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

被引:714
|
作者
Vimaleswaran, Karani S. [1 ,2 ]
Berry, Diane J. [1 ,2 ]
Lu, Chen [3 ]
Tikkanen, Emmi [4 ,5 ]
Pilz, Stefan [6 ,7 ]
Hiraki, Linda T. [8 ]
Cooper, Jason D. [9 ]
Dastani, Zari [10 ]
Li, Rui [11 ,12 ,13 ]
Houston, Denise K. [14 ]
Wood, Andrew R. [15 ]
Michaelsson, Karl [16 ]
Vandenput, Liesbeth [17 ]
Zgaga, Lina [18 ,19 ]
Yerges-Armstrong, Laura M. [20 ]
McCarthy, Mark I. [21 ,22 ,23 ]
Dupuis, Josee [3 ,24 ]
Kaakinen, Marika [25 ,26 ]
Kleber, Marcus E. [27 ,28 ]
Jameson, Karen [29 ]
Arden, Nigel [30 ,31 ]
Raitakari, Olli [32 ,33 ,34 ]
Viikari, Jorma [34 ,35 ]
Lohman, Kurt K. [36 ]
Ferrucci, Luigi [37 ]
Melhus, Hakan [38 ]
Ingelsson, Erik [39 ]
Byberg, Liisa [16 ]
Lind, Lars [38 ]
Lorentzon, Mattias [17 ]
Salomaa, Veikko [5 ]
Campbell, Harry [18 ]
Dunlop, Malcolm [40 ,41 ]
Mitchell, Braxton D. [20 ]
Herzig, Karl-Heinz [25 ,26 ,42 ,43 ]
Pouta, Anneli [44 ]
Hartikainen, Anna-Liisa [45 ]
Streeten, Elizabeth A. [20 ]
Theodoratou, Evropi [18 ]
Jula, Antti [5 ]
Wareham, Nicholas J. [46 ]
Ohlsson, Claes [17 ]
Frayling, Timothy M. [15 ]
Kritchevsky, Stephen B. [14 ]
Spector, Timothy D. [47 ]
Richards, J. Brent [11 ,12 ,13 ,47 ]
Lehtimaki, Terho [48 ,49 ]
Ouwehand, Willem H. [50 ,51 ,52 ]
Kraft, Peter [8 ]
Cooper, Cyrus [29 ]
机构
[1] UCL Inst Child Hlth, Ctr Paediat Epidemiol & Biostat, London, England
[2] UCL Inst Child Hlth, MRC Ctr Epidemiol Child Hlth, London, England
[3] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA USA
[4] Univ Helsinki, Inst Mol Med Finland FIMM, Helsinki, Finland
[5] Natl Inst Hlth & Welf, Helsinki, Finland
[6] Med Univ Graz, Div Endocrinol & Metab, Dept Internal Med, Graz, Austria
[7] Vrije Univ Amsterdam Med Ctr, EMGO Inst Hlth & Care Res, Dept Epidemiol & Biostat, Amsterdam, Netherlands
[8] Harvard Univ, Sch Publ Hlth, Program Mol & Genet Epidemiol, Boston, MA 02115 USA
[9] Univ Cambridge, Cambridge Inst Med Res, Dept Med Genet, Juvenile Diabet Res Fdn Wellcome Trust Diabet & I, Cambridge, England
[10] McGill Univ, Jewish Gen Hosp, Lady Davis Inst, Dept Epidemiol Biostat & Occupat Hlth, Montreal, PQ H3T 1E2, Canada
[11] McGill Univ, Jewish Gen Hosp, Lady Davis Inst, Dept Med, Montreal, PQ H3T 1E2, Canada
[12] McGill Univ, Jewish Gen Hosp, Lady Davis Inst, Dept Human Genet, Montreal, PQ H3T 1E2, Canada
[13] McGill Univ, Jewish Gen Hosp, Lady Davis Inst, Dept Epidemiol & Biostat, Montreal, PQ H3T 1E2, Canada
[14] Wake Forest Sch Med, Sect Gerontol & Geriatr Med, Dept Internal Med, Winston Salem, NC USA
[15] Univ Exeter, Peninsula Coll Med & Dent, Exeter, Devon, England
[16] Uppsala Univ, Dept Surg Sci, Uppsala, Sweden
[17] Univ Gothenburg, Inst Med, Dept Internal Med, Ctr Bone & Arthrit Res, Gothenburg, Sweden
[18] Univ Edinburgh, Ctr Populat Hlth Sci, Edinburgh, Midlothian, Scotland
[19] Univ Zagreb, Sch Med, Andrija Stampar Sch Publ Hlth, Zagreb 41001, Croatia
[20] Univ Maryland, Sch Med, Div Endocrinol, Baltimore, MD 21201 USA
[21] Univ Oxford, Churchill Hosp, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England
[22] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford, England
[23] Churchill Hosp, Oxford NIHR Biomed Res Ctr, Oxford OX3 7LJ, England
[24] NHLBI, Framingham, MA USA
[25] Univ Oulu, Inst Hlth Sci, Oulu, Finland
[26] Univ Oulu, Bioctr Oulu, Oulu, Finland
[27] LURIC Study Non Profit LLC, Freiburg, Germany
[28] Heidelberg Univ, Mannheim Inst Publ Hlth, Mannheim Med Fac, Social & Prevent Med, Mannheim, Germany
[29] Univ Southampton, MRC Lifecourse Epidemiol Unit, Southampton, Hants, England
[30] Botnar Res Ctr, NIHR Musculoskeletal BRU, Oxford, England
[31] Univ Southampton, MRC Lifecourse Epidemiol Unit, Southampton, Hants, England
[32] Univ Turku, Res Ctr Appl & Prevent Cardiovasc Med, Turku, Finland
[33] Univ Turku, Dept Clin Physiol & Nucl Med, Turku, Finland
[34] Turku Univ Hosp, FIN-20520 Turku, Finland
[35] Univ Turku, Dept Med, Turku, Finland
[36] Wake Sch Med, Div Publ Hlth Sci, Dept Biostat Sci, Winston Salem, NC USA
[37] Harbor Hosp, Clin Res Branch, Baltimore, MD USA
[38] Uppsala Univ, Dept Med Sci, Uppsala, Sweden
[39] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
[40] Univ Edinburgh, Inst Genet & Mol Med, Colon Canc Genet Grp & Acad Coloproctol, Edinburgh EH8 9YL, Midlothian, Scotland
[41] Western Gen Hosp Edinburgh, MRC Human Genet Unit, Edinburgh, Midlothian, Scotland
[42] Univ Oulu, Inst Biomed, Oulu, Finland
[43] Kuopio Univ Hosp, Dept Psychiat, SF-70210 Kuopio, Finland
[44] Univ Oulu, Dept Publ Hlth Sci & Gen Practice, Oulu, Finland
[45] Univ Oulu, Dept Obstet & Gynaecol & Publ Hlth & Gen Practice, Oulu, Finland
[46] Addenbrookes Hosp, Inst Metab Sci, MRC Epidemiol Unit, Cambridge, England
[47] Kings Coll London, Dept Twin Res & Genet Epidemiol, London WC2R 2LS, England
[48] Tampere Univ Hosp, Dept Clin Chem, Fimlab Labs, FIN-33521 Tampere, Finland
[49] Univ Tampere, FIN-33101 Tampere, Finland
[50] Univ Cambridge, Dept Haematol, Cambridge CB2 1TN, England
基金
英国医学研究理事会;
关键词
BODY-MASS INDEX; INSTRUMENTAL VARIABLES; 25-HYDROXYVITAMIN D; GENETIC-VARIANTS; D INSUFFICIENCY; D DEFICIENCY; PREVALENCE; RISK; ASSOCIATION; WEIGHT;
D O I
10.1371/journal.pmed.1001383
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 = 6.52x10(-27)). The BMI allele score was associated both with BMI (p = 6.30x10(-62)) and 25(OH) D (20.06% [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 <= 8.07x10(-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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页数:13
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