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Hippocampal atrophy and cognitive function in transient ischemic attack and minor stroke patients over three years

INTRODUCTION: Transient ischemic attack (TIA) and minor ischemic stroke (IS) is associated with a increased risk of late life dementia. In this study we aim to study the extent to which the rates of hippocampal atrophy in TIA/IS differ from healthy controls, and how they are correlated to neuropsych...

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Detalles Bibliográficos
Autores principales: Barber, Philip, Nestor, Sean M., Wang, Meng, Wu, Pauline, Ursenbach, Jake, Munir, Amlish, Gupta, Rani, Tariq, Sah Sana, Smith, Eric, Frayne, Richard, Black, Sandra E., Sajobi, Tolupe, Coutts, Shelagh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616379/
https://www.ncbi.nlm.nih.gov/pubmed/36324718
http://dx.doi.org/10.1016/j.cccb.2021.100019
Descripción
Sumario:INTRODUCTION: Transient ischemic attack (TIA) and minor ischemic stroke (IS) is associated with a increased risk of late life dementia. In this study we aim to study the extent to which the rates of hippocampal atrophy in TIA/IS differ from healthy controls, and how they are correlated to neuropsychological measurements. METHODS: TIA or minor stroke patients were tested with a neuropsychological battery including tests of executive function, and verbal and non-verbal memory at three time points out to 3 years. Annualized rates of hippocampal atrophy in TIA/IS patients were compared to controls. A linear-mixed regression model was used to assess the difference in rates of hippocampal atrophy after adjusting for time and demographic characteristics. RESULTS: TIA/IS patients demonstrated a higher hippocampal atrophy rate than healthy controls over a 3-year interval: the annual percentage change of the left hippocampal volume was 2.5% (78 mm(3) per year (SD 60)) for TIA/IS patients compared to 0.9% (29 mm(3) per year (SD 32)) for controls (p < 0.01); and the annual percentage change of the right hippocampal volume was 2.5% (80 mm(3) per year (SD 46)) for TIA/IS patients compared to 0.5% (17 mm(3) per year (SD 33)) for controls (P < 0.01). Patients with higher annual hippocampal atrophy were more likely to report higher TMT B times, but lower ROC total score, lower California Verbal Learning Test-II total recall, and lower ROC Figure recall scores longitudinally. CONCLUSION: TIA/IS patients experience a higher rate of hippocampal atrophy independent of TIA/IS recurrence that are associated with changes in episodic memory and executive function over 3 years.