Circulating Serum 25-Hydroxyvitamin D Levels and Bone Mineral Density: Mendelian Randomization Study

被引:41
|
作者
Larsson, Susanna C. [1 ]
Melhus, Hakan [2 ]
Michaelsson, Karl [3 ]
机构
[1] Karolinska Inst, Inst Environm Med, Unit Nutr Epidemiol, S-17177 Stockholm, Sweden
[2] Uppsala Univ, Dept Med Sci, Uppsala, Sweden
[3] Uppsala Univ, Dept Surg Sci, Unit Orthoped, Uppsala, Sweden
基金
瑞典研究理事会;
关键词
BONE MINERAL DENSITY; MENDELIAN RANDOMIZATION; OSTEOPOROSIS; SINGLE-NUCLEOTIDE POLYMORPHISMS; VITAMIN D; VITAMIN-D DEFICIENCY; CALCIUM-ABSORPTION; CONTROLLED-TRIAL; CLINICAL-TRIAL; OLDER WOMEN; DISEASE; OSTEOPOROSIS; METAANALYSIS; ASSOCIATION; MORTALITY;
D O I
10.1002/jbmr.3389
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There is considerable discussion of the importance for increased serum 25-hydroxyvitamin D (S-25OHD) concentration associated with adequacy for bone health. Accordingly, whether long-term high S-25OHD concentration in general positively affects bone mineral density (BMD) is uncertain. We used a Mendelian randomization design to determine the association between genetically increased S-25OHD concentrations and BMD. Five single-nucleotide polymorphisms (SNPs) in or near genes encoding enzymes and carrier proteins involved in vitamin D synthesis or metabolism were used as instrumental variables to genetically predict 1 standard deviation increase in S-25OHD concentration. Summary statistics data for the associations of the S-25OHD-associated SNPs with dual-energy X-ray absorptiometry (DXA)-derived femoral neck and lumbar spine BMD were obtained from the Genetic Factors for Osteoporosis (GEFOS) Consortium (32,965 individuals) and ultrasound-derived heel estimated BMD from the UK Biobank (142,487 individuals). None of the SNPs were associated with BMD at Bonferroni-corrected significance level, but there was a suggestive association between rs6013897 near CYP24A1 and femoral neck BMD (p=0.01). In Mendelian randomization analysis, genetically predicted 1 standard deviation increment of S-25OHD was not associated with higher femoral neck BMD (SD change in BMD 0.02; 95% confidence interval [CI] -0.03 to 0.07; p=0.37), lumbar spine BMD (SD change in BMD 0.02; 95% CI -0.04 to 0.08; p=0.49), or estimated BMD (g/cm(2) change in BMD -0.03; 95% CI -0.05 to -0.01; p=0.02). This study does not support a causal association between long-term elevated S-25OHD concentrations and higher BMD in generally healthy populations. These results suggest that more emphasis should be placed on the development of evidence-based cut-off points for vitamin D inadequacy rather than a general recommendation to increase S-25OHD. (C) 2018 American Society for Bone and Mineral Research.
引用
收藏
页码:840 / 844
页数:5
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