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dc.contributor.authorRobert Paulen_US
dc.contributor.authorTanakorn Apornpongen_US
dc.contributor.authorWasana Prasitsuebsaien_US
dc.contributor.authorThanyawee Puthanakiten_US
dc.contributor.authorVonthanak Saphonnen_US
dc.contributor.authorLinda Aurpibulen_US
dc.contributor.authorPope Kosalaraksaen_US
dc.contributor.authorSuparat Kanjanavaniten_US
dc.contributor.authorWicharn Luesomboonen_US
dc.contributor.authorChaiwat Ngampiyaskulen_US
dc.contributor.authorTulathip Suwanlerken_US
dc.contributor.authorKea Chettraen_US
dc.contributor.authorWilliam T. Sheareren_US
dc.contributor.authorVictor Valcouren_US
dc.contributor.authorJintanat Ananworanichen_US
dc.contributor.authorStephen Kerren_US
dc.date.accessioned2018-09-05T04:37:14Z-
dc.date.available2018-09-05T04:37:14Z-
dc.date.issued2018-01-01en_US
dc.identifier.issn10779450en_US
dc.identifier.issn15254135en_US
dc.identifier.other2-s2.0-85047724403en_US
dc.identifier.other10.1097/QAI.0000000000001619en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85047724403&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/59063-
dc.description.abstract© 2018 Wolters Kluwer Health, Inc. Background: HIV-infected children with long-term nonprogressive (LTNP) disease eventually convert to a progressive disease type, yet the extent to which these children experience the cognitive and emotional symptoms observed in typical progressive HIV (Progressors) is unknown. Methods: Eighty-eight LTNPs, 53 Progressors, and 323 healthy controls completed annual assessments of cognitive and emotional health as part of a prospective study. The 2 HIV-infected groups and the healthy controls were matched on age and sex distribution at enrollment. Plasma HIV RNA, T-cell counts/percentages, activated monocytes, perivascular monocytes, and markers of macrophage activation (sCD163 and sCD14) were compared by progression subtype. Cognitive and emotional outcomes were compared using cross-sectional linear regression analysis and longitudinal sensitivity models. Results: LTNPs exhibited the same cognitive phenotype and emotional dysregulation as Progressors, with worse outcomes in both groups compared with controls. In addition, cognitive and emotional symptoms were evident before children reached the minimum age for LTNP designation (8 years). Baseline plasma HIV RNA, sCD163, activated monocytes, and perivascular monocytes were lower in LTNPs versus Progressors, with no difference in T-cell counts/percentages or sCD14 levels. Most LTNPs converted to a progressive disease subtype during the study, with similar cognitive and emotion profiles between these subgroups. Conclusions: Pediatric LTNPs experience cognitive and emotional difficulties that mirror symptoms of progressive disease. The abnormalities are present at young ages and persist independent of plasma T-cell counts. The findings highlight the neurodevelopmental risk of pediatric HIV, even in those with early innate disease control.en_US
dc.subjectMedicineen_US
dc.titleCognition, emotional health, and immunological markers in children with long-term nonprogressive HIVen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Acquired Immune Deficiency Syndromesen_US
article.volume77en_US
article.stream.affiliationsMissouri Institute of Mental Healthen_US
article.stream.affiliationsThe HIV Netherlands Australia Thailand Research Collaborationen_US
article.stream.affiliationsChulalongkorn Universityen_US
article.stream.affiliationsUniversity of Health Sciencesen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsKhon Kaen Universityen_US
article.stream.affiliationsChiangrai Prachanukroh Hospitalen_US
article.stream.affiliationsQueen Savang Vadhana Memorial Hospitalen_US
article.stream.affiliationsNakornping Hospitalen_US
article.stream.affiliationsPrapokklao Hospitalen_US
article.stream.affiliationsSocial Health Clinicen_US
article.stream.affiliationsTexas Children's Hospital Houstonen_US
article.stream.affiliationsUniversity of California, San Franciscoen_US
article.stream.affiliationsHJFen_US
article.stream.affiliationsAcademic Medical Centre, University of Amsterdamen_US
article.stream.affiliationsUniversity of New South Wales (UNSW) Australiaen_US
Appears in Collections:CMUL: Journal Articles

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