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CN 34-1304/RISSN 1674-3679

Volume 29 Issue 2
Feb.  2025
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CHEN Mingyu, LIU Cong, TANG Xiaoping, LI Quanmin, LI Linghua, GU Jing, CAI Weiping. Long-term effect of AIDS infected individuals with hepatitis B virus infection on abnormal liver enzymes in Guangzhou[J]. CHINESE JOURNAL OF DISEASE CONTROL & PREVENTION, 2025, 29(2): 178-185. doi: 10.16462/j.cnki.zhjbkz.2025.02.009
Citation: CHEN Mingyu, LIU Cong, TANG Xiaoping, LI Quanmin, LI Linghua, GU Jing, CAI Weiping. Long-term effect of AIDS infected individuals with hepatitis B virus infection on abnormal liver enzymes in Guangzhou[J]. CHINESE JOURNAL OF DISEASE CONTROL & PREVENTION, 2025, 29(2): 178-185. doi: 10.16462/j.cnki.zhjbkz.2025.02.009

Long-term effect of AIDS infected individuals with hepatitis B virus infection on abnormal liver enzymes in Guangzhou

doi: 10.16462/j.cnki.zhjbkz.2025.02.009
Funds:

National Science and Technology Major Project of the Ministry of Science and Technology during the 13rd Five-Year Plan Period of China 2018ZX10715004

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  • Corresponding author: LI Linghua, E-mail: llheliza@126.com; GU Jing, E-mail: gujing5@mail.sysu.edu.cn
  • Received Date: 2024-03-01
  • Rev Recd Date: 2024-12-20
  • Available Online: 2025-03-08
  • Publish Date: 2025-02-10
  •   Objective  To analyze the impact of concurrent HBV infection on the occurrence of liver enzyme abnormalities in HIV-infected individuals during long-term antiviral therapy in Guangzhou City.  Methods  A retrospective cohort study was conducted in December 2023, using follow-up data from HIV-infected individuals who received antiviral treatment at the Eighth People′s Hospital of Guangzhou from January 1 2010, to June 30 2021, as recorded in the "Comprehensive AIDS Prevention and Control Data Information Management System." The study employed a joinpoint regression model to analyze the changing trend in the risk of liver enzyme abnormalities. Propensity score matching was applied to enhance comparability between individuals co-infected with HBV and those simple HIV infections. Additionally, a multilevel logistic regression model was used to analyze the impact of concurrent HBV infection on liver enzyme abnormalities.  Results  After applying the inclusion and exclusion criteria, 13 829 HIV-infected individuals were screened, and following propensity score matching, a total of 9 050 HIV-infected individuals were included in the analysis. Among individuals infected with HIV alone and those with HBV, 61.8% and 70.4% experienced liver enzyme abnormalities, respectively. The risk of occurrence showed a rapid decrease within 9 months of treatment, a slow decrease from 9 to 27 months of treatment, and a stable three stage period after 27 months of treatment. For HIV-infected individuals, the co-infection with HBV within the first 9 months of antiviral treatment is a risk factor for liver enzyme abnormalities (OR=1.637, 95% CI: 1.437-1.866), but after 9 months of continuous antiviral treatment, there was no association between ca-HBV and liver enzyme abnormalities (P>0.05).  Conclusions  In the follow-up and management of AIDS, the liver function of patients with HBV infection should be focused on in the first year after starting antiviral treatment.
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