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EDITORIAL ONLINE FIRST The Importance of Food I T HAS BEEN FIRMLY ESTABLISHED THAT LOW MA- ternal intake of folate creates a fetal nutrient deficiency that leads to incomplete development of the fetal nervous system. The critical period for maternal folate intake seems to be the first few weeks of fetal development. Ensuring adequate folate intake during this period is a vexing problem because the fact of pregnancy may not be known even to the mother at this early stage. The confluence of the problem of getting women of childbearing age to eat an adequate amount of folate with the observation that adequate folate helps prevent neural tube defects (NTDs) led to the addition of folic acid to grain foods in the US food supply starting in 1998.1 This strategy has been effective in getting folate to young potential mothers and also in reducing NTDs. 2 However, the strategy enhances an otherwise nutrient-poor food (refined grain foods are the primary focus of fortification; whole grain foods are naturally rich in folate) and increases folic acid in purified form to the total population. See also page 121 Despite the success of folate fortification in decreasing NTDs, in the broader context of a variety of dietary supplements, we are generally pessimistic about the value of purified supplements.3 Mursu et al3 studied consumption of 15 dietary supplements in 38 772 women initially aged 55 to 69 years with a median follow-up period of 19 years; after adjustment for lifestyle variables, 14 of the supplements were unassociated with total mortality or were associated with increased mortality. There is considerable evidence from randomized clinical trials (RCTs) that isolated supplements do not yield expected benefits and may even do harm.4 Of particular concern in regard to folic acid is the extended follow-up (median duration, 38 months) after 2 Norwegian RCTs that provided folate, pyridoxine hydrochloride (vitamin B6), and cyanocobalamin (vitamin B12) (median duration of treatment, 39 months) to men and women with ischemic heart disease.5 The pooled findings for these studies found a hazard ratio of 1.18 (95% CI, 1.04-1.33) for total mortality, 1.38 (95% CI, 1.07-1.79) for cancer mortality, and 1.21 (95% CI,1.03-1.41) for cancer incidence comparing the 3411 participants who were treated with folic acid plus cyanocobalamin and pyridoxine hydrochloride or folic acid plus cyanocobalamin with the 3426 participants who were treated with pyridoxine hydrochloride or placebo. Folate is a growth promoter, which is of benefit in the early fetal situation, but may be a detriment in cancer. Of great interest, given this conundrum of competing benefits (reduced NTDs) and risks (increased cancer or other chronic disease), Carmichael et al6 show that certain dietary patterns are strongly inversely related to reduced NTDs. Carmichaeletal6 appliedthedietpatternsconcepttoNTDs, although this approach has most commonly been used to study chronic diseases, such as cancer and cardiovascular disease,7-9 and has been used in other contexts, such as hypospadias.10 The importance of the findings of Carmichael et al6 lies in showing that women obtain benefit from the consumption of a high-quality diet, beyond the benefits derived throughgrainfortification.Thisraisesthequestionofwhether ahigh-qualitydietalonemaybesufficienttopreventNTDs—a strategy that would also remove the potential harm from fortification.5 Furthermore, a high-quality diet will contribute additional nutrients that may contribute to human development in as-yet unrecognized ways. Along these lines of thought, Carmichael et al6 contend that other constituents in food besides folate help to prevent NTDs, a notion supported by their data and in need of further investigation. For example, a living organism would likely activate a complementarypathwaytoinhibitfolate-inducedundesirablegrowth promotion. Such a complementary substance might be available in a food but not in folic acid as a supplement or added to food. We believe that a high-quality diet could have even greater benefits than those documented by Carmichael et al,6 in whose study diet patterns did not satisfy some optimality conditions. In particular, the authors did not separate whole-grain from refined-grain foods, nor dairy products by fat content, nor foods by predominant type of fat. We and others have made such distinctions,7-9 consistent with dietary recommendations. It would be interesting for Carmichael et al to use a dietary pattern score in the National Birth Defects Prevention Study that better reflects current nutritional knowledge. In addition, other databases might be queried to study data acquired prior to folate fortification; the point would be to examine the effect on NTDs of a high-quality diet in the absence of any form of folate supplementation. Food, deriving as it does from formerly living organisms, is a complex, nonrandom mixture of constituents that works well in keeping the organism alive.11 Nutrients repair deficiency conditions, such as folate in the case of NTD (deficient at least for the fetus). The fetus perhaps “doesn’t care” whether folate comes from food or supplements. Foods, however, are a balanced combination of nutrients and prevent a wide variety of chronic conditions, even in ARCH PEDIATR ADOLESC MED/ VOL 166 (NO. 2), FEB 2012 187 WWW.ARCHPEDIATRICS.COM Downloaded from www.archpediatrics.com at Kuopio University, on May 10, 2012 ©2012 American Medical Association. All rights reserved. the absence of deficiencies. The biologic systems involved in nutrition and disease are complex and not completely understood. We do know, however, that the human body did not evolve in the presence of a fortified food supply, and that some of the healthiest populations on the planet subsist, even thrive, on a whole food diet. Thus, we feel that it is reasonable to call for further exploration of the health effects, whether positive or negative, of adding isolated compounds to the food supply. The lesson from the article by Carmichael et al6 is an important one: people, including women of childbearing age, should eat good food. A good diet may be described as simply as the aphorism, “Eat food, not too much, mostly plants.”12 At the same time, we are reminded that more of a good thing is not always better. A nutrient may correct a deficiency condition but not necessarily be of benefit at higher doses in well-nourished people. The implication, based on many clinical trials of supplements, is that supplementation and its hidden partner in food, fortification, may have some dangers. Reduction of NTDs may be achievable by diet alone, at the same time reducing potential risk for other chronic diseases in the rest of the population. David R. Jacobs Jr, PhD Jaakko Mursu, PhD Katie A. Meyer, MPH, ScD Published Online: October 3, 2011. doi:10.1001 /archpediatrics.2011.184 Author Affiliations: Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis. Correspondence: Dr Jacobs, Division of Epidemiology and Community Health, School of Public Health, Uni- versity of Minnesota, 1300 S Second St, Ste 300, Minneapolis, MN 55454 ([email protected]). Financial Disclosure: None reported. REFERENCES 1. US Food and Drug Administration. Food standards: amendment of standards of identity for enriched grain products to require addition of folic acid. Fed Regist. 1996;61(4):8781-8797. 2. Wolff T, Witkop CT, Miller T, Syed SB; U.S. Preventive Services Task Force. Folic acid supplementation for the prevention of neural tube defects: an update of the evidence for the U.S. Preventive Services Task Force. Ann Intern Med. 2009; 150(9):632-639. 3. Mursu J, Robien K, Harnack LJ, Park K, Jacobs DR. Dietary supplements and mortality rate in older women: the Iowa Women’s Health Study. Arch Intern Med. 2011;171(18):1625-1633. 4. Bjelakovic G, Nikolova D, Gluud LL, Simonetti RG, Gluud C. Mortality in randomized trials of antioxidant supplements for primary and secondary prevention: systematic review and meta-analysis. JAMA. 2007;297(8):842-857. 5. Ebbing M, Bønaa KH, Nygård O, et al. Cancer incidence and mortality after treatment with folic acid and vitamin B12. JAMA. 2009;302(19):2119-2126. 6. Carmichael SL, Yang W, Feldkamp ML, et al; National Birth Defects Prevention Study. Reduced risks of neural tube defects and orofacial clefts with higher diet quality [published online October 3, 2011]. Arch Pediatr Adolesc Med. 2012; 166(2):121-126. 7. Lockheart MS, Steffen LM, Rebnord HM, et al. Dietary patterns, food groups and myocardial infarction: a case-control study. Br J Nutr. 2007;98(2):380-387. 8. Jacobs DR Jr, Sluik D, Rokling-Andersen MH, Anderssen SA, Drevon CA. Association of 1-y changes in diet pattern with cardiovascular disease risk factors and adipokines: results from the 1-y randomized Oslo Diet and Exercise Study. Am J Clin Nutr. 2009;89(2):509-517. 9. McCullough ML, Feskanich D, Stampfer MJ, et al. Diet quality and major chronic disease risk in men and women: moving toward improved dietary guidance. Am J Clin Nutr. 2002;76(6):1261-1271. 10. de Kort CA, Nieuwenhuijsen MJ, Mendez MA. Relationship between maternal dietary patterns and hypospadias. Paediatr Perinat Epidemiol. 2011;25(3):255264. 11. Jacobs DR Jr, Gross MD, Tapsell LC. Food synergy: an operational concept for understanding nutrition. Am J Clin Nutr. 2009;89(5):1543S-1548S. 12. Pollan M. In Defense of Foods. New York, NY: Penguin Press; 2008. ARCH PEDIATR ADOLESC MED/ VOL 166 (NO. 2), FEB 2012 188 WWW.ARCHPEDIATRICS.COM Downloaded from www.archpediatrics.com at Kuopio University, on May 10, 2012 ©2012 American Medical Association. All rights reserved.