• We are sorry, but NCBI web applications do not support your browser and may not function properly. More information
Logo of emborepLink to Publisher's site
EMBO Rep. Jul 2005; 6(Suppl 1): S20–S24.
PMCID: PMC1369274
Science and Society

Increasing longevity by tuning up metabolism

Abstract

To maximize human health and lifespan, scientists must abandon outdated models of micronutrients

Our daily intake of the 40 essential micronutrients—vitamins, minerals and other biochemicals—is commonly thought to be adequate. Indeed, classic deficiency diseases, such as scurvy, beriberi and pernicious anaemia, are now rare among the citizens of developed countries. The optimum amount of vitamins, minerals and essential biochemicals is the amount that maximizes a healthy lifespan, and is likely to be higher than the amount needed to prevent acute deficiency disease. Evidence suggests, however, that much chronic metabolic damage occurs at levels above the level that causes acute micronutrient deficiency disease but below the recommended dietary allowances (RDAs). In addition, current RDAs may not be sufficient to prevent subtle metabolic damage: if one input in the metabolic network is inadequate, repercussions are felt in a large number of other systems. This could result in an increase in DNA damage (and cancer), neuron decay (and cognitive dysfunction) or mitochondrial decay (and accelerated ageing and degenerative diseases). In addition, the optimum amount of micronutrients varies with age and constitution—the requirements of the elderly for vitamins and metabolites are likely to be different from those of the young—and with genetic make-up. A tune-up of micronutrient metabolism should therefore markedly increase health at little cost. It is a distortion of priorities for much of the world's population to have an inadequate intake of vitamins or minerals—at great cost to health—when a year's supply of a daily multivitamin/mineral pill costs less than a few packs of cigarettes. The poor, in general, have the worst diets and have the most to gain from improving their multivitamin and mineral supplementation and diet.

It is a distortion of priorities for much of the world's population to have an inadequate intake of vitamins or minerals...when a year's supply of a daily multivitamin/mineral pill costs less than a few packs of cigarettes

ForFor most of human evolution, caloric shortage probably limited population growth. As food was mostly calorie-poor and unprocessed, the supply of micronutrients may have been fairly adequate. The advent of agriculture changed that and made diets less varied. The introduction of the potato to Europe from South America in the late sixteenth century caused a major increase in the European population over the next few centuries as the cultivation of potatoes spread and as cultivars were selected that thrived in each climate. “In 1845 close to 40% of the population of Ireland lived chiefly on potatoes. The emergence of the 'potato people' occurred against the background of the quadrupling of the population after 1700...” (Clarkston & Crawford, 2001). Similarly, the cultivation of rice varieties was a major factor enabling high population density in Asia. Although caloric shortage is now a thing of the past for many people in Europe, Asia and North America, the abundance of carbohydrate- and fat-rich food causes another problem. Inexpensive, processed foods and drinks are calorie-rich but poor in micronutrients, and as a consequence, the USA and other developed nations are now facing an epidemic of obesity associated with micronutrient malnutrition (Kant, 2000).

figure 6-7400426-i2

Although optimal nutrition clearly requires more than micronutrients, such as fibre, there are important reasons to focus on micronutrients and health. More than 20 years of effort to improve the American diet has not been particularly successful with less-educated people, although this education initiative must continue. A parallel approach that focuses on micronutrient malnutrition is overdue and might even be more successful—it should be easier to convince people to take a multivitamin/mineral pill than to change their diet. Such a pill is inexpensive, recognized as safe and supplies a range of required vitamins and minerals. Other micronutrients, such as essential omega-3 fatty acids, which are important for brain function and development (Simopoulos, 2001), and fibre, are also widely available and inexpensive.

Fortification of food is another useful approach, such as the addition of folate to flour, or calcium to juice. However, fortification of food does not allow for metabolic differences between individuals. Menstruating women, for instance, need more iron than men or older women, who in turn may be getting too much. That is why two types of vitamin pill are now marketed: one with iron for menstruating women and one without. With more knowledge of human micronutrient requirements, a variety of tailor-made multivitamin pills could therefore be developed to meet different needs depending on age, gender and genetics.

Micronutrient deficiencies can cause DNA damage, which may ultimately lead to cancer. Our strategy in the laboratory has been to use cultured human cell lines to show that deficiency of vitamins C, E, B12, B6, niacin, folic acid, iron or zinc appears to mimic radiation by causing single- and double-strand DNA breaks, oxidative lesions or both. This has serious implications as half of the US population may be deficient in at least one of these micronutrients (Ames, 2001; Ames & Wakimoto, 2002). Micronutrient deficiency may thus contribute to the increase of cancer incidence in the quarter of the population that eat the fewest fruits and vegetables, as compared with the quarter who have the highest intake. Although 5–9 portions of fruit and vegetables a day are advised, 80% of American children and adolescents and 68% of adults do not eat five portions daily (Ames, 2001).

Fruits and vegetables are a main source of folate, and low folate intake has been associated with several types of cancer (Ames & Wakimoto, 2002). Folate deficiency causes chromosome breaks due to the massive incorporation of uracil in the DNA (Blount et al, 1997). Before the recent folate supplementation of flour in the USA, 25% of the population and close to half of poor urban minorities had levels of folate intake that are associated with high uracil content and DNA breaks. As one would expect from mechanistic considerations, and as our research has shown, deficiencies (less than 50% of the RDA) of vitamins B12 or B6 also cause high levels of uracil incorporation in human DNA and chromosome breaks (Crott et al, 2001a,b). We are now attempting to determine the level of these three vitamins that minimizes both nuclear and mitochondrial DNA damage in humans.humans.

figure 6-7400426-i3
Giuseppe Arcimboldo (1573) The Summer, oil on canvas. Original: Musée du Louvre, Paris, France. Image provided by Gerard Le Gall, RMN, Paris, France. With permission from bpk, Berlin, Germany.

Similarly, insufficient zinc causes oxidative DNA damage, inactivation of copper/ zinc superoxide dismutase, inactivation of tumour suppressor protein p53—a zinc protein—and inactivation of oxidative DNA repair in cultured human cells, and these effects can multiply to cause severe genetic damage (Ho & Ames, 2002; Ho et al, 2003). Zinc deficiency is associated with cancer in both humans and rodent models (Fong et al, 2005), but 10% of the US population ingest less than 50% of the RDA of zinc. Iron deficiency has also been shown to cause oxidative damage to mitochondria and mitochondrial DNA in rats (Walter et al, 2002; Atamna et al, 2002a). Among women of menstruating age in the USA, 25% ingest less than 50% of the RDA of iron. The poor are most affected as they have the lowest intake of these essential minerals (Frith-Terhune et al, 2000; Kumanyika & Krebssmith, 2001).

These common micronutrient deficiencies are likely to damage DNA by the same mechanism as radiation and many chemicals, but they seem to be more important by several orders of magnitude (Ames, 2001; Gold et al, 2002). Consequently, a sound public-health policy calls for micronutrient requirements to be set to minimize DNA damage (Fenech, 2003). The poor are clearly not well served if huge resources are put into preventing minor hypothetical risks, such as pesticide residues, while the major risk of poor nutrition is not addressed (Gold et al, 2002).

Vitamin-D deficiency is another major problem, particularly for people in northern areas. The hormone vitamin D is formed with the aid of ultraviolet (UV) light from sunlight, but too much exposure to UV light is dangerous. People who originate from northern areas with little UV radiation have light skin to maximize their exposure to UV rays, whereas people from southern areas have dark skin to minimize their UV light exposure. Dark-skinned people in northern parts of the USA are exposed to insufficient sunlight and individuals are often chronically vitamin-D deficient unless they drink fortified milk or take a supplement. “Although both dark- and light-skinned individuals can produce vitamin D in response to UV light, this response is much more limited in dark-skinned individuals. The 25-hydroxyvitamin D (25(OH)D) levels in African-Americans and Hispanics are, therefore, lower than Caucasians in the US” (Abrams, 2002). A study in the Boston area showed that 80% of African-Americans and 60% of Hispanics were vitamin-D deficient (Holick, 1994).

Vitamin D is necessary for calcium mobilization in bone formation, and a deficiency causes brittle bones. In addition, there is an inverse relationship between vitamin-D intake and the risk of several types of cancer, primarily colorectal cancer and colorectal adenomas; there is also evidence for a link to prostate cancer (Platz et al, 2000a,b; Levine et al, 2001; Holt et al, 2002). A plausible mechanism by which vitamin-D deficiency could increase cancer is the known inhibitory effect of vitamin-D metabolites on cell proliferation (Holt et al, 2002). African-Americans have almost double the prostate cancer rate of Caucasian Americans and also have lower levels of the vitamin-D metabolite 25-hydroxyvitamin D in their blood (Platz et al, 2000b). Recent epidemiological studies suggest that much of the increased cancer rate among African-Americans is in fact due to a vitamin-D deficiency.

Micronutrient deficiency may thus contribute to the increase of cancer incidence in the quarter of the population that eat the fewest fruits and vegetables...

Dark-skinned people such as African-Americans and some Hispanics tend not to drink milk as adults, because of lactose intolerance. Europeans and other northern people domesticated cows thousands of years ago and over time developed the ability to metabolize lactose, a major sugar in cow's milk. Most of the rest of the world cannot use lactose as adults: 70% of African-Americans, 53% of Mexican-Americans and 90% of Asians are lactose intolerant compared with 15% of northern Europeans and their descendants. As African-Americans and Hispanics also tend not to take vitamin supplements, these individuals are all the more likely to be calcium, magnesium, potassium, folate and vitamin-D deficient (Kumanyika & Krebssmith, 2001). This illustrates why understanding genetics is important in some cases to develop appropriate interventions for populations at risk.

In addition to contributing to cancer and disease risk, micronutrient deficiencies have an effect on mitochondrial metabolism and thus accelerate cellular ageing. Haem biosynthesis takes place predominantly in the mitochondria and interfering with this process causes specific loss of haem-a, a component of complex IV, with a subsequent release of oxidants (Atamna et al, 2002a,b). Iron deficiency thus causes the release of oxidants and mitochondrial decay, presumably through the lack of haem-a (Walter et al, 2002; Atamna et al, 2002a). Biotin deficiency, which is quite common (Mock et al, 2002a,b), also causes defects in mitochondrial complex IV and induces oxidant leakage (H. Atamna et al, in preparation). There is also evidence that deficiencies in copper and pantothenate decrease levels of complex IV (Brambl & Plesofsky-Vig, 1986; Rossi et al, 1998). Zinc deficiency causes an increased release of oxidants, owing to the inactivation of δ-aminolevulinate dehydratase, an enzyme of haem biosynthesis that contains eight zinc atoms (Jaffe, 1995; Ho & Ames, 2002; Ho et al, 2003). The consequences of these various micronutrient deficiencies are likely to be accelerated ageing and neural decay (Atamna et al, 2002b; Atamna & Frey, 2004).

The poor are clearly not well served if huge resources are put into preventing minor hypothetical risks...while the major risk of poor nutrition is not addressed

The importance of vitamins and minerals for disease pathology is also highlighted by the fact that various diseases can be treated in part with high doses of micronutrients. As much as one-third of all gene mutations results in the corresponding enzyme having an increased Michaelis constant and thus a decreased binding affinity for its coenzyme, which results in a lower rate of reaction. Thus, many of the human genetic diseases that are due to defective enzymes can be remedied or ameliorated by the administration of high doses of the B-vitamin component of the corresponding coenzyme, which partially restores enzymatic activity (Ames et al, 2002). Some examples include C677T/Ala222Val methylenetetrahydrofolate reductase (NADPH) and the cofactor FAD in relation to cardiovascular disease, migraines and rages; the C609T/Pro187Ser mutation in NAD(P):quinone oxidoreductase 1 and FAD in relation to cancer; the C131G/Ala44Gly mutation in glucose-6-phosphate 1-dehydrogenase and NADP in relation to favism and haemolytic anaemia; and the Glu487Lys mutation, common in Asians, in aldehyde dehydrogenase and NAD in relation to alcohol intolerance, Alzheimer's disease and cancer. The importance of binding affinity is also likely to be relevant for mitochondrial ageing as well as for human nutrition.

In fact, we are making progress in reversing some of the mitochondrial decay in aged rats by feeding them high levels of the normal metabolites acetyl carnitine (ALC) and R-lipoic acid (LA). The rationale behind this research is based on the observation that, with increasing age, oxidative damage to proteins causes a deformation in the structure of key enzymes, which reduces their affinity for the substrate (Liu et al, 2002a). The effect of age on decreasing the binding affinity of carnitine acyl transferase (CAT) for ALC or acetyl CoA can be mimicked by combining CAT with malondialdehyde, a lipid-peroxidation product that accumulates with age. Feeding rats ALC and LA restores the speed of the reaction for ALC transferase and mitochondrial function (Liu et al, 2002a). LA is an effective inducer of phase II antioxidant enzymes, including glutathione synthesis, as well as being a potent mitochondrial antioxidant (Suh et al, 2004a,b; Smith et al, 2004).

"The main distinguishing characteristic between man and the lower animals is the desire to take pills."

In old rats, we can see that mitochondrial membrane potential, cardiolipin levels, respiratory control ratio and cellular oxygen uptake are lower when compared with young rats, whereas the ratio of oxidant by-product to oxygen consumed, neuron RNA oxidation and mutagenic aldehydes from lipid peroxidation are higher. Feeding these old rats ALC and LA for a few weeks restores mitochondrial function, lowers oxidant levels, neuron RNA oxidation and mutagenic aldehydes and increases rat ambulatory activity and cognition (Liu et al, 2002a,b; Hagen et al, 2002a). ALC and LA are also effective in protecting the ageing rat heart against cardiovascular decay (Hagen et al, 2002b). There is evidence that this might also benefit humans. A recent meta-analysis of 21 double-blind clinical trials of ALC in the treatment of mild cognitive impairment and mild Alzheimer's disease showed significant efficacy versus placebo (Montgomery et al, 2003). A meta-analysis of four clinical trials of LA for the treatment of neuropathic deficits in diabetes also showed significant efficacy compared with placebo (Ziegler, 2002).

In addition to the various deleterious effects on chromosomes and mitochondria described above, micronutrient deficiencies might have another serious effect on public health. The USA and other developed countries are facing an epidemic of obesity with related insulin resistance and type II diabetes. Although this epidemic is widespread in all groups, it is most prevalent among the poor and particularly in African-Americans and Hispanics. Sturm (2002) has estimated that the toll on health will be comparable with that of smoking. An energy-rich and micronutrient-poor diet could contribute in numerous ways to shortening life (Kant, 2000). Although the question has not been addressed experimentally, we hypothesize that micronutrient deficiency counteracts the normal feeling of satiety after sufficient calories are eaten. This may be a biological strategy for obtaining missing nutrients, which is important in fertility. Results from the Coronary Artery Disease Risk Development in Young Adults (CARDIA) study suggest that dairy-product consumption, the main source of calcium, is inversely related to obesity, diabetes and insulin resistance (Pereira et al, 2002).

Evidence is accumulating that a multivitamin/mineral supplement is good health insurance and would markedly protect us against heart disease, cancer, immune deficiencies and cataracts (Bendich et al, 1997; Oakley, 1998; Fairfield & Fletcher, 2002). The caveat, of course, is that too much of many minerals, such as iron, zinc, copper and selenium, and some vitamins, are toxic. Mae West's dictum about sex—“Too much of a good thing is wonderful”—does not apply to micronutrients. Advice on taking a multivitamin should always be coupled with advice on eating a good diet, as we also need fibre, omega-3 fatty acids and other ingredients (Willett, 2001). It is also good to keep Mark Twain's observation in mind: “The main distinguishing characteristic between man and the lower animals is the desire to take pills.”

A metabolic tune-up through an improved supply of micronutrients is likely to have great health benefits, particularly for those with inadequate diets, such as many of the poor, young, obese and elderly. The issues discussed here highlight the need to educate the public about the crucial importance of nutrition and the potential health benefits of a simple and affordable daily multivitamin/mineral supplement. Tuning up metabolism to maximize human health and lifespan will require scientists, clinicians and educators to abandon outdated models and explore more meaningful ways to prevent chronic disease and achieve optimum health. It is becoming clear that unbalanced diets will soon become the largest contributor to ill health, with smoking following close behind.

figure 6-7400426-i1
Table 1
Micronutrient deficiencies in individuals in the USA

Acknowledgments

This paper has been adapted in part from Ames BN (2004) A role for supplements in optimizing health: the metabolic tune-up. Arch Biochem Biophys 423: 227–234.

References

  • Abrams SA (2002) Nutritional rickets: an old disease returns. Nutr Rev 60: 111–115 [PubMed]
  • Ames BN (2001) DNA damage from micronutrient deficiencies is likely to be a major cause of cancer. Mutat Res 475: 7–20 [PubMed]
  • Ames BN, Wakimoto P (2002) Are vitamin and mineral deficiencies a major cancer risk? Nat Rev Cancer 2: 694–704 [PubMed]
  • Ames BN, Elsonschwab I, Silver EA (2002) High-dose vitamin therapy stimulates variant enzymes with decreased coenzyme binding affinity (increased K(m)): relevance to genetic disease and polymorphisms. Am J Clin Nutr 75: 616–658 [PubMed]
  • Atamna H, Frey WH 2nd (2004) A role for heme in Alzheimer's disease: heme binds amyloid β and has altered metabolism. Proc Natl Acad Sci USA 101: 11153–11158 [PMC free article] [PubMed]
  • Atamna H, Walter PB, Ames BN (2002a) The role of heme and ironsulfur clusters in mitochondrial biogenesis, maintenance, and decay with age. Arch Biochem Biophys 397: 345–353 [PubMed]
  • Atamna H, Killilea DW, Killilea AN, Ames BN (2002b) Heme deficiency may be a factor in the mitochondrial and neuronal decay of aging. Proc Natl Acad Sci USA 99: 14807–14812 [PMC free article] [PubMed]
  • Bendich A, Mallick R, Leader S (1997) Potential health economic benefits of vitamin supplementation. West J Med 166: 306–312 [PMC free article] [PubMed]
  • Blount BC, Mack MM, Wehr CM, MacGregor JT, Hiatt RA, Wang G, Wickramasinghe SN, Everson RB, Ames BN (1997) Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage. Proc Natl Acad Sci USA 94: 3290–3295 [PMC free article] [PubMed]
  • Brambl R, Plesofsky-Vig N (1986) Pantothenate is required in Neurospora crassa for assembly of subunit peptides of cytochrome c oxidase and ATPase/ATP synthase. Proc Natl Acad Sci USA 83: 3644–3648 [PMC free article] [PubMed]
  • Clarkston LA, Crawford ME (2001) Feast and famine: A History of Food and Nutrition in Ireland 1500–1920. Oxford, UK: Oxford University Press
  • Crott JW, Mashiyama ST, Ames BN, Fenech MF (2001a) Methylenetetrahydrofolate reductase C677T polymorphism does not alter folic acid deficiency-induced uracil incorporation into primary human lymphocyte DNA in vitro. Carcinogenesis 22: 1019–1025 [PubMed]
  • Crott JW, Mashiyama ST, Ames BN, Fenech MF (2001b) The effect of folic acid deficiency and MTHFR C677T polymorphism on chromosome damage in human lymphocytes in vitro. Cancer Epidemiol Biomarkers Prev 10: 1089–1096 [PubMed]
  • Fairfield KM, Fletcher RH (2002) Vitamins for chronic disease prevention in adults: scientific review. JAMA 287: 3116–3126 [PubMed]
  • Fenech M (2003) Nutritional treatment of genome instability: a paradigm shift in disease prevention and in the setting of recommended dietary allowances. Nutr Res Rev 16: 109–122 [PubMed]
  • Fong LY, Zhang L, Jiang Y, Farber JL (2005) Dietary zinc modulation of COX-2 expression and lingual and esophageal carcinogenesis in rats. J Natl Cancer Inst 97: 40–50 [PubMed]
  • Frith-Terhune AL, Cogswell ME, Khan LK, Will JC, Ramakrishnan U (2000) Iron deficiency anemia: higher prevalence in Mexican American than in non-Hispanic white females in the third National Health and Nutrition Examination Survey, 1988–1994. Am J Clin Nutr 72: 963–968 [PubMed]
  • Gold LS, Slone TH, Manley NB, Ames BN (2002) Misconceptions About the Causes of Cancer. Vancouver, BC, Canada: The Fraser Institute
  • Hagen TM, Liu J, Lykkesfeldt J, Wehr CM, Ingersoll RT, Vinarsky V, Bartholomew JC, Ames BN (2002a) Feeding acetyl-L-carnitine and lipoic acid to old rats significantly improves metabolic function while decreasing oxidative stress. Proc Natl Acad Sci USA 99: 1870–1875 [PMC free article] [PubMed]
  • Hagen TM, Moreau R, Suh JH, Visioli F (2002b) Mitochondrial decay in the aging rat heart: evidence for improvement by dietary supplementation with acetyl-L-carnitine and/or lipoic acid. Ann NY Acad Sci 959: 491–507 [PubMed]
  • Ho E, Ames BN (2002) Low intracellular zinc induces oxidative DNA damage, disrupts p53, NFκB, and AP1 DNA-binding, and affects DNA repair in a rat glioma cell line. Proc Natl Acad Sci USA 99: 16770–16775 [PMC free article] [PubMed]
  • Ho E, Courtemanche C, Ames BN (2003) Zinc deficiency induces oxidative DNA damage and increases p53 expression in human lung fibroblasts. J Nutr 133: 2543–2548 [PubMed]
  • Holick MF (1994) McCollum Award Lecture, 1994: vitamin D—new horizons for the 21st century. Am J Clin Nutr 60: 619–630 [PubMed]
  • Holt PR et al. (2002) Colonic epithelial cell proliferation decreases with increasing levels of serum 25-hydroxy vitamin D. Cancer Epidemiol Biomarkers Prev 11: 113–119 [PubMed]
  • Jaffe EK (1995) Porphobilinogen synthase, the first source of heme's asymmetry. J Bioenerg Biomembr 27: 169–179 [PubMed]
  • Kant AK (2000) Consumption of energy-dense, nutrient-poor foods by adult Americans: nutritional and health implications. The Third National Health and Nutrition Examination Survey, 1988–1994. Am J Clin Nutr 72: 929–936 [PubMed]
  • Kumanyika SK, Krebssmith SM (2001) Preventive nutrition issues in ethnic and socioeconomic groups in the United States. In Bendich A, Deckelbaum RJ (eds) Primary and Secondary Preventive Nutrition pp325–356. Totowa, NJ, USA: Humana
  • Levine AJ, Harper JM, Ervin CM, Chen YH, Harmon E, Xue S, Lee ER, Frankel HD, Haile RW (2001) Serum 25-hydroxyvitamin D, dietary calcium intake, and distal colorectal adenoma risk. Nutr Cancer 39: 35–41 [PubMed]
  • Liu J, Killilea D, Ames BN (2002a) Age-associated mitochondrial oxidative decay: improvement of carnitine acetyltransferase substrate-binding affinity and activity in brain by feeding old rats acetyl-L-carnitine and/or R-α-lipoic acid. Proc Natl Acad Sci USA 99: 1876–1881 [PMC free article] [PubMed]
  • Liu J, Head E, Gharib AM, Yuan W, Ingersoll RT, Hagen TM, Cotman CW, Ames BN (2002b) Memory loss in old rats is associated with brain mitochondrial decay and RNA/DNA oxidation: partial reversal by feeding acetyl-L-carnitine and/or R-α-lipoic acid. Proc Natl Acad Sci USA 99: 2356–2361 [PMC free article] [PubMed]
  • Mock DM, Henrich CL, Carnell N, Mock NI (2002a) Indicators of marginal biotin deficiency and repletion in humans: validation of 3-hydroxyisovaleric acid excretion and a leucine challenge. Am J Clin Nutr 76: 1061–1068 [PMC free article] [PubMed]
  • Mock DM, Quirk JG, Mock NI (2002b) Marginal biotin deficiency during normal pregnancy. Am J Clin Nutr 75: 295–299 [PMC free article] [PubMed]
  • Montgomery SA, Thal LJ, Amrein R (2003) Meta-analysis of double blind randomized controlled clinical trials of acetyl-L-carnitine versus placebo in the treatment of mild cognitive impairment and mild Alzheimer's disease. Int Clin Psychopharmacol 18: 61–71 [PubMed]
  • Oakley GP Jr (1998) Eat right and take a multivitamin. N Engl J Med 338: 1060–1061 [PubMed]
  • Pereira MA, Jacobs DR Jr, Van Horn L, Slattery ML, Kartashov AI, Ludwig DS (2002) Dairy consumption, obesity, and the insulin resistance syndrome in young adults: the CARDIA Study. JAMA 287: 2081–2089 [PubMed]
  • Platz EA, Hankinson SE, Hollis BW, Colditz GA, Hunter DJ, Speizer FE, Giovannucci E (2000a) Plasma 1,25-dihydroxy- and 25-hydroxyvitamin D and adenomatous polyps of the distal colorectum. Cancer Epidemiol Biomarkers Prev 9: 1059–1065 [PubMed]
  • Platz EA, Rimm EB, Willett WC, Kantoff PW, Giovannucci E (2000b) Racial variation in prostate cancer incidence and in hormonal system markers among male health professionals. J Natl Cancer Inst 92: 2009–2017 [PubMed]
  • Rossi L, Lippe G, Marchese E, De Martino A, Mavelli I, Rotilio G, Ciriolo MR (1998) Decrease of cytochrome c oxidase protein in heart mitochondria of copper-deficient rats. Biometals 11: 207–212 [PubMed]
  • Simopoulos AP (2001) n-3 fatty acids and human health: defining strategies for public policy. Lipids 36: S83–S89 [PubMed]
  • Smith AR, Shenvi SV, Widlansky M, Suh JH, Hagen TM (2004) Lipoic acid as a potential therapy for chronic diseases associated with oxidative stress. Curr Med Chem 11: 1135–1146 [PubMed]
  • Sturm R (2002) The effects of obesity, smoking, and drinking on medical problems and costs. Health Aff (Millwood) 21: 245–253 [PubMed]
  • Suh JH, Shenvi SV, Dixon BM, Liu H, Jaiswal AK, Liu RM, Hagen TM (2004a) Decline in transcriptional activity of Nrf2 causes age-related loss of glutathione synthesis, which is reversible with lipoic acid. Proc Natl Acad Sci USA 101: 3381–3386 [PMC free article] [PubMed]
  • Suh JH, Wang H, Liu RM, Liu J, Hagen TM (2004b) (R)-α-lipoic acid reverses the age-related loss in GSH redox status in post-mitotic tissues: evidence for increased cysteine requirement for GSH synthesis. Arch Biochem Biophy 423: 126–135 [PubMed]
  • Wakimoto P, Block G (2001) Dietary intake, dietary patterns, and changes with age: an epidemiological perspective. J Gerontol A Biol Sci Med Sci 56(S2): 65–80 [PubMed]
  • Walter PB, Knutson MD, Paler-Martinez A, Lee S, Xu Y, Viteri FE, Ames BN (2002) Iron deficiency and iron excess damage mitochondria and mitochondrial DNA in rats. Proc Natl Acad Sci USA 99: 2264–2269 [PMC free article] [PubMed]
  • Willett WC (2001) Eat, Drink and be Healthy. New York, NY, USA: Simon & Schuster
  • Ziegler D (2002) The terrible twins: neuropathy and diabetes. Diabetes Monitor p1–6

Articles from EMBO Reports are provided here courtesy of The European Molecular Biology Organization
PubReader format: click here to try

Formats:

Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...

Links

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...