Population-based studies of brain imaging patterns in cerebral palsy
- PMID: 23937113
- DOI: 10.1111/dmcn.12228
Population-based studies of brain imaging patterns in cerebral palsy
Abstract
Aim: The aim of this study was to review the distribution of neuroimaging findings from a contemporary population cohort of individuals with cerebral palsy (CP) and to facilitate standardization of imaging classification.
Method: Publications from 1995 to 2012 reporting imaging findings in population cohorts were selected through a literature search, and review of the titles, abstracts, and content of studies. Relevant data were extracted, including unpublished data from Victoria, Australia. The proportions for each imaging pattern were tabulated, and heterogeneity was assessed for all individuals with CP, and for subgroups based on gestational age, CP subtype, and Gross Motor Function Classification System level.
Results: Studies from three geographic regions met the inclusion criteria for individuals with CP, and two additional studies reported on specific CP subtypes. Brain abnormalities were observed in 86% of scans, but were observed least often in children with ataxia (24-57%). White matter injury was the most common imaging pattern (19-45%), although the proportions showed high heterogeneity. Additional patterns were grey matter injury (21%), focal vascular insults (10%), malformations (11%), and miscellaneous findings (4-22%).
Interpretation: This review suggests areas where further dialogue will facilitate progress towards standardization of neuroimaging classification. Standardization will enable future collaborations aimed at exploring the relationships among magnetic resonance imaging patterns, risk factors, and clinical outcomes, and, ultimately, lead to better understanding of causal pathways and opportunities for prevention.
© 2013 Mac Keith Press.
Comment in
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Providing important evidence for the major causal contributors to cerebral palsy in Africa.Acta Paediatr. 2016 Jun;105(6):572-3. doi: 10.1111/apa.13389. Acta Paediatr. 2016. PMID: 27153365 No abstract available.
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