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Aging, comorbidities, and the importance of finding biomarkers for HIV-associated neurocognitive disorders
Jacqueline Rosenthal1,2, William Tyor3,4
1Atlanta VA Medical Center, Decatur, GA, USA.
Insights
HIV-associated neurocognitive disorders (HAND) are common in people with HIV, even with treatment. Diagnosis is challenging due to aging and other conditions, requiring new biomarkers for accuracy.
Area of Science:
- Neuroscience
- Infectious Diseases
- Geriatrics
Background:
- HIV-associated neurocognitive disorders (HAND) persist despite combined antiretroviral therapy (cART).
- Milder forms of HAND are increasingly prevalent.
- HAND pathogenesis is multifactorial, involving pre-cART CNS damage, immune activation, cART neurotoxicity, and comorbidities.
Purpose of the Study:
- To address the diagnostic challenges of mild HAND in an aging HIV-positive population.
- To highlight the need for age-appropriate differential diagnoses for HAND.
- To emphasize the necessity of developing reliable biomarkers for early and accurate HAND diagnosis.
Main Methods:
- Review of current literature on HAND pathogenesis and diagnosis in the context of aging and cART.
- Analysis of factors contributing to cognitive impairment in aging individuals with HIV.
- Discussion of shared pathologies between HAND and other neurodegenerative diseases.
Main Results:
- Aging HIV-positive individuals face complex cognitive challenges due to multifactorial HAND causes.
- Premature aging and comorbidities like cardiovascular disease exacerbate cognitive impairment.
- Shared pathologies with diseases like Alzheimer's complicate HAND diagnosis.
Conclusions:
- Accurate diagnosis of mild HAND in aging populations is challenging.
- Biomarkers are crucial for early, reliable HAND diagnosis.
- Development of specific biomarkers is essential for future targeted HAND treatments.
Abstract:
HIV-associated neurocognitive disorders (HAND) continue to affect a large proportion of persons living with HIV despite effective viral suppression with combined antiretroviral therapy (cART). Importantly, milder versions of HAND have become more prevalent. The pathogenesis of HAND in the era of cART appears to be multifactorial with contributions from central nervous system (CNS) damage that occur prior to starting cART, chronic immune activation, cART neurotoxicity, and various age-related comorbidities (i.e., cardiovascular and cerebrovascular disease, diabetes, hyperlipidemia). Individuals with HIV may experience premature aging, which could also contribute to cognitive impairment. Likewise, degenerative disorders aside from HAND increase with age and there is evidence of shared pathology between HAND and other neurodegenerative diseases, such as Alzheimer's disease, which can occur with or without co-existing HAND. Given the aforementioned complex interactions associated with HIV, cognitive impairment, and aging, it is important to consider an age-appropriate differential diagnosis for HAND as the HIV-positive population continues to grow older. These factors make the accuracy and reliability of the diagnosis of mild forms of HAND in an aging population of HIV-infected individuals challenging. The complexity of current diagnosis of mild HAND also highlights the need to develop reliable biomarkers. Ultimately, the identification of a set of specific biomarkers will be required to achieve early and accurate diagnosis, which will be necessary assuming specific treatments for HAND are developed.
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