University of Birmingham, Institute of Applied Health Research, Birmingham, B15 2TT, UK.
Christian Medical College, Vellore, India.
Arthritis Res Ther. 2022 Aug 19;24(1):201. doi: 10.1186/s13075-022-02885-9.
Granulomatosis with polyangiitis (GPA) is small vessel vasculitis with heterogeneous clinical presentation. In the present population-based cohort study, we classified patients with GPA based on clinical features at presentation using an unsupervised clustering approach and compared their mortality, infections and frequency of comorbidities.
In this open cohort study, de-identified primary care data of patients with GPA included in the IQVIA Medical Research Data database between 1 January 1995 and 25 September 2019 was analysed retrospectively. Latent class analysis was performed to create symptom clusters of patients based on 16 categories of symptoms representing various organ involvement. All-cause mortality of resultant clusters was compared after adjusting for age, sex, Townsend deprivation quintile and smoking status at index date using extended Cox proportional hazards models. Prescription of antibiotics, considered as an indirect indicator of recurrent bacterial infection, was compared using a recurrent event model, after adjusting for quarterly use of steroid as a time-dependent covariate. Cumulative frequencies of common comorbidities were compared among the clusters at index visit, 1-year and 3-year follow-up.
Altogether, 649 patients with GPA [median age 60.0 (IQR: 49.6-70.1)] were included. Three clusters were identified: patients with limited disease mainly with involvement of ENT and cough were classified into cluster 1 (n = 426); cluster 2 had generalised non-renal disease (n = 176); while patients in cluster 3 had renal-predominant disease (n = 47). Many patients in cluster 1 developed generalised disease at the end of 1 year. Mortality in clusters 2 and 3 was higher compared with cluster 1. Mortality in cluster 1 itself was 68% higher than the general population without GPA. The duration of antibiotics prescription and frequency of coexisting medical illnesses was also higher in clusters 2 and 3.
In a primary care setting, patients with GPA can be classified into three distinct clusters with different prognosis, susceptibility to recurrent infections and presence of comorbidities. The tendency of cluster 1 to evolve into a more generalised disease raises questions about current immunosuppressive treatment approaches in these patients.
肉芽肿性多血管炎(GPA)是一种小血管血管炎,临床表现多样。在本项基于人群的队列研究中,我们使用无监督聚类方法根据患者就诊时的临床特征对 GPA 患者进行分类,并比较了他们的死亡率、感染率和合并症的频率。
在这项开放队列研究中,回顾性分析了 1995 年 1 月 1 日至 2019 年 9 月 25 日期间 IQVIA 医疗研究数据库中包含的 GPA 患者的去识别初级保健数据。基于代表各种器官受累的 16 类症状,对患者进行症状聚类的潜在类别分析。使用扩展 Cox 比例风险模型,在校正索引日期时的年龄、性别、汤森贫困五分位数和吸烟状况后,比较了不同聚类的全因死亡率。使用复发性事件模型,在校正季度使用类固醇作为时变协变量后,比较了抗生素的处方情况,抗生素被认为是细菌感染复发的间接指标。在校正索引就诊时、1 年和 3 年随访时的常见合并症累积频率后,比较了聚类之间的差异。
共纳入 649 例 GPA 患者(中位年龄 60.0[四分位距:49.6-70.1])。确定了三个聚类:以 ENT 受累和咳嗽为主要表现的局限性疾病患者归入聚类 1(n=426);聚类 2 为全身性非肾疾病(n=176);而聚类 3 为以肾脏为主的疾病患者(n=47)。许多聚类 1 的患者在 1 年末发展为全身性疾病。与聚类 1 相比,聚类 2 和 3 的死亡率更高。聚类 1 本身的死亡率比没有 GPA 的一般人群高 68%。聚类 2 和 3 的抗生素处方持续时间和并存疾病的频率也更高。
在初级保健环境中,GPA 患者可分为具有不同预后、易发生复发性感染和存在合并症的三个不同聚类。聚类 1 向更广泛的疾病发展的趋势引发了对这些患者当前免疫抑制治疗方法的质疑。