4.7 Article

Associations among 25-Hydroxyvitamin D, Diet Quality, and Metabolic Disturbance Differ by Adiposity in Adults in the United States

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JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
卷 95, 期 8, 页码 3814-3827

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ENDOCRINE SOC
DOI: 10.1210/jc.2010-0410

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  1. National Institute on Aging, (NIA/NIH)

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Context: Recent evidence indicates that a higher plasma level of 25-hydroxyvitamin D [25(OH) D] is associated with lower adiposity and a reduced number of metabolic disturbances (MetD). Objectives: We examined associations among dietary quality, 25(OH) D, percent body fat (% BF), and MetD, and a pathway linking them, across central obesity. Design: This cross-sectional nationally representative study used extensive data from the National Health and Nutrition Examination Surveys of 2001-2004. Participants: U. S. adults aged at least 20 yr were stratified by central obesity (CO) status. Sample sizes ranged from 1943 (all MetD combined) to 7796 (each component). Main Outcome Measures: % BF was measured using dual-energy x-ray absorptiometry, and MetD was measured with individual continuous nonadiposity outcomes (e. g. fasting plasma glucose) and with a composite count index of binary MetD with prespecified cutoff points (Index I). Results: A higher 25(OH) D was associated with better dietary quality, lower % BF, and lower number of MetD. These inverse 25(OH) D-% BF and 25(OH) D-MetD associations (i.e. fasting blood glucose, homeostatic model assessment of insulin resistance, C-reactive protein, and Index I) were significantly stronger among the CO+ group. Finally, the pathway linking the dairy component of the Healthy Eating Index (HEIdairy) to Index I through 25(OH) D and % BF indicated complete mediation among the CO- group, but HEIdairy and 25(OH) D had direct inverse associations with Index I among the CO+ group. Conclusions: Due to potential genetic differences between CO- and CO+ groups, empowering U. S. adults with central obesity to make related behavioral changes may be especially effective in improving their vitamin D status and metabolic profile. (J Clin Endocrinol Metab 95: 3814-3827, 2010)

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