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PMID: 18218107 Published · epublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

FTO gene SNPs associated with extreme obesity in cases, controls and extremely discordant sister pairs.

BMC medical genetics ·Vol. 9 ·2008-01-24 ·Pages 4

Price RA, Li WD, Zhao H

Abstract

FTO is a gene located in chromosome region 16q12.2. Recently two studies have found associations of several single nucleotide polymorphisms (SNPs) in FTO with body mass index (BMI) and obesity, particularly rs1421085, rs17817449, and rs9939609. We examined these three SNPs in 583 extremely obese women with current BMI greater than 35 kg/m2 and lifetime BMI greater than 40 kg/m2, and 544 controls who were currently normal weight (BMI<25 kg/m2) and had never been overweight during their lifetimes. We detected highly significant associations of obesity with alleles in all three SNPs (p < 10-9). The strongest association was with rs1421085 (p = 3.04 x 10-10, OR = 1.75, CI = 1.47-2.08). A subset of 99 cases had extremely discordant sisters with BMI<25 kg/m2. The discordant sisters differed in allele and genotype frequencies in parallel with the overall case and control sample. The strongest association was with rs17817449 (z = 3.57, p = 3.6 x 10-4). These results suggest common variability in FTO is associated with increased obesity risk or resistance and may in part account for differences between closely related individuals.

MeSH Terms
Adolescent Adult Aged Alpha-Ketoglutarate-Dependent Dioxygenase FTO Body Mass Index Case-Control Studies Female Genetic Markers Humans Linkage Disequilibrium Middle Aged Obesity, Morbid/genetics Polymorphism, Single Nucleotide Proteins/genetics
Chemicals
Genetic Markers Proteins Alpha-Ketoglutarate-Dependent Dioxygenase FTO FTO protein, human
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Price R Arlen
Center for Neurobiology and Behavior, Department of Psychiatry, University of Pennsylvania, Philadelphia, Pennsylvania, USA. [email protected]
Li Wei-Dong
Zhao Hongyu
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Article Info
Journal
BMC medical genetics
Abbr.
BMC Med Genet
ISSN
1471-2350
Published
2008-01-24
Epub
2008-00-24
Pages
4
Language
English
Region
England
NLM ID
100968552
PMCID
PMC2254593
Subset
IM
Grants
NIDDK NIH HHS · R01 DK044073 · United States
NIDDK NIH HHS · R01 DK056210 · United States
NIDDK NIH HHS · R01DK44073 · United States
NIDDK NIH HHS · R01DK56210 · United States
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