IF 8.2 1区 医学 Q1 IMMUNOLOGY
Jesica Martín-Carmona, Anaïs Corma-Gómez, Francisco Téllez, Dolores Arenga-Barrios, Miriam Serrano-Fuentes, Luis Morano, Diana Corona-Mata, Miguel Nicolás Navarrete Lorite, Francisco Jesús Vera-Méndez, Juan Carlos Alados, Rosario Palacios, Ignacio de los Santos, Paloma Geijo, Arkaitz Imaz, Dolores Merino, Sergio Javier Reus-Bañuls, Maria Jose Galindo, Miguel Ángel López-Ruz, Carlos Galera, Juan A Pineda, Juan Macías
{"title":"No impact of HIV coinfection on the mortality in patients with hepatitis C virus infection after sustained virological response","authors":"Jesica Martín-Carmona, Anaïs Corma-Gómez, Francisco Téllez, Dolores Arenga-Barrios, Miriam Serrano-Fuentes, Luis Morano, Diana Corona-Mata, Miguel Nicolás Navarrete Lorite, Francisco Jesús Vera-Méndez, Juan Carlos Alados, Rosario Palacios, Ignacio de los Santos, Paloma Geijo, Arkaitz Imaz, Dolores Merino, Sergio Javier Reus-Bañuls, Maria Jose Galindo, Miguel Ángel López-Ruz, Carlos Galera, Juan A Pineda, Juan Macías","doi":"10.1093/cid/ciae473","DOIUrl":null,"url":null,"abstract":"Background In patients with hepatitis C virus (HCV) chronic infection and advanced liver disease, the impact of human immunodeficiency virus (HIV) coinfection on the clinical outcome after sustained virological response (SVR) has not been sufficiently clarified. The aim of this study was to compare the mortality after SVR of patients bearing HCV chronic infection and advanced liver fibrosis, with and without HIV-coinfection after a prolonged follow-up. Methods This was a prospective multicenter cohort study including individuals with HIV/HCV-coinfection and patients with HCV-monoinfection from Spain, fulfilling: 1) Liver stiffness (LS) ≥9.5 kPa before treatment; 2) SVR with a direct-acting antiviral (DAA) based regimen; 3) LS measurement available at SVR. The main outcome was overall survival. Mortality attributable to liver disease and non-hepatic causes was also assessed. Results 1,118 patients were included, of whom 676 (60.5%) were living with HIV. The median (Q1-Q3) follow-up was 76 months (57-83). After SVR, 46 (10%) HCV-monoinfected and 74 (11%) HIV/HCV-coinfected patients died. The overall mortality rate (95% CI) was 1.9 (1.6-2.2) per 100 person-years, 1.9 (1.4-2.5) per 100 person-years in patients with HCV-monoinfection and 1.8 (1.6-2.3) per 100 person-years in people living with HIV. In the multivariable analysis, HIV-coinfection was not associated with a shorter survival [0.98 HR (95% confidence interval, CI) = (0.61-1.58), p=0.939]. Conclusions In patients with HCV chronic infection and advanced fibrosis, HIV-coinfection does not reduce the overall survival after SVR.","PeriodicalId":10463,"journal":{"name":"Clinical Infectious Diseases","volume":null,"pages":null},"PeriodicalIF":8.2000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/cid/ciae473","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景 在丙型肝炎病毒(HCV)慢性感染和晚期肝病患者中,人类免疫缺陷病毒(HIV)合并感染对持续病毒学应答(SVR)后临床结果的影响尚未得到充分阐明。本研究的目的是比较长期随访后,HCV 慢性感染和晚期肝纤维化患者 SVR 后的死亡率,包括合并和未合并 HIV 感染者。方法 这是一项前瞻性多中心队列研究,研究对象包括西班牙的 HIV/HCV 合并感染者和 HCV 单感染者:1) 治疗前肝硬度(LS)≥9.5 kPa;2) 采用基于直接作用抗病毒药物(DAA)的方案进行 SVR;3) SVR 时可测量肝硬度。主要结果为总生存期。还评估了肝病和非肝病原因导致的死亡率。结果 共纳入 1,118 名患者,其中 676 人(60.5%)为 HIV 感染者。随访中位数(Q1-Q3)为 76 个月(57-83)。SVR 后,46 名(10%)HCV 单感染者和 74 名(11%)HIV/HCV 合并感染者死亡。总死亡率(95% CI)为 1.9(1.6-2.2)/100 人年,HCV 单感染患者为 1.9(1.4-2.5)/100 人年,HIV 感染者为 1.8(1.6-2.3)/100 人年。在多变量分析中,HIV 合并感染与生存期缩短无关[0.98 HR(95% 置信区间,CI)= (0.61-1.58),P=0.939]。结论 在HCV慢性感染和晚期纤维化患者中,HIV合并感染不会降低SVR后的总生存率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
No impact of HIV coinfection on the mortality in patients with hepatitis C virus infection after sustained virological response
Background In patients with hepatitis C virus (HCV) chronic infection and advanced liver disease, the impact of human immunodeficiency virus (HIV) coinfection on the clinical outcome after sustained virological response (SVR) has not been sufficiently clarified. The aim of this study was to compare the mortality after SVR of patients bearing HCV chronic infection and advanced liver fibrosis, with and without HIV-coinfection after a prolonged follow-up. Methods This was a prospective multicenter cohort study including individuals with HIV/HCV-coinfection and patients with HCV-monoinfection from Spain, fulfilling: 1) Liver stiffness (LS) ≥9.5 kPa before treatment; 2) SVR with a direct-acting antiviral (DAA) based regimen; 3) LS measurement available at SVR. The main outcome was overall survival. Mortality attributable to liver disease and non-hepatic causes was also assessed. Results 1,118 patients were included, of whom 676 (60.5%) were living with HIV. The median (Q1-Q3) follow-up was 76 months (57-83). After SVR, 46 (10%) HCV-monoinfected and 74 (11%) HIV/HCV-coinfected patients died. The overall mortality rate (95% CI) was 1.9 (1.6-2.2) per 100 person-years, 1.9 (1.4-2.5) per 100 person-years in patients with HCV-monoinfection and 1.8 (1.6-2.3) per 100 person-years in people living with HIV. In the multivariable analysis, HIV-coinfection was not associated with a shorter survival [0.98 HR (95% confidence interval, CI) = (0.61-1.58), p=0.939]. Conclusions In patients with HCV chronic infection and advanced fibrosis, HIV-coinfection does not reduce the overall survival after SVR.
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
Clinical Infectious Diseases
Clinical Infectious Diseases 医学-传染病学
CiteScore
25.00
自引率
2.50%
发文量
900
审稿时长
3 months
期刊介绍: Clinical Infectious Diseases (CID) is dedicated to publishing original research, reviews, guidelines, and perspectives with the potential to reshape clinical practice, providing clinicians with valuable insights for patient care. CID comprehensively addresses the clinical presentation, diagnosis, treatment, and prevention of a wide spectrum of infectious diseases. The journal places a high priority on the assessment of current and innovative treatments, microbiology, immunology, and policies, ensuring relevance to patient care in its commitment to advancing the field of infectious diseases.
×
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