Fast Fibrosis Progression Between Repeated Liver Biopsies in Patients Coinfected with Human Immunodeficiency Virus/hepatitis C Virus
Overview
Authors
Affiliations
Unlabelled: A few studies have assessed the observed fibrosis progression between serial liver biopsies (LB) in human immunodeficiency virus (HIV) / hepatitis C virus (HCV)-coinfected patients. Approximately half of the patients progressed at least one fibrosis stage over a short period of time. The risk factors for this fast progression need clarification. Because of this, we evaluated the observed fibrosis progression rates of HIV/HCV-coinfected patients and the risk factors for accelerated progression. Overall, 135 HIV-infected patients with positive serum HCV RNA, without other possible causes of liver disease, who underwent two LB, separated at least by 1 year, were included in this retrospective cohort study. The median (Q1-Q3) time between both LBs was 3.3 (2.0-5.2) years. Patients showed the following changes in fibrosis stage: regression >or =1 stage: 23 (17%), no change: 52 (39%), progression 1 stage: 38 (28%), and progression > or =2 stages: 22 (16%). Seventeen (13%) patients had cirrhosis in the second biopsy. Factors independently associated with progression > or =1 stage were undetectable plasma HIV RNA during the follow-up (relative risk [RR] [95% confidence interval, 95% CI] 0.61 [0.39-0.93], P = 0.03), moderate-to-severe lobular necroinflammation (1.77 [1.16-2.7], P = 0.009), time between biopsies (1.11 [1.08-1.2], P = 0.01), and end of treatment response to anti-HCV therapy (0.41 [0.19-0.88], P = 0.02).
Conclusion: Fibrosis progresses with high frequency in HIV/HCV-coinfected patients over a period of time of 3 years. Absent-to-mild lobular necroinflammation at baseline, achievement of response with anti-HCV treatment, and effective antiretroviral therapy are associated with slower fibrosis progression.
SASLT guidelines: Update in treatment of hepatitis C virus infection, 2024.
Alghamdi A, Alghamdi H, Alserehi H, Babatin M, Alswat K, Alghamdi M Saudi J Gastroenterol. 2024; 30(Supp 1):S1-S42.
PMID: 38167232 PMC: 10856511. DOI: 10.4103/sjg.sjg_333_23.
Lin W, Wang X, Zhang J, Wen C, Kang W, Mao L Lancet Reg Health West Pac. 2023; 36:100749.
PMID: 37547041 PMC: 10398601. DOI: 10.1016/j.lanwpc.2023.100749.
Aimla K, Kowalska J, Matulionyte R, Mulabdic V, Vassilenko A, Bolokadze N Vaccines (Basel). 2023; 11(5).
PMID: 37243084 PMC: 10222000. DOI: 10.3390/vaccines11050980.
Singh G, Lata S, Swu A, Virk N, Singh J, Thakkar S J Family Med Prim Care. 2023; 11(10):6250-6254.
PMID: 36618149 PMC: 9810970. DOI: 10.4103/jfmpc.jfmpc_788_22.
Lateral flow assays for viruses diagnosis: Up-to-date technology and future prospects.
Ince B, Sezginturk M Trends Analyt Chem. 2022; 157:116725.
PMID: 35815063 PMC: 9252863. DOI: 10.1016/j.trac.2022.116725.