Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis in China: Epidemiology, Management, Prognosis, and Outlook.

IF 3.2 4区 医学 Q1 UROLOGY & NEPHROLOGY
Kidney Diseases Pub Date : 2024-08-05 eCollection Date: 2024-10-01 DOI:10.1159/000540514
Su-Fang Chen, Zhi-Ying Li, Ming-Hui Zhao, Min Chen
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引用次数: 0

Abstract

Background: Increasing evidence indicates that clinicopathologic phenotypes and ANCA serotypes may differ ethnically and geographically. This review highlights the progress in the prevalence, pathogenesis, management, and outcomes of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) in China.

Summary: AAV is not rare in China. Cumulative evidence has demonstrated a significant preponderance of microscopic polyangiitis (MPA) and myeloperoxidase (MPO)-ANCA AAV in China. Even in patients with granulomatosis with polyangiitis (GPA), there is a predominance of MPO-ANCA over proteinase 3 (PR3)-ANCA, presenting a unique subset. The pathogenesis of AAV is multifactorial, with the role of complement activation being highlighted during recent years. Treatment strategies for AAV in China have also been refined recently. A rapid tapering of glucocorticoids to minimize exposure has been recommended by the Chinese guidelines. Along with a better understanding of the disease, B cell-targeted therapy and complement-targeted therapy are developing. A considerable number of patients in China received rituximab treatment and achieved remission. However, infection risk and associated mortality still remain concerns. Therefore, less rituximab exposure should be considered and evaluated in Chinese AAV patients. Prognostic factors have been reviewed. Of note, along with improved outcomes, there is an increase of cardiovascular and malignant-related death, warranting specific care. Recently, a modified renal risk score model has been validated for early risk prediction in Chinese AAV patients. Moreover, emerging biomarkers for AAV, including complement components, have been identified in Chinese patients.

Key messages: There is a preponderance of MPA and MPO-ANCA in China. Treatment strategies for Chinese AAV patients generally align with those in western countries, and to some extent, less aggressive. Prognostic factors and emerging biomarkers for AAV in China have been identified. Further challenges include optimizing interventions, minimizing treatment-related comorbidities, improving disease monitoring, and enhancing life qualities of AAV patients.

中国的抗中性粒细胞胞浆抗体相关血管炎:中国抗中性粒细胞胞浆抗体相关性血管炎:流行病学、管理、预后与展望》。
背景:越来越多的证据表明,临床病理表型和ANCA血清型在种族和地域上可能存在差异。本综述重点介绍了中国抗中性粒细胞胞浆抗体(ANCA)相关性血管炎(AAV)的发病率、发病机制、管理和预后方面的进展。累积的证据表明,在中国,显微镜下多血管炎(MPA)和髓过氧化物酶(MPO)-ANCA相关性血管炎的发病率很高。即使在肉芽肿伴多血管炎(GPA)患者中,MPO-ANCA 也比蛋白酶 3(PR3)-ANCA 占优势,这是一个独特的亚群。AAV的发病机制是多因素的,近年来补体激活的作用受到重视。近年来,中国的 AAV 治疗策略也在不断完善。中国指南建议快速减量糖皮质激素,以尽量减少暴露。随着对该病认识的加深,B细胞靶向治疗和补体靶向治疗也在不断发展。在中国,相当多的患者接受了利妥昔单抗治疗并获得了缓解。然而,感染风险和相关死亡率仍然令人担忧。因此,应考虑减少中国 AAV 患者的利妥昔单抗暴露,并对其进行评估。我们对预后因素进行了回顾。值得注意的是,随着预后的改善,与心血管和恶性肿瘤相关的死亡也在增加,因此需要特别注意。最近,一种改良的肾脏风险评分模型得到了验证,可用于中国 AAV 患者的早期风险预测。此外,在中国患者中发现了包括补体成分在内的AAV新兴生物标志物:关键信息:在中国,MPA 和 MPO-ANCA 患者居多。中国 AAV 患者的治疗策略总体上与西方国家一致,在一定程度上不那么激进。中国 AAV 的预后因素和新兴生物标志物已经确定。进一步的挑战包括优化干预措施、尽量减少与治疗相关的合并症、改善疾病监测以及提高 AAV 患者的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Kidney Diseases
Kidney Diseases UROLOGY & NEPHROLOGY-
CiteScore
6.00
自引率
2.70%
发文量
33
审稿时长
27 weeks
期刊介绍: ''Kidney Diseases'' aims to provide a platform for Asian and Western research to further and support communication and exchange of knowledge. Review articles cover the most recent clinical and basic science relevant to the entire field of nephrological disorders, including glomerular diseases, acute and chronic kidney injury, tubulo-interstitial disease, hypertension and metabolism-related disorders, end-stage renal disease, and genetic kidney disease. Special articles are prepared by two authors, one from East and one from West, which compare genetics, epidemiology, diagnosis methods, and treatment options of a disease.
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