Heavy alcohol consumption (three drinks or more/day for women and four drinks or more/day for men) is linked to alterations in immune function among people with HIV.
While it has been known that alcohol impacts immune function, it’s been unclear the effect of alcohol on immune function in the context of HIV, a disease whose progression is dependent on immune dysfunction.
Researchers from Boston University School of Medicine (BUSM) looked at biological markers of innate immune function, a kind of immune response that acts quickly and non-specifically to new infections and pathogens. They investigated biological markers of three specific immune processes: systemic inflammation, monocyte activation and altered coagulation. Higher levels of biological markers for these processes have previously been associated with higher risk of death. In the current study, the researchers assessed self-reported alcohol use over time (three times over two years) and also measured alcohol use using a blood-based marker of alcohol consumption called PEth (phosphatidylethanol) that detects alcohol consumption up to about 21 days after drinking. Additionally they measured other behaviors and health conditions that could obscure the true relationship between alcohol consumption and these biomarkers.
“We found that people who reported drinking more alcohol or had high PEth had higher levels of these biomarkers of immune function. The fact that heavy alcohol consumption was linked to elevated levels of these biomarkers, which are linked to mortality, suggests that alcohol may be contributing to mortality risk through immune dysfunction among people with HIV,” said corresponding author Kaku So-Armah, PhD, assistant professor of medicine at BUSM.
According to the researchers, it is important to note they observed elevated levels of these biomarkers of immune activity in a relatively young HIV population with a low occurrence of chronic inflammatory diseases of aging like diabetes, obesity or renal disease. “Further we observed that the relationship between alcohol consumption and some of these biomarkers was not linear, suggesting a complex relationship between alcohol use and biomarkers of systemic inflammation and monocyte activation.”
While the researchers stress that this is an observational study and the findings do not prove causality, they hope the study highlights the harms associated with heavy alcohol consumption among people living with HIV.
These findings appear online in the journal PLoS One.
Funding for this study was provided by grants from the National Institute on Alcohol Abuse and Alcoholism (NIAAA) in support of URBAN ARCH: U01AA021989, U01AA020780, U24AA020779, U24AA020778; National Heart, Lung, and Blood Institute (K01 HL1314701); and by the Providence/Boston Center for AIDS Research (P30AI042853) and Tennessee Center for AIDS Research (P30AI110527).
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