Appetite regulation genes are associated with body mass index in black South African adolescents: a genetic association study

被引:32
作者
Lombard, Zane [1 ,2 ]
Crowther, Nigel J. [2 ,3 ]
van der Merwe, Lize [4 ,5 ]
Pitamber, Punita [1 ,2 ]
Norris, Shane A. [6 ]
Ramsay, Michele [1 ,2 ]
机构
[1] Natl Hlth Lab Serv, Fac Hlth Sci, Sch Pathol, Div Human Genet, Johannesburg, South Africa
[2] Univ Witwatersrand, Johannesburg, South Africa
[3] Natl Hlth Lab Serv, Dept Chem Pathol, Sch Pathol, Fac Hlth Sci, Johannesburg, South Africa
[4] MRC, Biostat Unit, Cape Town, South Africa
[5] Univ Western Cape, Dept Stat, Cape Town, South Africa
[6] Univ Witwatersrand, MRC Wits Dev Pathways Hlth Res Unit, Dept Paediat, Sch Clin Med,Fac Hlth Sci, Johannesburg, South Africa
来源
BMJ OPEN | 2012年 / 2卷 / 03期
基金
新加坡国家研究基金会; 英国惠康基金; 英国医学研究理事会;
关键词
GENOME-WIDE ASSOCIATION; Y2 RECEPTOR GENES; POPULATION-STRUCTURE; LEPTIN GENE; WEST AFRICANS; PEPTIDE YY; OBESITY; VARIANTS; POLYMORPHISM; ADIPOSITY;
D O I
10.1136/bmjopen-2012-000873
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Obesity is a complex trait with both environmental and genetic contributors. Genome-wide association studies have identified several variants that are robustly associated with obesity and body mass index (BMI), many of which are found within genes involved in appetite regulation. Currently, genetic association data for obesity are lacking in Africans-a single genome-wide association study and a few replication studies have been published in West Africa, but none have been performed in a South African population. Objective: To assess the association of candidate loci with BMI in black South Africans. The authors focused on single nucleotide polymorphisms (SNPs) in the FTO, LEP, LEPR, MC4R, NPY2R and POMC genes. Design: A genetic association study. Participants: 990 randomly selected individuals from the larger Birth to Twenty cohort (a longitudinal birth cohort study of health and development in Africans). Measures: The authors genotyped 44 SNPs within the six candidate genes that included known BMI-associated SNPs and tagSNPs based on linkage disequilibrium in an African population for FTO, LEP and NPY2R. To assess population substructure, the authors included 18 ancestry informative markers. Weight, height, sex, sex-specific pubertal stage and exact age collected during adolescence (13 years) were used to identify loci that predispose to obesity early in life. Results: Sex, sex-specific pubertal stage and exact age together explain 14.3% of the variation in log(BMI) at age 13. After adjustment for these factors, four SNPs were individually significantly associated with BMI: FTO rs17817449 (p=0.022), LEP rs10954174 (p=0.0004), LEP rs6966536 (p=0.012) and MC4R rs17782313 (p=0.045). Together the four SNPs account for 2.1% of the variation in log(BMI). Each risk allele was associated with an estimated average increase of 2.5% in BMI. Conclusions: The study highlighted SNPs in FTO and MC4R as potential genetic markers of obesity risk in South Africans. The association with two SNPs in the 39 untranslated region of the LEP gene is novel.
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页数:10
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