Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

被引:1290
作者
Barrett, Jeffrey C. [2 ]
Clayton, David G. [1 ,2 ]
Concannon, Patrick [3 ]
Akolkar, Beena [4 ]
Cooper, Jason D. [2 ]
Erlich, Henry A. [5 ]
Julier, Cecile [6 ]
Morahan, Grant [7 ,8 ]
Nerup, Jorn [9 ,10 ]
Nierras, Concepcion [11 ]
Plagnol, Vincent [2 ]
Pociot, Flemming [9 ,10 ]
Schuilenburg, Helen [2 ]
Smyth, Deborah J. [2 ]
Stevens, Helen [2 ]
Todd, John A. [2 ]
Walker, Neil M. [2 ]
Rich, Stephen S. [3 ,12 ]
机构
[1] Univ Virginia, Dept Biochem & Mol Genet, Charlottesville, VA 22903 USA
[2] Univ Cambridge, Addenbrookes Hosp, Cambridge Inst Med Res,Juvenile Diabet Res Fdn, Dept Med Genet,Wellcom Trust Diabet & Inflammat L, Cambridge CB2 2QQ, England
[3] Univ Virginia, Ctr Publ Hlth Genom, Charlottesville, VA USA
[4] NIDDK, Div Diabet Endocrinol & Metab Dis, NIH, Bethesda, MD USA
[5] Roche Mol Syst, Pleasanton, CA USA
[6] INSERM, U958, Ctr Natl Genotypage, Evry, France
[7] Western Australia Inst Med Res, Ctr Diabet Res, Perth, WA, Australia
[8] Univ Western Australia, Med Res Ctr, Perth, WA 6009, Australia
[9] Steno Diabet Ctr, DK-2820 Gentofte, Denmark
[10] Hagedorn Res Inst, Gentofte, Denmark
[11] Juvenile Diabet Res Fdn, New York, NY USA
[12] Univ Virginia, Dept Publ Hlth Sci, Div Biostat & Epidemiol, Charlottesville, VA USA
基金
英国医学研究理事会; 英国惠康基金;
关键词
SUSCEPTIBILITY LOCUS; CHROMOSOME; DISEASE; REGION; GENES; HLA; VARIANTS; MELLITUS; PTPN22; TESTS;
D O I
10.1038/ng.381
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Type 1 diabetes (T1D) is a common autoimmune disorder that arises from the action of multiple genetic and environmental risk factors. We report the findings of a genome-wide association study of T1D, combined in a meta-analysis with two previously published studies. The total sample set included 7,514 cases and 9,045 reference samples. Forty-one distinct genomic locations provided evidence for association with T1D in the meta-analysis (P < 10(-6)). After excluding previously reported associations, we further tested 27 regions in an independent set of 4,267 cases, 4,463 controls and 2,319 affected sib-pair (ASP) families. Of these, 18 regions were replicated (P < 0.01; overall P < 5 x 10(-8)) and 4 additional regions provided nominal evidence of replication (P < 0.05). The many new candidate genes suggested by these results include IL10, IL19, IL20, GLIS3, CD69 and IL27.
引用
收藏
页码:703 / 707
页数:5
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