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 3′ untranslated region of the
LEP
gene is novel.