European lactase persistence genotype shows evidence of association with increase in body mass index

被引:45
|
作者
Kettunen, Johannes [1 ,2 ]
Silander, Kaisa [2 ]
Saarela, Olli [2 ]
Amin, Najaf [4 ]
Mueller, Martina [5 ,6 ,7 ]
Timpson, Nicholas [8 ]
Surakka, Ida [2 ]
Ripatti, Samuli [2 ]
Laitinen, Jaana [9 ]
Hartikainen, Anna-Liisa [10 ]
Pouta, Anneli [10 ,11 ,12 ]
Lahermo, Paeivi [3 ]
Anttila, Verneri [1 ]
Maennistoe, Satu [2 ]
Jula, Antti [2 ]
Virtamo, Jarmo [2 ]
Salomaa, Veikko [2 ]
Lehtimaeki, Terho [13 ,14 ]
Raitakari, Olli [15 ,16 ]
Gieger, Christian [6 ]
Wichmann, Erich H. [6 ,7 ,17 ]
Van Duijn, Cornelia M. [4 ]
Smith, George Davey [5 ]
McCarthy, Mark I. [18 ,19 ]
Jaervelin, Marjo-Riitta [20 ,21 ,22 ,23 ]
Perola, Markus [2 ,24 ]
Peltonen, Leena [1 ,2 ,24 ,25 ]
机构
[1] Wellcome Trust Genome Campus, Wellcome Trust Sanger Inst, Cambridge CB10 1HH, England
[2] Natl Inst Hlth & Welf, Dept Chron Dis Prevent, FIN-00251 Helsinki, Finland
[3] Univ Helsinki, Inst Mol Med Finland, Finnish Genome Ctr, FIN-00251 Helsinki, Finland
[4] Erasmus Univ, Med Ctr MC, Dept Epidemiol, NL-3000 CA Rotterdam, Netherlands
[5] Klinikum Grosshadern, Dept Med 1, D-81377 Munich, Germany
[6] Helmholtz Zentrum Munchen, German Res Ctr Environm Hlth, Inst Epidemiol, D-85764 Neuherberg, Germany
[7] Univ Munich, Inst Med Informat Biometry & Epidemiol, Chair Epidemiol, D-81377 Munich, Germany
[8] Univ Bristol, MRC Ctr Causal Anal Translat Epidemiol, Bristol BS8 2BN, Avon, England
[9] Finnish Natl Inst Occupat Hlth, FIN-90220 Oulu, Finland
[10] Univ Oulu, Dept Clin Sci Obstet & Gynecol, FIN-90014 Oulu, Finland
[11] Natl Publ Hlth Inst, FIN-90101 Oulu, Finland
[12] Univ Oulu, FIN-90101 Oulu, Finland
[13] Tampere Univ Hosp, Dept Clin Chem, FIN-33521 Tampere, Finland
[14] Univ Tampere, FIN-33521 Tampere, Finland
[15] Univ Turku, Dept Clin Physiol, FIN-20521 Turku, Finland
[16] Turku Univ, Cent Hosp, FIN-20521 Turku, Finland
[17] Univ Munich, Klinikum Grosshadern, D-81377 Munich, Germany
[18] Oxford Ctr Diabet Endocrinol & Metab, Oxford OX3 7LJ, England
[19] Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
[20] Univ London Imperial Coll Sci Technol & Med, Dept Epidemiol & Publ Hlth, London W2 1PG, England
[21] Univ Oulu, Inst Hlth Sci, FIN-90014 Oulu, Finland
[22] Natl Publ Hlth Inst, Dept Child & Adolescent Hlth, FIN-90101 Oulu, Finland
[23] Univ Oulu, Bioctr Oulu, FIN-90014 Oulu, Finland
[24] Univ Helsinki, Dept Med Genet, FIN-00014 Helsinki, Finland
[25] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
基金
英国惠康基金; 芬兰科学院;
关键词
DEFINED LACTOSE-MALABSORPTION; GENOME-WIDE ASSOCIATION; ADULT-TYPE HYPOLACTASIA; BRITISH WOMENS HEART; GEOGRAPHICAL VARIATION; CARDIOVASCULAR RISK; MILK CONSUMPTION; CALCIUM INTAKE; OBESITY; VARIANT;
D O I
10.1093/hmg/ddp561
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The global prevalence of obesity has increased significantly in recent decades, mainly due to excess calorie intake and increasingly sedentary lifestyle. Here, we test the association between obesity measured by body mass index (BMI) and one of the best-known genetic variants showing strong selective pressure: the functional variant in the cis-regulatory element of the lactase gene. We tested this variant since it is presumed to provide nutritional advantage in specific physical and cultural environments. We genetically defined lactase persistence (LP) in 31 720 individuals from eight European population-based studies and one family study by genotyping or imputing the European LP variant (rs4988235). We performed a meta-analysis by pooling the beta-coefficient estimates of the relationship between rs4988235 and BMI from the nine studies and found that the carriers of the allele responsible for LP among Europeans showed higher BMI (P = 7.9 x 10(-5)). Since this locus has been shown to be prone to population stratification, we paid special attention to reveal any population substructure which might be responsible for the association signal. The best evidence of exclusion of stratification came from the Dutch family sample which is robust for stratification. In this study, we highlight issues in model selection in the genome-wide association studies and problems in imputation of these special genomic regions.
引用
收藏
页码:1129 / 1136
页数:8
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