People with HIV are at higher risk of ageing-related genetic changes
We don’t know enough about biological processes in people who are aging with HIV—a new study sheds light on the matter.
Forty years after the first diagnosis of HIV/AIDS, Australian scientists from the Kirby Institute at UNSW Sydney and the Peter MacCallum Cancer Center have uncovered a vital link in the relationship between HIV and aging. The results were published today in the journal Nature Medicine.
In this world-leading study, the research team evaluated age-related genetic changes in over 400 participants from nine sites at hospitals and community practices. Half of the participants had HIV, and half did not.
The study found that people living with HIV had a higher rate of clonal haematopoiesis (CH) – a common condition among older people caused by a genetic mutation in a small number of blood stem cells.
“One in ten older people in the general population have these mutations in their blood cells, but our study found that one in five people with HIV have these mutations,” says Dr. Nila Dharan from the Kirby Institute, co-lead author on the paper.
“As people with HIV have more cardiovascular disease and blood cancers than the general population, this finding suggests new pathways behind the development of medical conditions in people with HIV, and may in the future help identify preventive measures to reduce these conditions and optimize the health of aging people with HIV.”
An HIV diagnosis used to be a death sentence, but thanks to incredible scientific advances in antiretroviral treatments, people with HIV are living long, healthy lives.
“The good news is that globally, people with HIV are living longer, and the question of how HIV affects the aging process, and what we can do to maximize the health and quality of life of older adults with HIV, is becoming an increasingly important field of research,” says Dr. Dharan.
The link between inflammation, aging and HIV
According to the research team, this discovery is centered around the relationship between HIV, inflammation, and aging. HIV attacks cells in the lymph nodes and in lymphatic tissue, and this causes inflammation. While HIV treatment slows this process, people with HIV may still have higher levels of inflammation than people without HIV.
“Our study found that people with HIV and CH had higher markers of inflammation, suggesting that the underlying chronic inflammation seen in people with HIV may create an environment that facilitates the emergence of clonal haematopoiesis mutations,” says Dr. Paul Yeh from the Peter MacCallum Cancer Center, who is also co-lead author on the paper. “Because inflammation increases as part of the aging process, older people with HIV may have multiple risk factors for the development of CH.”
The research casts new light on the biological processes occurring in people who are aging with HIV, and outlines directions for future research.
“Our research has demonstrated that people with HIV have an increased chance of developing clonal haematopoiesis mutations. Importantly, however, in this study we did not find that people who have HIV and CH had more adverse health outcomes, but more research is needed,” says Dr. Yeh, who is also a physician hematologist.
“As there are many other factors that determine whether or not a person with or without HIV develops stroke, cardiovascular disease or blood cancer—such as age, gender and lifestyle factors like smoking—further research is critical to understanding the role that clonal haematopoiesis plays among all of these.”
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