Neurocognitive SuperAging in Older Adults Living With HIV: Demographic, Neuromedical and Everyday Functioning Correlates.

TitleNeurocognitive SuperAging in Older Adults Living With HIV: Demographic, Neuromedical and Everyday Functioning Correlates.
Publication TypeJournal Article
Year of Publication2019
AuthorsSaloner, R, Campbell, LM, Serrano, V, Montoya, JL, Pasipanodya, E, Paolillo, EW, Franklin, D, Ellis, RJ, Letendre, SL, Collier, AC, Clifford, DB, Gelman, BB, Marra, CM, J McCutchan, A, Morgello, S, Sacktor, N, Jeste, DV, Grant, I, Heaton, RK, Moore, DJ
Corporate AuthorsCHARTER and HNRP Groups
JournalJ Int Neuropsychol Soc
Volume25
Issue5
Pagination507-519
Date Published2019 05
ISSN1469-7661
KeywordsActivities of Daily Living, Cognition, Cognitive Aging, Cognitive Reserve, Employment, Female, Healthy Lifestyle, HIV Infections, Humans, Male, Marijuana Use, Middle Aged, Quality of Life
Abstract

OBJECTIVES: Studies of neurocognitively elite older adults, termed SuperAgers, have identified clinical predictors and neurobiological indicators of resilience against age-related neurocognitive decline. Despite rising rates of older persons living with HIV (PLWH), SuperAging (SA) in PLWH remains undefined. We aimed to establish neuropsychological criteria for SA in PLWH and examined clinically relevant correlates of SA.METHODS: 734 PLWH and 123 HIV-uninfected participants between 50 and 64 years of age underwent neuropsychological and neuromedical evaluations. SA was defined as demographically corrected (i.e., sex, race/ethnicity, education) global neurocognitive performance within normal range for 25-year-olds. Remaining participants were labeled cognitively normal (CN) or impaired (CI) based on actual age. Chi-square and analysis of variance tests examined HIV group differences on neurocognitive status and demographics. Within PLWH, neurocognitive status differences were tested on HIV disease characteristics, medical comorbidities, and everyday functioning. Multinomial logistic regression explored independent predictors of neurocognitive status.RESULTS: Neurocognitive status rates and demographic characteristics differed between PLWH (SA=17%; CN=38%; CI=45%) and HIV-uninfected participants (SA=35%; CN=55%; CI=11%). In PLWH, neurocognitive groups were comparable on demographic and HIV disease characteristics. Younger age, higher verbal IQ, absence of diabetes, fewer depressive symptoms, and lifetime cannabis use disorder increased likelihood of SA. SA reported increased independence in everyday functioning, employment, and health-related quality of life than non-SA.CONCLUSIONS: Despite combined neurological risk of aging and HIV, youthful neurocognitive performance is possible for older PLWH. SA relates to improved real-world functioning and may be better explained by cognitive reserve and maintenance of cardiometabolic and mental health than HIV disease severity. Future research investigating biomarker and lifestyle (e.g., physical activity) correlates of SA may help identify modifiable neuroprotective factors against HIV-related neurobiological aging. (JINS, 2019, 25, 507-519).

DOI10.1017/S1355617719000018
Alternate JournalJ Int Neuropsychol Soc
PubMed ID30890191
PubMed Central IDPMC6705613
Grant ListHHSN271201000030C / MH / NIMH NIH HHS / United States
U24 MH100928 / MH / NIMH NIH HHS / United States
HHSN271201000036C / MH / NIMH NIH HHS / United States
R24 MH059745 / MH / NIMH NIH HHS / United States
T32 DA031098 / DA / NIDA NIH HHS / United States
T32 AA013525 / AA / NIAAA NIH HHS / United States
N01MH22005 / MH / NIMH NIH HHS / United States
P30 MH062512 / MH / NIMH NIH HHS / United States
U01 MH083506 / MH / NIMH NIH HHS / United States
F31 AA027198 / AA / NIAAA NIH HHS / United States
K24 MH097673 / MH / NIMH NIH HHS / United States
N01 MH022005 / MH / NIMH NIH HHS / United States
R01 MH099987 / MH / NIMH NIH HHS / United States
R01 MH107345 / MH / NIMH NIH HHS / United States
U24 MH100930 / MH / NIMH NIH HHS / United States