A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä

Microstructural abnormality in white matter, regulatory T lymphocytes, and depressive symptoms after stroke




TekijätYasuno F, Taguchi A, Yamamoto A, Kajimoto K, Kazui H, Kudo T, Kikuchi-Taura A, Sekiyama A, Kishimoto T, Iida H, Nagatsuka K

KustantajaWILEY-BLACKWELL

Julkaisuvuosi2014

JournalPsychogeriatrics

Tietokannassa oleva lehden nimiPSYCHOGERIATRICS

Lehden akronyymiPSYCHOGERIATRICS

Vuosikerta14

Numero4

Aloitussivu213

Lopetussivu221

Sivujen määrä9

ISSN1346-3500

DOIhttps://doi.org/10.1111/psyg.12084


Tiivistelmä
BackgroundThe purpose of the present study was to investigate the existence of microstructure abnormalities in the white matter circuit in stroke patients and its relationship to depressive episodes. To target the prevention of depression, we also investigated the relationship between lymphocyte subsets and cerebral abnormalities in patients.MethodsParticipants included 18 patients with acute ischemic stroke and 22 healthy control subjects. Diffusion tensor imaging was performed. Whole-brain voxel-based analysis was used to compare fractional anisotropy (FA) between groups. Blood samples were obtained, and the lymphocyte subsets were evaluated using flow cytometry. Follow-up examinations were conducted on 12 patients at 6 months.ResultsFA was decreased in the bilateral anterior limb of the internal capsule in stroke patients. At the 6-month follow-up examination, there was a significant increase in FA, which was associated with a lower depression scale score. Patients showed a decreased percentage of circulated regulatory T lymphocytes, and the degree of reduction was related to the decrease in the FA value in the internal capsule.ConclusionsFA reductions in the anterior limb of the internal capsule cause abnormality in the frontal-subcortical circuits and confer a biological vulnerability, which in combination with environmental stressors results in the onset of depression. Our findings also demonstrated the possibility of preventing post-stroke depression by targeting the role of regulatory T lymphocytes in brain tissue repair and regeneration after stroke.



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