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|Title:||Atrophy of Ipsilesional Hippocampal Subfields Vary Over First Year After Ischemic Stroke.||Austin Authors:||Khlif, Mohamed Salah;Werden, Emilio ;Bird, Laura J;Egorova-Brumley, Natalia;Brodtmann, Amy||Affiliation:||Eastern Cognitive Disorders Clinic, Box Hill Hospital, Monash University, Box Hill, Victoria, Australia..
The Florey Institute of Neuroscience and Mental Health
Melbourne School of Psychological Sciences, University of Melbourne, Melbourne, Australia..
Department of Neurology, Royal Melbourne Hospital, Parkville, Victoria, Australia..
|Issue Date:||Jul-2022||metadata.dc.date:||2021||Publication information:||Journal of magnetic resonance imaging : JMRI 2022; 56(1): 273-281||Abstract:||The structural integrity of hippocampal subfields has been investigated in many neurological disorders and was shown to be better associated with cognitive performance than whole hippocampus. In stroke, hippocampal atrophy is linked to cognitive impairment, but it is unknown whether the hippocampal subfields atrophy differently. To evaluate longitudinal hippocampal subfield atrophy in first year poststroke, in comparison with atrophy in healthy individuals. Cohort. A total of 92 ischemic stroke (age: 67 ± 12 years, 63 men) and 39 healthy participants (age: 69 ± 7 years, 24 men). A3 T/T1-MPRAGE, T2-SPACE, and T2-FLAIR. FreeSurfer (6.0) was used to delineate 12 hippocampal subfields. Whole hippocampal volume was computed as sum of subfield volumes excluding hippocampal fissure volume. Separate assessments were completed for contralesional and ipsilesional hippocampi. A mixed-effect regression model was used to compare subfield volumes cross-sectionally between healthy and stroke groups and longitudinally between 3-month and 12-month timepoints. False discovery rate at 0.05 significance level was used to correct for multiple comparisons. Also, a receiver operating characteristic (ROC) curve analysis was performed to assess differentiation between healthy and stroke participants based on subfield volumes. There were no volume differences between groups at 3 months, but there was a significant difference (P = 0.027) in whole hippocampal volume reduction over time between control and stroke ipsilesionally. Thus, the ipsilesional whole hippocampal volume in stroke became significantly smaller (P = 0.035) at 12 months. The hippocampal tail was the highest single-region contributor (22.7%) to ipsilesional hippocampal atrophy (1.19%) over 9 months. The cornu ammonis areas (CA1) subfield volume reduction was minimal in controls and stroke contralesionally but significant ipsilesionally (P = 0.007). CA1 volume significantly outperformed whole hippocampal volume (P < 0.01) in discriminating between stroke participants and healthy controls in ROC curve analysis. Greater stroke-induced effects were observed in the ipsilesional hippocampus anteriorly in CA1 and posteriorly in the hippocampal tail. Atrophy of CA1 and hippocampal tail may provide a better link to cognitive impairment than whole hippocampal atrophy. 2 TECHNICAL EFFICACY STAGE: 3.||URI:||https://ahro.austin.org.au/austinjspui/handle/1/30414||DOI:||10.1002/jmri.28009||ORCID:||https://orcid.org/0000-0002-0096-434X
|PubMed URL:||34837426||PubMed URL:||https://pubmed.ncbi.nlm.nih.gov/34837426/||Type:||Journal Article||Subjects:||FreeSurfer
|Appears in Collections:||Journal articles|
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