Repeated Kidney Biopsy in Membranoproliferative Glomerulonephritis.

IF 3.2 4区 医学 Q1 UROLOGY & NEPHROLOGY
Kidney Diseases Pub Date : 2025-04-04 eCollection Date: 2025-01-01 DOI:10.1159/000545727
Ai-Hui Li, Yang Li, Meng-Shi Li, Zhuo-Ran Song, Ji-Cheng Lv, Hong Zhang, Xiao-Juan Yu, Xu-Jie Zhou
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引用次数: 0

Abstract

Introduction: Membranoproliferative glomerulonephritis (MPGN) is a heterogeneous pattern of glomerular injury. Repeated kidney biopsies may elucidate pathogenic mechanisms and guide diagnostic strategies.

Methods: We included 82 patients diagnosed with MPGN by kidney biopsy who underwent at least two biopsies between 1997 and 2023 at Peking University First Hospital. Clinical and pathological data were analyzed retrospectively.

Results: Of 342 MPGN patients, 95 (28%) had repeated biopsies (0.9-4.0 years apart). This incidence was higher than in other glomerulonephropathies under immunosuppression. Among the 82 patients analyzed (excluding kidney transplants and ≤3-month biopsy intervals), 42 were initially diagnosed with non-MPGN pathology. At the second biopsy, proteinuria increased (from 2.9 to 6.3 g/day), eGFR declined (from 76 to 47 mL/min/1.73 m2), and renal C3 deposition was stronger (p = 0.04). Thirty patients (37%) had etiological reclassification, mostly to monoclonal gammopathy of renal significance (MGRS). Compared to idiopathic MPGN, MGRS patients were older (53 vs. 35 years) and had worse renal function (eGFR 57 vs. 81 mL/min/1.73 m2) but slower eGFR decline (-7 vs. -12 mL/min/1.73 m2/year). Most MGRS patients (64%) remained negative for monoclonal protein in serum or urine immunofixation, necessitating repeat biopsy and clone-directed therapy.

Conclusion: In this study, about half and one-third of patients underwent morphological and etiological reclassification, respectively. Stronger complement deposition may drive morphological changes. Repeated kidney biopsies are crucial for diagnosing MGRS, especially in patients with negative immunofixation.

膜增生性肾小球肾炎的重复肾活检。
膜增生性肾小球肾炎(MPGN)是一种异质性肾小球损伤。反复肾活检可能阐明致病机制和指导诊断策略。方法:我们纳入了82例经肾活检诊断为MPGN的患者,这些患者于1997年至2023年间在北京大学第一医院接受了至少两次活检。回顾性分析临床及病理资料。结果:在342例MPGN患者中,95例(28%)重复活检(间隔0.9-4.0年)。这一发生率高于免疫抑制的其他肾小球肾病。在分析的82例患者中(不包括肾移植和≤3个月的活检间隔),42例最初诊断为非mpgn病理。第二次活检时,蛋白尿增加(从2.9 g/天增加到6.3 g/天),eGFR下降(从76 mL/min/1.73 m2下降到47 mL/min/1.73 m2),肾C3沉积更强(p = 0.04)。30例(37%)患者进行病因重新分类,主要为肾性单克隆γ病(MGRS)。与特发性MPGN相比,MGRS患者年龄较大(53岁vs. 35岁),肾功能较差(eGFR 57 vs. 81 mL/min/1.73 m2),但eGFR下降较慢(-7 vs. -12 mL/min/1.73 m2/年)。大多数MGRS患者(64%)在血清或尿液免疫固定中单克隆蛋白呈阴性,需要重复活检和克隆定向治疗。结论:在本研究中,约有一半和三分之一的患者分别进行了形态学和病因学的重新分类。较强的补体沉积可能导致形态变化。反复的肾脏活检对于诊断MGRS至关重要,特别是在免疫固定阴性的患者中。
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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