High Plasma Soluble CD163 During Infancy Is a Marker for Neurocognitive Outcomes in Early-Treated HIV-Infected Children
dc.contributor.author | Benki-Nugent, Sarah F. | |
dc.contributor.author | Martopullo, Ira | |
dc.contributor.author | Laboso, Tony | |
dc.contributor.author | Tamasha, Nancy | |
dc.contributor.author | Wamalwa, Dalton C. | |
dc.contributor.author | Tapia, Kenneth | |
dc.contributor.author | Langat, Agnes | |
dc.contributor.author | Obimbo, Elizabeth Maleche | |
dc.contributor.author | Marra, Christina M. | |
dc.contributor.author | Bangirana, Paul | |
dc.contributor.author | Boivin, Michael J. | |
dc.contributor.author | Stewart, Grace C. John | |
dc.date.accessioned | 2022-02-10T19:56:36Z | |
dc.date.available | 2022-02-10T19:56:36Z | |
dc.date.issued | 2019 | |
dc.description.abstract | Monocyte activation may contribute to neuronal injury in aviremic HIV-infected adults; data are lacking in children. We examined the relation between monocyte activation markers and early and long-term neurodevelopmental outcomes in early-treated HIV-infected children.Prospective study of infant and child neurodevelopmental outcomes nested within a randomized clinical trial () and extended cohort study in Kenya.HIV-infected infants (N=67) initiated ART at age <5 months. Plasma soluble (s) CD163 (sCD163), sCD14 and neopterin were measured pre-ART (entry) and 6 months later. Milestone attainment was ascertained monthly during 24 months and neuropsychological tests (NPTs) were performed at 5.8–8.2 years post-initiation of ART (N=27). The relationship between neurodevelopment and sCD163, sCD14 and neopterin at entry and 6 months post-ART was assessed using Cox proportional hazards models and linear regression.Infants with high entry sCD163 had unexpected earlier attainment of supported sitting (5 vs 6 mo.; P=0.006) and supported walking (10 vs 12 mo.; P =0.02) with trends in adjusted analysis. Infants with high 6-month post-ART sCD163 attained speech later (17 vs 15 mo.; P=0.006; aHR, 0.47; P=0.02), threw toys later (18 vs 17 mo.; P =0.01; aHR, 0.53; P =0.04), and at median 6.8 years post-ART, had worse NPT scores (adj. mean z-score differences, cognition, −0.42; P =0.07; short-term memory, −0.52; P =0.08; nonverbal test performance, −0.39, P =0.05).Prior to ART, monocyte activation may reflect transient neuroprotective mechanisms in infants. Following ART and viral suppression, monocyte activation may predict worse short- and long-term neurodevelopment outcomes. | en_US |
dc.identifier.citation | Benki-Nugent, S. F., Martopullo, I., Laboso, T., Tamasha, N., Wamalwa, D. C., Tapia, K., ... & John-Stewart, G. C. (2019). High plasma soluble CD163 during infancy is a marker for neurocognitive outcomes in early treated HIV-infected children. Journal of acquired immune deficiency syndromes (1999), 81(1), 102.https://dx.doi.org/10.1097%2FQAI.0000000000001979 | en_US |
dc.identifier.uri | https://nru.uncst.go.ug/xmlui/handle/123456789/2044 | |
dc.language.iso | en | en_US |
dc.publisher | Journal of acquired immune deficiency syndromes | en_US |
dc.subject | monocyte, neurocognitive, antiretroviral, perinatal HIV, CD163, neurodevelopment | en_US |
dc.title | High Plasma Soluble CD163 During Infancy Is a Marker for Neurocognitive Outcomes in Early-Treated HIV-Infected Children | en_US |
dc.type | Article | en_US |
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