Villacorta Javier, Diaz-Crespo Francisco, Acevedo Mercedes, Guerrero Carmen, Mollejo Manuela, Fernandez-Juarez Gema
Nephrology, Toledo, Spain.
Pathology, Toledo, Spain.
Nephrology (Carlton). 2016 Apr;21(4):301-7. doi: 10.1111/nep.12608.
Pauci-immune extracapillary glomerulonephritis (PEGN) is one of the most common causes of rapidly progressive glomerulonephritis and is usually associated with circulating anti-neutrophil cytoplasmic antibodies (ANCAs). However, a significant number of individuals with PEGN test negative for ANCA and this study aimed to analyze the characteristics of this subgroup of patients.
Patients from two centres who were diagnosed with PEGN between 1997 and 2014 were studied retrospectively. Clinicopathological characteristics and renal outcome were compared between patients presenting with pauci-immune necrotizing extracapillary glomerulonephritis associated or not with the presence of circulating ANCA.
Among the 114 patients with PEGN, 29 (25.4%) were ANCA negative. Compared with the 85 ANCA-positive patients, ANCA-negative patients were younger at the onset (54.8 ± 17.2 vs. 62 ± 14.0 years; P < 0.05). The median level of urinary protein excretion was significantly higher among ANCA-negative patients (3.1 vs. 1 g/24 h; P < 0.001), whereas no differences were found in renal function and need for dialysis between ANCA-negative and positive groups. Extrarenal involvement was present independently of ANCA status. Histological analysis showed that ANCA-negative patients were more likely to have mesangial proliferation (P < 0.05). Renal and global survival were similar between ANCA-negative and positive patients, and treatment response and relapse rates were comparable in both groups.
ANCA-negative pauci-immune extracapillary glomerulonephritis is not a rare condition and is part of a systemic vasculitis disease. Although ANCA-negative patients have renal and histological characteristics that differ from ANCA-positive patients, renal survival and treatment response in PEGN are independent of ANCA status.
寡免疫性毛细血管外增生性肾小球肾炎(PEGN)是快速进展性肾小球肾炎最常见的病因之一,通常与循环抗中性粒细胞胞浆抗体(ANCA)相关。然而,相当数量的PEGN患者ANCA检测呈阴性,本研究旨在分析该亚组患者的特征。
对1997年至2014年间在两个中心被诊断为PEGN的患者进行回顾性研究。比较寡免疫性坏死性毛细血管外增生性肾小球肾炎患者中伴有或不伴有循环ANCA的临床病理特征及肾脏转归。
114例PEGN患者中,29例(25.4%)ANCA阴性。与85例ANCA阳性患者相比,ANCA阴性患者发病时年龄更小(54.8±17.2岁对62±14.0岁;P<0.05)。ANCA阴性患者尿蛋白排泄中位数显著更高(3.1对1g/24小时;P<0.001),而ANCA阴性和阳性组在肾功能及透析需求方面未发现差异。肾外受累情况与ANCA状态无关。组织学分析显示,ANCA阴性患者更易出现系膜增生(P<0.05)。ANCA阴性和阳性患者的肾脏及总体生存率相似,两组的治疗反应及复发率相当。
ANCA阴性的寡免疫性毛细血管外增生性肾小球肾炎并非罕见疾病,是系统性血管炎疾病的一部分。尽管ANCA阴性患者的肾脏及组织学特征与ANCA阳性患者不同,但PEGN的肾脏生存率及治疗反应与ANCA状态无关。