Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits
Open accessAbstract
The obesity epidemic is responsible for a substantial economic burden in developed countries and is a major risk factor for type 2 diabetes and cardiovascular disease. The disease is the result not only of several environmental risk factors, but also of genetic predisposition. To take advantage of recent advances in gene-mapping technology, we executed a genome-wide association scan to identify genetic variants associated with obesity-related quantitative traits in the genetically isolated population of Sardinia. Initial analysis suggested that several SNPs in the FTO and PFKP genes were associated with increased BMI, hip circumference, and weight. Within the FTO gene, rs9930506 showed the strongest association with BMI (p = 8.6 x10(-7)), hip circumference (p = 3.4 x 10(-8)), and weight (p = 9.1 x 10(-7)). In Sardinia, homozygotes for the rare "G" allele of this SNP (minor allele frequency = 0.46) were 1.3 BMI units heavier than homozygotes for the common "A" allele. Within the PFKP gene, rs6602024 showed very strong association with BMI (p = 4.9 x 10(-6)). Homozygotes for the rare "A" allele of this SNP (minor allele frequency = 0.12) were 1.8 BMI units heavier than homozygotes for the common "G" allele. To replicate our findings, we genotyped these two SNPs in the GenNet study. In European Americans (N = 1,496) and in Hispanic Americans (N = 839), we replicated significant association between rs9930506 in the FTO gene and BMI (p-value for meta-analysis of European American and Hispanic American follow-up samples, p = 0.001), weight (p = 0.001), and hip circumference (p = 0.0005). We did not replicate association between rs6602024 and obesity-related traits in the GenNet sample, although we found that in European Americans, Hispanic Americans, and African Americans, homozygotes for the rare "A" allele were, on average, 1.0-3.0 BMI units heavier than homozygotes for the more common "G" allele. In summary, we have completed a whole genome-association scan for three obesity-related quantitative traits and report that common genetic variants in the FTO gene are associated with substantial changes in BMI, hip circumference, and body weight. These changes could have a significant impact on the risk of obesity-related morbidity in the general population.
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The underlying loci of these two SNPs, FTO and MC4R, are well established obesity-related loci.
“The underlying loci of these two SNPs, FTO and MC4R, are well established obesity-related loci [35, 36, 45].”
From Causal relationship between obesity and serum testosterone status in men: A bi-directional mendelian randomization analysis (2017) · cites this paper as [35]
Similar results were also obtained using a genetic risk score based solely on the SNP in the FTO gene.
“Secondly, similar results were also obtained using a genetic risk score based solely on the SNP in the FTO gene, which is a gene that has been found to be associated with BMI in numerous studies, where none of the cohorts used in the present study were included [34–36].”
From Causal relationship between obesity and serum testosterone status in men: A bi-directional mendelian randomization analysis (2017) · cites this paper as [35]
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References 57 · Cited by 1,724
Research works printed but not linked: 1
- Chen WM, Abecasis GR (2007) Family Based Association Tests for Genome Wide Association Scans. Am J Hum Genet. In press.
- Authors
- Scuteri, A., Sanna, S., Chen, W.-M., Uda, M., Albai, G., Strait, J., Najjar, S., Nagaraja, R., Orrú, M., Usala, G., Dei, M., Lai, S., Maschio, A., Busonero, F., Mulas, A., Ehret, G. B., Fink, A. A., Weder, A. B., Cooper, R. S., Galan, P., Chakravarti, A., Schlessinger, D., Cao, A., Lakatta, E., & Abecasis, G. R.
- Affiliations
- National Institute on Aging (US)
- University of Michigan (US)
- Institute of Genetic and Biomedical Research (IT)
- Johns Hopkins University (US)
- Loyola University Chicago (US)
- Conservatoire National des Arts et Métiers (FR)
- Corresponding author
- Schlessinger, David
- Abecasis, Gonçalo R
- ORCID
- Venue
- PLoS Genetics
- Publisher
- Public Library of Science (PLoS)
- Published
- 2007-07-20
- Volume
- 3
- Issue
- 7
- Pages
- e115
- ISSN
- 1553-7390 (ISSN-L)
- 1553-7404
- PMC
- PMC1934391
- OpenAlex
- W2110678911
- Cited by
- 1,724
- References
- 57
- Citations by year
- 2026: 25 · 2025: 42 · 2024: 58 · 2023: 68 · 2022: 69 · 2021: 87 · 2020: 89 · 2019: 71 · 2018: 88 · 2017: 81 · 2016: 90 · 2015: 98 · 2014: 104 · 2013: 122 · 2012: 117
- FWCI
- 71.33
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- PLoS Genetics (publishedVersion, public-domain)
- Europe PMC (PubMed Central) (publishedVersion, other-oa)
- PubMed Central (publishedVersion, public-domain)
- PubMed (publishedVersion)
- Civil War Book Review (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- UNICA IRIS Institutional Research Information System (University of Cagliari) (submittedVersion)
- UnissResearch (Università degli Studi di Sassari) (submittedVersion)
- Funders
- University of Michigan
- National Institutes of Health (NO1-AG-1–2109, 263-MA-410953)
- U.S. Public Health Service (263-MA-410953)
- National Institute on Aging (N01-AG-12109)
- National Heart, Lung, and Blood Institute (U01HL084729, HL-084729)
- National Human Genome Research Institute (HG02651, R01HG002651)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Physical Performance
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Nutrition, Genetics, and Disease
- Keywords
- FTO, obesity, body mass index, hip circumference, weight, single nucleotide polymorphisms, genetic susceptibility, Sardinian population, Hispanic Americans, African Americans, obesity-related traits, type 2 diabetes risk, cardiovascular risk
- MeSH terms
- Alpha-Ketoglutarate-Dependent Dioxygenase FTO, Adolescent, Adult, Aged, Aged, 80 and over, Alleles, Body Weight, Female, Humans, Male, Middle Aged, Obesity, Proteins, Genetic Variation, Linkage Disequilibrium, Genome, Human, Body Mass Index, Genetic Predisposition to Disease, Polymorphism, Single Nucleotide, Phosphofructokinases, Quantitative Trait Loci, Adiposity
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