Risk of serious infection with JAK inhibitors in immune-mediated inflammatory skin diseases: a meta-analysis of randomized clinical trials

被引:0
|
作者
Su, Xinhong [1 ,2 ]
Ou, Yushan [1 ,2 ]
Ruan, Shifan [1 ,2 ]
Lv, Xiaoqing [1 ,2 ]
Qin, Kun [1 ,2 ]
Mao, Jing [1 ,2 ]
Ji, Chao [1 ,2 ]
机构
[1] Fujian Med Univ, Affiliated Hosp 1, Dept Dermatol, 20 Chazhong Rd, Fuzhou 350000, Fujian, Peoples R China
[2] Fujian Med Univ, Affiliated Hosp 1, Fujian Dermatol & Venereol Res Inst, Fuzhou, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
JAK inhibitors; serious infection; immune-mediated inflammatory skin diseases; atopic dermatitis; psoriasis; vitiligo; alopecia areata; lichen planus; hidradenitis suppurativa; SEVERE ATOPIC-DERMATITIS; DOUBLE-BLIND; PLAQUE PSORIASIS; PHASE; 2B; PLACEBO; EFFICACY; SAFETY; MODERATE; TOFACITINIB; MULTICENTER;
D O I
10.1080/09546634.2025.2474507
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
BackgroundEmerging research suggests that Janus kinase-signal transducer and activator of transcription (JAK-STAT) inhibitors may be associated with a higher risk of serious infection for patients with rheumatoid arthritis. However, there is no consensus on whether JAK inhibitors increase the risk of serious infection in patients with Immune-mediated inflammatory skin diseases (IMISDs).ObjectivesTo ascertain the correlation between JAK inhibitor use and the risk of serious infection in patients with IMISDs.MethodsPubMed, Cochrane Central Register of Controlled Trials (CENTRAL), and registered Clinical Trials were searched up to June 1, 2024, using specific search terms related to JAK inhibitors and IMISDs. Randomized clinical trials (RCTs) comparing JAK inhibitors with a control group in patients with IMISDs were included. Studies focusing on cohort studies, case reports, case series, review articles, pooled analysis studies, post hoc analyses and topical JAK inhibitors were excluded. Data were extracted independently by two authors, focusing on serious infections defined according to each study's criteria. Crude numbers for serious infections were pooled and underwent meta-analysis. We assessed the primary outcome regarding the occurrence of severe infections for each study.ResultsThirty-two randomized clinical trials involving 11,917 patients were included. Serious infections were reported in 0.62% of patients receiving JAK inhibitors and 0.51% of controls. Meta-analysis found no significant increase in risk of serious infection (I2=0.00%, RR, 0.68; 95% CI, 0.43-1.07). Subgroup analyses revealed no significant heterogeneity based on condition (p = .56) or medication (p = .69).ConclusionsThis meta-analysis demonstrates that JAK inhibitors do not significantly increase the risk of serious infections in IMISD patients compared to control treatments. These findings support the safety of JAK inhibitors in this population. Future research should focus on real-world evidence to further assess their risk-benefit profile in dermatological practice.
引用
收藏
页数:8
相关论文
共 50 条
  • [1] Cardiovascular and Venous Thromboembolic Risk With JAK Inhibitors in Immune-Mediated Inflammatory Skin Diseases A Systematic Review and Meta-Analysis
    Ingrassia, Jenne P.
    Maqsood, Muhammad Haisum
    Gelfand, Joel M.
    Weber, Brittany N.
    Bangalore, Sripal
    Lo Sicco, Kristen I.
    Garshick, Michael S.
    JAMA DERMATOLOGY, 2024, 160 (01) : 28 - 36
  • [2] Risk of herpes zoster associated with JAK inhibitors in immune-mediated inflammatory diseases: a systematic review and network meta-analysis
    Xu, Qingling
    He, Liyuan
    Yin, Yufeng
    FRONTIERS IN PHARMACOLOGY, 2023, 14
  • [3] Cardiovascular and Venous Thromboembolic Risk With Janus Kinase Inhibitors in Immune-Mediated Inflammatory Diseases: A Systematic Review and Meta-Analysis of Randomized Trials
    Maqsood, Muhammad Haisum
    Weber, Brittany N.
    Haberman, Rebecca H.
    Lo Sicco, Kristen, I
    Bangalore, Sripal
    Garshick, Michael S.
    ACR OPEN RHEUMATOLOGY, 2022, 4 (10) : 912 - 922
  • [4] The correlation between DPP4 inhibitors and the risk of skin diseases: a meta-analysis of randomized clinical trials
    Zhang, Rui
    Zheng, Hongting
    Zou, Houdi
    Tong, Qiang
    Guan, Lingzhi
    Wang, Hui
    DIABETES-METABOLISM RESEARCH AND REVIEWS, 2015, 31 : 54 - 54
  • [5] ANALYSIS OF ADVERSE EFFECTS IN IMMUNE-MEDIATED INFLAMMATORY DISEASES TREATED WITH JAK INHIBITORS IN A SINGLE CENTER
    Sada, Guillen
    Pineiro, Irene
    Ibarrola, Libe
    Astigarraga, Uxue
    Lopez I Gomez, Marta
    Mendizabal, Javier
    Fito Manteca, Concepcion
    JCR-JOURNAL OF CLINICAL RHEUMATOLOGY, 2023, 29 : S24 - S24
  • [6] JAK inhibitors and the risk of infection: a meta-analysis
    Ran, Hao-Long
    Liu, Huan
    Xu, Wen-Ting
    Zhang, Jin-Rui
    Chen, Wei
    Dong, Han-Yue
    Li, Hongmin
    Tan, Cheng
    ARCHIVES OF DERMATOLOGICAL RESEARCH, 2025, 317 (01)
  • [7] Cardiotoxicity of immune checkpoint inhibitors: A meta-analysis of randomized clinical trials
    Agostinetto, E.
    Eiger, D.
    Lambertini, M.
    Ceppi, M.
    Bruzzone, M.
    Ponde, N. F.
    Plummer, C.
    Awada, A. H.
    Piccart, M.
    de Azambuja, E.
    ANNALS OF ONCOLOGY, 2020, 31 : S1432 - S1432
  • [8] Infection risk with JAK inhibitors in dermatoses: a meta-analysis
    Ireland, Patrick A.
    Verheyden, Matthew
    Jansson, Nicholas
    Sebaratnam, Deshan
    Sullivan, John
    INTERNATIONAL JOURNAL OF DERMATOLOGY, 2025, 64 (01) : 24 - 36
  • [9] Polymorphism of VEGF gene in susceptibility to chronic immune-mediated inflammatory diseases: a meta-analysis
    Ni Wei
    Zijia Chen
    Zhifeng Xue
    Yuelan Zhu
    Rheumatology International, 2015, 35 : 1351 - 1360
  • [10] Polymorphism of VEGF gene in susceptibility to chronic immune-mediated inflammatory diseases: a meta-analysis
    Wei, Ni
    Chen, Zijia
    Xue, Zhifeng
    Zhu, Yuelan
    RHEUMATOLOGY INTERNATIONAL, 2015, 35 (08) : 1351 - 1360