Heli Liu, Long Zhou, Ziping Song, Ruijun Zhang, Yuying Kang
{"title":"中重度银屑病生物治疗和浅表真菌感染风险:荟萃分析。","authors":"Heli Liu, Long Zhou, Ziping Song, Ruijun Zhang, Yuying Kang","doi":"10.1111/myc.70081","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Biologic agents have become a key treatment option for moderate-to-severe plaque psoriasis; however, the associated risk of superficial fungal infections, such as Candida and dermatophytes infections, remains unclear. This study aims to systematically assess the impact of different biologic agents on these infection risks and to compare the differences between them.</p><p><strong>Methods: </strong>Research questions and keywords were developed based on the Population, Intervention, Control and Outcome (PICO) framework. A systematic search of PubMed, EMBASE, the Cochrane Library and Web of Science was conducted for randomised controlled trials (RCTs) published up to December 2024, using the keywords 'psoriasis', 'biologics', 'anti-IL-17', 'anti-IL-12/23', 'anti-TNF', 'superficial fungal infections', 'dermatophyte infections', 'Candida' and 'onychomycosis'. Meta-analyses were performed using RevMan 5.4 and STATA 16.0 software.</p><p><strong>Results: </strong>A total of 644 records were identified, with 29 articles included in the final analysis. Meta-analysis indicated that compared with placebo, interleukin-17 (IL-17) inhibitors notably raised the risk of Candida infections (OR = 2.39, 95% CI = 1.84-3.11, p < 0.00001), whereas tumour necrosis factor-alpha (TNF-α) inhibitors (OR = 1.75, 95% CI = 0.53-5.82, p = 0.36) and interleukin-12/23 (IL-12/23) inhibitors (OR = 1.11, 95% CI = 0.27-4.63, p = 0.88) showed no significant differences. Cross-comparison demonstrated that IL-17 inhibitors had a higher risk of Candida infection compared to TNF-α inhibitors (OR = 2.23, 95% CI = 1.08-4.57, p = 0.03) and IL-12/23 inhibitors (OR = 4.21, 95% CI = 2.71-6.55, p < 0.00001). For dermatophyte infections, the overall risk associated with biologic agents was increased (OR = 1.89, 95% CI = 1.19-3.01, p = 0.007), IL-17 inhibitors showed a higher risk compared to IL-12/23 inhibitors (OR = 2.70 95% CI = 1.29-5.63, p = 0.008). Overall, biologic agents significantly increased the risk of superficial fungal infections compared to placebo (OR = 2.10, 95% CI = 1.73-2.55, p < 0.00001).</p><p><strong>Conclusion: </strong>Biologic agents, particularly IL-17 inhibitors, notably increase the risk of superficial fungal infections in psoriasis patients. In clinical practice, targeted monitoring protocols should be established, including regular follow-up to promptly detect superficial fungal infections and initiate antifungal treatment as necessary.</p><p><strong>Trial registration: </strong>PROSPERO: CRD42025636705.</p>","PeriodicalId":18797,"journal":{"name":"Mycoses","volume":"68 6","pages":"e70081"},"PeriodicalIF":3.1000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Biologic Therapy and Superficial Fungal Infection Risk in Moderate-to-Severe Psoriasis: A Meta-Analysis.\",\"authors\":\"Heli Liu, Long Zhou, Ziping Song, Ruijun Zhang, Yuying Kang\",\"doi\":\"10.1111/myc.70081\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Biologic agents have become a key treatment option for moderate-to-severe plaque psoriasis; however, the associated risk of superficial fungal infections, such as Candida and dermatophytes infections, remains unclear. This study aims to systematically assess the impact of different biologic agents on these infection risks and to compare the differences between them.</p><p><strong>Methods: </strong>Research questions and keywords were developed based on the Population, Intervention, Control and Outcome (PICO) framework. A systematic search of PubMed, EMBASE, the Cochrane Library and Web of Science was conducted for randomised controlled trials (RCTs) published up to December 2024, using the keywords 'psoriasis', 'biologics', 'anti-IL-17', 'anti-IL-12/23', 'anti-TNF', 'superficial fungal infections', 'dermatophyte infections', 'Candida' and 'onychomycosis'. Meta-analyses were performed using RevMan 5.4 and STATA 16.0 software.</p><p><strong>Results: </strong>A total of 644 records were identified, with 29 articles included in the final analysis. Meta-analysis indicated that compared with placebo, interleukin-17 (IL-17) inhibitors notably raised the risk of Candida infections (OR = 2.39, 95% CI = 1.84-3.11, p < 0.00001), whereas tumour necrosis factor-alpha (TNF-α) inhibitors (OR = 1.75, 95% CI = 0.53-5.82, p = 0.36) and interleukin-12/23 (IL-12/23) inhibitors (OR = 1.11, 95% CI = 0.27-4.63, p = 0.88) showed no significant differences. Cross-comparison demonstrated that IL-17 inhibitors had a higher risk of Candida infection compared to TNF-α inhibitors (OR = 2.23, 95% CI = 1.08-4.57, p = 0.03) and IL-12/23 inhibitors (OR = 4.21, 95% CI = 2.71-6.55, p < 0.00001). For dermatophyte infections, the overall risk associated with biologic agents was increased (OR = 1.89, 95% CI = 1.19-3.01, p = 0.007), IL-17 inhibitors showed a higher risk compared to IL-12/23 inhibitors (OR = 2.70 95% CI = 1.29-5.63, p = 0.008). Overall, biologic agents significantly increased the risk of superficial fungal infections compared to placebo (OR = 2.10, 95% CI = 1.73-2.55, p < 0.00001).</p><p><strong>Conclusion: </strong>Biologic agents, particularly IL-17 inhibitors, notably increase the risk of superficial fungal infections in psoriasis patients. 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引用次数: 0
摘要
目的:生物制剂已成为中重度斑块型银屑病的主要治疗选择;然而,表面真菌感染的相关风险,如念珠菌和皮肤真菌感染,仍不清楚。本研究旨在系统评估不同生物制剂对这些感染风险的影响,并比较它们之间的差异。方法:根据人口、干预、控制和结果(PICO)框架制定研究问题和关键词。系统检索PubMed、EMBASE、Cochrane Library和Web of Science,检索截至2024年12月发表的随机对照试验(rct),检索关键词为“牛皮癣”、“生物制剂”、“抗il -17”、“抗il -12/23”、“抗tnf”、“浅表真菌感染”、“皮肤真菌感染”、“念珠菌”和“甲真菌病”。采用RevMan 5.4和STATA 16.0软件进行meta分析。结果:共识别644条记录,最终纳入29篇。荟萃分析显示,与安慰剂相比,白介素-17 (IL-17)抑制剂显著增加念珠菌感染的风险(OR = 2.39, 95% CI = 1.84-3.11, p)。结论:生物制剂,特别是IL-17抑制剂显著增加银屑病患者浅表真菌感染的风险。在临床实践中,应建立有针对性的监测方案,包括定期随访,及时发现浅表真菌感染,必要时进行抗真菌治疗。试验注册:PROSPERO: CRD42025636705。
Biologic Therapy and Superficial Fungal Infection Risk in Moderate-to-Severe Psoriasis: A Meta-Analysis.
Purpose: Biologic agents have become a key treatment option for moderate-to-severe plaque psoriasis; however, the associated risk of superficial fungal infections, such as Candida and dermatophytes infections, remains unclear. This study aims to systematically assess the impact of different biologic agents on these infection risks and to compare the differences between them.
Methods: Research questions and keywords were developed based on the Population, Intervention, Control and Outcome (PICO) framework. A systematic search of PubMed, EMBASE, the Cochrane Library and Web of Science was conducted for randomised controlled trials (RCTs) published up to December 2024, using the keywords 'psoriasis', 'biologics', 'anti-IL-17', 'anti-IL-12/23', 'anti-TNF', 'superficial fungal infections', 'dermatophyte infections', 'Candida' and 'onychomycosis'. Meta-analyses were performed using RevMan 5.4 and STATA 16.0 software.
Results: A total of 644 records were identified, with 29 articles included in the final analysis. Meta-analysis indicated that compared with placebo, interleukin-17 (IL-17) inhibitors notably raised the risk of Candida infections (OR = 2.39, 95% CI = 1.84-3.11, p < 0.00001), whereas tumour necrosis factor-alpha (TNF-α) inhibitors (OR = 1.75, 95% CI = 0.53-5.82, p = 0.36) and interleukin-12/23 (IL-12/23) inhibitors (OR = 1.11, 95% CI = 0.27-4.63, p = 0.88) showed no significant differences. Cross-comparison demonstrated that IL-17 inhibitors had a higher risk of Candida infection compared to TNF-α inhibitors (OR = 2.23, 95% CI = 1.08-4.57, p = 0.03) and IL-12/23 inhibitors (OR = 4.21, 95% CI = 2.71-6.55, p < 0.00001). For dermatophyte infections, the overall risk associated with biologic agents was increased (OR = 1.89, 95% CI = 1.19-3.01, p = 0.007), IL-17 inhibitors showed a higher risk compared to IL-12/23 inhibitors (OR = 2.70 95% CI = 1.29-5.63, p = 0.008). Overall, biologic agents significantly increased the risk of superficial fungal infections compared to placebo (OR = 2.10, 95% CI = 1.73-2.55, p < 0.00001).
Conclusion: Biologic agents, particularly IL-17 inhibitors, notably increase the risk of superficial fungal infections in psoriasis patients. In clinical practice, targeted monitoring protocols should be established, including regular follow-up to promptly detect superficial fungal infections and initiate antifungal treatment as necessary.
期刊介绍:
The journal Mycoses provides an international forum for original papers in English on the pathogenesis, diagnosis, therapy, prophylaxis, and epidemiology of fungal infectious diseases in humans as well as on the biology of pathogenic fungi.
Medical mycology as part of medical microbiology is advancing rapidly. Effective therapeutic strategies are already available in chemotherapy and are being further developed. Their application requires reliable laboratory diagnostic techniques, which, in turn, result from mycological basic research. Opportunistic mycoses vary greatly in their clinical and pathological symptoms, because the underlying disease of a patient at risk decisively determines their symptomatology and progress. The journal Mycoses is therefore of interest to scientists in fundamental mycological research, mycological laboratory diagnosticians and clinicians interested in fungal infections.