Genetic and environmental risk factors for rheumatoid arthritis in a UK African ancestry population: the GENRA case-control study

被引:13
|
作者
Traylor, Matthew [1 ]
Curtis, Charles [2 ]
Patel, Hamel [2 ]
Breen, Gerome [2 ]
Lee, Sang Hyuck [2 ]
Xu, Xiaohui [2 ]
Newhouse, Stephen [2 ]
Dobson, Richard [2 ]
Steer, Sophia [3 ]
Cope, Andrew P. [4 ]
Markus, Hugh S. [5 ]
Lewis, Cathryn M. [1 ,2 ]
Scott, Ian C. [1 ,4 ,6 ,7 ]
机构
[1] Kings Coll London, Dept Med & Mol Genet, London, England
[2] Kings Coll London, Inst Psychiat Psychol & Neurosci, SGDP Ctr, London, England
[3] Kings Coll Hosp London, Dept Rheumatol, London, England
[4] Kings Coll London, Ctr Mol & Cellular Biol Inflammat, Acad Dept Rheumatol, London, England
[5] Univ Cambridge, Dept Clin Neurosci, Neurol Unit, Cambridge, England
[6] Haywood Hosp, Dept Rheumatol, Burslem, England
[7] Keele Univ, Res Inst Primary Care & Hlth Sci, Keele, Staffs, England
关键词
arthritis; rheumatoid; African continental ancestry group; genetic susceptibility; smoking; GENOME-WIDE ASSOCIATION; SUSCEPTIBILITY LOCI; HLA-DRB1; DISEASE; ETHNICITY; SEVERITY; SMOKING;
D O I
10.1093/rheumatology/kex048
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. To evaluate whether genetic and environmental factors associated with RA in European and Asian ancestry populations are also associated with RA in African ancestry individuals. Methods. A case-control study was undertaken in 197 RA cases and 868 controls of African ancestry (Black African, Black Caribbean or Black British ethnicity) from South London. Smoking and alcohol consumption data at RA diagnosis was captured. Genotyping was undertaken (Multi-Ethnic Genotyping Array) and human leukocyte antigen (HLA) alleles imputed. The following European/Asian RA susceptibility factors were tested: 99 genome-wide loci combined into a genetic risk score; HLA region [20 haplotypes; shared epitope (SE)]; smoking; and alcohol consumption. The SE was tested for its association with radiological erosions. Logistic regression models were used, including ancestry-informative principal components, to control for admixture. Results. European/Asian susceptibility loci were associated with RA in African ancestry individuals. The genetic risk score provided an odds ratio (OR) for RA of 1.53 (95% CI: 1.31, 1.79; P = 1.3 x 10(-7)). HLA haplotype ORs in European and African ancestry individuals were highly correlated (r = 0.83, 95% CI: 0.56, 0.94; P = 1.1 x 10(-4)). Ever-smoking increased (OR = 2.36, 95% CI: 1.46, 3.82; P = 4.6 x 10(-4)) and drinking alcohol reduced (OR = 0.34, 95% CI: 0.20, 0.56; P = 2.7 x 10(-5)) RA risk in African ancestry individuals. The SE was associated with erosions (OR = 2.61, 95% CI: 1.36, 5.01; P = 3.9 x 10(-3)). Conclusion. Gene-environment RA risk factors identified in European/Asian ancestry populations are relevant in African ancestry individuals. As modern statistical methods facilitate analysing ancestrally diverse populations, future genetic studies should incorporate African ancestry individuals to ensure their implications for precision medicine are universally applicable.
引用
收藏
页码:1282 / 1292
页数:11
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