4.3 Article Proceedings Paper

Ethnic/Racial Disparities in Longitudinal Neurocognitive Decline in People With HIV

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAI.0000000000002922

关键词

Hispanic Americans; African Americans; cognitive disorders; health status disparities

资金

  1. NIH [T32DA031098, T32 AA013525, K23MH105297, P30AG059299, N01 MH22005, HHSN271201000036C, HHSN271201000030C, R01 MH107345]

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This study examined neurocognitive decline among Latino, non-Latino Black, and non-Latino White people with HIV and explored factors that may explain ethnic/racial disparities. The findings showed that Latino individuals with HIV may be at a higher risk of early neurocognitive decline compared to Black and White individuals. Comorbidities accounted for some, but not all, of the increased risk among Latino individuals. Further research is needed to understand the institutional, sociocultural, and biomedical factors contributing to these disparities.
Background: To examine longitudinal neurocognitive decline among Latino, non-Latino Black, and non-Latino White people with HIV (PWH) and factors that may explain ethnic/racial disparities in neurocognitive decline. Methods: Four hundred ninety nine PWH (13.8% Latino, 42.7% Black, 43.5% White; baseline age: M = 43.5) from the CNS HIV Anti-Retroviral Therapy Effects Research (CHARTER) study completed neurocognitive, neuromedical, and laboratory assessments every 6-12 months with up to 5 years of follow-up. Longitudinal neurocognitive change was determined via published regression-based norms. Survival analyses investigated the relationship between ethnicity/race and neurocognitive change, and baseline and time-dependent variables that may explain ethnic/racial disparities in neurocognitive decline, including socio-demographic, HIV-disease, medical, psychiatric, and substance use characteristics. Results: In Cox proportional hazard models, hazard ratios for neurocognitive decline were increased for Latino compared with White PWH (HR = 2.25, 95% CI = 1.35 to 3.73, P = 0.002), and Latino compared with Black PWH (HR = 1.86, 95% CI = 1.14 to 3.04, P = 0.013), with no significant differences between Black and White PWH (P = 0.40). Comorbidities, including cardiometabolic factors and more severe neurocognitive comorbidity classification, accounted for 33.6% of the excess hazard for Latino compared with White PWH, decreasing the hazard ratio associated with Latino ethnicity (HR = 1.83, 95% CI = 1.06 to 3.16, P = 0.03), but did not fully account for elevated risk of decline. Conclusions: Latino PWH may be at higher risk of early neurocognitive decline compared with Black and White PWH. Comorbidities accounted for some, but not all, of this increased risk among Latino PWH. Future research examining institutional, sociocultural, and biomedical factors, including structural discrimination and age-related biomarkers, may further explain the observed disparities.

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