Cognitive Performance and Neuro-Metabolites in HIV Using 3T Magnetic Resonance Spectroscopy: A Cross-Sectional Study
K Gupta1, Shivabalan2, V Kumar2
1Department of Internal Medicine, All India Institute of Medical Sciences, New Delhi, India.
Current HIV Research
|October 27, 2020
Summary
Cognitive impairment is common in human immunodeficiency virus (HIV) patients not on antiretroviral therapy (ART). Brain metabolite levels did not differ between HIV patients with or without cognitive impairment.
Area of Science:
- Neuroscience
- Infectious Diseases
- Radiology
Background:
- Cognitive impairment in human immunodeficiency virus (HIV) is linked to increased morbidity.
- The prevalence of brain metabolite changes associated with cognitive impairment in ART-naïve HIV patients is not well-established.
Purpose of the Study:
- To determine the prevalence of neurometabolites linked to cognitive impairment in ART-naïve HIV patients.
Main Methods:
- A cross-sectional study was conducted on 43 ART-naïve HIV patients (aged 18-50) in India.
- Cognition was assessed using the Post Graduate Institute battery, evaluating memory, attention, executive function, perceptual skills, and motor skills.
- Brain metabolites (tNAA, tCr, Glx) were measured using 3T magnetic resonance spectroscopy; cognitive impairment was defined as impairment in ≥2 domains.
Main Results:
- Over half (51.2%) of the participants had cognitive impairment, with deficits most common in simple motor skills (46.5%) and memory (44%).
- While trends suggested higher frontal lobe concentrations of tNAA, tGlx, and tCr in those with cognitive impairment, these differences were not statistically significant (p>0.05).
- No significant differences in metabolite concentrations were observed in the basal ganglia between groups.
Conclusions:
- A high prevalence of cognitive impairment exists in ART-naïve HIV patients.
- No significant differences in measured brain metabolites were found between HIV patients with or without cognitive impairment.
- Further longitudinal studies are needed to elucidate the pathophysiology of cognitive impairment in this population.


