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

Karani S. Vimaleswaran(University College London), Diane J. Berry(University College London), Lu Chen(Boston University), Emmi Tikkanen(University of Helsinki), Stefan Pilz(Medical University of Graz), Linda T. Hiraki(Harvard University), Jason D. Cooper(University of Cambridge), Zari Dastani(Jewish General Hospital), Rui Li(Jewish General Hospital), Denise K. Houston(Wake Forest University), Andrew R. Wood(University of Exeter), Karl Michaëlsson(Uppsala University), Liesbeth Vandenput(University of Gothenburg), Lina Zgaga(University of Zagreb), Laura M. Yerges-Armstrong(University of Maryland, Baltimore), Mark I. McCarthy(Centre for Human Genetics), Josée Dupuis(Boston University), Marika Kaakinen(University of Oulu), Marcus E. Kleber(University of Mannheim), Anthony James(MRC Lifecourse Epidemiology Unit), Nigel Arden(NIHR Oxford Musculoskeletal Biomedical Research Centre), Olli Raitakari(University of Turku), Jorma Viikari(University of Turku), Kurt K. Lohman(Wake Forest University), Luigi Ferrucci(MedStar Harbor Hospital), Håkan Melhus(Uppsala University), Erik Ingelsson(Karolinska Institutet), Liisa Byberg(Uppsala University), Lars Lind(Uppsala University), Mattias Lorentzon(University of Gothenburg), Veikko Salomaa(Finnish Institute for Health and Welfare), Harry Campbell(University of Edinburgh), Malcolm G. Dunlop(Western General Hospital), Braxton D. Mitchell(University of Maryland, Baltimore), Karl-Heinz Herzig(Kuopio University Hospital), Anneli Pouta(University of Oulu), Anna-Liisa Hartikainen(University of Oulu), Elizabeth A. Streeten(University of Maryland, Baltimore), Evropi Τheodoratou(University of Edinburgh), Antti Jula(Finnish Institute for Health and Welfare), Nicholas J. Wareham(Addenbrooke's Hospital), Claes Ohlsson(University of Gothenburg), Timothy M. Frayling(University of Exeter), Stephen B. Kritchevsky(Wake Forest University), Timothy D. Spector(King's College London), J. Brent Richards(King's College London), Terho Lehtimäki(Tampere University), Willem H. Ouwehand(NHS Blood and Transplant), Peter Kraft(Harvard University), Cyrus Cooper(MRC Lifecourse Epidemiology Unit), Winfried März(University of Mannheim), Chris Power(University College London), Ruth J. F. Loos(Addenbrooke's Hospital), Thomas J. Wang(Massachusetts General Hospital), Marjo‐Riitta Järvelin(Finnish Institute for Health and Welfare), John C. Whittaker(GlaxoSmithKline (United Kingdom)), Aroon D. Hingorani(University College London), Elina Hyppönen(University College London)
PLoS Medicine
February 5, 2013
Cited by 1,053Open Access
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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.


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