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Published on: September 11, 2019
Survival of HIV-infected patients with compensated liver cirrhosis
Paula Tuma1, Inmaculada Jarrin, Julia Del Amo
1Department of Infectious Diseases, Hospital Carlos III, Spain.
Insights
Mortality in HIV patients with liver cirrhosis is high, with older age, low CD4 counts, and detectable HIV RNA being key predictors. Hepatic elastometry and MELD scores accurately predict mortality in this population.
Area of Science:
- Hepatology and Infectious Diseases
- HIV/AIDS Research
- Clinical Outcomes and Prognosis
Background:
- Liver-related mortality is a leading cause of non-AIDS deaths in HIV-infected patients on HAART.
- Chronic hepatitis B and C are primary drivers of end-stage liver disease in this population.
Purpose of the Study:
- To examine mortality incidence and predictors in HIV-infected patients with compensated liver cirrhosis.
- To evaluate the predictive accuracy of elastometry, Child-Pugh, and MELD scores for mortality.
Main Methods:
- Prospective follow-up of 194 HIV-positive cirrhotic patients from October 2004 to December 2008.
- Analysis of mortality rates and associated factors using multivariate analyses.
- Assessment of elastometry, Child-Pugh, and MELD scores for mortality prediction.
Main Results:
- Overall mortality rate was 5.8 deaths per 100 patient-years.
- Independent predictors of mortality included age ≥50, CD4 <200 cells/µL, and detectable plasma HIV-RNA.
- MELD score ≥11 and hepatic elastometry >28.75 kPa were significant predictors of mortality.
Conclusions:
- HIV patients with compensated cirrhosis have a high annual mortality rate (5.8%) in the HAART era.
- Older age, low CD4 counts, and detectable HIV RNA are associated with increased mortality.
- Hepatic elastometry and MELD scores demonstrate strong predictive accuracy for mortality in this cohort.
Introduction:
Since the advent of HAART, liver-related mortality has become the leading cause of non-AIDS deaths in HIV-infected patients in western countries, complications of end-stage liver disease due to chronic hepatitis B, chronic hepatitis C or both being mainly responsible.
Method:
The incidence and predictors of mortality were examined in HIV-infected patients with compensated liver cirrhosis. The accuracy of three different methods (elastometry, Child-Pugh and Model for End-Stage Liver Disease scores) to predict mortality was further examined. Cirrhosis was defined for hepatic elastometry values above 14.5 kPa.
Results:
A total of 194 (11.4%) out of 1706 HIV-positive individuals were cirrhotic and were prospectively followed since October 2004 until December 2008. Overall, 89% of cirrhotic individuals had chronic hepatitis C, 10.3% chronic hepatitis B, 4.6% hepatitis delta and 4.1% liver disease of other causes or unknown cause. The overall mortality rate was 5.8 deaths per 100 patient-years. Multivariate analyses showed that age of at least 50 years (hazard ratio 4.76, 95% confidence interval 1.66-13.59, P = 0.004), CD4 cell counts below 200 cells/microl (hazard ratio 3.01, 95% confidence interval 1.26-7.23, P = 0.03) and detectable plasma HIV-RNA (hazard ratio 3.97, 95% CI, 1.53-10.27, P = 0.005) were associated with mortality. A baseline Model for End-stage Liver Disease score of at least 11 (P = 0.03) and hepatic elastometry values above 28.75 kPa (P = 0.001) were independent predictors of mortality.
Conclusion:
The death rate in HIV-infected patients with compensated liver cirrhosis in the HAART era is 5.8% yearly, higher than mortality previously reported for either HIV-uninfected individuals with cirrhosis or noncirrhotic HIV-positive patients. Factors associated with mortality were older age, low CD4 cell counts and detectable plasma HIV-RNA. Both Model for End-Stage Liver Disease and especially hepatic elastometry accurately predicted mortality in this population.
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