Journal article
Cortical Features in Child and Adolescent Carriers of Mutant Huntingtin (mHTT)
Journal of Huntington's disease, Vol.11(2), pp.173-178
06/03/2022
DOI: 10.3233/JHD-210512
PMCID: PMC9177765
PMID: 35275555
Abstract
Molecular studies provide evidence that mutant huntingtin (mHTT) affects early cortical development; however, cortical development has not been evaluated in child and adolescent carriers of mHTT.
To evaluate the impact of mHTT on the developmental trajectories of cortical thickness and surface area.
Children and adolescents (6-18 years) participated in the KidsHD study. mHTT carrier status was determined for research purposes only to classify participants as gene expanded (GE) and gene non-expanded (GNE). Cortical features were extracted from 3T neuroimaging using FreeSurfer. Nonlinear mixed effects models were conducted to determine if age, group, and CAG repeat were associated with cortical morphometry.
Age-related changes in cortical morphometry were similar across groups. Expanded CAG repeat was not significantly associated with cortical features.
While striatal development is markedly different in GE and GNE, developmental change of the cortex appears grossly normal among child and adolescent carrier of mHTT.
Details
- Title: Subtitle
- Cortical Features in Child and Adolescent Carriers of Mutant Huntingtin (mHTT)
- Creators
- Erin E Reasoner - University of IowaEllen van der Plas - University of IowaDouglas R Langbehn - University of IowaAmy L Conrad - University of IowaTimothy R Koscik - University of IowaEric A Epping - University of IowaVincent A Magnotta - University of IowaPeggy C Nopoulos - University of Iowa
- Resource Type
- Journal article
- Publication Details
- Journal of Huntington's disease, Vol.11(2), pp.173-178
- DOI
- 10.3233/JHD-210512
- PMID
- 35275555
- PMCID
- PMC9177765
- NLM abbreviation
- J Huntingtons Dis
- ISSN
- 1879-6397
- eISSN
- 1879-6400
- Language
- English
- Electronic publication date
- 03/07/2022
- Date published
- 06/03/2022
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Neurology; Radiology; Psychiatry; Pediatric Psychology; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Craniofacial Anomalies Research Center
- Record Identifier
- 9984227002602771
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