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Clinicopathological Significance and Renal Outcomes of Light Microscopic Patterns in Complement Component 3 Glomerulopathy

机译:补体组分3肾小球病的临床病理学意义和肾脏结果

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Background: Complement component 3 glomerulopathy (C3G) is a disease diagnosed based on the predominance of C3 immunostaining in glomeruli. The popular electron microscopic subtyping of C3G into dense deposit disease and C3 glomerulonephritis (GN) is not without limitations. We aimed to study the light microscopic (LM) patterns of C3G along with their clinicopathological correlation and treatment outcome. Methods: C3G biopsies were classified into 4 LM patterns (membranoproliferative GN [MPGN], mesan-gial proliferative GN [MesPGN], diffuse proliferative GN [DPGN], and crescentic GN [CrGN]). These patterns were compared for clinicopathological profile, treatment outcome, and renal survival. Further, predictors of end-stage renal disease (ESRD) were determined using the Cox proportional hazards model. Results: Of 162 biopsies, there were 83 MPGN, 36 DPGN, 22 MesPGN, and 21 CrGN. Majority of the patients were young, with males being more than females. About half (48%) of the patients received immunosuppres-sion, steroids alone (29%) or steroids with other immuno-suppressants (19%). The overall remission rate was 32.7% (median follow-up = 14 months). CKD developed in 46 patients and 31 patients progressed to ESRD. Predictors of progression to ESRD were older age (hazard ratio [HR] = 1.04, p < 0.01), advanced renal failure at presentation (HR = 3.73, p < 0.01), glomerulosclerosis (HR = 5.07, p < 0.01), and severity of interstitial fibrosis and tubular atrophy (HR = 8.25, p = 0.01). Conclusions: The LM patterns differed in their clinicopathological profiles, without any significant difference in their renal outcomes. Glomerulosclerosis and interstitial fibrosis portend a poor prognosis. Besides CrGN, MesPGN pattern of C3G presented as a severe form of disease.
机译:背景:补体组分3肾小球疗法(C3G)是一种诊断为基于肾小球C3免疫染色的优势的疾病。流行的电子显微镜亚型C3g成致密的沉积疾病和C3肾小球肾炎(GN)并非没有限制。我们旨在研究C3G的光学显微镜(LM)模式以及它们的临床病理相关性和治疗结果。方法:将C3G活组织检查分为4 LM图案(膜上促乳液GN [MPGN],中霉素增殖性GN [MSPGN],弥漫性增殖GN型,和Crescencic GN [Crgn])。比较这些模式,用于临床病理分布,治疗结果和肾脏存活。此外,使用COX比例危害模型确定终级肾病(ESRD)的预测因子。结果:162个活组织检查,有83mpgn,36dpgn,22 mesmgn和21 crgn。大多数患者年轻,男性比女性更多。大约一半(48%)患者接受免疫抑制剂,单独的类固醇(29%)或类固醇与其他免疫抑制剂(19%)。整体缓解率为32.7%(中位后续= 14个月)。 CKD在46名患者中开发,31例患者进入ESRD。 ESRD进展预测因素是较老龄(危害比[HR] = 1.04,P <0.01),呈现晚期肾功能衰竭(HR = 3.73,P <0.01),肾盂粥样硬化(HR = 5.07,P <0.01)和严重程度间质纤维化和管状萎缩(HR = 8.25,P = 0.01)。结论:LM模式在其临床病理学谱不同,没有任何显着差异的肾果菌。肾小球粥样硬化和间质纤维化移植预后差。除CRGN外,C3G的MESGN模式呈现为严重的疾病。

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