Diffusion tensor imaging point to ongoing functional impairment in HIV-infected children at age 5, undetectable using standard neurodevelopmental assessments

dc.contributor.authorAckermann, Christelle
dc.contributor.authorAndronikou, Savvas
dc.contributor.authorSaleh, Muhammad G
dc.contributor.authorKidd, Martin
dc.contributor.authorCotton, Mark F
dc.contributor.authorMeintjes, Ernesta M
dc.contributor.authorLaughton, Barbara
dc.date.accessioned2020-05-26T08:09:12Z
dc.date.available2020-05-26T08:09:12Z
dc.date.issued2020-05-19
dc.date.updated2020-05-24T03:44:21Z
dc.description.abstractBackground Perinatal HIV infection negatively impacts cognitive functioning of children, main domains affected are working memory, processing speed and executive function. Early ART, even when interrupted, improves neurodevelopmental outcomes. Diffusion tension imaging (DTI) is a sensitive tool assessing white matter damage. We hypothesised that white matter measures in regions showing HIV-related alterations will be associated with lower neurodevelopmental scores in specific domains related to the functionality of the affected tracts. Methods DTI was performed on children in a neurodevelopmental sub study from the Children with HIV Early Antiretroviral (CHER) trial. Voxel-based group comparisons to determine regions where fractional anisotropy and mean diffusion differed between HIV+ and uninfected children were done. Locations of clusters showing group differences were identified using the Harvard–Oxford cortical and subcortical and John Hopkins University WM tractography atlases provided in FSL. This is a second review of DTI data in this cohort, which was reported in a previous study. Neurodevelopmental assessments including GMDS and Beery-Buktenica tests were performed and correlated with DTI parameters in abnormal white matter. Results 38 HIV+ children (14 male, mean age 64.7 months) and 11 controls (4 male, mean age 67.7 months) were imaged. Two clusters with lower fractional anisotropy and 7 clusters with increased mean diffusion were identified in the HIV+ group. The only neurodevelopmental domain with a trend of difference between the HIV+ children and controls (p = 0.08), was Personal Social Quotient which correlated to improved myelination of the forceps minor in the control group. As a combined group there was a negative correlation between visual perception and radial diffusion in the right superior longitudinal fasciculus and left inferior longitudinal fasciculus, which may be related to the fact that these tracts, forming part of the visual perception pathway, are at a crucial state of development at age 5. Conclusion Even directed neurodevelopmental tests will underestimate the degree of microstructural white matter damage detected by DTI. The visual perception deficit detected in the entire study population should be further examined in a larger study.en_US
dc.identifier.apacitationAckermann, C., Andronikou, S., Saleh, M. G., Kidd, M., Cotton, M. F., Meintjes, E. M., & Laughton, B. (2020). Diffusion tensor imaging point to ongoing functional impairment in HIV-infected children at age 5, undetectable using standard neurodevelopmental assessments. <i>AIDS Research and Therapy</i>, 17(1), 20. en_ZA
dc.identifier.chicagocitationAckermann, Christelle, Savvas Andronikou, Muhammad G Saleh, Martin Kidd, Mark F Cotton, Ernesta M Meintjes, and Barbara Laughton "Diffusion tensor imaging point to ongoing functional impairment in HIV-infected children at age 5, undetectable using standard neurodevelopmental assessments." <i>AIDS Research and Therapy</i> 17, 1. (2020): 20. en_ZA
dc.identifier.citationAckermann, C., Andronikou, S., Saleh, M.G., Kidd, M., Cotton, M.F., Meintjes, E.M. & Laughton, B. 2020. Diffusion tensor imaging point to ongoing functional impairment in HIV-infected children at age 5, undetectable using standard neurodevelopmental assessments. <i>AIDS Research and Therapy.</i> 17(1):20. en_ZA
dc.identifier.ris TY - Journal Article AU - Ackermann, Christelle AU - Andronikou, Savvas AU - Saleh, Muhammad G AU - Kidd, Martin AU - Cotton, Mark F AU - Meintjes, Ernesta M AU - Laughton, Barbara AB - Background Perinatal HIV infection negatively impacts cognitive functioning of children, main domains affected are working memory, processing speed and executive function. Early ART, even when interrupted, improves neurodevelopmental outcomes. Diffusion tension imaging (DTI) is a sensitive tool assessing white matter damage. We hypothesised that white matter measures in regions showing HIV-related alterations will be associated with lower neurodevelopmental scores in specific domains related to the functionality of the affected tracts. Methods DTI was performed on children in a neurodevelopmental sub study from the Children with HIV Early Antiretroviral (CHER) trial. Voxel-based group comparisons to determine regions where fractional anisotropy and mean diffusion differed between HIV+ and uninfected children were done. Locations of clusters showing group differences were identified using the Harvard–Oxford cortical and subcortical and John Hopkins University WM tractography atlases provided in FSL. This is a second review of DTI data in this cohort, which was reported in a previous study. Neurodevelopmental assessments including GMDS and Beery-Buktenica tests were performed and correlated with DTI parameters in abnormal white matter. Results 38 HIV+ children (14 male, mean age 64.7 months) and 11 controls (4 male, mean age 67.7 months) were imaged. Two clusters with lower fractional anisotropy and 7 clusters with increased mean diffusion were identified in the HIV+ group. The only neurodevelopmental domain with a trend of difference between the HIV+ children and controls (p = 0.08), was Personal Social Quotient which correlated to improved myelination of the forceps minor in the control group. As a combined group there was a negative correlation between visual perception and radial diffusion in the right superior longitudinal fasciculus and left inferior longitudinal fasciculus, which may be related to the fact that these tracts, forming part of the visual perception pathway, are at a crucial state of development at age 5. Conclusion Even directed neurodevelopmental tests will underestimate the degree of microstructural white matter damage detected by DTI. The visual perception deficit detected in the entire study population should be further examined in a larger study. DA - 2020-05-19 DB - OpenUCT DP - University of Cape Town IS - 1 J1 - AIDS Research and Therapy KW - HIV KW - Cognitive functioning KW - ARV KW - DTI KW - Functional anisotropy KW - White matter LK - https://open.uct.ac.za PY - 2020 T1 - Diffusion tensor imaging point to ongoing functional impairment in HIV-infected children at age 5, undetectable using standard neurodevelopmental assessments TI - Diffusion tensor imaging point to ongoing functional impairment in HIV-infected children at age 5, undetectable using standard neurodevelopmental assessments UR - ER - en_ZA
dc.identifier.urihttps://doi.org/10.1186/s12981-020-00278-z
dc.identifier.urihttps://hdl.handle.net/11427/31986
dc.identifier.vancouvercitationAckermann C, Andronikou S, Saleh MG, Kidd M, Cotton MF, Meintjes EM, et al. Diffusion tensor imaging point to ongoing functional impairment in HIV-infected children at age 5, undetectable using standard neurodevelopmental assessments. AIDS Research and Therapy. 2020;17(1):20. .en_ZA
dc.language.isoenen_US
dc.language.rfc3066en
dc.publisher.departmentMRC/UCT Medical Imaging Research Uniten_US
dc.publisher.facultyFaculty of Health Sciencesen_US
dc.rights.holderThe Author(s)
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceAIDS Research and Therapyen_US
dc.source.journalissue1en_US
dc.source.journalvolume17en_US
dc.source.pagination20en_US
dc.source.urihttps://aidsrestherapy.biomedcentral.com/
dc.subjectHIVen_US
dc.subjectCognitive functioningen_US
dc.subjectARVen_US
dc.subjectDTIen_US
dc.subjectFunctional anisotropyen_US
dc.subjectWhite matteren_US
dc.titleDiffusion tensor imaging point to ongoing functional impairment in HIV-infected children at age 5, undetectable using standard neurodevelopmental assessmentsen_US
dc.typeJournal Articleen_US
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