Causal Relationship Between Obesity and Vitamin D Status: Bi-Directional Mendelian Randomization Analysis of Multiple Cohorts

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Author
Vimaleswaran, Karani S.
Berry, Diane J.
Lu, Chen
Tikkanen, Emmi
Pilz, Stefan
Cooper, Jason D.
Dastani, Zari
Li, Rui
Houston, Denise K.
Wood, Andrew R.
Michaëlsson, Karl
Vandenput, Liesbeth
Zgaga, Lina
Yerges-Armstrong, Laura M.
McCarthy, Mark I.
Dupuis, Josée
Kaakinen, Marika
Kleber, Marcus E.
Jameson, Karen
Arden, Nigel
Raitakari, Olli
Viikari, Jorma
Lohman, Kurt K.
Ferrucci, Luigi
Melhus, Håkan
Ingelsson, Erik
Byberg, Liisa
Lind, Lars
Lorentzon, Mattias
Salomaa, Veikko
Campbell, Harry
Dunlop, Malcolm
Mitchell, Braxton D.
Herzig, Karl-Heinz
Pouta, Anneli
Hartikainen, Anna-Liisa
Streeten, Elizabeth A.
Theodoratou, Evropi
Jula, Antti
Wareham, Nicholas J.
Ohlsson, Claes
Frayling, Timothy M.
Kritchevsky, Stephen B.
Spector, Timothy D.
Richards, J. Brent
Lehtimäki, Terho
Ouwehand, Willem H.
Kraft, Peter
Cooper, Cyrus
März, Winfried
Power, Chris
Loos, Ruth J. F.
Järvelin, Marjo-Riitta
Whittaker, John C.
Hingorani, Aroon D.
Hyppönen, Elina
Genetic Investigation of Anthropometric Traits (GIANT) consortium
Note: Order does not necessarily reflect citation order of authors.
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https://doi.org/10.1371/journal.pmed.1001383Metadata
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Vimaleswaran, Karani S., Diane J. Berry, Chen Lu, Emmi Tikkanen, Stefan Pilz, Linda T. Hiraki, Jason D. Cooper, and et al. 2013. Causal relationship between obesity and vitamin D status: Bi-directional Mendelian randomization analysis of multiple cohorts. PLoS Medicine 10(2): e1001383.Abstract
Background: Obesity is associated with vitamin D deficiency, and both are areas of active public health concern. We explored the causality and direction of the relationship between body mass index (BMI) and 25-hydroxyvitamin D [25(OH)D] using genetic markers as instrumental variables (IVs) in bi-directional Mendelian randomization (MR) analysis. Methods and findings: We used information from 21 adult cohorts (up to 42,024 participants) with 12 BMI-related SNPs (combined in an allelic score) to produce an instrument for BMI and four SNPs associated with 25(OH)D (combined in two allelic scores, separately for genes encoding its synthesis or metabolism) as an instrument for vitamin D. Regression estimates for the IVs (allele scores) were generated within-study and pooled by meta-analysis to generate summary effects. Associations between vitamin D scores and BMI were confirmed in the Genetic Investigation of Anthropometric Traits (GIANT) consortium (n = 123,864). Each \(1 kg/m^{2}\) higher BMI was associated with 1.15% lower 25(OH)D \((p = 6.52×10^{−27})\). The BMI allele score was associated both with BMI \((p = 6.30×10^{−62})\) and 25(OH)D (−0.06% [95% CI −0.10 to −0.02], p = 0.004) in the cohorts that underwent meta-analysis. The two vitamin D allele scores were strongly associated with 25(OH)D \((p≤8.07×10^{−57}\) for both scores) but not with BMI (synthesis score, p = 0.88; metabolism score, p = 0.08) in the meta-analysis. A 10% higher genetically instrumented BMI was associated with 4.2% lower 25(OH)D concentrations (IV ratio: −4.2 [95% CI −7.1 to −1.3], p = 0.005). No association was seen for genetically instrumented 25(OH)D with BMI, a finding that was confirmed using data from the GIANT consortium (p≥0.57 for both vitamin D scores). Conclusions: On the basis of a bi-directional genetic approach that limits confounding, our study suggests that a higher BMI leads to lower 25(OH)D, while any effects of lower 25(OH)D increasing BMI are likely to be small. Population level interventions to reduce BMI are expected to decrease the prevalence of vitamin D deficiency. Please see later in the article for the Editors' Summary.Other Sources
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3564800/pdf/Terms of Use
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