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 citas
Cómo se estudió
- Diseño
- Ensayo clínico controlado (indexado por PubMed)
- Estudiado en
- Personas
- Resultado principal
- Marcadores de salud y funcionamiento
Quién lo pagó
- Financiación
- Financiación independiente
- Gobierno
- Forskningsrådet om Hälsa, Arbetsliv och Välfärd
- Gobierno
- Medical Research Council
- Subvenciones
- Medical Research Council (MC_PC_17228)
Según 2 financiadores declarados.
Publicación
- Publicado
- 2018-01-16 · J Bone Miner Res · vol. 33 · número 5 · págs. 840–844
- Editorial
- Oxford University Press
- Citado
- 53 citas · más que el 96% de estudios similares · 4.6× el promedio de su campo
- Impacto
- Entre el 10 % más citado de su campo
- Referencias
- 50 trabajos
- Acceso
- Lectura gratuita
- Áreas de investigación
- Vitamin D Research Studies · Bone health and osteoporosis research · Folate and B Vitamins Research
- Palabras clave
- 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 autores
- Susanna C. Larsson🇸🇪 · autor de correspondenciaKarolinska Institutet
- Håkan Melhus🇸🇪Uppsala University
- Karl Michaëlsson🇸🇪Uppsala University
Resumen
El texto original del estudio, en el idioma en que se publicó.
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.
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