| Title | Use of Neuronal-Enriched Extracellular Vesicles to Distinguish Cognitive Impairment Levels and Sex Differences in People with HIV. |
| Publication Type | Journal Article |
| Year of Publication | 2026 |
| Authors | Tang N, Xia F, Freasier H, Tien PC, Glesby MJ, Merenstein D, French AL, McKay H, Diaz MM, Ofotokun I, Lake JE, Margolick JB, Kim E-Y, Levine SR, Fischl MA, Li W, Martinson J, Pulliam L |
| Journal | Cells |
| Volume | 15 |
| Issue | 17 |
| Date Published | 2026 Aug 31 |
| ISSN | 2073-4409 |
| Keywords | Adult, Biomarkers, Cognitive Dysfunction, Extracellular Vesicles, Female, HIV Infections, Humans, Male, Middle Aged, Neurons, Sex Characteristics |
| Abstract | Cognitive impairment still occurs despite well-controlled HIV but with milder symptoms. People with and without HIV have different neuronal protein changes that may differentiate the asymptomatic neurocognitive impairment (ANI) condition from normal cognition (NPN) and mild neurocognitive disorder (MND). Plasma neuronal-enriched extracellular vesicles (nEVs) were isolated from people with HIV (PWH) with NPN, ANI, or MND, and HIV seronegative controls with NPN (HIV-). Two different platforms were used to delineate protein patterns between sexes and cognitive conditions. When combining results from men and women, the nEV cargo in many cases showed little difference between cognitive conditions. However, when separated, there were different patterns between the sexes for some nEV cargo that distinguished the HIV- groups and HIV+ cognition groups. PWH with NPN had higher nEV toxic proteins compared to individuals without HIV. Women with HIV showed perfect separation between NPN and ANI with Aβ42 and NCAM-1 and perfect separation between ANI and MND with Aβ40 and NCAM-1. Men with HIV with MND had significantly higher NCAM-1 when compared to ANI, and lower GLRX when compared to NPN. This study shows distinct markers for different HIV cognitive categories, many of which differed between men and women. |
| DOI | 10.3390/cells15171581 |
| Alternate Journal | Cells |
| PubMed ID | 42738875 |
| PubMed Central ID | PMC13565498 |
| Grant List | U01 HL146245 / HL / NHLBI NIH HHS / United States R01 MH121121 / MH / NIMH NIH HHS / United States U01 HL146208 / HL / NHLBI NIH HHS / United States UL1 TR001409 / TR / NCATS NIH HHS / United States U01 HL146192 / HL / NHLBI NIH HHS / United States U01 HL146242 / HL / NHLBI NIH HHS / United States TL1 TR001431 / TR / NCATS NIH HHS / United States U01 HL146193 / HL / NHLBI NIH HHS / United States P30 AI027763 / AI / NIAID NIH HHS / United States U01 HL146194 / HL / NHLBI NIH HHS / United States U01 HL146241 / HL / NHLBI NIH HHS / United States P30 AI027767 / AI / NIAID NIH HHS / United States P30 AI050409 / AI / NIAID NIH HHS / United States U01 HL146333 / HL / NHLBI NIH HHS / United States U01 HL146205 / HL / NHLBI NIH HHS / United States P30 MH116867 / MH / NIMH NIH HHS / United States L.P. R01MH121121 / MH / NIMH NIH HHS / United States KL2 TR001432 / TR / NCATS NIH HHS / United States P30 AI073961 / AI / NIAID NIH HHS / United States U01 HL146201 / HL / NHLBI NIH HHS / United States U01 HL146204 / HL / NHLBI NIH HHS / United States U01 HL146202 / HL / NHLBI NIH HHS / United States UL1 TR001881 / TR / NCATS NIH HHS / United States UL1 TR000004 / TR / NCATS NIH HHS / United States U01 HL146240 / HL / NHLBI NIH HHS / United States U01 HL146203 / HL / NHLBI NIH HHS / United States UL1 TR003098 / TR / NCATS NIH HHS / United States P30 AI050410 / AI / NIAID NIH HHS / United States |
