2022年hiv相关肾病。

Frederick Berro Rivera, Marie Francesca Mapua Ansay, Jem Marie Golbin, Pia Gabrielle I Alfonso, Gerard Francis E Mangubat, Rajiv Hans Solita Menghrajani, Siena Placino, Marianne Katharina Vicera Taliño, Deogracias Villa De Luna, Nicolo Cabrera, Carlo Nemesio Trinidad, Amir Kazory
{"title":"2022年hiv相关肾病。","authors":"Frederick Berro Rivera,&nbsp;Marie Francesca Mapua Ansay,&nbsp;Jem Marie Golbin,&nbsp;Pia Gabrielle I Alfonso,&nbsp;Gerard Francis E Mangubat,&nbsp;Rajiv Hans Solita Menghrajani,&nbsp;Siena Placino,&nbsp;Marianne Katharina Vicera Taliño,&nbsp;Deogracias Villa De Luna,&nbsp;Nicolo Cabrera,&nbsp;Carlo Nemesio Trinidad,&nbsp;Amir Kazory","doi":"10.1159/000526868","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>HIV-associated nephropathy (HIVAN) is a renal parenchymal disease that occurs exclusively in people living with HIV. It is a serious kidney condition that may possibly lead to end-stage kidney disease, particularly in the HIV-1 seropositive patients.</p><p><strong>Summary: </strong>The African-American population has increased susceptibility to this comorbidity due to a strong association found in the <i>APOL1</i> gene, specifically two missense mutations in the G1 allele and a frameshift deletion in the G2 allele, although a \"second-hit\" event is postulated to have a role in the development of HIVAN. HIVAN presents with proteinuria, particularly in the nephrotic range, as with other kidney diseases. The diagnosis requires biopsy and typically presents with collapsing subtype focal segmental glomerulosclerosis and microcyst formation in the tubulointerstitial region. Gaps still exist in the definitive treatment of HIVAN - concurrent use of antiretroviral therapy and adjunctive management with like renal-angiotensin-aldosterone system inhibitors, steroids, or renal replacement therapy showed benefits.</p><p><strong>Key message: </strong>This study reviews the current understanding of HIVAN including its epidemiology, mechanism of disease, related genetic factors, clinical profile, and pathophysiologic effects of management options for patients.</p>","PeriodicalId":73177,"journal":{"name":"Glomerular diseases","volume":"3 1","pages":"1-11"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/1d/ef/gdz-0003-0001.PMC9936764.pdf","citationCount":"0","resultStr":"{\"title\":\"HIV-Associated Nephropathy in 2022.\",\"authors\":\"Frederick Berro Rivera,&nbsp;Marie Francesca Mapua Ansay,&nbsp;Jem Marie Golbin,&nbsp;Pia Gabrielle I Alfonso,&nbsp;Gerard Francis E Mangubat,&nbsp;Rajiv Hans Solita Menghrajani,&nbsp;Siena Placino,&nbsp;Marianne Katharina Vicera Taliño,&nbsp;Deogracias Villa De Luna,&nbsp;Nicolo Cabrera,&nbsp;Carlo Nemesio Trinidad,&nbsp;Amir Kazory\",\"doi\":\"10.1159/000526868\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>HIV-associated nephropathy (HIVAN) is a renal parenchymal disease that occurs exclusively in people living with HIV. It is a serious kidney condition that may possibly lead to end-stage kidney disease, particularly in the HIV-1 seropositive patients.</p><p><strong>Summary: </strong>The African-American population has increased susceptibility to this comorbidity due to a strong association found in the <i>APOL1</i> gene, specifically two missense mutations in the G1 allele and a frameshift deletion in the G2 allele, although a \\\"second-hit\\\" event is postulated to have a role in the development of HIVAN. HIVAN presents with proteinuria, particularly in the nephrotic range, as with other kidney diseases. The diagnosis requires biopsy and typically presents with collapsing subtype focal segmental glomerulosclerosis and microcyst formation in the tubulointerstitial region. Gaps still exist in the definitive treatment of HIVAN - concurrent use of antiretroviral therapy and adjunctive management with like renal-angiotensin-aldosterone system inhibitors, steroids, or renal replacement therapy showed benefits.</p><p><strong>Key message: </strong>This study reviews the current understanding of HIVAN including its epidemiology, mechanism of disease, related genetic factors, clinical profile, and pathophysiologic effects of management options for patients.</p>\",\"PeriodicalId\":73177,\"journal\":{\"name\":\"Glomerular diseases\",\"volume\":\"3 1\",\"pages\":\"1-11\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/1d/ef/gdz-0003-0001.PMC9936764.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Glomerular diseases\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1159/000526868\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Glomerular diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000526868","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

背景:HIV相关性肾病(HIV -associated nephropathy, HIVAN)是一种仅发生在HIV感染者身上的肾实质疾病。这是一种严重的肾脏疾病,可能导致终末期肾脏疾病,特别是在HIV-1血清阳性患者中。摘要:非裔美国人对这种共病的易感性增加,这是由于APOL1基因中发现的强烈关联,特别是G1等位基因的两个错义突变和G2等位基因的移码缺失,尽管“二次命中”事件被认为在HIVAN的发展中起作用。与其他肾脏疾病一样,hiv表现为蛋白尿,尤其是肾病。诊断需要活检,典型表现为塌陷亚型局灶节段性肾小球硬化和小管间质区微囊肿形成。在hiv的明确治疗方面仍然存在差距——同时使用抗逆转录病毒治疗和辅助管理如肾-血管紧张素-醛固酮系统抑制剂、类固醇或肾脏替代治疗显示出益处。本研究综述了目前对hiv的认识,包括其流行病学、发病机制、相关遗传因素、临床概况以及患者治疗方案的病理生理影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

HIV-Associated Nephropathy in 2022.

HIV-Associated Nephropathy in 2022.

HIV-Associated Nephropathy in 2022.

Background: HIV-associated nephropathy (HIVAN) is a renal parenchymal disease that occurs exclusively in people living with HIV. It is a serious kidney condition that may possibly lead to end-stage kidney disease, particularly in the HIV-1 seropositive patients.

Summary: The African-American population has increased susceptibility to this comorbidity due to a strong association found in the APOL1 gene, specifically two missense mutations in the G1 allele and a frameshift deletion in the G2 allele, although a "second-hit" event is postulated to have a role in the development of HIVAN. HIVAN presents with proteinuria, particularly in the nephrotic range, as with other kidney diseases. The diagnosis requires biopsy and typically presents with collapsing subtype focal segmental glomerulosclerosis and microcyst formation in the tubulointerstitial region. Gaps still exist in the definitive treatment of HIVAN - concurrent use of antiretroviral therapy and adjunctive management with like renal-angiotensin-aldosterone system inhibitors, steroids, or renal replacement therapy showed benefits.

Key message: This study reviews the current understanding of HIVAN including its epidemiology, mechanism of disease, related genetic factors, clinical profile, and pathophysiologic effects of management options for patients.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信