Variation in FTO contributes to childhood obesity and severe adult obesity

被引:1537
作者
Dina, Christian [1 ]
Meyre, David
Gallina, Sophie
Durand, Emmanuelle
Koerner, Antje
Jacobson, Peter
Carlsson, Lena M. S.
Kiess, Wieland
Vatin, Vincent
Lecoeur, Cecile
Delplanque, Jerome
Vaillant, Emmanuel
Pattou, Francois
Ruiz, Juan
Weill, Jacques
Levy-Marchal, Claire
Horber, Fritz
Potoczna, Natascha
Hercberg, Serge
Le Stunff, Catherine
Bougneres, Pierre
Kovacs, Peter
Marre, Michel
Balkau, Beverley
Cauchi, Stephane
Chevre, Jean-Claude
Froguel, Philippe
机构
[1] Inst Pasteur, CNRS 8090, Inst Biol, F-59019 Lille, France
[2] Univ Leipzig, Univ Hosp Children & Adolescents, D-7010 Leipzig, Germany
[3] Univ Gothenburg, Sahlgrenska Acad, Inst Med, Dept Mol & Clin Med, S-40020 Gothenburg, Sweden
[4] Univ Lille 2, INSERM, U859, F-59045 Lille, France
[5] CHU Vaudois, Lausanne, Switzerland
[6] Jeanne Flandre Hosp, Paediat Endocrine Unit, Lille, France
[7] Hop Robert Debre, INSERM, U690, F-75019 Paris, France
[8] Klin Lindberg, Winterthur, Switzerland
[9] INRA, U1125, Bobigny, France
[10] INSERM, U557, Bobigny, France
[11] CNAM, EA3200, Paris, France
[12] Univ Paris 13, Paris, France
[13] CRNH, Paris, France
[14] Univ Paris 05, St Vincent Paul Hosp, Dept Pediat Endocrinol, F-75005 Paris, France
[15] Univ Paris 05, St Vincent Paul Hosp, INSERM U561, F-75005 Paris, France
[16] Univ Leipzig, Dept Internal Med 2, D-7010 Leipzig, Germany
[17] Univ Leipzig, Interdisciplinary Ctr Clin Res, D-7010 Leipzig, Germany
[18] Hop Bichat Claude Bernard, AP HP, Dept Diabetol, F-75877 Paris 18, France
[19] INSERM, U780, IFR69, Villejuif, France
[20] Univ Paris Sud, Villejuif, France
[21] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, London SW7 2AY, England
基金
英国医学研究理事会;
关键词
D O I
10.1038/ng2048
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We identified a set of SNPs in the first intron of the FTO (fat mass and obesity associated) gene on chromosome 16q12.2 that is consistently strongly associated with early-onset and severe obesity in both adults and children of European ancestry with an experiment-wise P value of 1.67 x 10(-26) in 2,900 affected individuals and 5,100 controls. The at- risk haplotype yields a proportion of attributable risk of 22% for common obesity. We conclude that FTO contributes to human obesity and hence may be a target for subsequent functional analyses.
引用
收藏
页码:724 / 726
页数:3
相关论文
共 12 条
  • [1] The SU.VI.MAX study -: A randomized, placebo-controlled trial of the health effects of antioxidant vitamins and minerals
    Hercberg, S
    Galan, P
    Preziosi, P
    Bertrais, S
    Mennen, L
    Malvy, D
    Roussel, AM
    Favier, P
    Briançon, S
    [J]. ARCHIVES OF INTERNAL MEDICINE, 2004, 164 (21) : 2335 - 2342
  • [2] Spouse resemblance in body mass index:: Effects on adult obesity prevalence in the offspring generation
    Jacobson, Peter
    Torgerson, Jarl S.
    Sjostrom, Lars
    Bouchard, Claude
    [J]. AMERICAN JOURNAL OF EPIDEMIOLOGY, 2007, 165 (01) : 101 - 108
  • [3] Evaluation of regulatory potential and conservation scores for detecting cis-regulatory modules in aligned mammalian genome sequences
    King, DC
    Taylor, J
    Elnitski, L
    Chiaromonte, F
    Miller, W
    Hardison, RC
    [J]. GENOME RESEARCH, 2005, 15 (08) : 1051 - 1060
  • [4] KORNER A, 2007, J CLIN ENDOCRINOL ME
  • [5] Increased insulin resistance to obese children who have both 972 IRS-1 and 1057 IRS-2 polymorphisms
    Le Fur, S
    Le Stunff, C
    Bougnères, P
    [J]. DIABETES, 2002, 51 : S304 - S307
  • [6] Loos RJF, 2007, SCIENCE, V315, DOI [10.1126/science.1130012, 10.1126/science.1129402, 10.1126/science.1130571]
  • [7] A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other
    Nyholt, DR
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (04) : 765 - 769
  • [8] Association of genetic loci - Replication or not, that is the question
    Ott, J
    [J]. NEUROLOGY, 2004, 63 (06) : 955 - 958
  • [9] Mouse Chromosome 2
    Peters, J
    Church, D
    Zuberi, AR
    Selley, R
    [J]. MAMMALIAN GENOME, 1999, 10 (10) : 941 - 941
  • [10] Anisomastia associated with interstitial duplication of chromosome 16, mental retardation, obesity, dysmorphic facies, and digital anomalies:: Molecular mapping of a new syndrome by fluorescent in situ hybridization and microsatellites to 16q13 (D16S419-D16S503)
    Stratakis, CA
    Lafferty, A
    Taymans, SE
    Gafni, RI
    Meck, JM
    Blancato, J
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (09) : 3396 - 3401