单克隆伽玛病和肾病患者的临床表现、肾脏组织病理学发现和预后

IF 1.7 Q3 UROLOGY & NEPHROLOGY
International Journal of Nephrology Pub Date : 2021-05-12 eCollection Date: 2021-01-01 DOI:10.1155/2021/8859340
Gaetano Alfano, Alice Delrio, Francesco Fontana, Giacomo Mori, Silvia Cazzato, Annachiara Ferrari, Rossella Perrone, Silvia Giovanella, Giulia Ligabue, Riccardo Magistroni, Gianni Cappelli
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引用次数: 2

摘要

单克隆伽玛病与急性和慢性肾损伤有关。分泌的单克隆(M)蛋白的肾毒性与其生物学特性和血药浓度有关。关于肾脏疾病患者单克隆伽玛病的流行病学、临床表现和预后知之甚少。我们回顾性收集了2000年1月至2017年3月期间接受肾活检的所有患者(n = 1334)的人口统计学、临床表现和肾脏组织学病变数据。174例(13%)患者检测到单克隆伽玛病,平均年龄66.4±13.1岁。单克隆伽玛病包括未确定意义的单克隆伽玛病(MGUS)(52.8%)、多发性骨髓瘤(MM)(25.2%)、原发性淀粉样变性(AL)(9.1%)、阴烧型MM (SMM)(4%)、非霍奇金淋巴瘤(NHL)(6.8%)和霍奇金淋巴瘤(HL)(1.7%)。肾意义单克隆γ病变(MGRS)在MGUS患者中占6.5%,在SMM患者中占14.2%。肾活检评估显示m蛋白直接参与MM肾损伤(93.1%)。MM是唯一与肾损伤风险增加显著相关的伽玛病(比值比[OR] = 47.5, CI 95%, 13.7-164.9;P≤0.001)。虽然在终末期肾脏疾病或透析进展方面没有显著差异(P = 0.776),但在随访结束时,单克隆伽玛病与不同的死亡风险相关(P = 0.047)。总之,单克隆伽玛病在接受肾活检的患者中是一个常见的发现(13%)。m蛋白在恶性前体细胞(56.8%)和恶性细胞(43.2%)中均有分泌。肾活检在MGUS(6.5%)和SMM(14.2%)患者中识别MGRS具有关键作用。在单克隆伽玛病中,只有MM与活检证实的肾损伤显著相关。单克隆伽玛病的终末期肾病或透析率相似,而NHL、MM和SMM的死亡率更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical Presentation, Renal Histopathological Findings, and Outcome in Patients with Monoclonal Gammopathy and Kidney Disease.

Clinical Presentation, Renal Histopathological Findings, and Outcome in Patients with Monoclonal Gammopathy and Kidney Disease.

Clinical Presentation, Renal Histopathological Findings, and Outcome in Patients with Monoclonal Gammopathy and Kidney Disease.

Clinical Presentation, Renal Histopathological Findings, and Outcome in Patients with Monoclonal Gammopathy and Kidney Disease.

Monoclonal gammopathies are associated with acute and chronic kidney injury. Nephrotoxicity of the secreted monoclonal (M)-protein is related to its biological properties and blood concentration. Little is known about epidemiology, clinical manifestations, and outcome of monoclonal gammopathies in patients with kidney disease. We retrospectively collected data about demographics, clinical manifestations, and renal histological lesions of all patients (n = 1334) who underwent kidney biopsy between January 2000 and March 2017. Monoclonal gammopathy was detected in 174 (13%) patients with a mean age of 66.4 ± 13.1 years. The spectrum of monoclonal gammopathies comprised monoclonal gammopathy of undetermined significate (MGUS) (52.8%), multiple myeloma (MM) (25.2%), primary amyloidosis (AL) (9.1%), smoldering MM (SMM) (4%), non-Hodgkin lymphoma (NHL) (6.8%), and Hodgkin lymphoma (HL) (1.7%). Monoclonal gammopathy of renal significance (MGRS) accounted for 6.5% in patients with MGUS and 14.2% in patients with SMM. Evaluation of kidney biopsy revealed that M-protein was directly involved in causing kidney injury in MM (93.1%). MM was the only gammopathy significantly associated with an increased risk of kidney injury (odds ratio [OR] = 47.5, CI 95%, 13.7-164.9; P ≤ 0.001). While there were no significant differences in the progression toward end-stage renal disease or dialysis (P = 0.776), monoclonal gammopathies were associated with a different risk of death (P = 0.047) at the end of the follow-up. In conclusion, monoclonal gammopathy was a frequent finding (13%) in patients who underwent kidney biopsy. M-protein was secreted by both premalignant (56.8%) and malignant (43.2%) lymphoproliferative clones. Kidney biopsy had a key role in identifying MGRS in patients with MGUS (6.5%) and SMM (14.2%). Among monoclonal gammopathies, only MM was significantly associated with biopsy-proven kidney injury. The rate of end-stage renal disease or dialysis was similar among monoclonal gammopathies, whereas NHL, MM, and SMM showed a higher rate of deaths.

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来源期刊
International Journal of Nephrology
International Journal of Nephrology UROLOGY & NEPHROLOGY-
CiteScore
3.40
自引率
4.80%
发文量
44
审稿时长
17 weeks
期刊介绍: International Journal of Nephrology is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies focusing on the prevention, diagnosis, and management of kidney diseases and associated disorders. The journal welcomes submissions related to cell biology, developmental biology, genetics, immunology, pathology, pathophysiology of renal disease and progression, clinical nephrology, dialysis, and transplantation.
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