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Association between Coagulation Function and Cerebral Microbleeds in Ischemic Stroke Patients with Atrial Fibrillation and/or Rheumatic Heart Disease
Cerebral microbleeds (CMBs), which indicate hemorrhage-prone disease, may associate with hemostatic abnormalities, but the association between CMBs and coagulation function is uncertain. We aimed to examine this possible association. The following coagulation function indicators were evaluated in 85...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
JKL International LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362173/ https://www.ncbi.nlm.nih.gov/pubmed/28400980 http://dx.doi.org/10.14336/AD.2016.0715 |
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author | Liu, Junfeng Wang, Deren Xiong, Yao Liu, Bian Lin, Jing Zhang, Shihong Wu, Bo Wei, Chenchen Liu, Ming |
author_facet | Liu, Junfeng Wang, Deren Xiong, Yao Liu, Bian Lin, Jing Zhang, Shihong Wu, Bo Wei, Chenchen Liu, Ming |
author_sort | Liu, Junfeng |
collection | PubMed |
description | Cerebral microbleeds (CMBs), which indicate hemorrhage-prone disease, may associate with hemostatic abnormalities, but the association between CMBs and coagulation function is uncertain. We aimed to examine this possible association. The following coagulation function indicators were evaluated in 85 consecutive ischemic stroke patients diagnosed with atrial fibrillation and/or rheumatic heart disease: prothrombintime (PT), activated partial thromboplastin time (APTT), and levels of D-dimer and fibrinogen. Indicators were assessed within 24 h after admission. CMBs were identified based on published criteria by two experienced stroke neurologists working independently. PT, APPT, and levels of D-dimer and fibrinogen were compared between patients with and without CMBs using univariate and multivariate analysis. CMBs were detected in 48 patients (56.5%), and fibrinogen levels in these patients were independently and significantly higher than in patients without CMBs after adjustment (OR 2.16, 95% CI 1.20-3.90, P=0.01), whereas the two types of patients did not differ significantly in PT, APPT, or D-dimer levels. The presence of CMBs in ischemic stroke patients with atrial fibrillation and/or rheumatic heart disease is associated with elevated levels of fibrinogen. Larger prospective studies are needed to verify this association and explore the mechanisms involved. |
format | Online Article Text |
id | pubmed-5362173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | JKL International LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53621732017-04-12 Association between Coagulation Function and Cerebral Microbleeds in Ischemic Stroke Patients with Atrial Fibrillation and/or Rheumatic Heart Disease Liu, Junfeng Wang, Deren Xiong, Yao Liu, Bian Lin, Jing Zhang, Shihong Wu, Bo Wei, Chenchen Liu, Ming Aging Dis Short Communication Cerebral microbleeds (CMBs), which indicate hemorrhage-prone disease, may associate with hemostatic abnormalities, but the association between CMBs and coagulation function is uncertain. We aimed to examine this possible association. The following coagulation function indicators were evaluated in 85 consecutive ischemic stroke patients diagnosed with atrial fibrillation and/or rheumatic heart disease: prothrombintime (PT), activated partial thromboplastin time (APTT), and levels of D-dimer and fibrinogen. Indicators were assessed within 24 h after admission. CMBs were identified based on published criteria by two experienced stroke neurologists working independently. PT, APPT, and levels of D-dimer and fibrinogen were compared between patients with and without CMBs using univariate and multivariate analysis. CMBs were detected in 48 patients (56.5%), and fibrinogen levels in these patients were independently and significantly higher than in patients without CMBs after adjustment (OR 2.16, 95% CI 1.20-3.90, P=0.01), whereas the two types of patients did not differ significantly in PT, APPT, or D-dimer levels. The presence of CMBs in ischemic stroke patients with atrial fibrillation and/or rheumatic heart disease is associated with elevated levels of fibrinogen. Larger prospective studies are needed to verify this association and explore the mechanisms involved. JKL International LLC 2017-04-01 /pmc/articles/PMC5362173/ /pubmed/28400980 http://dx.doi.org/10.14336/AD.2016.0715 Text en Copyright: © 2017 Liu, et al. http://creativecommons.org/licenses/by/2.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Short Communication Liu, Junfeng Wang, Deren Xiong, Yao Liu, Bian Lin, Jing Zhang, Shihong Wu, Bo Wei, Chenchen Liu, Ming Association between Coagulation Function and Cerebral Microbleeds in Ischemic Stroke Patients with Atrial Fibrillation and/or Rheumatic Heart Disease |
title | Association between Coagulation Function and Cerebral Microbleeds in Ischemic Stroke Patients with Atrial Fibrillation and/or Rheumatic Heart Disease |
title_full | Association between Coagulation Function and Cerebral Microbleeds in Ischemic Stroke Patients with Atrial Fibrillation and/or Rheumatic Heart Disease |
title_fullStr | Association between Coagulation Function and Cerebral Microbleeds in Ischemic Stroke Patients with Atrial Fibrillation and/or Rheumatic Heart Disease |
title_full_unstemmed | Association between Coagulation Function and Cerebral Microbleeds in Ischemic Stroke Patients with Atrial Fibrillation and/or Rheumatic Heart Disease |
title_short | Association between Coagulation Function and Cerebral Microbleeds in Ischemic Stroke Patients with Atrial Fibrillation and/or Rheumatic Heart Disease |
title_sort | association between coagulation function and cerebral microbleeds in ischemic stroke patients with atrial fibrillation and/or rheumatic heart disease |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362173/ https://www.ncbi.nlm.nih.gov/pubmed/28400980 http://dx.doi.org/10.14336/AD.2016.0715 |
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