Abstract
Obesity is a major health problem. Although heritability is substantial, genetic mechanisms predisposing to obesity are not very well understood. We have performed a genome wide association study (GWA) for early onset (extreme) obesity. a) GWA (Genome-Wide Human SNP Array 5.0 comprising 440,794 single nucleotide polymorphisms) for early onset extreme obesity based on 487 extremely obese young German individuals and 442 healthy lean German controls; b) confirmatory analyses on 644 independent families with at least one obese offspring and both parents. We aimed to identify and subsequently confirm the 15 SNPs (minor allele frequency > or =10%) with the lowest p-values of the GWA by four genetic models: additive, recessive, dominant and allelic. Six single nucleotide polymorphisms (SNPs) in FTO (fat mass and obesity associated gene) within one linkage disequilibrium (LD) block including the GWA SNP rendering the lowest p-value (rs1121980; log-additive model: nominal p = 1.13 x 10(-7), corrected p = 0.0494; odds ratio (OR)(CT) 1.67, 95% confidence interval (CI) 1.22-2.27; OR(TT) 2.76, 95% CI 1.88-4.03) belonged to the 15 SNPs showing the strongest evidence for association with obesity. For confirmation we genotyped 11 of these in the 644 independent families (of the six FTO SNPs we chose only two representing the LD bock). For both FTO SNPs the initial association was confirmed (both Bonferroni corrected p<0.01). However, none of the nine non-FTO SNPs revealed significant transmission disequilibrium. Our GWA for extreme early onset obesity substantiates that variation in FTO strongly contributes to early onset obesity. This is a further proof of concept for GWA to detect genes relevant for highly complex phenotypes. We concurrently show that nine additional SNPs with initially low p-values in the GWA were not confirmed in our family study, thus suggesting that of the best 15 SNPs in the GWA only the FTO SNPs represent true positive findings.
MeSH Terms
Adipose Tissue/metabolism
Adolescent
Alpha-Ketoglutarate-Dependent Dioxygenase FTO
Child
Genome, Human
Humans
Obesity/genetics
Organ Size
Polymorphism, Single Nucleotide
Proteins/genetics
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Chemicals
Proteins
Alpha-Ketoglutarate-Dependent Dioxygenase FTO
FTO protein, human
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Hinney Anke
Department of Child and Adolescent Psychiatry, University of Duisburg-Essen, Essen, Germany.
[email protected]
Nguyen Thuy Trang
Scherag André
Friedel Susann
Brönner Günter
Müller Timo Dirk
Grallert Harald
Illig Thomas
Wichmann H-Erich
Rief Winfried
Schäfer Helmut
Hebebrand Johannes
References (17)
17 references, click to expand
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
Nature. 2007 Jun 7;447(7145):661-78
PMID: 17554300
-
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits.
PLoS Genet. 2007 Jul;3(7):e115
PMID: 17658951
-
Association of the low-density lipoprotein receptor gene with obesity in Native American populations.
Hum Genet. 2000 May;106(5):546-52
PMID: 10914685
-
Association of estrogen receptor-alpha genotypes with body mass index in normal healthy postmenopausal Caucasian women.
J Clin Endocrinol Metab. 2000 Aug;85(8):2748-51
PMID: 10946876
-
Association of polymorphisms in the estrogen receptor alpha gene with body fat distribution.
Int J Obes Relat Metab Disord. 2003 Sep;27(9):1020-7
PMID: 12917706
-
Association of HincII RFLP of low density lipoprotein receptor gene with obesity in essential hypertensives.
Clin Genet. 1995 Mar;47(3):118-21
PMID: 7634533
-
Power and sample size calculations in the presence of phenotype errors for case/control genetic association studies.
BMC Genet. 2005;6:18
PMID: 15819990
-
A common genetic variant is associated with adult and childhood obesity.
Science. 2006 Apr 14;312(5771):279-83
PMID: 16614226
-
The human obesity gene map: the 2005 update.
Obesity (Silver Spring). 2006 Apr;14(4):529-644
PMID: 16741264
-
Significant association of a M129V independent polymorphism in the 5' UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study.
J Med Genet. 2006 Oct;43(10):e53
PMID: 17047093
-
A genome-wide association study identifies novel risk loci for type 2 diabetes.
Nature. 2007 Feb 22;445(7130):881-5
PMID: 17293876
-
What genome-wide association studies can do for medicine.
N Engl J Med. 2007 Mar 15;356(11):1094-7
PMID: 17360987
-
Upward bias in odds ratio estimates from genome-wide association studies.
Genet Epidemiol. 2007 May;31(4):288-95
PMID: 17266119
-
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity.
Science. 2007 May 11;316(5826):889-94
PMID: 17434869
-
Variation in FTO contributes to childhood obesity and severe adult obesity.
Nat Genet. 2007 Jun;39(6):724-6
PMID: 17496892
-
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.
Science. 2007 Jun 1;316(5829):1341-5
PMID: 17463248
-
Heterogeneity in meta-analyses of genome-wide association investigations.
PLoS One. 2007;2(9):e841
PMID: 17786212