Circulating Serum 25-Hydroxyvitamin D Levels and Bone Mineral Density: Mendelian Randomization Study
Larsson SC, Melhus H, Michaëlsson K
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 41 citations
How it was studied
- Design
- Controlled clinical trial (indexed by PubMed)
- Studied in
- People
- Main outcome
- Health markers and function
Who paid for it
- Funding
- Independent funding
- Government
- Forskningsrådet om Hälsa, Arbetsliv och Välfärd
- Government
- Medical Research Council
- Grants
- Medical Research Council (MC_PC_17228)
Based on 2 listed funder(s).
Publication
- Published
- 2018-01-16 · J Bone Miner Res · vol. 33 · issue 5 · pp. 840–844
- Publisher
- Oxford University Press
- Cited
- 53 citations · more than 96% of similar papers · 4.6× the field average
- Impact
- Top 10% most cited in its field
- References
- 50 works
- Access
- Free to read
- Research areas
- Vitamin D Research Studies · Bone health and osteoporosis research · Folate and B Vitamins Research
- Keywords
- Mendelian randomization, Bone mineral, Medicine, Femoral neck, Internal medicine, Single-nucleotide polymorphism, Vitamin D and neurology, Osteoporosis, Endocrinology, Parathyroid hormone, Bone density, Biology, Genetics, Genotype, Calcium, Genetic variants
- MeSH
- femur neck, lumbar vertebrae, humans, vitamin d, absorptiometry, photon, bone density, polymorphism, single nucleotide, female, male, mendelian randomization analysis
3 authors
From SE
- Susanna C. Larsson · correspondingKarolinska Institutet
- Håkan MelhusUppsala University
- Karl MichaëlssonUppsala University
Abstract
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/cm2 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. © 2018 American Society for Bone and Mineral Research.
Abstract via Europe PMC. Copyright remains with the authors or publisher.
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