WASHINGTON (Feb. 22, 2021) --- People living with the human immunodeficiency virus (HIV) who have a history of severe immunosuppression and at least one copy of the Alzheimer's disease-related gene variant APOE4, might see a compounded adverse effect on the circuitry that impacts memory. This could eventually lead to an increased risk for dementia after age 65, according to Georgetown University Medical Center investigators and colleagues.
The researchers used MRI scans to examine the brain, with a focus on two regions - the hippocampus, which is critical for memory and is often affected in Alzheimer's disease, and the caudate nucleus, which sits deep in the center of the brain and is often affected in people with HIV. Based on the MRI images, they found that connectivity between the two regions was affected by APOE4 in people with HIV. A history of severe immunosuppression further exacerbated the impact of APOE4.
The finding appears online this month in the journal AIDS.
"We know that the hippocampus plays a critical role in memory and the caudate is a key region involved in HIV-associated neurocognitive disorders," said Xiong Jiang, PhD, an assistant professor at Georgetown who heads the Cognitive Neuroimaging Laboratory. "We wanted to understand whether HIV disease and APOE4 may concomitantly and/or interactively affect these areas of brain function."
The AIDS crisis began in mostly young men in the early 1980s, and by now nearly half of people living with HIV in the U.S. today are 50 or older. There have been significant advances in therapies for HIV that help account for the older survivors, including a combination antiretroviral therapy, or cART. This therapy stops HIV infection from progressing to full-blown AIDS in many people and transforms HIV-infection from a rapidly fatal illness to a chronic, manageable condition. Despite the advent of cART, people living with HIV can still develop neurological conditions known as HIV-associated neurocognitive disorders. Longevity now poses emerging additional risks related to other brain-related diseases, including Alzheimer's.
To try to better understand this risk, the researchers recruited 104 people with HIV from the Washington, DC, metropolitan area. To image areas of memory and other brain functions, the clinicians used resting-state functional MRI where no tasks or stimuli were given during the scan.
The investigators found that APOE4 was associated with reduced functional connectivity (the ability of two distinct areas of the brain to communicate) between the hippocampus and the caudate in people with HIV. This reduced functional connectivity was associated with poorer memory function. Importantly, a history of severe immunosuppression led to further reduction in functional connectivity that contributed to reduced memory performance in APOE4 carriers, but not in APOE4 non-carriers. The investigators concluded that a history of severe immunosuppression may compound the effects of APOE4. They also found that executive function, primarily the ability to conduct everyday chores, was not impaired in these same people.
Most treatments in development for Alzheimer's are focusing on signal pathways related to the hippocampus and associated regions, where new memories are formed and where the earliest signs of the disease are seen. However, in people with HIV, this study suggests that in addition to the hippocampus, the regions they identified, such as the caudate, might need to be considered and included in a treatment plan.
"A helpful study would be to compare HIV-positive people ages 18 to 40 with those over age 70 to investigate whether, and how, age interacts with APOE4 and HIV disease in affecting brain function," said Jiang. "Also, we're exploring a possible therapeutic investigation that uses transcranial direct current stimulation. A constant electrical current is delivered via electrodes placed on the scalp that indirectly stimulates the caudate or hippocampus of people with HIV to try to lessen functional deterioration of memory."
In addition to Jiang, authors of the manuscript at Georgetown include Fan Nils Yang, Margarita Bronshteyn, Sarah A. Flowers, Princy Kumar, G. William Rebeck and R. Scott Turner. Other authors include Matthew Dawson, David J. Moore, and Ronald J. Ellis at the University of California, San Diego.
Author and his/her co-authors report having no personal financial interests related to the study.
This research was supported by grant (1R01MH108466) from the National Institutes of Health.
About Georgetown University Medical Center
Georgetown University Medical Center (GUMC) is an internationally recognized academic health and science center with a four-part mission of research, teaching, service and patient care (through MedStar Health). GUMC's mission is carried out with a strong emphasis on public service and a dedication to the Catholic, Jesuit principle of cura personalis -- or "care of the whole person." The Medical Center includes the School of Medicine and the School of Nursing & Health Studies, both nationally ranked; Georgetown Lombardi Comprehensive Cancer Center, designated as a comprehensive cancer center by the National Cancer Institute; and the Biomedical Graduate Research Organization, which accounts for the majority of externally funded research at GUMC including a Clinical and Translational Science Award from the National Institutes of Health. Connect with GUMC on Facebook (Facebook.com/GUMCUpdate), Twitter (@gumedcenter).