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Dynamic changes of peripheral blood lymphocyte subsets in acute ischemic stroke and prognostic value
OBJECTIVE: To explore dynamic changes of peripheral blood lymphocyte subsets in patients with acute ischemic stroke (AIS) and the relationship with stroke severity and long‐term outcomes. METHODS: A total of 96 consecutive patients with AIS and 28 age‐ and gender‐matched healthy controls were recrui...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821621/ https://www.ncbi.nlm.nih.gov/pubmed/33111494 http://dx.doi.org/10.1002/brb3.1919 |
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author | Xiao, Jun Qiu, Qian‐Wen Qin, Chuan Tao, Ran Qiao, Su‐Ya Chen, Man Pan, Deng‐Ji Tian, Dai‐Shi |
author_facet | Xiao, Jun Qiu, Qian‐Wen Qin, Chuan Tao, Ran Qiao, Su‐Ya Chen, Man Pan, Deng‐Ji Tian, Dai‐Shi |
author_sort | Xiao, Jun |
collection | PubMed |
description | OBJECTIVE: To explore dynamic changes of peripheral blood lymphocyte subsets in patients with acute ischemic stroke (AIS) and the relationship with stroke severity and long‐term outcomes. METHODS: A total of 96 consecutive patients with AIS and 28 age‐ and gender‐matched healthy controls were recruited. Peripheral blood samples were collected, and the percentages of lymphocyte subsets were analyzed by flow cytometry. The dynamic changes in lymphocyte subsets and their correlation with clinical parameters, such as National Institutes of Health Stroke Scale (NIHSS) scores at onset and modified Rankin scale (mRS) scores 3 months later, were evaluated. RESULTS: In our study, we observed a decrease in the percentages of T‐lymphocytes (T cells), helper/inducible T‐lymphocytes (Th cells) and suppressor/cytotoxic T‐lymphocytes (Ts cells) in AIS patients as compared to controls. The frequencies of T cells and Ts cells on day 8–14 after stroke in NIHSS ≤4 group were significantly higher than those in NIHSS >4 group. The percentages of T cells and Th cells on day 1–3 after stroke in the mRS ≤2 group were higher than those in the mRS >2 group. CONCLUSION: The frequencies of T cells, Th cells, and Ts cells in AIS are declined dramatically at least 14 days after stroke. Lower frequencies of T cells and Ts cells on day 8–14 after stroke represent more severe disease conditions, and the percentages of T cells and Th cells within 72 hr after stroke are negatively correlated with 3‐month outcomes, which might have a potential for predicting long‐term prognosis of stroke. |
format | Online Article Text |
id | pubmed-7821621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78216212021-01-29 Dynamic changes of peripheral blood lymphocyte subsets in acute ischemic stroke and prognostic value Xiao, Jun Qiu, Qian‐Wen Qin, Chuan Tao, Ran Qiao, Su‐Ya Chen, Man Pan, Deng‐Ji Tian, Dai‐Shi Brain Behav Original Research OBJECTIVE: To explore dynamic changes of peripheral blood lymphocyte subsets in patients with acute ischemic stroke (AIS) and the relationship with stroke severity and long‐term outcomes. METHODS: A total of 96 consecutive patients with AIS and 28 age‐ and gender‐matched healthy controls were recruited. Peripheral blood samples were collected, and the percentages of lymphocyte subsets were analyzed by flow cytometry. The dynamic changes in lymphocyte subsets and their correlation with clinical parameters, such as National Institutes of Health Stroke Scale (NIHSS) scores at onset and modified Rankin scale (mRS) scores 3 months later, were evaluated. RESULTS: In our study, we observed a decrease in the percentages of T‐lymphocytes (T cells), helper/inducible T‐lymphocytes (Th cells) and suppressor/cytotoxic T‐lymphocytes (Ts cells) in AIS patients as compared to controls. The frequencies of T cells and Ts cells on day 8–14 after stroke in NIHSS ≤4 group were significantly higher than those in NIHSS >4 group. The percentages of T cells and Th cells on day 1–3 after stroke in the mRS ≤2 group were higher than those in the mRS >2 group. CONCLUSION: The frequencies of T cells, Th cells, and Ts cells in AIS are declined dramatically at least 14 days after stroke. Lower frequencies of T cells and Ts cells on day 8–14 after stroke represent more severe disease conditions, and the percentages of T cells and Th cells within 72 hr after stroke are negatively correlated with 3‐month outcomes, which might have a potential for predicting long‐term prognosis of stroke. John Wiley and Sons Inc. 2020-10-27 /pmc/articles/PMC7821621/ /pubmed/33111494 http://dx.doi.org/10.1002/brb3.1919 Text en © 2020 The Authors. Brain and Behavior published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Xiao, Jun Qiu, Qian‐Wen Qin, Chuan Tao, Ran Qiao, Su‐Ya Chen, Man Pan, Deng‐Ji Tian, Dai‐Shi Dynamic changes of peripheral blood lymphocyte subsets in acute ischemic stroke and prognostic value |
title | Dynamic changes of peripheral blood lymphocyte subsets in acute ischemic stroke and prognostic value |
title_full | Dynamic changes of peripheral blood lymphocyte subsets in acute ischemic stroke and prognostic value |
title_fullStr | Dynamic changes of peripheral blood lymphocyte subsets in acute ischemic stroke and prognostic value |
title_full_unstemmed | Dynamic changes of peripheral blood lymphocyte subsets in acute ischemic stroke and prognostic value |
title_short | Dynamic changes of peripheral blood lymphocyte subsets in acute ischemic stroke and prognostic value |
title_sort | dynamic changes of peripheral blood lymphocyte subsets in acute ischemic stroke and prognostic value |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821621/ https://www.ncbi.nlm.nih.gov/pubmed/33111494 http://dx.doi.org/10.1002/brb3.1919 |
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