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乙型和/或丙型肝炎对HIV感染患者肝功能及抗逆转录病毒治疗反应的影响:一项罗马尼亚队列研究

The Impact of Hepatitis B and/or C on Liver Function and on the Response to Antiretroviral Therapy in HIV-Infected Patients: A Romanian Cohort Study.

作者信息

Marin Ruxandra-Cristina, Tit Delia Mirela, Bungău Gabriela, Moleriu Radu Dumitru

机构信息

Doctoral School of Biological and Biomedical Sciences, University of Oradea, 410087 Oradea, Romania.

Department of Pharmacy, Faculty of Medicine and Pharmacy, University of Oradea, 410028 Oradea, Romania.

出版信息

Pharmaceuticals (Basel). 2025 May 7;18(5):688. doi: 10.3390/ph18050688.


DOI:10.3390/ph18050688
PMID:40430507
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12114873/
Abstract

: Hepatitis B (HBV) and C (HCV) virus coinfections remain major contributors to liver-related morbidity and mortality among people living with HIV (PLWH). This study aimed to assess the prevalence of HBV and/or HCV coinfections in a Romanian HIV cohort and to evaluate their impact on immunological, virological, and liver function parameters under antiretroviral therapy (ART). We retrospectively analyzed 462 HIV-infected patients (2018-2021) from the National Institute of Infectious Diseases, Bucharest, stratified into four groups: HIV mono-infection ( = 176), HIV/HBV ( = 114), HIV/HCV ( = 97), and HIV/HBV/HCV ( = 75) coinfections. Immunological (CD4 count, CD8 count, and CD4/CD8 ratio), virological (HIV-1 RNA), and hepatic parameters (ALT, AST, GGT, bilirubin, amylase, and lipase) were compared. No significant differences were observed between groups regarding the immune recovery (mean CD4 count = 0.89, HIV-RNA suppression = 0.78). However, liver and pancreatic parameters showed statistically significant deterioration in the coinfected groups. ALT ( < 0.001), GGT ( = 0.009), total bilirubin ( = 0.011), amylase ( = 0.010), and lipase ( < 0.001) were significantly higher in the triple-infection (HIV/HBV/HCV) group compared to HIV mono-infected patients. Coinfection was also associated with a longer duration of illness ( = 0.002) and therapy ( = 0.021) and with a higher number of ART regimens used ( = 0.013). While HIV suppression and immune recovery were not significantly impaired by HBV/HCV coinfections, liver and pancreatic injuries were significantly more prevalent and severe in coinfected patients. Regular monitoring of hepatic function and integrated management strategies are recommended to minimize liver-related complications in this population.

摘要

乙型肝炎病毒(HBV)和丙型肝炎病毒(HCV)合并感染仍然是导致人类免疫缺陷病毒(HIV)感染者(PLWH)肝脏相关发病和死亡的主要因素。本研究旨在评估罗马尼亚HIV队列中HBV和/或HCV合并感染的患病率,并评估它们在抗逆转录病毒治疗(ART)下对免疫、病毒学和肝功能参数的影响。我们回顾性分析了来自布加勒斯特国家传染病研究所的462例HIV感染患者(2018 - 2021年),将其分为四组:HIV单一感染(n = 176)、HIV/HBV(n = 114)、HIV/HCV(n = 97)和HIV/HBV/HCV(n = 75)合并感染。比较了免疫(CD4计数、CD8计数和CD4/CD8比值)、病毒学(HIV - 1 RNA)和肝脏参数(ALT、AST、GGT、胆红素、淀粉酶和脂肪酶)。在免疫恢复(平均CD4计数 = 0.89,HIV - RNA抑制 = 0.78)方面,各组之间未观察到显著差异。然而,合并感染组的肝脏和胰腺参数显示出统计学上的显著恶化。与HIV单一感染患者相比,三重感染(HIV/HBV/HCV)组的ALT(p < 0.001)、GGT(p = 0.009)、总胆红素(p = 0.011)、淀粉酶(p = 0.010)和脂肪酶(p < 0.001)显著更高。合并感染还与更长的病程(p = 0.002)和治疗时间(p = 0.021)以及更多的ART方案使用次数(p = 0.013)相关。虽然HBV/HCV合并感染并未显著损害HIV抑制和免疫恢复,但合并感染患者的肝脏和胰腺损伤明显更为普遍和严重。建议对该人群定期监测肝功能并采取综合管理策略,以尽量减少肝脏相关并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d250/12114873/0b10d7580ea6/pharmaceuticals-18-00688-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d250/12114873/55c3606d6ab9/pharmaceuticals-18-00688-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d250/12114873/c659bdb0cf52/pharmaceuticals-18-00688-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d250/12114873/f628daf08753/pharmaceuticals-18-00688-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d250/12114873/099f6a27fc72/pharmaceuticals-18-00688-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d250/12114873/0b10d7580ea6/pharmaceuticals-18-00688-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d250/12114873/55c3606d6ab9/pharmaceuticals-18-00688-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d250/12114873/c659bdb0cf52/pharmaceuticals-18-00688-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d250/12114873/f628daf08753/pharmaceuticals-18-00688-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d250/12114873/099f6a27fc72/pharmaceuticals-18-00688-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d250/12114873/0b10d7580ea6/pharmaceuticals-18-00688-g005a.jpg

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引用本文的文献

[1]
From Management to Cure: The Shifting Paradigm in HIV and Chronic Viral Hepatitis.

Pharmaceuticals (Basel). 2025-7-11

本文引用的文献

[1]
Prevalence of HDV, HCV, and HIV Infection in the Population of Patients Infected with HBV in a Romanian Cohort.

Microorganisms. 2025-1-9

[2]
Estimating the Current Routes of Transmission in HIV-1 F1 Subtype Infected Persons in Romania: Differences Between Self-Reporting and Phylogenetic Data.

Pathogens. 2024-11-4

[3]
Hospitalizations and deaths among people coinfected with HIV and HCV.

Sci Rep. 2024-11-19

[4]
World Medical Association Declaration of Helsinki: Ethical Principles for Medical Research Involving Human Participants.

JAMA. 2025-1-7

[5]
Hepatitis B and C viral coinfection and associated factors among HIV-positive patients attending ART clinics of Afar regional state, northeast Ethiopia.

PLoS One. 2024

[6]
Trends of pre-treatment drug resistance in antiretroviral-naïve people with HIV-1 in the era of second-generation integrase strand-transfer inhibitors in Taiwan.

J Antimicrob Chemother. 2024-5-2

[7]
Efficacy, safety, and tolerability of dolutegravir-based ART regimen in Durban, South Africa: a cohort study.

BMC Infect Dis. 2024-3-21

[8]
Factors associated with immunological non-response after ART initiation: a retrospective observational cohort study.

BMC Infect Dis. 2024-1-29

[9]
Associations of modern initial antiretroviral therapy regimens with all-cause mortality in people living with HIV in resource-limited settings: a retrospective multicenter cohort study in China.

Nat Commun. 2023-9-2

[10]
Bictegravir, emtricitabine, and tenofovir alafenamide versus dolutegravir, emtricitabine, and tenofovir disoproxil fumarate for initial treatment of HIV-1 and hepatitis B coinfection (ALLIANCE): a double-blind, multicentre, randomised controlled, phase 3 non-inferiority trial.

Lancet HIV. 2023-10

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