Genetically Proxied Interleukin-13 Inhibition Is Associated With Risk of Psoriatic Disease: A Mendelian Randomization Study

被引:0
|
作者
Zhao, Sizheng Steven [1 ]
Hyrich, Kimme [2 ]
Yiu, Zenas [3 ,4 ]
Barton, Anne [2 ]
Bowes, John [1 ]
机构
[1] Univ Manchester, Ctr Musculoskeletal Res, Manchester, England
[2] Univ Manchester, Ctr Musculoskeletal Res, NIHR Manchester Biomed Res Ctr, Manchester, England
[3] NIHR Manchester Biomed Res Ctr, Manchester, England
[4] Northern Care Alliance NHS Fdn Trust, Manchester, England
关键词
GENOME-WIDE ASSOCIATION; 2-PHASE; 3; TRIALS; SUSCEPTIBILITY LOCI; DUPILUMAB; IDENTIFICATION; PLACEBO; IL-13; UC;
D O I
10.1002/art.42942
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectiveInhibitors of the interleukin 13 (IL-13) pathway, such as dupilumab, are licensed for atopic dermatitis and asthma. Adverse events resembling psoriatic disease after dupilumab initiation have been reported, but evidence is limited to case reports with uncertain causality. We aimed to investigate whether genetically mimicked IL-13 inhibition (IL-13i) is associated with risk of psoriatic arthritis (PsA) and psoriasis.MethodsWe instrumented IL-13i using a protein-coding variant in the IL13 gene, rs20541, that is associated with circulating eosinophil count (biomarker of IL-13i) at genome-wide significance in a study of 563,946 individuals. Outcome genetic data were taken from studies of PsA, psoriasis, and related spondyloarthritis traits in up to 10,588 cases and 209,287 controls. Colocalization analysis was performed to examine genetic confounding. We additionally used circulating IgE as a biomarker to test whether associations were replicated, both in the test and in an independent genetic dataset. We also replicated analyses using individual-level data from the UK Biobank.ResultsGenetically proxied IL-13i was associated with increased risk of PsA (odds ratio [OR] 37.39; 95% confidence interval [95% CI] 11.52-121.34; P = 1.64 x 10-9) and psoriasis (OR 20.08; 95% CI 4.38-92.01; P = 1.12 x 10-4). No consistent associations were found for Crohn disease, ulcerative colitis, ankylosing spondylitis, or iritis. Colocalization showed no strong evidence of genetic confounding for psoriatic disease. Results were replicated using circulating IgE for the exposure, using independent outcome data and using individual-level data.ConclusionWe provide supportive genetic evidence that IL-13i is linked to increased risk of PsA and psoriasis. Physicians prescribing IL-13 inhibitors should be vigilant for these adverse events. imageConclusionWe provide supportive genetic evidence that IL-13i is linked to increased risk of PsA and psoriasis. Physicians prescribing IL-13 inhibitors should be vigilant for these adverse events. image image
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收藏
页码:1602 / 1610
页数:9
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