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African Journal of Traditional, Complementary, and Alternative Medicines logoLink to African Journal of Traditional, Complementary, and Alternative Medicines
. 2014 Apr 3;11(3):248–258. doi: 10.4314/ajtcam.v11i3.35

Dietary Supplements in the Management of Hypertension and Diabetes - A Review

Anthony Jide Afolayan 1,, Olubunmi Abosede Wintola 1
PMCID: PMC4202446  PMID: 25371590

Abstract

Background

The use of alternative therapies like herbs and dietary supplements is very common among hypertensive and diabetic patients all over the globe. Hypertension is a silent disease that causes increase in cardiovascular, cerebrovascular, renal morbidity and mortality whereas diabetic complications cause heart attack, stroke, blindness and kidney disease. These are serious and chronic metabolic disorders that have a significant impact on the health, quality of life, and life expectancy of patients, as well as on the health care systems. Orthodox drugs used for the treatment of hypertension and diabetes produce side effects such as headache, nausea, vomiting, stomach pain, constipation, diarrhea, weakness, fatigue and erectile dysfunction. The need for considering alternate therapies in the form of dietary supplements known to promote good health, having little or no side effects therefore arises.

Materials and methods

This review was carried out using comprehensive and systematic literature reports on the concurrent use of dietary supplements in the management of diabetes and hypertension. Empirical searches were conducted using Google scholar (http://scholar.google.com), and Science Direct (http://www.sciencedirect.com). In addition to these databases, the University database was also used. Searches were also undertaken using keyword combinations such as dietary supplements and the names of the diseases in question.

Result and Discussion

This review chronicled the therapeutic values of vitamins, minerals, amino acids, fruits, vegetables, herbs and other botanicals used as dietary supplements. Results show that these supplements provided better and safe substitutes to toxic and expensive conventional drugs. Generally dietary supplements are free from major side effects, readily available and affordable. It is envisaged that the use of dietary supplement will promote good health and improve the status of hypertensive and diabetic patients.

Conclusion

Medical doctors are therefore encouraged to incorporate dietary supplements into the regimen employed for hypertension and diabetes management.

Keywords: Blood pressure, blood glucose, botanicals, minerals, vitamins

Introduction

The practice of using nature as pharmacy dates back to antecedent/s and continues till date as many of the medications currently in use are derived from plants. Dietary supplements are food products, extracts or concentrates that are intended to supplement diets because they contain certain dietary ingredients such as vitamins, minerals, herbs, and amino acids (Halsad, 2003). They are usually found in many forms including tablet, capsule, powder, liquid, bar, soft-gel and gel-cap.

Dietary supplements are generally regarded as classes of foods not drugs. This is because like foods, most dietary supplements are not screened for safety and effectiveness following their removal from the regulatory authority of the Federal Food, Drug and Cosmetic Act of 1958. This prevents dietary supplements labels from assertions showing their intended ability to treat, diagnose, mitigate, prevent or cure diseases (DSHEA, 1994). The line between permissible and impermissible health claims for supplements is not always clear to the consumer, who naturally may misunderstand the apparent bounty of medicinal-sounding risk-free benefits. However, while many supplements may be beneficial, they are not without risks. Generally, several claims have been put forward regarding the beneficial attributes of dietary supplements including prevention of acne, reduction of fats, low cholesterol content, rich fibre content, and the promotion of healthy skin (DSHEA, 1994).

Dietary supplements occur in different forms ranging from vitamins, minerals, amino acids and botanicals. Vitamins are organic compounds that cannot be synthesized by the body, but are necessary for its proper functioning. There are two types of vitamins namely; fat soluble and water soluble vitamins. Fat soluble vitamins are A, D, E and K which can be stored in the body for future use. Vitamins B and C are water soluble that cannot be stored by the body and therefore need to be replenished regularly through diet in order to avoid deficiencies which can interfere with normal metabolic processes and cause severe illness (Bellow and More, 2012). For instance, pellagra and beriberi diseases result from niacin (vitamin B3), and thiamin (vitamin B1) deficiencies while scurvy is a disorder arising from ascorbic acid (vitamin C), deficiency (Beckman et al., 2001; Gaede et al., 2001; Pemberton, 2006).

Minerals are inorganic elements derived from soil and water which are absorbed by plants and eaten by animals. Some of these minerals are required in large amounts by the body e.g. calcium for bone development. Others like chromium, copper, iron, selenium and zinc often called trace minerals are needed in very small amounts. These minerals are chemical elements required by all living organisms along with carbon, hydrogen, nitrogen and oxygen for proper growth and development (Soetan et al., 2010).

Amino acids are the building blocks of proteins and they can be categorized into three groups namely indispensable (essential), conditionally indispensable and dispensable (non-essential). Indispensable amino acids must be consumed in the diet while conditionally indispensable amino acids can be synthesized by human body under most conditions but may require dietary supplementation under certain patho-physiological conditions such as catabolic stress or neonatal prematurity (Morris et al., 2002). Five amino acids are dispensable, meaning that they can be synthesized from other amino acids or complex metabolites (Engelhart et al. 2002).

Other dietary supplements include metabolites and extracts. Metabolites are substances that are produced by metabolic actions or are necessary for metabolic processes while extracts are substances usually biologically active ingredients of plant or animal tissues prepared by the use of solvents to separate the substance from the original material. A herbal remedy is a plant or plant part (root, flower, leaf, and fruit), that is used for its medicinal or therapeutic properties (Awoyemi et al., 2012). The potency of herbal products varies depending on each plant's growing conditions, level of maturity when harvested and the processes used to dry and store each ingredient.

The popularity and increase in the use of dietary supplements have been reported by the media, government agencies and published studies in medical journals (De Smet, 2000; Litovitz et al., 2001; Spencer, 2004; Wise, 2004). Reports showed significant difference/s in dietary supplement usage by age, with higher prevalence in older age groups for all supplements and for single ingredient vitamins/minerals. There is also a significant difference in supplement use by sex, with women having the upper hand than men for all supplements except herbs and botanicals. A significant difference also exists with respect to race/ethnicity, with higher use amongst whites than any other groups for all supplements including multivitamins/minerals. Household income as well as the level of education of users also shows some level of significance difference for all supplement, multivitamins/multi-minerals and herbs users (Timbo et al., 2006).

Methodology

This review was carried out by a comprehensive and systematic literature search on the concurrent use of dietary supplements in the management of diabetes and hypertension. Empirical researches were conducted using Google scholar (http:// scholar. google.com) and Science Direct (http://www.sciencedirect.com). In addition to these databases, the University of Fort Hare's online database were also used. Significant inquiries were also made using keyword combinations such as dietary supplements and the names of the diseases in question.

Specific disease and types of dietary supplements used in its management

Dietary supplements used in the management of Hypertension includes cod liver oil, garlic, Co-enzyme Q10, beta glucan, lipoic acid, whole grains, vitamins E, B6, C, potassium, magnesium, sodium, polyphenol, botanicals and vanadium.

Dietary supplements used in the management of Diabetes includes Alpha-lipoic, chromium, omega 3 fatty acids, polyphenols, garlic, magnesium, coenzyme Q10, vanadium, folic acid, selenium, vitamins B6, C and E, zinc and copper.

Hypertension

Hypertension is a highly prevalent chronic medical condition in which blood pressure in the arteries is elevated (Tabassum and Ahmad, 2011). It is a global health burden affecting both developed and developing countries (Kearney et al., 2005). The condition is becoming an increasingly common problem and this may be attributed to the increasing longevity and prevalence of contributing factors such as obesity, physical inactivity and unhealthy diets (Singh et al., 2000; Yusuf et al., 2001). It is a silent disease, which if untreated or sub-optimally controlled, could lead to increase in cardiovascular, cerebrovascular as well as renal morbidity and mortality.

The proportion of global disease burden attributed to hypertension is substantially affecting 32% of men and 30% of women aged 16 and above in England (WHO, 2003; Huisman et al., 2004). The high prevalence of hypertension globally contributes to the present anticipated pandemic of cardiovascular diseases (CVD), which is of particular concern in developing countries (Kearney et al., 2005). The control of hypertension, together with other associated risk factors such as dyslipidemia and diabetes mellitus, constitute the ideal approach to primary prevention of atherosclerotic disease, and remains a major challenge for communities. The trend towards comprehensive cardiovascular risk factor management is the internationally accepted model of care (WHO, 2002).

Hypertension is more prevalent in men than in women and even more in those of low socio-economic status though menopause tends to decrease this difference (Carretero and Oparil, 2000). This gender disparity is common in hypertension (Du et al., 2006). Before menopause, blood pressure (BP) is significantly lower in women than in age-matched men. However, the incidence/s of hypertension increases dramatically in women following menopause, eventually approximating the incidence in men (Kotchen et al., 1982; Spence, 1996). Although the mechanism underlying this increase is unknown, the loss of oestrogen traditionally has been considered the primary factor (Kearney et al., 2005).

Dietary supplements used in the management of hypertension

Dietary interventions have been shown to reduce the occurrence of high blood pressure (Appel et al., 2006). In the United States, the combined use of herbal supplements as home remedies for the management of hypertension was put at 48% (Mansoor, 2001). Furthermore, in a survey performed within a primary care setting in Alabama, 41% of patients were taking nutritional supplements and 26% were taking herbal products (Phillips and Osborne, 2000). In another report by Winslow and Kroll (1998), up to 90% of hypertensive patients take either over-the-counter medications or supplements depending on the definitions used.

Studies in other patient populations including those suffering from hypertension have also shown a significant prevalence of supplements, herbs and other alternative therapy use (Gulla and Singer, 2000; Cappuccio et al., 2001). It is therefore a common practice among patients attending a medical care setting to use dietary supplements. Unfortunately, most patients do not reveal the use of such treatments to their health care providers (Gulla and Singer, 2000). Common dietary supplements used in the management of hypertension, their health benefits and limitations are presented in Table 1.

Table 1.

Common dietary supplements used in the management of hypertension

S/no Dietary
supplement
Nutrients/ food
sources
Form found Target organ/cell Health benefits Limitations Reference
1. Cod liver oil Vitamin A, D, and
omega-3 fatty acids.
Fish oils, flax seed,
primrose, borage
and flaxseed oils.
Herring haddock,
Atlantic salmon, trout,
tuna, cod and mackerel.
Cardiovascular
system.
Reduces cardio
metabolic risk factors,
protects sudden cardiac
death after myocardial
infraction, reduces
raised plasma
triglycerides, reduces
blood pressure and
ameliorates atherogenic
effects.
High doses required for
reduction of blood
pressure may have side
effects.
Warner, 2000;
Marchioli et al., 2002; Hooper et al., 2006;
Apel et al., 2006;
Abeywardena and Patten, 2011; Trofimiuk and Braszko, 2011.
2. Garlic Gamma glutamyl
peptides, flavonol
magnesium, ajoenes
phosphorus,
adenosine, allicin
and sulphur
Allium sativum, aglio,
ail, Da-suan,
Knoblauch, La-juan,
rustic treacle, stinking
rose
Cardiovascular
system.
Reduces cardiovascular
diseases by lowering
blood pressure and
increases levels of
antioxidant enzymes.
Inhibits platelet
aggregation which may
prolong bleeding time.
Mohamadi et al., 2000;
Weiss, 2000;
Mansoor, 2001.
3. Coenzyme Q-10 B vitamins; B6,
B12, niacin and
folic acid. Fatty
fish, organ meats
and peanut.
Reduced or oxidized
form of CoQ10 in
dry powder capsules
dispersed in oil,
surfactants and
emulsifiers such as
lecithin and polysorbate
80 to improve
absorption.
Heart, lung and liver Strengthens heart
muscle and improves a
variety of heart
conditions.
Low level compromises
myocardial energy
generation leading to
“energy starvation” of the
myocardium, considered
to be a
pathogenic mechanism of
chronic heart failure (CHF).
Mohamadi et al., 2000;
Weiss, 2000;
Mansoor, 2001.
4. Beta glucan Sorghum, rye,
maize, triticale,
wheat, rice, seaweed
and mushrooms.
Oat and barley
bran.
Heart Immune enhancer and
cholesterol-lowering effect.
Delay stomach emptying. Mohamadi et al., 2000;
Weiss, 2000;
Mansoor, 2001.
5. Lipoic acid Liver, spinach,
broccoli and potato.
Lipoic acid in tablet and
capsule.
Nerve cell, kidney,
heart and liver.
Lowers blood pressure
in persons with
hypertension.
Pregnant women or
nursing mothers should
avoid lipoic acid
supplements at
pharmacologic doses.
Mohamadi et al., 2000;
Weiss, 2000;
Mansoor, 2001.
6. Whole grains Brown rice, wheat,
barley, rye, maize.
Oat meal, polenta,
wheat pasta, wheat
bread, corn meal.
Heart and liver Reduces systolic and
diastolic pressures
along with mean arterial
pressure (MAP).
Intake of three servings a
day must be ensured for
positive result.
Anderson et al., 2000.
7. (i) Potassium Fruits and
vegetables
such as apricots,
bananas, tomatoes
and carrots.
Citrate and chloride. Cell membranes. Reduces blood pressure. Potassium depletion in
normal individuals causes
sodium retention and
increased blood pressure.
Kotchen and McCarron, 1998.
(ii)
Magnesium
Fat or fibre (from
fruits, vegetables
and cereal grains.
Citrate, stearate and
sulphate forms.
Heart and kidney. Inhibits platelet
dependent thrombosis.
dequate levels may
se loose stool in
sitive individuals.
Touyz, 1991; Burgess et al., 1999.
(iii) Sodium Fat or fibre from
fruits, vegetables
and cereal grains.
Additive in commercial
processed foods.
Heart and blood
vessels.
Moderate intake
reduces mean arterial
pressure as well as
morbidity and
mortality.
Excess sodium in the diet
can lead to or complicate
high blood pressure.
McCarron, 1997
Burgess et al., 1999;
Kotchen and McCarron, 1998.
8. Vitamin E Vegetable oil,
sunflower nuts,
avocado, carrot,
peanut, almonds,
hazelnuts.
Alpha - Tocopherol Heart, brain, lung,
and muscle
Reduces elevated blood
pressure caused by
excess endogenous
aldehydes in insulin
resistance hypertension.
Large doses of α-tocopherol
inhibits normal
blood coagulation.
Jiang et al., 2001;
Vasdev et al., 2002.
9. Vitamin B6 Brown rice, oats,
wheat germ,
molasses, cereals,
potato, banana,
plum and salmon
fish.
Pyridoxine Jejunum, ileum,
heart.
Prevents heart attacks
and nerve damage.
Excess doses over long
period of time result into
painful and ultimately
irreversible neurological
problem.
Schaumburg et al., 1983;
Bendich and Cohen, 1990;
McCormick, 2006.
10. Vitamin C Fruits and
vegetables.
Ascorbic acid Blood plasma, brain,
spleen, lung, liver,
kidney and pancreas.
Lowers blood pressure
in persons with
hypertension, helpful
for long term health
maintenance of arteries.
Causes diuretic effect
which gets rid of fluids.
Ness et al., 1997;
Vasdev et al., 2002.
11. Polyphenol Fruits and
vegetables, nuts and
their products.
Catechin and
epicatechin.
Heart Inhibits oxidation of
low density lipoprotein
(LDL), inhibits platelet
aggregation and
vascular relaxation
through the production
of nitric oxide.
Safety should be carefully
tested in relation to the
disease status of potential
users.
Frankel et al., 1993;
McCarron, 1997;
Dubick and Omaye, 2001;
Halsad, 2003;
Carlson et al., 2008.
12. Botanicals Prickly pear, cactus,
Coccinea indica,
Aloe vera,
fenugreek, bitter
melon, Ginseng.
Herbs Liver, bones, skin
and heart.
Prevents hypertension
and ulcerative colitis.
Lack of dose regimen and
limited research on the
efficacy of these botanicals.
Merchant and Andre, 2001;
Van Breemen et al., 2007.
13. Vanadium Black pepper,
mushroom, shell
fish parsley, fresh
fruits and
vegetables.
Chelate and sulphates. Muscles, liver, heart
and body fluids.
Lowers blood pressure. GI irritation and tissue
accumulation, uncertain
long term safety profile.
Bhanot et al., 1994a;
Bhanot et al., 1994b
Cohen et al., 1995;
Goldfine et al., 1995;
Boden et al., 1996;;
Preuss et al., 1998.

Dietary folate and plasma ascorbic acid have been found to be inversely associated with blood pressure in observational studies (Forman et al., 2005). However, intervention trials with vitamin C yielded inconsistent results (Ness et al., 1997). While in two small trials, folic acid was effective at lowering blood pressure, the finding of a lower risk of elevated blood pressure in the multiple supplement groups suggests that there was a relationship between these nutrients and blood pressure (van Dijk et al., 2001; Mangoni et al., 2002).

Some studies have reported the concurrent use of dietary supplements and conventional antihypertensive drugs. For example, Co-enzyme Q10 has been reported to exhibit significant reduction of systolic blood pressure (SBP), and diastolic blood pressure (DBP), when added to conventional antihypertensive drugs (Singh et al., 1999; Rasmussen et al., 2012). Similarly, the systolic blood pressure (SBP) and diastolic blood pressure (DBP) were reported to have decreased by 6 mm Hg and 5 mmHg respectively in a trial where hypertensive men received fish oil (eicosapentaenoic acid, docosahexaenoic acid) for 4 months followed by a 2 month reassessment period (Prisco et al., 1998).

Diabetes

Diabetes, borrowed from a Greek word meaning siphon, is a metabolic disorder marked by high levels of blood glucose resulting from defects in insulin production, insulin action or both which can lead to serious complications and premature death (Afolayan and Sunmonu, 2010). However, people with the condition, working together with their support network and their health care providers can take steps to control the disease and lower the risk of complications.

Diabetes mellitus is a serious disease that has a significant impact on the health, quality of life and life expectancy of patients as well as the health care system (Dey et al., 2002). It is a disorder affecting the metabolism of carbohydrates, fats, proteins and electrolytes in the body leading to acute, sub-acute and chronic complications (Rang et al., 1991). Hyperglycemia, ketoacidosis and non ketotic syndromes are some of the complications of acute diabetes (Knentz and Nattras, 1991), while thirst, polyuria, visual blurriness, weight loss and lack of energy are experienced in sub-acute diabetes incidence (Kumar and Clark, 2002). Chronic hyperglycemia complication causes bonding of a protein or lipid molecules with a sugar molecule (glycation) which may eventually affect the eye, kidney, nerves and arteries (Sharma, 1993; Afolayan and Sunmonu, 2010).

Three main forms of diabetes were recognized by the world Health Organization; these are type 1, type 2, and gestational diabetes (WHO, 1999). These three forms of diabetes showed common symptoms but differs in their causes, diagnosis, population distribution and treatment. The causes of diabetes are due to the beta cells of the pancreas being unable to produce sufficient insulin to prevent hyperglycemia (Rother, 2007). Type 1, diabetes previously called insulin-dependent diabetes mellitus (IDDM), or juvenile-onset diabetes is usually due to auto-immune destruction of the pancreatic beta cells which produce insulin. It develops when the body's immune system destroys pancreatic beta cells, the only cells in the body that produce the hormone insulin that regulates blood glucose (Holt, 2004). People with type 1 diabetes must have insulin delivered by injection or a pump. It usually strikes children and young adults, although disease onset can occur at any age. Type 2 previously called non-insulin-dependent diabetes mellitus (NIDDM), usually begins as insulin resistance, a disorder in which the cells do not use insulin properly (Holt, 2004). It is characterized by tissue-wide insulin resistance and varies widely; it sometimes progresses to loss of beta cell function. As the need for insulin rises, the pancreas gradually loses its ability to produce insulin. Type 2, diabetes is associated with older age, obesity, family history of diabetes, history of gestational diabetes, impaired glucose metabolism, physical inactivity, and race/ethnicity. Gestational diabetes occurs during pregnancy, it is similar to type 2, diabetes, which involves insulin resistance. The hormones of pregnancy cause insulin resistance in those women genetically predisposed to developing this condition.

The World Health Organization (WHO) estimated diabetes in adults to be around 173 million, and about two-thirds of these patients live in developing countries (Wild et al., 2004; Sunmonu and Afolayan, 2013). The prevalence of diabetes is on the increase worldwide, and this is still expected to increase by 5.4% in 2025 (Moller and Flier, 1991; Sunmonu and Afolayan, 2013). Women suffer from diabetes in both developed and developing countries. Approximately, 2.1 million women die of diabetes each year in the world, making diabetes the ninth leading cause of death among women (IDF, 2011). Increase in sedentary lifestyle, consumption of energy-rich diet and obesity are some of the factors causing the rise in the number of diabetics. According to the American Diabetes Association (1997), Asia and Africa are regions with the greatest potential where diabetics could rise to two or threefold above the present level (Sunmonu and Afolayan, 2010).

Dietary supplements used in the management of diabetes

The management of diabetic condition has advanced considerably over the past 50 years. Today, people living with diabetes are able to use advanced equipment and treatments such as electronic monitors which gives accurate readings of their glucose levels. There are also insulin pumps about the size of a beeper, strapped to a belt which gives measured insulin injections under the skin. Despite this development, dietary supplements are still used to a very large extent in the management of diabetes (Table 2). Some dietary supplements that have been studied in clinical trials include alpha-lipoic acid, chromium and omega-3 fatty acids (Martin et al., 2006).

Table 2.

Common dietary supplements used in the management of diabetes

S/no Dietary
supplement
Nutrients/ food source Form found Target organ/cell Health benefits Limitations Reference
1. Alpha-lipoic
acid
Liver, spinach, broccoli
and potato.
lipoic acid in tablet
and capsule.
Nerve cell, kidney
and liver.
Prevents cell damage,
improves the body's ability
to use insulin.
May lower blood
sugar too much.
Jacob et al., 1995; 1996;
Konrad et al., 1999.
2. Chromium Trace element,
meat, whole grain
products, some fruits,
vegetables and spices.
Capsule and tablets
sold as chromium
picolinate, chromium
chloride, chromium
nicotinate.
Pancreas Keeps pancreas working
well and lowers blood sugar
levels.
Lower doses are
safer as high doses
can cause kidney
problem.
McCarty, 1999;
Althuis et al., 2002;
Cefalu and He, 2004;
Balk et al., 2007;
Jellin and Gregory, 2007.
3. Omega-3fatty
acids
Poly unsaturated fatty
acids. Oil, vegetable oil
(canola and soybean),
walnuts, and wheat
germ.
Capsule or oil. Liver and heart. Maintains blood glucose
levels.
Safer at low to
moderate doses,
may interfere with
certain medications.
Hartweg et al., 2007;
Hartweg et al., 2008.
4. Polyphenols Tea and dark chocolate. Green tea Vascular tissue Lowers blood glucose
levels by enhancing insulin
action.
Contains caffeine,
which can cause, in
some people,
insomnia, anxiety,
or irritability.
Green tea also has
small amounts of
vitamin K, which
can make
anticoagulant drugs,
such as warfarin,
less effective.
Fukino et al., 2005;
Ryu et al., 2006
Collins et al., 2007; Kim et al., 2007;
Mackenzie et al., 2007; Potenza et al., 2007.
5. Garlic Allium sativum S-ally cysteine
sulphoxide (SACS).
Pancreas Reduces fasting blood
glucose and lower serum
cholesterol levels.
Inhibits platelet
Aggregation and
may prolong
bleeding time.
Sheela and Augusti, 1992;
Kaczmar, 1998.
Banerjee and Maulik, 2002.
6. Magnissium Fat or fibre from fruits,
vegetables, cereals and
grain.
Citrate, chloride,
sulphate and stearate.
Heart, kidney and
muscle.
Improves insulin response
and glucose handling
in the elderly and in type 2
diabetics.
Causes loose stool
in sensitive
individuals.
Begon et al., 2000;
Larsson and Wolk, 2007;
Schulze et al., 2007.
7. Coenzyme Q10 B vitamins i.e. niacin
and folic acid. Fatty
fish, organ meat,
peanuts, spinach.
Oil Heart, liver and
lungs.
Improves long-term
glycemic control in type 2
diabetics.
Body stores of Co-Q10
can be reduced
when used
alongside prescribed
diabetic medications
such as glyburide.
Andersonet al, 2001;
Hodgson et al., 2002;
Bonadkdar and Guarneri, 2005.
8. Vanadium Black pepper,
mushroom , shell fish
parsley, fresh fruits and
vegetables.
Chelate and
sulphates.
Muscles, liver and
body fluids.
Helps cells of both the liver
and muscles use insulin
more effectively, controls
glucose and insulin
sensitizers.
Adverse reactions of
diarrhea, green
Tongue, nausea,
vomiting and
cramps are reported.
Cusi et al., 2001.
9. Folic Acid Vitamin B9, spinach
broccoli, avocado,
oranges, tomatoes,
banana.
Oxidized synthetic
folate tablet form.
Liver and kidney Along with B12, folic acid
prevents strokes and loss of
limbs due to diabetic
complications.
High dosages cause
neural damage.
Salardi et al., 2000.
10. Selenium Broccoli, raddish,
cabbage, onion, garlic,
cereals, meat,
mushroom, fish , nuts
and egg.
Chelate Small intestine,
kidney
Helps take blood sugar into
cells, protects against blood
vessel and nerve damage
from elevated blood sugars.
Low blood selenium
predisposes to
cancer, coronary
heart disease and
diabetes.
Mukherjee et al., 1998;
Stapleton, 2000.
11. Vitamin B6 All bran, brown rice,
oats, molasses, wheat
germ, banana, plum,
fish and salmon.
Pyridoxine Jejunum, ileum Pyridoxine with folic acid,
B12 and B6 helps prevent
diabetic blindness and
vision loss.
Excessive vitamin
B6 produces
painful, disfiguring
dermatological
lesions.
Bendich and Cohen, 1990;
Ellis et al., 1991;
McCormick, 2006.
12. Vitamin C Fruit and vegetables Ascorbic acid Endothelial cells Improves insulin stimulated
glucose metabolism.
May raise blood
sugar level.
Paolisso et al., 1994;
1995.
13. Vitamin E Vegetable oil,
sunflower, nuts, whole
grain, green leafy
avocado, carrot,
peanuts, almond,
hazelnuts.
Tocopherol Kidney, brain,
muscles, heart and
lung.
Produces a significant
improvement in insulin
mediated glucose
utilization in healthy people
and type-2 diabetics.
Large doses of α-tocopherol
are known to deplete
plasma and tissue γ-tocopherol.
Paolisso et al., 1993;
Barbagallo et al., 1999;
Jiang et al., 2001.
14. Zinc Minerals Zinc (picolinate) Immune and
metabolic cells.
Assists normal production,
storage and secretion of
insulin, necessary for the
conformational integrity of
insulin, helps blood sugar
get into cells.
Significantly higher
doses may cause nausea, vomiting,
headache and drowsiness.
Paolisso et al., 1993;
Barbagallo et al., 1999;
Jiang et al., 2001.
15. Copper Oat, bran, apple,
almond.
Copper picolinate Pancreas, blood
vessels and nerves.
Protects pancreatic cells,
prevents diabetes-related
damage to blood vessels
and nerves and lowers
blood sugar levels.
Health benefits
impaired by high
intake of zinc.
Johnson et al., 1998;
Sitasawad et al., 2001.

Alpha-lipoic acid (ALA), also known as lipoic acid or thioctic acid and acts as an antioxidant substance that protects against cell damage. ALA has been researched for its effect on insulin sensitivity, glucose metabolism and diabetic neuropathy (Jacob et al., 1996). Diabetic patients also take chromium in an effort to improve their blood glucose control. Chromium supplementation in diabetics has been researched but not with some controversies. While some researchers have found benefits, others have indicated little or no benefits (Cefalu and Hu, 2004). Therefore, additional high-quality research is needed to prove its efficacy. Omega-3 fatty acids are another class of compound that has been researched for their effect on controlling glucose and reducing heart disease risk in people with Type 2, diabetes. Studies showed that omega-3 fatty acids lower triglycerides, but do not affect blood glucose control, total cholesterol or HDL (good), cholesterol in people with diabetes (De Luis et al., 2009).

Complementary medicine is mostly used along with conventional medicine while alternative medicine is replacing conventional medicine (Egede et al., 2002). For example, ALA, Chromium supplements, cinnamon and host of other supplements have proved successful for quite some time in the treatment for peripheral neuropathy. ALA has been reported to lower blood glucose level even though; there is no evidence that the supplement prevents neuropathy (Ziegler et al., 1995; Reljanovic et al., 1999). However, chromium supplement on A1C, glucose, and insulin levels have shown little effect in a trial among diabetes and non diabetic patients, other studies have shown some benefit on these same markers in subjects who were chromium deficient (Althius et al., 2002). Similar reports was reported where participant received 1, 3, or 6 g of cinnamon daily for 40 days to have lowered the blood glucose levels of participants from 18 to 29%. There was further reduction in the glucose level for up to 20 days for the participants who consumed the least quantity (1g) of the supplement even after the discontinuation of its use (Khan et al., 2003). Despite insufficient data on supplement safety and effectiveness, the fact remains that people with diabetes do and will continue to use dietary supplements.

Reasons for the use of dietary supplements in the management of hypertension and diabetes

Several reasons can be attributed to the upsurge in the use of dietary supplements for the management of diseases. Diabetes and hypertension represent huge financial cost to the government and affected individuals, which is predicted to increase over the next 20 years. Not everyone can afford the latest technology and advancements in the treatment of these diseases; dietary supplements and pharmacological interventions are therefore necessary (Bastaki, 2005).

Another important factor is lack of response and unwanted side effects arising from the use of conventional treatments which have forced many patients to explore dietary supplements as alternative therapy (Halat and Dennehy, 2003). The properties of dietary supplements used to treat hypertension and diabetic neuropathy are well described (Halat and Dennehy, 2003; Gupta and Guptha, 2010) Comparisons of these supplements with regard to dosages, frequencies and adverse effects described in medical literatures help with selection of the most appropriate supplements for individual patient. Majority of hypertensive patients (especially those with mild elevated blood pressure), claim they obtained little or no benefit from drug therapy and that the risks of some orthodox drugs far outweigh the benefits (Mansoor, 2001). Therefore, diet and other non-pharmacological approaches represent a safer approach to treating diabetes and hypertension with the added benefit of reduced cost (Halat and Dennehy, 2003).

Shortcomings of dietary supplements

Notwithstanding the popularity and widespread use of dietary supplements, a number of shortcomings have been recorded against them. Some of the risks involved include allergic reactions, competitive inhibition for absorption of other nutrients and drug-nutrient interactions resulting in long-term adverse effects. (Palmer and Howland, 2001; Palmer and Betz, 2002). Most of the dietary supplements including herbs and botanicals do not undergo the same stringent regulatory approval process as drugs. Food and drug laws do not require demonstration of safety and efficacy to support legal marketing of dietary supplements. There is lack of standardization among brands of supplements and the bioactive ingredients in products can vary widely (van Breemen et al., 2007). For instance, few clinical trial reports are available to support the use of herbal and botanical supplements in the prevention or treatment of high blood pressure or heart disease. At a minimum, health care professionals should ask their patients about the use of herbal products and educate them on the possibility of herb-drug interactions. The active compound of a particular herb may not be known or if known may not be on the label. Furthermore, the amount of the active substance stated may not be accurate. Quality control measures vary from company to company and from product to product. Consumers should consider buying from manufacturers that have obtained Pharmacopeia standards for product purity and content reliability, thus at least ensuring some standards are followed during manufacture.

Conclusion

Dietary supplements used presently occur in a variety of forms including vitamins, minerals, herbals, botanicals, amino acids and enzymes. Deficiency in the consumption of some recommended foods requires the use of supplements. This may help ensure adequate amounts of essential nutrients and help promote optimal health and performance. Scientific evidence supporting the benefits of some dietary supplements is well established for certain health conditions like hypertension and diabetes. In affected individuals, inadequate nutritional intake of essential vitamins and minerals may worsen their conditions. Therefore, additional nutrients from supplements can help patients meet their medical needs and requirements. We envisage that the application of dietary supplements in the management of hypertension and diabetes is an opportunity for health care professionals to work in partnership with patients to educate and support beneficial self-care behaviors.

Acknowledgments

This research was supported by grants from NRF and Govan Mbeki Research and Development Centre, University of Fort Hare, South Africa.

References

  • 1.Abeywardena MY, Patten GS. Role of omega 3 Long chain polyunsaturated fatty acids in reducing cardio-metabolic risk factors. End Metabol and Immune Disorder-Drug Target. 2011;11(3):232–246. doi: 10.2174/187153011796429817. [DOI] [PubMed] [Google Scholar]
  • 2.Afolayan AJ, Sunmonu T O. In vivo studies on Antidiabetic plants used in South Africa Herbal medicine. J Clin Biochem Nutri. 2010;47:98–106. doi: 10.3164/jcbn.09-126R. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Althuis MD, Jordan NE, Ludington EA, Wittes JT. Glucose and insulin responses to dietary chromium supplements: A meta-analysis. Am J Clin Nutr. 2002;76(1):148–155. doi: 10.1093/ajcn/76.1.148. [DOI] [PubMed] [Google Scholar]
  • 4.American Diabetes Association, author. Standards of medical care for patients with diabetes mellitus (position statement) Diabetes Care. 1997;20(1):518–520. [Google Scholar]
  • 5.Anderson JW, Hanna TJ, Xuejun Peng BS, Kryscio RJ. Whole grain food and heart disease risk. J Ame College of Nutri. 2000;19(3):291–299. doi: 10.1080/07315724.2000.10718963. [DOI] [PubMed] [Google Scholar]
  • 6.Anderson RA, Evans ML, Ellis GR, Graham J, Morris K, Jackson SK, Lewis MJ, Rees A, Frenneaux MP. The relationships between post-prandial lipaemia, endothelial function and oxidative stress in healthy individuals and patients with type 2 diabetes. Atherosclerosis. 2001;154:475–483. doi: 10.1016/s0021-9150(00)00499-8. [DOI] [PubMed] [Google Scholar]
  • 7.Appel LJ, Brands MW, Daniels SR, Karanja N, Elmer PJ, Sacks FM. Dietary approaches to prevent and treat hypertension. A scientific statement from the American Heart Association. Hypertension. 2006;47:296–308. doi: 10.1161/01.HYP.0000202568.01167.B6. [DOI] [PubMed] [Google Scholar]
  • 8.Awoyemi OK, Ewa EE, Abdulkarim IA, Adepoju AR. Ethnobotanical assessment of herbal plants in South-Western Nigeria. Acad Res Intern. 2012;2(3):50–57. [Google Scholar]
  • 9.Balk EM, Tatsioni A, Lichtenstein AH, Lau J, Pittas AG. Effect of chromium supplementation on glucose metabolism and lipids: a systematic review of randomized controlled trials. Diabetes Care. 2007;30(8):2154–2163. doi: 10.2337/dc06-0996. [DOI] [PubMed] [Google Scholar]
  • 10.Banerjee SK, Maulik SK. Effect of garlic on cardiovascular disorders: A review. Nutri Journal. 2002;1(1):4. doi: 10.1186/1475-2891-1-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Barbagallo M, Dominguez LJ, Tagliamonte MR, Resnick LM, Paolisso G. Effect of vitamin E and glutathione on glucose metabolism: Role of magnesium. Hyper. 1999;34:1002–1006. doi: 10.1161/01.hyp.34.4.1002. [DOI] [PubMed] [Google Scholar]
  • 12.Bastaki S. Review: Diabetes mellitus and its treatments. Int J Dia Metabol. 2005;13:111–134. [Google Scholar]
  • 13.Beckman JA, Goldfine AB, Gordon MB, Craeger MA. Ascorbate restores endothelium-dependent vasodilation impaired by acute hyperglycemia in humans. Circulation. 2001;103:1618–1623. doi: 10.1161/01.cir.103.12.1618. [DOI] [PubMed] [Google Scholar]
  • 14.Begon S, Pickering G, Eschalier A, Dubray C. Magnesium and MK-801 have a similar effect in two experimental models of neuropathic pain. Brain Res. 2000;887:436–439. doi: 10.1016/s0006-8993(00)03028-6. [DOI] [PubMed] [Google Scholar]
  • 15.Bellows I, Moore R. Water-soluble vitamins: B- complex and vitamin C. Colorado State University; 2012. Cooperative Extension fact sheet No. 9.312. [Google Scholar]
  • 16.Bendich A, Cohen M. Vitamin B6 safety issues. Annals of New York Academy of Sci. 1990;585:321–330. doi: 10.1111/j.1749-6632.1990.tb28064.x. [DOI] [PubMed] [Google Scholar]
  • 17.Bhanot S, Bryer-Ash M, Cheung A, McNeill JH. Bis (maltolato) oxovanadium (IV) attenuates hyperinsulinemia and hypertension in spontaneously hypertensive rats. Diabetes. 1994a;43:857–861. doi: 10.2337/diab.43.7.857. [DOI] [PubMed] [Google Scholar]
  • 18.Bhanot S, McNeill JH, Bryer-Ash M. Vanadyl sulfate prevent fructose-induced hyperinsulinemia and hypertension in rats. Hyperten. 1994b;23:308–312. doi: 10.1161/01.hyp.23.3.308. [DOI] [PubMed] [Google Scholar]
  • 19.Boden G, Chen X, Ruiz J, van Rossum GDV, Turco S. Effects of vanadyl sulfate on carbohydrate and lipid metabolism in patients with non-insulin-dependent diabetes mellitus. Metabol. 1996;45:1130–1135. doi: 10.1016/s0026-0495(96)90013-x. [DOI] [PubMed] [Google Scholar]
  • 20.Bonadkdar RA, Guarneri E. Coenzyme Q10. American Family Physician. 2005;72(6):1065–1069. [PubMed] [Google Scholar]
  • 21.Burgess E, Lewanczuk R, Bolli P, Chockalingam A, Cutler H, Taylor G, Hamet P. Recommendations on potassium, magnesium, and calcium. Can Med Ass. 1999;160(9):35–45. [PMC free article] [PubMed] [Google Scholar]
  • 22.Cappuccio FP, Duneclift SM, Atkinson RW, Cook DG. Use of alternative medicines in a multi-ethnic population. Ethnic and Dis. 2001;11:11–18. [PubMed] [Google Scholar]
  • 23.Carlson S, Peng N, Prasain JK, Wyss JM. Effects of Botanical dietary supplements on cardiovascular, cognitive and metabolic function in males and females. Gender Med. 2008;5:76–90. doi: 10.1016/j.genm.2008.03.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Carretero OA, Oparil S. Essential hypertension. Part I: definition and etiology. Circulation. 2000;101(3):329–335. doi: 10.1161/01.cir.101.3.329. [DOI] [PubMed] [Google Scholar]
  • 25.Cefalu WT, Hu FB. Role of chromium in human health and in diabetes. Diabetes Care. 2004;27:2741–2751. doi: 10.2337/diacare.27.11.2741. [DOI] [PubMed] [Google Scholar]
  • 26.Cohen N, Halberstasm M, Slimovitch P, Shammon H, Rosetti L. Oral vanadyl sulfate improves hepatic and peripheral insulin sensitivity in patients with non-insulin-dependent diabetes mellitus. J Clin Invest. 1995;95:2501–2509. doi: 10.1172/JCI117951. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Collins QF, Liu HY, Pi J, Liu Z, Quon MJ, Cao W. Epigallocatechin-3-gallate (EGCG), a green tea polyphenol, suppresses hepatic gluconeogenesis through 5-AMP activated protein kinase. J Bio Chem. 2007;282(41):30143–30149. doi: 10.1074/jbc.M702390200. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Cusi K, Cukier S, DeFronzo RA, Torres M, Puchulu FM, Redondo JC. Vanadyl sulfate improves hepatic and muscle insulin sensitivity in type 2 diabetes. J Clin Endocrinol Metab. 2001;86:1410–1417. doi: 10.1210/jcem.86.3.7337. [DOI] [PubMed] [Google Scholar]
  • 29.De Luis DA, Conde R, Aller R, Izaola O, Gonzalez Sagrado M, Perez Castrillon JL, Duenas A, Romero E. Effect of omega-3 fatty acids on cardiovascular risk factors in patients with type 2 diabetes mellitus and hypertriglyceridemia: an open study. Eur Rev Med Pharmacol Sci. 2009;13:51–55. [PubMed] [Google Scholar]
  • 30.De Smet PA. Herbal remedies. New Engl J Med. 2000;347:2046–2056. doi: 10.1056/NEJMra020398. [DOI] [PubMed] [Google Scholar]
  • 31.Dey L, Attele AS, SuYuan C. Alternative therapies for type 2 diabetes. Alt Med Rev. 2002;7(1):45–48. [PubMed] [Google Scholar]
  • 32.DSHEA, author. Dietery supplements Health and Education Act. 1994. [11/04/2013]. www.wikipedia.
  • 33.Du XJ, Fang L, Kiriazis H. Sex dimorphism in cardiac pathophysiology: Experimental findings, hormonal mechanisms, and molecular mechanisms. Pharmacol Ther. 2006;111:434–475. doi: 10.1016/j.pharmthera.2005.10.016. [DOI] [PubMed] [Google Scholar]
  • 34.Dubick M, Omaye ST. Modification of atherogenesis and heart disease by grape wine and tea polyphenols. In: Wildman REC, editor. Handbook of nutraceuticals and functional foods. Boca Raton, FL: CRC Press; 2001. pp. 235–260. [Google Scholar]
  • 35.Egede LE, Ye X, Zheng D, Silverstein MD. The prevalence and pattern of complementary and alternative medicine use in individuals with diabetes. Dia Care. 2002;25:324–329. doi: 10.2337/diacare.25.2.324. [DOI] [PubMed] [Google Scholar]
  • 36.Ellis JM, Folkers K, Minadeo M, Vanbuskirk R, Xia LJ, Tamagawa H. A deficiency of vitamin B6 is a plausible molecular basis of the retinopathy of patients with diabetes mellitus. Biochem Biophy Res Comm. 1991;179:615–619. doi: 10.1016/0006-291x(91)91416-a. [DOI] [PubMed] [Google Scholar]
  • 37.Engelhart MJ, Geerlings MI, Ruitenberg A, van Swieten JC, Hofman A, Witteman JC, Breteler MM. Dietary intake of antioxidants and risk of Alzheimer disease. J Am Med Ass. 2002;287:3223–3229. doi: 10.1001/jama.287.24.3223. [DOI] [PubMed] [Google Scholar]
  • 38.Forman JP, Rimm EB, Stampfer MJ, Curhan GC. Folate intake and the risk of incident hypertension among US women. JAMA. 2005;293:320–329. doi: 10.1001/jama.293.3.320. [DOI] [PubMed] [Google Scholar]
  • 39.Frankel EN, Kanner J, German JB, Parks E, Kinsella JE. Inhibition of oxidation of human low-density lipoprotein by phenolic substances in red wine. Lancet. 1993;341:454–457. doi: 10.1016/0140-6736(93)90206-v. [DOI] [PubMed] [Google Scholar]
  • 40.Fukino Y, Shimbo M, Aoki N, Okubo T, Iso H. Randomized controlled trial for an effect of green tea consumption on insulin resistance and inflammation markers. J Nutr Sci Vitaminol. 2005;51(5):335–342. doi: 10.3177/jnsv.51.335. [DOI] [PubMed] [Google Scholar]
  • 41.Gaede P, Poulson HE, Parving HH, Pederson O. Double-blind, randomised study of the effect of combined treatment with vitamin C and E on albuminuria in Type 2 diabetic patients. Diabet Med. 2001;18:756–760. doi: 10.1046/j.0742-3071.2001.00574.x. [DOI] [PubMed] [Google Scholar]
  • 42.Goldfine AB, Simonson DC, Folli F, Patti ME, Kahn CR. Metabolic effects of sodium metavanadate in humans with insulin-dependent and non-insulin-dependent diabetes mellitus. J Clin Endocrinol Metabol. 1995;80:3311–3320. doi: 10.1210/jcem.80.11.7593444. [DOI] [PubMed] [Google Scholar]
  • 43.Gulla J, Singer AJ. Use of alternative therapies among emergency department patients. Ann Emerge Med. 2000;35:226–228. doi: 10.1016/s0196-0644(00)70072-2. [DOI] [PubMed] [Google Scholar]
  • 44.Gupta R, Guptha S. Strategies for initial management of hypertension. Indian J Med Res. 2010;132:531–542. [PMC free article] [PubMed] [Google Scholar]
  • 45.Halat KM, Dennehy CE. Botanicals and dietary supplements in diabetic peripheral neuropathy. J Am Board Family Pract. 2003;16:47–57. doi: 10.3122/jabfm.16.1.47. [DOI] [PubMed] [Google Scholar]
  • 46.Halsad CH. Dietary supplements and functional foods: 2 sides of a coin. American J Clinic Nutri. 2003;77:1001–1007. doi: 10.1093/ajcn/77.4.1001S. [DOI] [PubMed] [Google Scholar]
  • 47.Hartweg J, Farmer AJ, Perera R, Holman R R, Neil HA. Meta-analysis of the effects of n-3 polyunsaturated fatty acids on lipoproteins and other emerging lipid cardiovascular risk markers in patients with type 2 diabetes. Diabetologia. 2007;50(8):1593–1602. doi: 10.1007/s00125-007-0695-z. [DOI] [PubMed] [Google Scholar]
  • 48.Hartweg J, Perera R, Montori VM, Dinneen SF, Neil AHAWN, Farmer AJ. Omega-3 polyunsaturated fatty acids (PUFA) for type 2 diabetes mellitus. Cochrane Database of Systematic Reviews. 2008;2008 doi: 10.1002/14651858.CD003205.pub2. Issue 1.Art. No.: CD003205. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Hodgson JM, Watts GF, Playford DA, Burke V, Croft KD. Coenzyme Q10 improves blood pressure and glycemic control: A controlled trial in subjects with type 2 diabetes. Eur J Clinic Nutri. 2002;56:1137–1142. doi: 10.1038/sj.ejcn.1601464. [DOI] [PubMed] [Google Scholar]
  • 50.Holt RIG. Diagnosis, epidemiology and pathogenesis of diabetes mellitus: an update for psychiatrists. The British Journal of Psychiatry. 2004;184:47–55. doi: 10.1192/bjp. [DOI] [PubMed] [Google Scholar]
  • 51.Hooper L, Thompson RL, Harrison RA, Summerbell CD, Ness AR, Moore HJ, Worthington HV, Durrington PN, Higgins JPT, Capps NE, Riemersma RA, Ebrahim SBJ, Davey Smith G. Risks and benefits of omega-3 fats for mortality, cardiovascular disease and cancer: a systematic review. Achieves of British Med Journal. 2006;332:752–760. doi: 10.1136/bmj.38755.366331.2F. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Huisman M, Kunst AE, Andersen O, Bopp M, Borgan JK, Borrell C, Costa G, Deboosere P, Desplanques G, Donkin A, Gadeyne S, Minder C, Regidor E, Spadea T, Valkonen T, Mackenbach JP. Socio-economic inequalities in mortality among the elderly in 11 European populations. J Epidemiol Comm Health. 2004;58:468–475. doi: 10.1136/jech.2003.010496. International Diabetes Federation (2011) [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Jacob S, Henriksen EJ, Schiemann AL, Simon I, Clancy DE, Tritschler HJ, Jung WI, Augustin HJ, Dietze GJ. Enhancement of glucose disposal in patients with type 2 diabetes by alpha-lipoic acid. Arzneimittel-Forschung. 1995;45(8):872–874. [PubMed] [Google Scholar]
  • 54.Jacob S, Henriksen EJ, Tritschler HJ, Augustin HJ, Dietze GJ. Improvement of insulin-stimulated glucose-disposal in type 2 diabetes after repeated parenteral administration of thioctic acid. Exp Clin Endocrinol Diabetes. 1996;104(3):284–288. doi: 10.1055/s-0029-1211455. [DOI] [PubMed] [Google Scholar]
  • 55.Jellin JM, Gregory PJ. Pharmacist's Letter/Prescriber's Letter NaturalMedicines Comprehensive Database. 9th ed. Stockton, CA: Therapeutic Research Faculty; 2007. [Google Scholar]
  • 56.Jiang Q, Chrieten S, Shigenaga MK, Ames BN. γ-Tocopherol, the major form of Vitamin E in the US diet deserves more attention. Ame Soc Clinic Nutri. 2001;74(6):714–722. doi: 10.1093/ajcn/74.6.714. [DOI] [PubMed] [Google Scholar]
  • 57.Johnson MA, Smith MM, Edmonds JT. Copper, iron, zinc, and manganese in Dietary supplements, infant formulas, and ready-to-eat breakfast cereals. Ame J Clinic Nutri. 1998:1035, 1040. doi: 10.1093/ajcn/67.5.1035S. [DOI] [PubMed] [Google Scholar]
  • 58.Kaczmar T. Herbal support for diabetes management. Clinical Nutrition Insights CNI608 5/98. 1998;6(8) [Google Scholar]
  • 59.Kearney PM, Whelton M, Reynolds K, Muntner P, Whelton PK, He J. Global burden of hypertension: analysis of worldwide data. Lancet. 2005;365:217–223. doi: 10.1016/S0140-6736(05)17741-1. [DOI] [PubMed] [Google Scholar]
  • 60.Khan A, Safdar M, Ali Khan MM, Khattak KN, Anderson RA. Cinnamon improves glucose and lipids of people with type 2 diabetes. Diabetes Care. 2003;26:3215–3218. doi: 10.2337/diacare.26.12.3215. [DOI] [PubMed] [Google Scholar]
  • 61.Kim JA, Formoso G, Li Y, Potenza MA, Marasciulo FL, Montagnani M, Quon MJ. Epigallocatechin gallate, a green tea polyphenol, mediates NO-dependent vasodilation using signaling pathways in vascular endothelium requiring reactive oxygen species and Fyn. J Bio Chem. 2007;282(18):13736–13745. doi: 10.1074/jbc.M609725200. [DOI] [PubMed] [Google Scholar]
  • 62.Knentz AJ, Nattras M. Diabetic ketoacidosis, non ketotic hyperosmolar coma and lactic Acidosis. In: Pickup JC, Williams G, editors. Handbook of diabetes. 2nd edition. Blackwell Science; 1991. pp. 479–494. [Google Scholar]
  • 63.Konrad T, Vicini P, Kusterer K, Hoflich A, Assadkhani A, Bohles HJ, Sewell A, Tritschler HJ, Cobelli C, Usadel KH. α-Lipoic acid treatment decreases serum lactate and pyruvate concentrations and improves glucose effectiveness in lean and obese patients with type 2 diabetes. Dia Care. 1999;22:280–287. doi: 10.2337/diacare.22.2.280. [DOI] [PubMed] [Google Scholar]
  • 64.Kotchen TA, McCarron DA. Dietary electrolytes and blood pressure: A statement For Healthcare Professionals from the American Heart Association Nutrition Committee. Circulation. 1998;98:613–617. doi: 10.1161/01.cir.98.6.613. [DOI] [PubMed] [Google Scholar]
  • 65.Kotchen JM, McKean HE, Kotchen TA. Blood pressure trends with aging. Hypertension. 1982;4:128–134. doi: 10.1161/01.hyp.4.5_pt_2.iii128. [DOI] [PubMed] [Google Scholar]
  • 66.Kumar PJ, Clark M. Textbook of clinical medicine. London: Saunders; 2002. pp. 1099–1121. [Google Scholar]
  • 67.Larsson SC, Wolk A. Magnesium intake and risk of type 2 diabetes: a meta-analysis. J Intern Med. 2007;262(2):208–214. doi: 10.1111/j.1365-2796.2007.01840.x. [DOI] [PubMed] [Google Scholar]
  • 68.Litovitz TL, Klein-Schwartz W, White S, Cobaugh DJ, Youniss J, Omslaer JC, Drab A, Benson BE. 2000 Annual report of the American Association of Poison Control Centers Toxic Exposure Surveillance System. Ame J Emergency Med. 2001;19:337–395. doi: 10.1053/ajem.2001.25272. [DOI] [PubMed] [Google Scholar]
  • 69.Mackenzie T, Leary L, Brooks WB. The effect of an extract of green and black tea on glucose control in adults with type 2 diabetes mellitus: double-blind randomized study. Metabol. 2007;56(10):1340–1344. doi: 10.1016/j.metabol.2007.05.018. [DOI] [PubMed] [Google Scholar]
  • 70.Mangoni AA, Sherwood RA, Swift CG, Jackson SH. Folic acid enhances endothelial function and reduces blood pressure in smokers: a randomized controlled trial. J Internal Med. 2002;252:497–503. doi: 10.1046/j.1365-2796.2002.01059.x. [DOI] [PubMed] [Google Scholar]
  • 71.Mansoor GA. Herbs and alternative therapies in the hypertension clinic. American J Hyperten. 2001;14:971–975. doi: 10.1016/s0895-7061(01)02172-0. [DOI] [PubMed] [Google Scholar]
  • 72.Marchioli R, Barzi F, Bomba E, Chieffo C, Di Gregorio D, Di Mascio R, Franzosi MG, Geraci E, Levantesi G, Maggioni AP, Mantini L, Marfisi RM, Mastrogiuseppe G, Mininni N, Nicolosi GL, Santini M, Schweiger C, Tavazzi L, Tognoni G, Tucci C, Valagussa F GISSI-Prevenzione Investigators, author. Early Protection against death by n-3 polyunsaturated fatty acid after myocardial infarction: time-course analysis of the results of the Gruppo Italiano per lo studio della Sopravvienza nell'Infarto Miocardico (GISSI)-Prevenzione. Circulation. 2002;105:1897–1903. doi: 10.1161/01.cir.0000014682.14181.f2. [DOI] [PubMed] [Google Scholar]
  • 73.Martin J, Wang ZQ, Zhang XH, Wachtel D, Volaufova J, Mathews DE, Cefalu WT. Chromium picolinate supplementation attenuates body weight gain and Increases insulin sensitivity in subjects with type 2 diabetes. Dia Care. 2006;29(8):1826–1832. doi: 10.2337/dc06-0254. [DOI] [PubMed] [Google Scholar]
  • 74.McCarron DA. Role of adequate dietary calcium intake in the prevention and management of salt-sensitive hypertension. Am J Clinic Nutri. 1997;65:712–716. doi: 10.1093/ajcn/65.2.712S. [DOI] [PubMed] [Google Scholar]
  • 75.McCarty MF. High-dose biotin, an inducer of glucokinase expression, may synergize With chromium picolinate to enable a definitive nutritional therapy for type II diabetes. Med Hypotheses. 1999;52:401–406. doi: 10.1054/mehy.1997.0682. [DOI] [PubMed] [Google Scholar]
  • 76.McCormick D. Vitamin B6. In: Bowman B, Russell R, editors. Present Knowledge in Nutrition. 9th ed. Washington, DC: International Life Sciences Institute; 2006. [Google Scholar]
  • 77.Merchant RE, Andre CA. Nutritional supplement Chlorella pyrenoidosa in the treatment of fibromyalgia, hypertension and ulcerative colitis. Alternative Therapies in Health and Medicine. 2001;7(3):79–91. [PubMed] [Google Scholar]
  • 78.Mohamadi A, Jarrell ST, Shi SJ, Andrawis NS, Myers A, Clouatre D, Preuss HG. Effects of wild versus cultivated garlic on blood pressure and other parameters in hypertensive rats. Heart Dis. 2000;2:3–9. [PubMed] [Google Scholar]
  • 79.Moller D E, Flier J S. “Insulin resistance-mechanisms, syndromes, and implications,”. The New England J Med. 1991;325(13):938–948. doi: 10.1056/NEJM199109263251307. 1991. [DOI] [PubMed] [Google Scholar]
  • 80.Morris MC, Evans DA, Bienias JL, Tangney CC, Bennett CC, Aggarwal N. Dietary intake of antioxidant nutrients and the risk of incident Alzheimer disease in a biracial community study. J Am Med Ass. 2002;287:3230–3237. doi: 10.1001/jama.287.24.3230. [DOI] [PubMed] [Google Scholar]
  • 81.Mukherjee B, Anbazhagan S, Roy A, Ghosh R, Chatterjee M. Novel implications of the potential role of selenium on antioxidant status in streptozotocin induced diabetic mice. Biomed Pharmacother. 1998;52(2):89–95. doi: 10.1016/S0753-3322(98)80008-5. [DOI] [PubMed] [Google Scholar]
  • 82.Ness AR, Chee D, Elliott P. Vitamin C and blood pressure: an overview. [19 February 2013];J Human Hyperten. 1997 11:343–350. doi: 10.1038/sj.jhh.1000423. National Institutes of Health Office of Dietary Supplements: Dietary supplement fact sheet: chromium[article online]. Available from http://ods.od.nih.gov/factsheets/chromium.asp#en35. [DOI] [PubMed] [Google Scholar]
  • 83.Palmer ME, Howland MA. Herbals and dietary supplements. In: Ford M, et al., editors. Clinical toxicology. Philadelphia: WB Saunders; 2001. pp. 316–331. [Google Scholar]
  • 84.Palmer M, Plants Betz J. In: Goldfrank's toxicologic emergencies. 7th edn. Goldfrank LR, Flomenbaum NE, Lewin NA, et al., editors. New York: McGraw-Hill; 2002. pp. 1150–1182. [Google Scholar]
  • 85.Paolisso G, D'Amore A, Giugliano D, Ceriello A, Varricchio M, D'Onofrio F. Pharmacologic doses of vitamin E improve insulin action in healthy subjects and non-insulin dependent diabetic patients. Am J Clinic Nutri. 1993;57:650–656. doi: 10.1093/ajcn/57.5.650. [DOI] [PubMed] [Google Scholar]
  • 86.Paolisso G, D'Amore A, Balbi V, Volpe C, Galzerano D, Giugliano D, Sgambato S, Varricchio M, D'Onofrio F. Plasma vitamin C affects glucose homeostasis in healthy subjects and in non-insulin dependent diabetes. Am J Physiol. 1994;266:261–268. doi: 10.1152/ajpendo.1994.266.2.E261. [DOI] [PubMed] [Google Scholar]
  • 87.Paolisso G, Balbi V, Volpe C, Varricchio G, Gambardella A, Saccomanno F, Ammendola S, Varricchio M, D'Onofrio F. Metabolic benefits deriving from chronic vitamin C supplementation in aged non-insulin dependent diabetics. J Am Coll Nutr. 1995;14:387–392. doi: 10.1080/07315724.1995.10718526. [DOI] [PubMed] [Google Scholar]
  • 88.Pemberton J. “Medical experiments carried out in Sheffield on conscientious objectors to military service during the 1939–45 war”. Int J Epidemiol. 2006;35(3):556–558. doi: 10.1093/ije/dyl020. [DOI] [PubMed] [Google Scholar]
  • 89.Phillips AW, Osborne JA. Survey of alternative and nonprescription therapy use. Am J Health Syst Pharm. 2000;57:1361–1362. doi: 10.1093/ajhp/57.14.1361. [DOI] [PubMed] [Google Scholar]
  • 90.Potenza MA, Marasciulo FL, Tarquinio M, Tiravanti E, Colantuono G, Federici A, Kim JA, Quon MJ, Montagnani M. EGCG, a green tea polyphenol, improves endothelial function and insulin sensitivity, reduces blood pressure, and protects against myocardial I/R injury in SHR. Am J Physiol Endocrinol Metab. 2007;292:1378–1387. doi: 10.1152/ajpendo.00698.2006. [DOI] [PubMed] [Google Scholar]
  • 91.Preuss HG, Jarrell ST, Scheckenbach R, Lieberman S, Anderson RA. Comparative Effects of Chromium, Vanadium and Gymnema Sylvestre on Sugar Induced Blood Pressure Elevations in SHR. J Am College Nutri. 1998;17(2):116–123. doi: 10.1080/07315724.1998.10718736. [DOI] [PubMed] [Google Scholar]
  • 92.Prisco D, Paniccia R, Bandinelli B, Filippini M, Francalanci I, Giusti B, Giuriani L, Gensini GF, Abbate R, Neri Serneri GG. Effect of medium-term supplementation with a moderate dose of n-3 polyunsaturated fatty acids on blood pressure in mild hypertensive patients. Thromb Res. 1998;91:105–112. doi: 10.1016/s0049-3848(98)00046-2. [DOI] [PubMed] [Google Scholar]
  • 93.Rang HP, Dale MM, Ritters JM. In: The endocrine pancreas and the control of blood glucose, in pharmacology. Simmons B, Beasley S, editors. UK: Longman Group Ltd; 1991. pp. 403–410. [Google Scholar]
  • 94.Rasmussen CB, Glisson JK, Minor DS. Dietary Supplements and HypertensionPot ential Benefits and Precautions - A review. The J Clinical Hyperten. 2012;14(7):467–471. doi: 10.1111/j.1751-7176.2012.00642.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 95.Reljanovic M, Reichel G, Rett K, Lobisch M, Schuette K, Moller W, Tritschler HJ, Mehnert H. reatment of diabetic polyneuropathy with the antioxidantthioctic acid (alpha-lipoic acid): a two year multicenter randomized double blind placebo controlled trial. Free Radic Biol Med. 1999;31:171–179. doi: 10.1080/10715769900300721. [DOI] [PubMed] [Google Scholar]
  • 96.Rother KI. “Diabetes Treatment- Bridging the Divide”. N Engl J Med. 2007;356(15):1499–1501. doi: 10.1056/NEJMp078030. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 97.Ryu OH, Lee J, Lee KW, Kim HY, Seo JA, Kim SG, Kim NH, Baik SH, Choi DS, Choi KM. Effects of green tea consumption on inflammation, insulin resistance and pulse wave velocity in type 2 diabetes patients. Diabetes Res Clinic Practice. 2006;71(3):356–358. doi: 10.1016/j.diabres.2005.08.001. [DOI] [PubMed] [Google Scholar]
  • 98.Salardi S, Cacciari E, Sassi S, Grossi G, Mainetti B, Casa CD, Pirazzoli P, Cicognani A, Gualandi S. Homocysteinemia, serum folate and vitamin B12 in very young patients with diabetes mellitus type 1. J Pediatr Endocrinol Metab. 2000;13:1621–1627. doi: 10.1515/jpem.2000.13.9.1621. [DOI] [PubMed] [Google Scholar]
  • 99.Schaumburg H, Kaplan J, Widebank A, Vick N, Rasmus S, Pleasure D, Brown MJ. Sensory neuropathy from pyridoxine abuse. A new megavitamin syndrome. New Engl J Med. 1983;309:445–448. doi: 10.1056/NEJM198308253090801. [DOI] [PubMed] [Google Scholar]
  • 100.Schulze MB, Schulz M, Heidemann C, Schienkiewitz A, Hoffmann K, Boeing H. Fiber and magnesium intake and incidence of type 2 diabetes: a prospective study and meta-analysis. Archives Intern Med. 2007;167(9):956–965. doi: 10.1001/archinte.167.9.956. [DOI] [PubMed] [Google Scholar]
  • 101.Sharma AK. In: Diabetes mellitus and its complications: An update. Galadari EO, Behara I, Manchandra M, Abdulrazzaq SK, Mehra MK, editors. New Delhi: Macmillian; 1993. [Google Scholar]
  • 102.Sheela CG, Augusti KT. Antidiabetic effects of S-ally cysteine sulphoxide isolated from garlic Allium sativum Linn. Ind J Experiment Bio. 1992;30:523–526. [PubMed] [Google Scholar]
  • 103.Singh RB, Sul IL, Singh VP, Chaithiraphan S, Laothavorn P, Sy RG, Babilonia NA, Rahman ARA, Sheikh S, Tomlinson B, Sarraf-Zadigan N. Hypertension and stroke in Asia: prevalence, control and strategies in developing countries for prevention. J Human Hyperten. 2000;14:749–763. doi: 10.1038/sj.jhh.1001057. [DOI] [PubMed] [Google Scholar]
  • 104.Singh RB, Niaz MA, Rastogi SS, Shukla PK, Thakur AS. Effect of hydrosoluble coenzyme Q10 on blood pressures and insulin resistance in hypertensive patients with coronary artery disease. J Hum Hypertens. 1999;13:203–208. doi: 10.1038/sj.jhh.1000778. [DOI] [PubMed] [Google Scholar]
  • 105.Sitasawad S, Deshpande M, Katdare M, Tirth S, Parab P. Beneficial effect of supplementation with copper sulfate on STZ-diabetic mice (IDDM) Diabetes Res Clin Pract. 2001;52:77–84. doi: 10.1016/s0168-8227(00)00249-7. [DOI] [PubMed] [Google Scholar]
  • 106.Soetan KO, Olaiya CO, Oyewole OE. The importance of mineral elements for humans, domestic animals and plants; A review. Afr J Food Sci. 2010;4(5):200–222. [Google Scholar]
  • 107.Spence JD. Cerebral consequences of hypertension:Where do they lead? J Hypertens. 1996;(Suppl 14):S139–S145. [PubMed] [Google Scholar]
  • 108.Spencer J. The risk of mixing drugs and herbs. Wall Street Journal. 2004 Jun 22;2004:D1. [Google Scholar]
  • 109.Stapleton SR. Selenium: an insulin-mimetic. Cell Mol Life Sci. 2000;57:1874–1879. doi: 10.1007/PL00000669. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 110.Sunmonu T O, Afolayan AJ. Evaluation of Antidiabetic Activity and Associated Toxicity of Artemisia afra Aqueous Extract in Wistar Rats. Evidence-Based. Complementary and Alternative Medicine. 2013;2013 doi: 10.1155/2013/929074. Article ID 929074, 8 pages. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 111.Tabassum N, Ahmad F. Role of natural herbs in the treatment of hypertension. Pharmacog Rev. 2011;5:30–40. doi: 10.4103/0973-7847.79097. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 112.Timbo BB, Ross MP, McCarthy PV, Lin CJ. Dietary supplements in a National Survey: Prevalence of Use and Reports of Adverse Events. J Am Diet Ass. 2006;106:1966–1974. doi: 10.1016/j.jada.2006.09.002. [DOI] [PubMed] [Google Scholar]
  • 113.Touyz RM. Magnesium supplementation as an adjuvant to synthetic calcium channel antagonists in the treatment of hypertension. Med Hypotheses. 1991;36:140–141. doi: 10.1016/0306-9877(91)90256-x. [DOI] [PubMed] [Google Scholar]
  • 114.Trofimiuk E, Braszko JJ. Long-term administration of cod liver oil ameliorates cognitive impairment induced by chronic stress in rats. Lipids. 2011;46(5):417–423. doi: 10.1007/s11745-011-3551-3. [DOI] [PubMed] [Google Scholar]
  • 115.Van Breemen RB, Fong HH, Farnsworth NR. The role of quality assurance and standardization in the safety of botanical dietary supplements. Chem Res Toxicol. 2007;20:577–582. doi: 10.1021/tx7000493. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 116.Van Dijk RA, Rauwerda JA, Steyn M, Twisk JW, Stehouwer CD. Long-term homocysteine-lowering treatment with folic acid plus pyridoxine is associated with decreased blood pressure but not with improved brachial artery endothelium-dependent vasodilation or carotid artery stiffness: a 2-year, randomized, placebo-controlled trial. Arteriole Thrombo Vas Bio. 2001;21:2072–2079. doi: 10.1161/hq1201.100223. [DOI] [PubMed] [Google Scholar]
  • 117.Vasdev S, Longerich L, Gill V, Singal P. Dietary management of hypertension. Kuwait Med Journ. 2002;34(1):2–11. [Google Scholar]
  • 118.Warner MG. Complementary and alternative therapies for hypertension. Complementary Health Practice Review. 2000;6:11–19. [Google Scholar]
  • 119.Weiss D. Cardiovascular disease: risk factors and fundamental nutrition. International J Integra Med. 2000;2:6–12. [Google Scholar]
  • 120.World Health Organization Department of Non-communicable Disease Surveillance, author. Definition, Diagnosis and Classification of Diabetes Mellitus and its Complications (PDF) 1999 [Google Scholar]
  • 121.World Health Organization, author. Integrated management of cardiovascular risk. Geneva: 2002. [Google Scholar]
  • 122.WHO, author. 2002. [20 June, 2012]. http://whqlibdoc.who.int/publications/9241562242.pdf.
  • 123.World Health Organisation, author. The world health report 2003. International Society of Hypertension (ISH) statement on management of hypertension. J Hyper. 2003;21:1983–1992. doi: 10.1097/00004872-200311000-00002. [DOI] [PubMed] [Google Scholar]
  • 124.Wild S, Roglic G, Green Sicree R, King H. “Global prevalence of diabetes: estimates for the year 2000 and projections for 2030,”. Diabetes Care. 2004;27(5):1047–1053. doi: 10.2337/diacare.27.5.1047. [DOI] [PubMed] [Google Scholar]
  • 125.Winslow LC, Kroll DJ. Herbs as medicine. Arch Intern Med. 1998;158:2192–2199. doi: 10.1001/archinte.158.20.2192. [DOI] [PubMed] [Google Scholar]
  • 126.Wise E. Twelve dangerous dietary supplements identified by ‘Consumer Reports’ widely used herbs linked to several serious ailments. USA Today. 2004 April 8, 9D. [Google Scholar]
  • 127.Dietery supplement. www.wikipedia.org. Retrieved 14/102/2014.
  • 128.Yosefy C, Viskoper JR, Laszt A, Priluk R, Guita E, Varon D, Illan Z, Berry EM, Savion N, Adan Y, Lugassy G, Schneider R, Raz A. The effects of fish oil on hypertension, plasma lipids and hemostatis in hypertensive, obese yslipidemic patients with and without diabetes mellitus. Prostaglandins Leukot Essent Fatty Acids. 1999;61:83–87. doi: 10.1054/plef.1999.0075. [DOI] [PubMed] [Google Scholar]
  • 129.Yusuf S, Reddy S, Ounpuu S, Anand S. Global burden of cardiovascular diseases. Part 1: General considerations, the epidemiologic transition risk factors and impact of urbanization. Circulation. 2001;104:2746–2753. doi: 10.1161/hc4601.099487. [DOI] [PubMed] [Google Scholar]
  • 130.Ziegler D, Hanefeld M, Ruhnau KJ, Meibner HP, Lobisch M, Schuette K, Gries FA. Treatment of symptomatic diabetic peripheral neuropathy with the anti-oxidant “lipoic acid”: a 3 week multicentre randomized controlled trial (ALADIN Study I) Diabetologia. 1995;38:1425–1433. doi: 10.1007/BF00400603. [DOI] [PubMed] [Google Scholar]

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