffy head"
106. 0 1 2 3 Crave bread or noodles
107. 0 1 2 3 Alternating constipation and diarrhea
108. 0 1 2 3 Crohn's disease (0 =no, 1=yes in the past,
2=currently mild condition, 3=severe)
109. 0 1 2 3 Wheat or grain sensitivity
110. 0 1 2 3 Dairy sensitivity
111. 0 1 Are there foods you could not give up (0=no,
1=yes)
112. 0 1 2 3 Asthma, sinus infections, stuffy nose
113. 0 1 2 3 Bizarre vivid dreams, nightmares
114. 0 1 2 3 Use over-the-counter pain medications
115. 0 1 2 3 Feel spacey or unreal

Section 4 – Large Intestine (58)
116. 0 1 2 3 Anus itches
117. 0 1 2 3 Coated tongue
118. 0 1 2 3 Feel worse in moldy or musty place
119. 0 1 2 3 Taken antibiotic for a total accumulated time of
(0=never, 1= <1 2="<3" 3="" month="" months="">3
months)
120. 0 1 2 3 Fungus or yeast infections
121. 0 1 2 3 Ring worm, "jock itch", "athletes foot", nail fungus
122. 0 1 2 3 Yeast symptoms increase with sugar, starch or
alcohol
123. 0 1 2 3 Stools hard or difficult to pass
124. 0 1 History of parasites (0=no, 1=yes)
125. 0 1 2 3 Less than one bowel movement per day
126. 0 1 2 3 Stools have corners or edges, are flat or ribbon
shaped
127. 0 1 2 3 Stools are not well formed (loose)
128. 0 1 2 3 Irritable bowel or mucus colitis
129. 0 1 2 3 Blood in stool
130. 0 1 2 3 Mucus in stool
131. 0 1 2 3 Excessive foul smelling lower bowel gas
132. 0 1 2 3 Bad breath or strong body odors
133. 0 1 2 3 Painful to press along outer sides of thighs
(Iliotibial Band)
134. 0 1 2 3 Cramping in lower abdominal region
135. 0 1 2 3 Dark circles under eyes

Section 5 – Mineral Needs (75)
136. 0 1 History of carpal tunnel syndrome (0=no, 1=yes)
137. 0 1 History of lower right abdominal pains or
ileocecal valve problems (0=no, 1=yes)
138. 0 1 History of stress fracture (0=no, 1=yes)
139. 0 1 2 3 Bone loss (reduced density on bone scan)
140. 0 1 Are you shorter than you used to be? (0=no,
1=yes)
141. 0 1 2 3 Calf, foot or toe cramps at rest
142. 0 1 2 3 Cold sores, fever blisters or herpes lesions
143. 0 1 2 3 Frequent fevers
144. 0 1 2 3 Frequent skin rashes and/or hives
145. 0 1 Herniated disc (0=no, 1=yes)
146. 0 1 2 3 Excessively flexible joints, "double jointed"
147. 0 1 2 3 Joints pop or click
148. 0 1 2 3 Pain or swelling in joints
149. 0 1 2 3 Bursitis or tendonitis
150. 0 1 History of bone spurs (0=no, 1=yes)
151. 0 1 2 3 Morning stiffness
152. 0 1 2 3 Nausea with vomiting
153. 0 1 2 3 Crave chocolate
154. 0 1 2 3 Feet have a strong odor
155. 0 1 2 3 History of anemia
156. 0 1 2 3 Whites of eyes (sclera) blue tinted
157. 0 1 2 3 Hoarseness
158. 0 1 2 3 Difficulty swallowing
159. 0 1 2 3 Lump in throat
160. 0 1 2 3 Dry mouth, eyes and/or nose
161. 0 1 2 3 Gag easily
162. 0 1 2 3 White spots on fingernails
163. 0 1 2 3 Cuts heal slowly and/or scar easily
164. 0 1 2 3 Decreased sense of taste or smell 

Section 6 – Essential Fatty Acids (22)
165. 0 1 Experience pain relief with aspirin (0=no, 1=yes)
166. 0 1 2 3 Crave fatty or greasy foods
167. 0 1 2 3 Low- or reduced-fat diet (0=never, 1=years ago,
2=within past year, 3=currently)
168. 0 1 2 3 Tension headaches at base of skull
169. 0 1 2 3 Headaches when out in the hot sun
170. 0 1 2 3 Sunburn easily or suffer sun poisoning
171. 0 1 2 3 Muscles easily fatigued
172. 0 1 2 3 Dry flaky skin or dandruff

Section 7 – Sugar Handling (39)
173. 0 1 2 3 Awaken a few hours after falling asleep, hard to
get back to sleep
174. 0 1 2 3 Crave sweets
175. 0 1 2 3 Binge or uncontrolled eating
176. 0 1 2 3 Excessive appetite
177. 0 1 2 3 Crave coffee or sugar in the afternoon
178. 0 1 2 3 Sleepy in afternoon
179. 0 1 2 3 Fatigue that is relieved by eating
180. 0 1 2 3 Headache if meals are skipped or delayed
181. 0 1 2 3 Irritable before meals
182. 0 1 2 3 Shaky if meals delayed
183. 0 1 2 3 Family members with diabetes (0=none, 1=1 or
2, 2=3 or 4, 3=more than 4)
184. 0 1 2 3 Frequent thirst
185. 0 1 2 3 Frequent urination

Section 8 – Vitamin Need (81)
186. 0 1 2 3 Muscles become easily fatigued
187. 0 1 2 3 Feel exhausted or sore after moderate exercise
188. 0 1 2 3 Vulnerable to insect bites
189. 0 1 2 3 Loss of muscle tone, heaviness in arms/legs
190. 0 1 2 3 Enlarged heart or congestive heart failure
191. 0 1 2 3 Pulse below 65 per minute (0=no, 1=yes)
192. 0 1 2 3 Ringing in the ears (Tinnitus)
193. 0 1 2 3 Numbness, tingling or itching in hands and feet
194. 0 1 2 3 Depressed
195. 0 1 2 3 Fear of impending doom
196. 0 1 2 3 Worrier, apprehensive, anxious
197. 0 1 2 3 Nervous or agitated
198. 0 1 2 3 Feelings of insecurity
199. 0 1 2 3 Heart races
200. 0 1 2 3 Can hear heart beat on pillow at night
201. 0 1 2 3 Whole body or limb jerk as falling asleep
202. 0 1 2 3 Night sweats
203. 0 1 2 3 Restless leg syndrome
204. 0 1 2 3 Cracks at corner of mouth (Cheilosis)
205. 0 1 2 3 Fragile skin, easily chaffed, as in shaving
206. 0 1 2 3 Polyps or warts
207. 0 1 2 3 MSG sensitivity
208. 0 1 2 3 Wake up without remembering dreams
209. 0 1 2 3 Small bumps on back of arms
210. 0 1 2 3 Strong light at night irritates eyes
211. 0 1 2 3 Nose bleeds and/or tend to bruise easily
212. 0 1 2 3 Bleeding gums especially when brushing teeth

Section 9 – Adrenal (78)
213. 0 1 2 3 Tend to be a "night person"
214. 0 1 2 3 Difficulty falling asleep
215. 0 1 2 3 Slow starter in the morning
216. 0 1 2 3 Tend to be keyed up, trouble calming down
217. 0 1 2 3 Blood pressure above 120/80
218. 0 1 2 3 Headache after exercising
219. 0 1 2 3 Feeling wired or jittery after drinking coffee
220. 0 1 2 3 Clench or grind teeth
221. 0 1 2 3 Calm on the outside, troubled on the inside
222. 0 1 2 3 Chronic low back pain, worse with fatigue
223. 0 1 2 3 Become dizzy when standing up suddenly
224. 0 1 2 3 Difficulty maintaining manipulative correction
225. 0 1 2 3 Pain after manipulative correction
226. 0 1 2 3 Arthritic tendencies
227. 0 1 2 3 Crave salty foods
228. 0 1 2 3 Salt foods before tasting
229. 0 1 2 3 Perspire easily
230. 0 1 2 3 Chronic fatigue, or get drowsy often
231. 0 1 2 3 Afternoon yawning
232. 0 1 2 3 Afternoon headache
233. 0 1 2 3 Asthma, wheezing or difficulty breathing
234. 0 1 2 3 Pain on the medial or inner side of the knee
235. 0 1 2 3 Tendency to sprain ankles or "shin splints"
236. 0 1 2 3 Tendency to need sunglasses
237. 0 1 2 3 Allergies and/or hives
238. 0 1 2 3 Weakness, dizziness

Section 10 – Pituitary (29)
239. 0 1 Height over 6' 6" (0=no, 1=yes)
240. 0 1 Early sexual development (before age 10) (0=no,
1=yes)
241. 0 1 2 3 Increased libido
242. 0 1 2 3 Splitting type headache
243. 0 1 2 3 Memory failing
244. 0 1 Tolerate sugar, feel fine when eating sugar
(0=no, 1=yes)
245. 0 1 Height under 4' 10" (0=no, 1=yes)
246. 0 1 2 3 Decreased libido
247. 0 1 2 3 Excessive thirst
248. 0 1 2 3 Weight gain around hips or waist
249. 0 1 2 3 Menstrual disorders
250. 0 1 Delayed sexual development (after age 13)
(0=no, 1=yes)
251. 0 1 2 3 Tendency to ulcers or colitis 

Section 11 – Thyroid (48)
252. 0 1 2 3 Sensitive/allergic to iodine
253. 0 1 2 3 Difficulty gaining weight, even with large
appetite
254. 0 1 2 3 Nervous, emotional, can't work under pressure
255. 0 1 2 3 Inward trembling
256. 0 1 2 3 Flush easily
257. 0 1 2 3 Fast pulse at rest
258. 0 1 2 3 Intolerance to high temperatures
259. 0 1 2 3 Difficulty losing weight
260. 0 1 2 3 Mentally sluggish, reduced initiative
261. 0 1 2 3 Easily fatigued, sleepy during the day
262. 0 1 2 3 Sensitive to cold, poor circulation (cold hands
and feet)
263. 0 1 2 3 Constipation, chronic
264. 0 1 2 3 Excessive hair loss and/or coarse hair
265. 0 1 2 3 Morning headaches, wear off during the day
266. 0 1 2 3 Loss of lateral 1/3 of eyebrow
267. 0 1 2 3 Seasonal sadness

Section 12 – Men Only (27)
268. 0 1 2 3 Prostate problems
269. 0 1 2 3 Difficulty with urination, dribbling
270. 0 1 2 3 Difficult to start and stop urine stream
271. 0 1 2 3 Pain or burning with urination
272. 0 1 2 3 Waking to urinate at night
273. 0 1 2 3 Interruption of stream during urination
274. 0 1 2 3 Pain on inside of legs or heels
275. 0 1 2 3 Feeling of incomplete bowel evacuation
276. 0 1 2 3 Decreased sexual function

Section 13 – Women Only (60)
277. 0 1 2 3 Depression during periods
278. 0 1 2 3 Mood swings associated with periods (PMS)
279. 0 1 2 3 Crave chocolate around periods
280. 0 1 2 3 Breast tenderness associated with cycle
281. 0 1 2 3 Excessive menstrual flow
282. 0 1 2 3 Scanty blood flow during periods
283. 0 1 2 3 Occasional skipped periods
284. 0 1 2 3 Variations in menstrual cycles
285. 0 1 2 3 Endometriosis
286. 0 1 2 3 Uterine fibroids
287. 0 1 2 3 Breast fibroids, benign masses
288. 0 1 2 3 Painful intercourse (dysparenia)
289. 0 1 2 3 Vaginal discharge
290. 0 1 2 3 Vaginal dryness
291. 0 1 2 3 Vaginal itchiness
292. 0 1 2 3 Gain weight around hips, thighs and buttocks
293. 0 1 2 3 Excess facial or body hair
294. 0 1 2 3 Hot flashes
295. 0 1 2 3 Night sweats (in menopausal females)
296. 0 1 2 3 Thinning skin

Section 14 – Cardiovascular (30)
297. 0 1 2 3 Aware of heavy and/or irregular breathing
298. 0 1 2 3 Discomfort at high altitudes
299. 0 1 2 3 "Air hunger" or sigh frequently
300. 0 1 2 3 Compelled to open windows in a closed room
301. 0 1 2 3 Shortness of breath with moderate exertion
302. 0 1 2 3 Ankles swell, especially at end of day
303. 0 1 2 3 Cough at night
304. 0 1 2 3 Blush or face turns red for no reason
305. 0 1 2 3 Dull pain or tightness in chest and/or radiate
into right arm, worse with exertion
306. 0 1 2 3 Muscle cramps with exertion

Section 15 – Kidney and Bladder (13)
307. 0 1 2 3 Pain in mid-back region
308. 0 1 2 3 Puffy around the eyes, dark circles under eyes
309. 0 1 History of kidney stones (0=no, 1=yes)
310. 0 1 2 3 Cloudy, bloody or darkened urine
311. 0 1 2 3 Urine has a strong odor

Section 16 – Immune system (30)
312. 0 1 2 3 Runny or drippy nose
313. 0 1 2 3 Catch colds at the beginning of winter
314. 0 1 2 3 Mucus producing cough
315. 0 1 2 3 Frequent colds or flu (0=1 or less per year, 1=2
to 3 times per year, 2=4 to 5 times per year, 3=6
or more times per year)
316. 0 1 2 3 Other infections (sinus, ear, lung, skin, bladder,
kidney, etc.) (0=1 or less per year, 1=2 to 3
times per year, 2=4 to 5 times per year, 3=6 or
more times per year)
317. 0 1 2 3 Never get sick (0 = sick only 1 or 2 times in last
2 years, 1 = not sick in last 2 years, 2 = not
sick in last 4 years, 3 = not sick in last 7 years)
318. 0 1 2 3 Acne (adult)
319. 0 1 2 3 Itchy skin (Dermatitis)
320. 0 1 2 3 Cysts, boils, rashes
321. 0 1 2 3 History of Epstein Bar, Mono, Herpes,
Shingles, Chronic Fatigue Syndrome, Hepatitis
or other chronic viral condition (0 = no, 1 = yes
in the past, 2 = currently mild condition, 3 = severe)

Health Questionnaire (NTAF)
* Please circle the appropriate number “0 - 3” on all questions below. 0 as the least/never to 3 as the most/always.
Name: _____________________________________Age: ______ Sex: ________ Date:

SECTION A
• Is your memory noticeably declining?
• Are you having a hard time remembering names
 and phone numbers?
• Is your ability to focus noticeably declining?
• Has it become harder for you to learn things?
• How often do you have a hard time remembering
 your appointments?
• Is your temperament getting worse in general?
• Are you losing your attention span endurance?
• How often do you find yourself down or sad?
• How often do you fatigue when driving compared
 to the past?
• How often do you fatigue when reading compared
 to the past?
• How often do you walk into rooms and forget why?
• How often do you pick up your cell phone and forget why?

SECTION B
• How high is your stress level?
• How often do you feel that you have something that
 must be done?
• Do you feel you never have time for yourself?
• How often do you feel you are not getting enough
 sleep or rest?
• Do you find it difficult to get regular exercise?
• Do you feel uncared for by the people in your life?
• Do you feel you are not accomplishing your
 life’s purpose?
• Is sharing your problems with someone difficult for you?

SECTION C
SECTION C1
• How often do you get irritable, shaky, or have
 lightheadedness between meals?
• How often do you feel energized after eating?
• How often do you have difficulty eating large
 meals in the morning?
• How often does your energy level drop in the afternoon?
• How often do you crave sugar and sweets in the afternoon?
• How often do you wake up in the middle of the night?
• How often do you have difficulty concentrating
 before eating?
• How often do you depend on coffee to keep yourself going?
• How often do you feel agitated, easily upset, and nervous
 between meals?

SECTION C2
• Do you get fatigued after meals?
• Do you crave sugar and sweets after meals?
• Do you feel you need stimulants such as coffee after meals?
• Do you have difficulty losing weight?
• How much larger is your waist girth compared to
 your hip girth?
• How often do you urinate?
• Have your thirst and appetite been increased?
• Do you have weight gain when under stress?
• Do you have difficulty falling asleep?

SECTION 1 - S
• Are you losing your pleasure in hobbies and interests?
• How often do you feel overwhelmed with ideas to manage?
• How often do you have feelings of inner rage (anger)?
• How often do you have feelings of paranoia?
• How often do you feel sad or down for no reason?
• How often do you feel like you are not enjoying life?
• How often do you feel you lack artistic appreciation?
• How often do you feel depressed in overcast weather?
• How much are you losing your enthusiasm for 
your favorite activities?
• How much are you losing enjoyment for
 your favorite foods?
• How much are you losing your enjoyment of
 friendships and relationships?
• How often do you have difficulty falling into
 deep restful sleep?
• How often do you have feelings of dependency
 on others?
• How often do you feel more susceptible to pain?
• How often do you have feelings of unprovoked anger?
• How much are you losing interest in life?

SECTION 2 - D
• How often do you have feelings of hopelessness?
• How often do you have self-destructive thoughts?
• How often do you have an inability to handle stress?
• How often do you have anger and aggression 
while under stress?
• How often do you feel you are not rested even 
after long hours of sleep?
• How often do you prefer to isolate yourself from others?
• How often do you have unexplained lack of 
concern for family and friends?
• How easily are you distracted from your tasks?
• How often do you have an inability to finish tasks?
• How often do you feel the need to consume 
caffeine to stay alert?
• How often do you feel your libido has been decreased?
• How often do you lose your temper for minor reasons?
• How often do you have feelings of worthlessness?

SECTION 3 - G
• How often do you feel anxious or panic for no reason?
• How often do you have feelings of dread or
 impending doom?
• How often do you feel knots in your stomach?
• How often do you have feelings of being 
overwhelmed for no reason?
• How often do you have feelings of guilt about
 everyday decisions?
• How often does your mind feel restless?
• How difficult is it to turn your mind off when you
 want to relax?
• How often do you have disorganized attention?
• How often do you worry about things you were
 not worried about before?
• How often do you have feelings of inner tension 
and inner excitability?

SECTION 4 - ACH
• Do you feel your visual memory (shapes & 
images) is decreased?
• Do you feel your verbal memory is decreased?
• Do you have memory lapses?
• Has your creativity been decreased?
• Has your comprehension been diminished?
• Do you have difficulty calculating numbers?
• Do you have difficulty recognizing objects & faces?
• Do you feel like your opinion about yourself
 has changed?
• Are you experiencing excessive urination?
• Are you experiencing slower mental response?
ideas to manage?
Do you have feelings of paranoia?

Symptom groups listed in this flyer are not intended to be used as a diagnosis of any disease condition.

For nutritional purposes only.

Medication History
Please circle any of the following medication you have been or are currently taking.

Acetylcholine Receptor Antagonist – Antimuscarinic Agents
Atropine, Ipratopium, Scopolamine, Tiotropium

Acetylcholine Receptor Antagonist - Ganlionic Blockers
Mecamylamine, Hexamethonium, Nicotine (high doses), Trimethaphan

Acetylcholinesterase Reactivators
Pralidoxime

Acetylcholine Receptor Antagonist - Neuromuscular Blockers
Atracurium, Cisatracurium, Doxacurium, Metocurine, Mivacurium, Pancuronium, Rocuronium, Uccinylcholine, Tubocurarine,
Vecuronium, Hemicholine

Agonist Modulator of GABA Receptor (benzodiazpines)
Xanax, Lexotanil, Lexotan, Librium, Klonopin, Valium, ProSon, Rohypnol, Dalmane, Ativan, Loramet, Sedoxil, Dormicum,
Megadon, Serax , Restoril, Halcion

Agonist Modulator of GABA Receptors (nonbenzodiazpines)
Ambien, Sonata, Lunesta, Imovane

Cholinesterase Inhibitors (irreversible)
Echotiophate, Isofl urophate, Organophosphate Insecticides, Organophosphate-containing nerve agents

Cholinesterase Inhibitors (reversible)
Donepezil, Galatamine, Rivastigmine, Tacrine, THC, Erophonium, Neostigmine, Phystigimine, Pyridostigmine,
Carbamate Insecticidses

Dopamine Reuptake Inhibitors
Wellbutrin (Bupropion)

Dopamine Receptor Agonists
Mirapex, Sifrol, Requip

D2 Dopamine Receptor Blockers (antipsychotics)
Thorazine, Prolixin, Trilafon, Compazine, Mellaril, Stelazine, Vesprin, Nozinan, Depixol, Navane, luanxol, Clopixol,
Acuphase, Haldol, Orap, Clozaril, Zyprexa, Zydis, Seroquel, Geodon, Solian, Invega, Abilify

GABA Antagonist Competitive binder
Flumazenil

Monoamine Oxidase Inhibitor (MAOI)
Marplan, Aurorix, Maneric, Moclodura, Nardil, Adlegiine, Elepryl, Azilect, Marsilid, Iprozid, Ipronid, Rivivol, Popilniazida, Zyvox, Zyvoxid

Noradrenergic and Specific Sertonergic Antidepressants (NaSSaa)
Remeron, Zispin, Avanza, Norset, Remergil, Axit

Selective Serotonin Reuptake Inhibitor
Paxil, Zoloft, Prozac, Celexa, Lexapro, Luvox, Cipramil , Emocal, Serpam, Seropram, Cipralex, Esteria, Fontex, Seromex, Seronil,
Sarafem, Fluctin, Faverin, Seroxat, Aropax, Deroxat, Rexetin, Xentor, Paroxat, Lustral, Serlain, Dapoxetine

Selective Serotonin Reuptake Enhancers
Stablon, Coaxil, Tatinol

Serotonin-Norepinephrine Reuptake Inhibitors (SNRIs)
Effexor, Pristiq, Meridia, Serzone, Dalcipran, Despramine, Duloxetine

Tricylic Antidepresseants (TCAs)
Elavil, Endep, Tryptanol, Trepiline, Asendin, Asendis, Defanyl, Demolox, Moxadil, Anafranil, Norpramin, Pertofrane, Prothiadin, Thanden, Adapin, Sinequan, Trofranil, Janamine, Gamanil, Aventyl, Pamelor, Opipramol, Vivactil, Rhotrimine, Surmontil

New Patient Health History
Please be assured that all information on this form and anything discussed during your consultation will be
confidential unless you grant permission otherwise
Name:______________________First Appt date:___________
Address:___________________City:___State:____ Zip_________
Day phone:___________ Evening phone:______ Cell:__________________
Referred by:______________________ YourEmail______________________
Date of Birth:________Age_____Height______Weight_______
Overall Health: circle one Excellent Good Fair Poor
Primary Reason for consultation:________________________
Previous treatments for this problem:____________________
Other concerns or problems____________________________
Current medications or supplements: ( please list all using extra paper if needed)
How many times in your life (approx) have you taken a course of antibiotics?
____1-5 ____5-10 ____more than 10 When was last course of antibiotics (approx.)?____________________
Are you currently under care with any physician or other health care provider. Please give names, date of last visit
and any problems identified at that time:

List all major illnesses or surgeries, accidents or injuries w/ approximate dates:

Please mark any scars on the body diagram included in the packet


List any dental work (fillings, crowns, root canals, extractions, bridges, gum problems)


Are you currently experiencing any dental issues that you are aware of?


Do you drink alcohol? Y N. If yes, how often and typical amount:_____________________________

Have you ever smoked Y N. Do you currently smoke? Y N. How much/day?

Marital Status (circle one) Single Divorced Partnered Married Widowed

How is health of partner? Excellent Good Fair Poor

Number of children if any_____

Do you have any health concerns for your children? Please describe briefly:


Any family history of serious illness or chronic conditions?
Cancer Diabetes Heart Mental Illness Depression/ Anxiety Alcoholism or Substance Abuse Other (please
note)


Any household pets or animals?


Where have you traveled outside of country and when?


What toxic chemicals do you know you are exposed to? Please consider hair chemicals, household cleaning
products, building materials, new furnishings, occupation-related chemicals, lawn, garden and household, etc.


Do you have a regular exercise program? If yes what is it?


What level of stress are you typically under? Low Medium High



What do you do to relieve stress?

What is your occupation and do you enjoy it?


Describe your sleep: ___hard time falling asleep ___broken sleep (wake up but fall back to sleep)
___fall asleep but wake up and can't get back to sleep ___wake up exhausted and dragging in a.m.


Do you live with other people that affect your food habits? What other things affect your food habits?


How willing are you to make dietary changes to address your health concerns?


___a few changes ____moderate _____substantial

Client Summary Sheet Name____________________________________
Special testing notes: ________________________Age: ____

Allergies:

Image result for body diagram
Image result for body diagram


Medication  &Contraindications



Weight
___/___/___ _____________
___/___/___ _____________
___/___/___ _____________
___/___/___ _____________
___/___/___ _____________

BMI
___/___/___ _____/______%
___/___/___ _____/______%
___/___/___ _____/______%

Weight Gain Pattern

T A L O P

Blood pressure


Date; BP

Medication ; Contraindications

Contract between Healthy Wealth Survival and
__________________________________ Print client name

The purpose of this contract is to serve as a memorandum of understanding for our work
together.

Here is what you can expect from me:
1. I am a consulting functional nutritionist; I am not a doctor. I do not diagnose illness or
prescribe medication. I am trained to think about how the body systems function, and to
understand health concerns in terms of overall function with a focus on the role of
nutrition. Function improves or degrades along a continuum and as it degrades, one
moves closer toward a diagnosable disease. However, long before a diagnosable
disease or condition happens, we can often identify nutritional deficiencies or other
things that are interfering with healthy functioning, and correct them. My role is to help
you understand how your body works and to look at your symptoms and health concerns
in the context of healthy functioning.

2. I believe in the body's ability to repair itself, if given the right ingredients (quality food, air,
water, and supplements from concentrated food, herbs, homeopathic remedies and
similar non-toxic agents). I believe that most health concerns and symptoms if caught
sooner rather than later can be addressed without the use of pharmaceutical medication,
which, while suppressing symptoms, usually interferes with the body's inherent ability to
self-repair. I do not judge your choice to use or not use pharmaceuticals, however I will
work with you to understand possible alternatives if you ask for that information. I will not
advise you to discontinue any medication that has been prescribed to you. I assume that
if you are choosing to work with me, you are open to learning how you can support your
body in this process of self-healing and I will do my best to share that knowledge with
you through dietary and life-style counseling and through helping you understand how
your body works.

3. I promise to keep our scheduled appointments and to be prepared, present, and ready to
give you the best attention I can.

Here is what I ask from you:
1. My expectation is that you will be open to what may be new ways of looking at your
health and healing, and that you are willing to accept as a goal, taking gradual but
consistent steps to improve your nutritional habits as needed to improve your health.

2. I reserve your appointment time for you, and no one else. Therefore, I respectfully

request that you give me at minimum 24 hours notice if you find it necessary to change your appointment time so that I may offer that spot to someone else. I do charge the
office visit fee for last minute cancellations with limited exceptions for true emergencies.

3. If we have agreed on certain supplements as part of your program, and you have any
concerns in between appointments about your supplements, I would like you to call me
and let me know your concerns rather than waiting until your next visit to have your
concerns addressed.

4. I ask you to agree to a schedule of visits so that we can work together over time to
improve your health and nutritional lifestyle.

5. I ask that if you are pleased with the care and the results you get from our work together
that you refer friends, family and co-workers to Nutrition Magician. Likewise if you have
concerns with your care, I hope you will discuss those with me so that we can find a
positive resolution.

Cost of Services
Initial Health Evaluation $200.00
includes Nutrition Response and Heart Rate Variability (HRV) Testing.
Visits 1-3 45-60 minutes $90
Follow-up Visit 20-25 minutes. $50
Extended Visit per ¼ hour $20.
Email Consultations per ¼ hour $20.
Dietary Consultation 30 / 60 min. $50. / $95.
HRV Testing and report $20.
Phone Consultations (visits 4 and beyond) $60
Center for Functional Nutrition Accepts Visa, Mastercard, Checks and Cash.

Referral Recognition
Our business grows when our clients share their good results with
friends, family, co-workers, and others they care about. We hope you
will support the growth of Healthy Wealth Survival  as we support you in
your health. In acknowledgement of the compliment you pay us when
you refer, we gratefully offer you coupons good for products or

services when someone you refer becomes a client. Thank you!