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A Protocol for Analyzing Hepatitis C Virus Replication
Published on: June 26, 2014
Neuropsychiatric impact of hepatitis C on advanced HIV
E L Ryan1, S Morgello, K Isaacs
1Departments of Psychiatry, The Mount Sinai Medical Center, New York, NY, USA. elizabeth.ryan@mssm.edu
Insights
Hepatitis C (HCV) infection appears to worsen central nervous system (CNS) dysfunction in individuals with advanced HIV. This coinfection is linked to poorer neurocognitive performance and increased rates of HIV-associated dementia.
Area of Science:
- Neuroscience
- Infectious Diseases
- Psychiatry
Background:
- Advanced HIV infection is associated with cognitive impairment.
- Hepatitis C virus (HCV) coinfection is common in HIV-positive individuals.
- The impact of HCV on CNS dysfunction in HIV patients requires further investigation.
Purpose of the Study:
- To determine if HCV coinfection contributes to central nervous system (CNS) dysfunction in individuals with advanced HIV.
- To compare the neuropsychiatric profiles of HIV+/HCV+ and HIV+/HCV- individuals.
Main Methods:
- Cross-sectional study design.
- Neurocognitive testing and psychiatric interviews.
- Serological testing for HCV and serum chemistries for hepatic function.
Main Results:
- HIV+/HCV+ individuals showed higher rates of past substance dependence and substance-induced depression.
- A trend towards worse neurocognitive performance was observed in HIV+/HCV+ participants, particularly in executive functioning and perseveration.
- Cognitive differences correlated with HCV serology but not liver disease severity.
- HIV+/HCV+ patients had higher rates of HIV-associated dementia.
Conclusions:
- HCV coinfection has a detectable neuropsychiatric impact in advanced HIV cohorts.
- The observed cognitive deficits are linked to HCV, independent of liver disease severity.
- Further research is warranted to understand the mechanisms underlying HCV's contribution to CNS dysfunction in HIV.
Objective:
To determine whether hepatitis C (HCV) contributes to CNS dysfunction among HIV-infected individuals.
Methods:
Using a cross-sectional design, the neuropsychiatric profile of individuals with advanced HIV coinfected with hepatitis C (HIV+/HCV+) was compared to similarly advanced HIV patients without HCV coinfection (HIV+/HCV-). Participants were derived from the Manhattan HIV Brain Bank and underwent neurocognitive testing and semistructured psychiatric interviews. Evidence of HCV infection was determined by serology performed prior to study entry. Hepatic function was determined by serum chemistries (bilirubin, creatinine, and international normalized ratio) at the time of the cognitive assessments.
Results:
Coinfected (HIV+/HCV+) individuals were significantly more likely to have had past opiate or cocaine or stimulant dependence. HIV+/HCV+ participants also had significantly greater rates of past substance-induced major depression. There were no significant differences in rates of primary mental disorders. Forty-two percent of both the HIV+/HCV+ and HIV+/HCV- participants met criteria for current major depression. There was a trend for HIV+/HCV+ patients to perform worse neurocognitively. On tests of executive functioning, HIV+/HCV+ individuals exhibited a greater rate of impairment and had significantly more perseveration. Differences in cognitive functioning were associated with serology but did not correlate with indices of liver disease severity. The HCV+ patients were also more likely to be diagnosed with HIV-associated dementia.
Conclusions:
There appears to be a neuropsychiatric impact of HCV that is detectable even among an advanced HIV cohort.
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