TY - JOUR
T1 - Relationship between Brain Arterial Pathology and Neurocognitive Performance among Individuals with Human Immunodeficiency Virus
AU - Gutierrez, Jose
AU - Byrd, Desiree
AU - Yin, Michael T.
AU - Morgello, Susan
N1 - Publisher Copyright:
© The Author(s) 2018.
PY - 2019/1/18
Y1 - 2019/1/18
N2 - Background. Human immunodeficiency virus-positive (HIV+) individuals have higher rates of cognitive impairment and cerebrovascular disease compared with uninfected populations. We hypothesize that cerebrovascular disease, specifically brain large artery disease, may play a role in HIV-associated neurocognitive disorders (HAND). Methods. Participants (N = 94) in the Manhattan HIV Brain Bank study were followed on average 32 ± 33 months with repeated neuropsychological examinations until death. We used five cognitive domains (motor, processing speed, working memory, verbal fluency, and executive functioning) to assess ante mortem performance. We quantified the diameter of the lumen and arterial wall thickness obtained during autopsy. The diagnoses of HAND were attributed using the American Academy of Neurology nosology. We used generalized linear mixed model to account for repeated measures, follow-up time, and codependence between arteries. Models were adjusted for demographics, viral loads, CD4 counts, history of opportunistic infections, and vascular risks. Results. We included 94 HIV+ individuals (mean age 56 ± 8.3, 68% men, 54% African American). In adjusted models, there was an association between arterial wall thickness and global cognitive score (B = ?0.176, P value = .03), processing speed (B = ?0.175, P = .05), and verbal fluency (B = ?0.253, P = .02). Participants with incident or worsening HAND had thicker brain arterial walls (B = 0.523 ± 0.234, P = .03) and smaller arterial lumen (B = ?0.633 ± 0.252, P = .01). Conclusions. We report here a novel association between brain arterial wall thickening and poorer ante mortem cognitive performance and diagnosis of.
AB - Background. Human immunodeficiency virus-positive (HIV+) individuals have higher rates of cognitive impairment and cerebrovascular disease compared with uninfected populations. We hypothesize that cerebrovascular disease, specifically brain large artery disease, may play a role in HIV-associated neurocognitive disorders (HAND). Methods. Participants (N = 94) in the Manhattan HIV Brain Bank study were followed on average 32 ± 33 months with repeated neuropsychological examinations until death. We used five cognitive domains (motor, processing speed, working memory, verbal fluency, and executive functioning) to assess ante mortem performance. We quantified the diameter of the lumen and arterial wall thickness obtained during autopsy. The diagnoses of HAND were attributed using the American Academy of Neurology nosology. We used generalized linear mixed model to account for repeated measures, follow-up time, and codependence between arteries. Models were adjusted for demographics, viral loads, CD4 counts, history of opportunistic infections, and vascular risks. Results. We included 94 HIV+ individuals (mean age 56 ± 8.3, 68% men, 54% African American). In adjusted models, there was an association between arterial wall thickness and global cognitive score (B = ?0.176, P value = .03), processing speed (B = ?0.175, P = .05), and verbal fluency (B = ?0.253, P = .02). Participants with incident or worsening HAND had thicker brain arterial walls (B = 0.523 ± 0.234, P = .03) and smaller arterial lumen (B = ?0.633 ± 0.252, P = .01). Conclusions. We report here a novel association between brain arterial wall thickening and poorer ante mortem cognitive performance and diagnosis of.
KW - Brain Arterial Remodeling
KW - Cerebrovascular Disease
KW - Dementia
KW - HIV
KW - HIV-Associated Neurocognitive Disorders
UR - http://www.scopus.com/inward/record.url?scp=85060176442&partnerID=8YFLogxK
U2 - 10.1093/cid/ciy501
DO - 10.1093/cid/ciy501
M3 - Article
C2 - 30107467
AN - SCOPUS:85060176442
SN - 1058-4838
VL - 68
SP - 490
EP - 497
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 3
ER -