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肾小球病塌陷。

Collapsing Glomerulopathy.

机构信息

Division of Nephrology, University of Washington, Seattle, Washington.

Department of Pathology, University of Washington, Seattle, Washington.

出版信息

Adv Kidney Dis Health. 2024 Jul;31(4):290-298. doi: 10.1053/j.akdh.2024.03.008.

DOI:10.1053/j.akdh.2024.03.008
PMID:39084754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11296495/
Abstract

Collapsing glomerulopathy (CG) is a pattern of kidney injury characterized by segmental or global collapse of the glomerular tuft associated with overlying epithelial cell hyperplasia. Although CG may be idiopathic, a wide range of etiologies have been identified that can lead to this pattern of injury. Recent advances have highlighted the role of inflammatory and interferon signaling pathways and upregulation of apolipoprotein L1 (APOL1) within podocytes in those carrying a high-risk APOL1 genotype. In this review, we describe the etiology, pathogenesis, pathology, and clinical course of CG, focusing on nonviral etiologies. We also describe current treatments and explore potential therapeutic options targeting interferon/APOL1 pathways in CG.

摘要

塌陷性肾小球病 (CG) 是一种肾脏损伤模式,其特征为肾小球簇的节段性或全球性塌陷,伴有上皮细胞过度增生。尽管 CG 可能是特发性的,但已经确定了广泛的病因,这些病因可能导致这种损伤模式。最近的进展强调了炎症和干扰素信号通路的作用,以及携带高风险 APOL1 基因型的足细胞中载脂蛋白 L1 (APOL1) 的上调。在这篇综述中,我们描述了 CG 的病因、发病机制、病理学和临床过程,重点介绍了非病毒病因。我们还描述了目前的治疗方法,并探讨了针对 CG 中干扰素/APOL1 途径的潜在治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46e7/11296495/a167ff7ca444/nihms-1990274-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46e7/11296495/d61479ccf952/nihms-1990274-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46e7/11296495/a167ff7ca444/nihms-1990274-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46e7/11296495/d61479ccf952/nihms-1990274-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46e7/11296495/a167ff7ca444/nihms-1990274-f0003.jpg

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本文引用的文献

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APOL1-mediated monovalent cation transport contributes to APOL1-mediated podocytopathy in kidney disease.APOL1 介导的单价阳离子转运有助于 APOL1 介导的肾脏病中的足细胞病变。
J Clin Invest. 2024 Jan 16;134(5):e172262. doi: 10.1172/JCI172262.
2
Inaxaplin for Proteinuric Kidney Disease in Persons with Two Variants.Inaxaplin 用于伴有两种变异的蛋白尿性肾病患者。
N Engl J Med. 2023 Mar 16;388(11):969-979. doi: 10.1056/NEJMoa2202396.
3
Collapsing glomerulopathy: unraveling varied pathogeneses.塌陷性肾小球病:解析多样的发病机制
Curr Opin Nephrol Hypertens. 2023 May 1;32(3):213-222. doi: 10.1097/MNH.0000000000000873. Epub 2023 Feb 9.
4
NLRP3 and pyroptosis blockers for treating inflammatory diseases.NLRP3 和焦亡抑制剂治疗炎症性疾病。
Trends Pharmacol Sci. 2022 Aug;43(8):653-668. doi: 10.1016/j.tips.2022.04.003. Epub 2022 May 3.
5
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Kidney Int. 2022 May;101(5):1017-1026. doi: 10.1016/j.kint.2022.01.033. Epub 2022 Feb 26.
6
The evolving story of apolipoprotein L1 nephropathy: the end of the beginning.载脂蛋白 L1 肾病的演变故事:开端的结束。
Nat Rev Nephrol. 2022 May;18(5):307-320. doi: 10.1038/s41581-022-00538-3. Epub 2022 Feb 25.
7
Longitudinal Outcomes of COVID-19-Associated Collapsing Glomerulopathy and Other Podocytopathies.COVID-19 相关的细胞性肾小球病及其他足细胞病的纵向转归。
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8
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