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
引用
收藏
页码:1602 / 1610
页数:9
相关论文
共 50 条
  • [1] Genetically Proxied Inhibition of Coagulation Factors and Risk of Cardiovascular Disease: A Mendelian Randomization Study
    Yuan, Shuai
    Burgess, Stephen
    Laffan, Mike
    Mason, Amy M.
    Dichgans, Martin
    Gill, Dipender
    Larsson, Susanna C.
    JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2021, 10 (08):
  • [2] Cardiovascular safety of genetically proxied interleukin-5 inhibition: A mendelian randomization study
    Alton, Philip
    Hughes, David M.
    Zhao, Sizheng Steven
    RESPIRATORY INVESTIGATION, 2023, 61 (02) : 149 - 152
  • [3] Genetically proxied therapeutic inhibition of lipid-lowering drug targets and risk of rheumatoid arthritis disease: a Mendelian randomization study
    Liang Qiao
    Shun Lv
    Kai Meng
    Jianmei Yang
    Clinical Rheumatology, 2024, 43 : 939 - 947
  • [4] Genetically proxied therapeutic inhibition of lipid-lowering drug targets and risk of rheumatoid arthritis disease: a Mendelian randomization study
    Qiao, Liang
    Lv, Shun
    Meng, Kai
    Yang, Jianmei
    CLINICAL RHEUMATOLOGY, 2024, 43 (03) : 1063 - 1071
  • [5] Relationship between genetically proxied vitamin D and psoriasis risk: a Mendelian randomization study
    Bohmann, Patricia
    Stein, Michael J.
    Konzok, Julian
    Tsoi, Lam C.
    Elder, James T.
    Leitzmann, Michael F.
    Baumeister, Sebastian-Edgar
    Baurecht, Hansjoerg
    CLINICAL AND EXPERIMENTAL DERMATOLOGY, 2023, 48 (06) : 642 - 647
  • [6] Association between genetically proxied PCSK9 inhibition and systemic lupus erythematosus risk: A mendelian randomization study
    Ji, Xincan
    Guo, Hao-Yang
    Han, Mengqi
    Peng, Hui
    Yuan, Hui
    INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES, 2024, 27 (04)
  • [7] Association between genetically proxied glucosamine and risk of cancer and non-neoplastic disease: A Mendelian randomization study
    Wu, Yingtong
    Che, Yinggang
    Zhang, Yong
    Xiong, Yanlu
    Shu, Chen
    Jiang, Jun
    Li, Gaozhi
    Guo, Lin
    Qiao, Tianyun
    Li, Shuwen
    Li, Ou
    Chang, Ning
    Zhang, Xinxin
    Zhang, Minzhe
    Qiu, Dan
    Xi, Hangtian
    Li, Jinggeng
    Chen, Xiangxiang
    Ye, Mingxiang
    Zhang, Jian
    FRONTIERS IN GENETICS, 2024, 15
  • [8] Association between genetically proxied HMGCR inhibition and male reproductive health: A Mendelian randomization study
    Yan, Zhaoqi
    Xu, Yifeng
    Li, Keke
    Liu, Liangji
    MEDICINE, 2023, 102 (39) : E34690
  • [9] Genetically proxied therapeutic inhibition of antihypertensive drug targets and risk of common cancers: A mendelian randomization analysis
    Yarmolinsky, James
    Diez-Obrero, Virginia
    Richardson, Tom M.
    Pigeyre, Marie E.
    Sjaarda, Jennifer Y.
    Pare, Guillaume
    Walker, Venexia
    Vincent, Emma
    Tan, Vanessa
    Obon-Santacana, Mireia
    Albanes, Demetrius K.
    Hampe, Jochen
    Gsur, Andrea
    Hampel, Heather
    Pai, Rish
    Jenkins, Mark I.
    Gallinger, Steven
    Casey, Graham M.
    Zheng, Wei
    Amos, Christopher
    Smith, George Davey
    Martin, Richard
    Moreno, Victor
    PRACTICAL consortium
    MEGASTROKE consortium
    PLOS MEDICINE, 2022, 19 (02)
  • [10] Genetically proxied therapeutic inhibition of antihypertensive drug targets and risk of pancreatic cancer: a mendelian randomization analysis
    Yao, Zehui
    Qin, Dailei
    Cao, Jianzhong
    Gao, Chun
    Xi, Pu
    Li, Shengping
    Wei, Ran
    BMC CANCER, 2025, 25 (01)