Division of Rheumatology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, 03722, Republic of Korea.
Division of Rheumatology, Department of Internal Medicine, Dongguk University Ilsan Hospital, Goyang, 10326, Republic of Korea.
Clin Rheumatol. 2024 Jan;43(1):367-376. doi: 10.1007/s10067-023-06720-7. Epub 2023 Aug 2.
Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) refers to a group of small vessel inflammatory disorders. Overlapping clinical phenotypes of AAV subgroups continually provoke controversies over their diagnostic and classification criteria.
Using the agglomerative hierarchical clustering method, we classified 210 Korean patients diagnosed with AAV into mutually exclusive clusters according to Birmingham Vasculitis Activity Score items, ANCA specificity, sex, and age. We analyzed the resulting clusters' outcomes to investigate the clinical significance of the classification. We proposed a distance-based algorithm of patient assignment and explored its clinically relevant modification.
In total, 116 patients (55%) had microscopic polyangiitis, 53 (25%) had granulomatosis with polyangiitis, and 42 (20%) had eosinophilic granulomatosis with polyangiitis. Our model grouped the patients into five clusters, namely, "limited proteinase 3 (PR3)-ANCA vasculitis," "generalized PR3-ANCA vasculitis," "ANCA-negative vasculitis," "renal-limited vasculitis," and "myeloperoxidase-ANCA vasculitis." Patients clustered under "generalized PR3-ANCA vasculitis" had a higher relapse rate (hazard ratio [HR] = 2.12, P = 0.067). The incidence of end-stage renal disease was higher in patients belonging to the "renal-limited vasculitis" cluster (HR=1.50, P=0.03), and those in the "ANCA-negative vasculitis" cluster experienced a relatively milder clinical course of AAV (mortality = 0).
Because the clusters were naturally derived from their distinguished phenotypes and have different clinical courses, our clustering method may be a more clinically relevant classification system for AAV, revealing its phenotypic diversity. We also proposed a simple and intuitive distance-based assignment algorithm, which can be easily modified according to specific clinical needs. Key Points • In this study with a single-center AAV cohort, we showed that AAV can be divided into five distinct subclasses with different disease courses based on the clinical and laboratory features of the patients. • Our study revealed ethnic differences in AAV manifestation and suggests that physicians may need to analyze their own AAV patients to assess the disease status of AAV patients. • We proposed a distance-based cluster membership assignment method that can be clinically modified to fit the specific purpose of grouping patients.
抗中性粒细胞胞质抗体(ANCA)相关性血管炎(AAV)是一组小血管炎症性疾病。AAV 亚组的重叠临床表型不断引发关于其诊断和分类标准的争议。
使用凝聚层次聚类方法,根据伯明翰血管炎活动评分项目、ANCA 特异性、性别和年龄,将 210 名韩国确诊为 AAV 的患者分为互不重叠的聚类。我们分析了产生的聚类结果,以研究分类的临床意义。我们提出了一种基于距离的患者分配算法,并探讨了其在临床相关方面的修改。
共有 116 名患者(55%)患有显微镜下多血管炎,53 名患者(25%)患有肉芽肿性多血管炎,42 名患者(20%)患有嗜酸性粒细胞肉芽肿性多血管炎。我们的模型将患者分为五个聚类,分别为“有限蛋白酶 3(PR3)-ANCA 血管炎”、“全身性 PR3-ANCA 血管炎”、“ANCA 阴性血管炎”、“肾局限性血管炎”和“髓过氧化物酶-ANCA 血管炎”。聚类在“全身性 PR3-ANCA 血管炎”下的患者复发率更高(风险比[HR] = 2.12,P = 0.067)。属于“肾局限性血管炎”聚类的患者发生终末期肾病的风险较高(HR=1.50,P=0.03),而属于“ANCA 阴性血管炎”聚类的患者 AAV 临床过程相对较轻(死亡率=0)。
由于聚类是根据其独特的表型自然产生的,并且具有不同的临床过程,因此我们的聚类方法可能是一种更具临床相关性的 AAV 分类系统,揭示了其表型多样性。我们还提出了一种简单直观的基于距离的分配算法,可根据特定的临床需求进行修改。关键点:• 在这项具有单中心 AAV 队列的研究中,我们表明,根据患者的临床和实验室特征,AAV 可以分为五个不同的亚类,具有不同的疾病过程。• 我们的研究揭示了 AAV 表现的种族差异,并表明医生可能需要分析自己的 AAV 患者,以评估 AAV 患者的疾病状况。• 我们提出了一种基于距离的聚类成员分配方法,可根据具体的分组目的进行临床修改。