Chien Ming-Hung, Wang Joshua, Lu Kuo-Cheng, Lu Chien-Lin
Division of Nephrology, Department of Internal Medicine, Fu Jen Catholic University Hospital, Fu Jen Catholic University, New Taipei City 24352, Taiwan.
Department of Research, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City 23142, Taiwan.
Biomedicines. 2025 Jul 2;13(7):1628. doi: 10.3390/biomedicines13071628.
Herpes zoster (HZ), resulting from the reactivation of latent varicella-zoster virus, has been increasingly observed in individuals following COVID-19. Given the shared immunological disturbances between the two conditions, this study aimed to investigate whether HZ following COVID-19 is associated with an elevated risk of renal, infectious, and autoimmune complications. This retrospective cohort study utilized data from the TriNetX global federated health network, encompassing over 9 million adults diagnosed with COVID-19 between January 2020 and January 2022. Patients who developed HZ within one year following COVID-19 diagnosis were compared to 1:1 propensity score-matched controls without HZ. Time-to-event analyses over a three-year follow-up period were conducted to estimate the risks of major adverse kidney events (MAKE; defined as acute kidney injury, dialysis dependence, or severely reduced kidney function with eGFR <30 mL/min/1.73 m), sepsis, systemic lupus erythematosus (SLE), and rheumatoid arthritis (RA), using Kaplan-Meier survival curves and Cox proportional hazards models. HZ following COVID-19 was significantly associated with increased risks of all four outcomes: MAKE (HR 1.940, 95% CI: 1.866-2.017), sepsis (HR 2.362, 95% CI: 2.250-2.479), SLE (HR 2.667, 95% CI: 2.254-3.156), and RA (HR 2.484, 95% CI: 2.267-2.730). Subgroup analyses identified older age, diabetes, impaired renal function, and elevated inflammatory markers as key risk-enhancing factors. HZ following COVID-19 may serve as a clinical indicator of systemic immune dysregulation and is independently associated with increased long-term risks of renal, infectious, and autoimmune sequelae. Enhanced monitoring of this high-risk population is warranted.
带状疱疹(HZ)由潜伏的水痘-带状疱疹病毒重新激活引起,在感染新冠病毒(COVID-19)后的个体中越来越多地被观察到。鉴于这两种疾病存在共同的免疫紊乱,本研究旨在调查COVID-19后发生的HZ是否与肾脏、感染和自身免疫并发症风险升高相关。这项回顾性队列研究利用了TriNetX全球联合健康网络的数据,该网络涵盖了2020年1月至2022年1月期间诊断为COVID-19的900多万成年人。将COVID-19诊断后一年内发生HZ的患者与1:1倾向评分匹配的无HZ对照进行比较。在三年随访期内进行事件发生时间分析,以使用Kaplan-Meier生存曲线和Cox比例风险模型估计主要不良肾脏事件(MAKE;定义为急性肾损伤、透析依赖或估算肾小球滤过率(eGFR)<30 mL/min/1.73 m2时肾功能严重下降)、败血症、系统性红斑狼疮(SLE)和类风湿关节炎(RA)的风险。COVID-19后的HZ与所有四种结局风险增加显著相关:MAKE(风险比[HR]1.940,95%置信区间[CI]:1.866-2.017)、败血症(HR 2.362,95%CI:2.250-2.479)、SLE(HR 2.667,95%CI:2.254-3.156)和RA(HR 2.484,95%CI:2.267-2.730)。亚组分析确定年龄较大、糖尿病、肾功能受损和炎症标志物升高是关键的风险增强因素。COVID-19后的HZ可能是全身免疫失调的临床指标,并与肾脏、感染和自身免疫后遗症的长期风险增加独立相关。有必要加强对这一高危人群的监测。