Metabolic disorders cause liver damage in people with HIV more often than viral hepatitis in lower-income countries

Keith Alcorn
Published:
01 March 2022
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Liver fibrosis in people with HIV in low- and middle-income countries was more often attributable to metabolic disorders than viral hepatitis, a six-country comparative study has found.

The findings, presented last month at the 2022 Conference on Retroviruses and Opportunistic Infections, suggest that prevention of type 2 diabetes and obesity will be critical for avoiding a growing burden of severe liver disease in people living with HIV as they age.

As the prevalence of hepatitis C has declined in people with HIV in higher-income countries due to direct-acting antiviral treatment, the contribution of metabolic disorders to liver disease has grown. But the role of metabolic disorders such as diabetes, obesity and raised lipid levels in causing liver damage in people with HIV in lower- and middle-income settings is less clear.

Glossary

FibroScan

A non-invasive test, used instead of a biopsy, to measure the stiffness or elasticity of the liver using an ultrasound probe.

steatosis

Abnormal fat deposits in the liver.

Researchers associated with two large international cohort studies of people with HIV on antiretroviral treatment investigated liver disease and its underlying causes in a subset of people with HIV enrolled into the cohorts in six countries (Brazil, Côte d'Ivoire, India, Kenya, Rwanda and Zambia).

The study looked at the prevalence of fibrosis, using non-invasive scanning, in adults with HIV on antiretroviral treatment aged 40 and over. Participants were also screened for viral hepatitis, metabolic disorders and hazardous alcohol use and multivariable analysis was used to identify factors associated with fibrosis and steatosis (liver fat accumulation).

The study analysed 1632 participants with a median age of 50 years who enrolled in the cohorts between June 2015 and August 2021. All participants had been taking antiretroviral treatment for at least six months and the median CD4 count was 545 cells. The study authors did not report the distribution of study participants between countries.

Screening for liver disease was carried out by Fibroscan transient elastography and showed that 11% had F2-F4 fibrosis, while 31% had steatosis. Prevalence of both conditions was highest in Brazil and India, where over 40% had steatosis and approximately 20% had fibrosis.

Multivariable analysis showed that people with HIV in India were between three and four times more likely to have liver fibrosis compared to people with HIV in Zambia, while people with HIV in Kenya were up to 90% less likely to have fibrosis compared to their counterparts in Zambia. Steatosis risk was similar for people with HIV in Zambia and Kenya, while the risk of liver fibrosis and steatosis was broadly similar for people with HIV in Zambia, Côte d'Ivoire and Rwanda.

The prevalence of viral hepatitis was relatively low compared to cohorts of people with HIV in Europe and Asia: 4.5% had hepatitis B and 3.4% had hepatitis C. Two-thirds of those with hepatitis B (67%) were taking tenofovir as part of their antiretroviral regimen (tenofovir also suppresses hepatitis B replication). People with chronic hepatitis B infection did not have an elevated risk of fibrosis but chronic hepatitis C infection raised the risk of fibrosis fivefold compared to no viral hepatitis.

Metabolic disorders were common in the study population. Nineteen per cent were obese (body mass index of 30 or more), 11% had type 2 diabetes, 24% had hypertension and 53% had dyslipidemia. Fifteen per cent had a hazardous level of alcohol use. In the multivariable analysis, obesity and type 2 diabetes were each associated with a 2.5-fold increase in the risk of fibrosis, while obesity raised the risk of steatosis fivefold. Type 2 diabetes tripled the risk of steatosis. Dyslipidemia and hypertension did not increase the risk of fibrosis or steatosis.

The researchers calculated what proportion of liver fibrosis in the study population was attributable to the risk factors that proved significant in multivariable analysis (the population attributable fraction). Eighteen per cent of fibrosis was attributable to obesity, 12% to type 2 diabetes, 8% to chronic hepatitis and 3% to hepatitis B.

Marie Plaisy of the University of Bordeaux, the study’s lead author, said that “as access to effective antiviral therapies against chronic viral hepatitis expands, preventive measures against diabetes and obesity for PLHIV [people living with HIV] are urgently needed.” Obesity in particular is a concern in people with HIV. Newer antiretroviral regimens are associated with substantial weight gain after starting treatment and in settings where body weight is high among people starting treatment, the weight gain may lead to obesity. Liver damage may prove to be a long-term complication of the weight gain associated with newer antiretroviral regimens, but larger prospective studies will be needed to investigate this potential risk.

Reference

Plaisy MK et al. Etiology of liver disease in adults with HIV in low and middle-income countries. Conference on Retroviruses and Opportunistic Infections, abstract 549, 2022.