4.7 Article

Free 25-hydroxyvitamin D is low in obesity, but there are no adverse associations with bone health

期刊

AMERICAN JOURNAL OF CLINICAL NUTRITION
卷 103, 期 6, 页码 1465-1471

出版社

AMER SOC NUTRITION-ASN
DOI: 10.3945/ajcn.115.120139

关键词

bone density; bone turnover; half-life; obesity; vitamin D; vitamin D-binding protein

资金

  1. Department of Health [024/0052]
  2. Sheffield National Institute for Health Research Clinical Research Facility
  3. Medical Research Council (MRC)
  4. Department for International Development (DFID) under the MRC/DFID Concordat [U105960371, U123261351]
  5. Medical Research Council [MC_U105960371, MR/K006312/1] Funding Source: researchfish
  6. Royal Osteoporosis Society [366] Funding Source: researchfish
  7. MRC [MC_U105960371, MR/K006312/1] Funding Source: UKRI

向作者/读者索取更多资源

Background: The mechanism and clinical significance of low circulating 25-hydroxyvitamin D [25(OH)D] in obese people are unknown. Low total 25(OH)D may be due to low vitamin D binding proteins (DBPs) or faster metabolic clearance. However, obese people have a higher bone mineral density (BMD), which suggests that low 25(OH)D may not be associated with adverse consequences for bone. Objective: We sought to determine whether 1) vitamin D metabolism and 2) its association with bone health differ by body weight. Design: We conducted a cross-sectional observational study of 223 normal-weight, overweight, and obese men and women aged 25-75 y in South Yorkshire, United Kingdom, in the fall and spring. A subgroup of 106 subjects was also assessed in the winter. We used novel techniques, including an immunoassay for free 25(OH)D, a stable isotope for the 25(OH)D-3 half-life, and high-resolution quantitative tomography, to make a detailed assessment of vitamin D physiology and bone health. Results: Serum total 25(OH)D was lower in obese and overweight subjects than in normal-weight subjects in the fall and spring (geometric means: 45.0 and 40.8 compared with 58.6 nmol/L, respectively; P < 0.001) but not in the winter. Serum 25(OH)D was inversely correlated with body mass index (BMI) in the fall and spring and in the winter. Free 25(OH)D and 1,25-dihydroxyvitamin D [1,25(OH)(2)D] were lower in obese subjects. DBP, the DBP genotype, and the 25(OH)D-3 half-life did not differ between BMI groups. Bone turnover was lower, and bone density was higher, in obese people. Conclusions: Total and free 25(OH)D and 1,25(OH)(2)D are lower at higher BMI, which cannot be explained by lower DBP or the shorter half-life of 25(OH)D-3. We speculate that low 25(OH)D in obesity is due to a greater pool of distribution. Lower 25(OH)D may not reflect at-risk skeletal health in obese people, and BMI should be considered when interpreting serum 25(OH)D as a marker of vitamin D status.

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