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Updated: Jan 27, 2026

Measurement of In Vitro Integration Activity of HIV-1 Preintegration Complexes
Published on: February 22, 2017
Effects of comorbidity burden and age on brain integrity in HIV
Rowan Saloner1,2, Robert K Heaton1, Laura M Campbell1,2
1Department of Psychiatry, University of California San Diego, La Jolla.
Insights
Comorbidities significantly impact brain health in people living with HIV (PLWH), affecting neuroimaging results. Older age worsens brain tissue injury, particularly in those with severe comorbidities.
Area of Science:
- Neuroimaging
- Neuroscience
- Infectious Diseases
Background:
- Neurocognitive comorbidities in people living with HIV (PLWH) can influence neuroimaging findings.
- Systematic evaluation of these confounding factors is crucial for understanding brain integrity in PLWH.
Purpose of the Study:
- To determine the association between comorbidity burden and brain integrity in PLWH.
- To examine the moderating effect of age on these associations.
Main Methods:
- Cross-sectional study of 288 PLWH using structural MRI and magnetic resonance spectroscopy.
- Comorbidity burden classified as incidental, contributing, or confounding based on Frascati criteria for HAND.
- Multiple regression modeling analyzed neuroimaging outcomes, comorbidity classification, age, and their interaction.
Main Results:
- Confounded participants showed reduced gray matter, abnormal white matter, and increased neuroinflammation compared to incidental/contributing groups.
- Older age exacerbated white matter abnormalities and reduced gray matter, especially in the confounded group.
- These findings were independent of HIV disease characteristics.
Conclusions:
- Neuroimaging in PLWH reveals distinct patterns associated with confounding neurocognitive conditions.
- Evaluating comorbidities is essential for diagnosing HAND in PLWH.
- Older age amplifies brain tissue injury in PLWH with severe comorbidities, necessitating focused attention as this population ages.
Objective:
The influence of confounding neurocognitive comorbidities in people living with HIV (PLWH) on neuroimaging has not been systematically evaluated. We determined associations between comorbidity burden and brain integrity and examined the moderating effect of age on these relationships.
Design:
Observational, cross-sectional substudy of the CNS HIV Antiretroviral Therapy Effects Research cohort.
Methods:
A total of 288 PLWH (mean age = 44.2) underwent structural MRI and magnetic resonance spectroscopy as well as neurocognitive and neuromedical assessments. Consistent with Frascati criteria for HIV-associated neurocognitive disorders (HAND), neuromedical and neuropsychiatric comorbidity burden was classified as incidental (mild), contributing (moderate), or confounding (severe-exclusionary) to a diagnosis of HAND. Multiple regression modeling predicted neuroimaging outcomes as a function of comorbidity classification, age, and their interaction.
Results:
Comorbidity classifications were 176 incidental, 77 contributing, and 35 confounded; groups did not differ in HIV disease characteristics. Relative to incidental and contributing participants, confounded participants had less cortical gray matter and more abnormal white matter and ventricular cerebrospinal fluid, alongside more neuroinflammation (choline, myo-inositol) and less neuronal integrity (N-acetylaspartate). Older age exacerbated the impact of comorbidity burden: to a greater extent in the confounded group, older age was associated with more abnormal white matter (P = 0.017), less total white matter (P = 0.015), and less subcortical gray matter (P = 0.014).
Conclusion:
Neuroimaging in PLWH reveals signatures associated with confounding neurocognitive conditions, emphasizing the importance of evaluating these among individuals with suspected HAND. Older age amplifies subcortical and white matter tissue injury, especially in PLWH with severe comorbidity burden, warranting increased attention to this population as it ages.
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