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
  • [41] The Risk of Infections Associated With JAK Inhibitors in Rheumatoid Arthritis A Systematic Review and Network Meta-analysis
    Alves, Carlos
    Penedones, Ana
    Mendes, Diogo
    Marques, Francisco Batel
    JCR-JOURNAL OF CLINICAL RHEUMATOLOGY, 2022, 28 (02) : E407 - E414
  • [42] The benefit-risk balance for biological agents in juvenile idiopathic arthritis: a meta-analysis of randomized clinical trials
    Cabrera, Natalia
    Avila-Pedretti, Gabriela
    Belot, Alexandre
    Larbre, Jean-Paul
    Mainbourg, Sabine
    Duquesne, Agnes
    Janiaud, Perrine
    Kassai, Behrouz
    Cucherat, Michel
    Lega, Jean-Christophe
    RHEUMATOLOGY, 2020, 59 (09) : 2226 - 2236
  • [43] Oral turmeric/curcumin effects on inflammatory markers in chronic inflammatory diseases: A systematic review and meta-analysis of randomized controlled trials
    White, C. Michael
    Pasupuleti, Vinay
    Roman, Yuani M.
    Li, Yangzhou
    Hernandez, Adrian V.
    PHARMACOLOGICAL RESEARCH, 2019, 146
  • [44] Efficacy and safety of topical calcineurin inhibitors for the treatment of atopic dermatitis: meta-analysis of randomized clinical trials
    Labedz, Natalia
    Pawliczak, Rafal
    POSTEPY DERMATOLOGII I ALERGOLOGII, 2019, 36 (06): : 752 - +
  • [45] Dipeptidyl peptidase-4 inhibitors and cardiovascular risk: a meta-analysis of randomized clinical trials
    Monami, M.
    Ahren, B.
    Dicembrini, I.
    Mannucci, E.
    DIABETES OBESITY & METABOLISM, 2013, 15 (02) : 112 - 120
  • [46] Dipeptidyl peptidase-4 inhibitors and pancreatitis risk: a meta-analysis of randomized clinical trials
    Monami, M.
    Dicembrini, I.
    Mannucci, E.
    DIABETES OBESITY & METABOLISM, 2014, 16 (01) : 48 - 56
  • [47] Risk of Immune Reconstitution Inflammatory Syndrome With Integrase Inhibitors Versus Other Classes of Antiretrovirals: A Systematic Review and Meta-analysis of Randomized Trials
    Zhao, Ying
    Hohlfeld, Ameer
    Namale, Phiona
    Meintjes, Graeme
    Maartens, Gary
    Engel, Mark E.
    JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2022, 90 (02) : 232 - 239
  • [48] Adalimumab safety and mortality rates from global clinical trials of six immune-mediated inflammatory diseases
    Burmester, G. R.
    Mease, P.
    Dijkmans, B. A. C.
    Gordon, K.
    Lovell, D.
    Panaccione, R.
    Perez, J.
    Pangan, A. L.
    ANNALS OF THE RHEUMATIC DISEASES, 2009, 68 (12) : 1863 - 1869
  • [49] Dipeptidyl Peptidase 4 Inhibitors and Risk of Inflammatory Bowel Disease Among Patients With Type 2 Diabetes: A Meta-analysis of Randomized Controlled Trials
    Li, Guangyao
    Crowley, Matthew J.
    Tang, Huilin
    Yang, Jeff Y.
    Sandler, Robert S.
    Wang, Tiansheng
    DIABETES CARE, 2019, 42 (07) : E119 - E121
  • [50] Premedication as primary prophylaxis does not influence the risk of acute infliximab infusion reactions in immune-mediated inflammatory diseases: A systematic review and meta-analysis
    Fumery, Mathurin
    Tilmant, Marion
    Yzet, Clara
    Brazier, Franck
    Loreau, Julien
    Turpin, Justine
    Le Mouel, Jean Philippe
    Goeb, Vincent
    Nguyen-Khac, Eric
    Singh, Siddarth
    Dupas, Jean-Louis
    Diouf, Momar
    DIGESTIVE AND LIVER DISEASE, 2019, 51 (04) : 484 - 488