病因学
肾小球疾病
发病机制
下调和上调
医学
病理
足细胞
免疫学
肾
生物信息学
生物
肾小球肾炎
内科学
遗传学
蛋白尿
基因
作者
Abbal Koirala,Shreeram Akilesh,J. Ashley Jefferson
标识
DOI:10.1053/j.akdh.2024.03.008
摘要
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.
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