Donovan Fariba M, Ramadan Ferris A, Lim James R, Buchfuhrer Julia E, Khan Rebia N, DeQuillfeldt Natalie P, Davis Natalie M, Kaveti Ashwini, De Shadarevian Melanie, Bedrick Edward J, Galgiani John N
Valley Fever Center for Excellence, University of Arizona College of Medicine-Tucson, Tucson, Arizona, USA.
University of Arizona College of Medicine-Tucson, Tucson, Arizona, USA.
Open Forum Infect Dis. 2022 Jan 27;9(3):ofac032. doi: 10.1093/ofid/ofac032. eCollection 2022 Mar.
The risk of coccidioidomycosis (CM) as a life-threatening respiratory illness or disseminated CM (DCM) increases as much as 150-fold in immunosuppressed patients. The safety of biologic response modifiers (BRMs) as treatment for patients with autoimmune disease (AI) in CM-endemic regions is not well defined. We sought to determine that risk in the Tucson and Phoenix areas.
We conducted a retrospective study reviewing demographics, Arizona residency length, clinical presentations, specific AI diagnoses, CM test results, and BRM treatments in electronic medical records of patients ≥18 years old with () codes for CM and AI from 1 October 2017 to 31 December 2019.
We reviewed 944 charts with overlapping codes for CM and AI, of which 138 were confirmed to have both diagnoses. Male sex was associated with more CM ( = .003), and patients with African ancestry were 3 times more likely than those with European ancestry to develop DCM (< .001). Comparing CM/AI (n = 138) with CM/AI (n = 449) patients, there were no significant differences in CM clinical presentations. Patients receiving BRMs had 2.4 times more DCM compared to pulmonary CM (PCM).
AI does not increase the risk of any specific CM clinical presentation, and BRM treatment of most AI patients does not lead to severe CM. However, BRMs significantly increase the risk of DCM, and prospective studies are needed to identify the immunogenetic subset that permits BRM-associated DCM.
球孢子菌病(CM)作为一种危及生命的呼吸道疾病或播散性CM(DCM),在免疫抑制患者中的风险增加多达150倍。在CM流行地区,生物反应调节剂(BRM)作为自身免疫性疾病(AI)患者治疗方法的安全性尚不明确。我们试图确定图森和凤凰城地区的这种风险。
我们进行了一项回顾性研究,回顾了2017年10月1日至2019年12月31日期间年龄≥18岁、有CM和AI()编码的患者电子病历中的人口统计学信息、在亚利桑那州的居住时长、临床表现、特定AI诊断、CM检测结果和BRM治疗情况。
我们回顾了944份有CM和AI重叠编码的病历,其中138份被确诊同时患有这两种疾病。男性与更多的CM相关(=0.003),非洲裔患者发生DCM的可能性是欧洲裔患者的3倍(<0.001)。比较CM/AI患者(n = 138)和CM/AI患者(n = 449),CM临床表现无显著差异。接受BRM治疗的患者发生DCM的几率是肺CM(PCM)患者的2.4倍。
AI不会增加任何特定CM临床表现的风险,大多数AI患者接受BRM治疗不会导致严重CM。然而,BRM会显著增加DCM的风险,需要进行前瞻性研究以确定允许BRM相关DCM发生的免疫遗传学亚组。