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Angiopoietin‐like protein 4 and clinical outcomes in ischemic stroke patients
AIMS: Angiopoietin‐like protein 4 (ANGPTL‐4) had been reported to be associated with the risk of ischemic stroke, but its prognostic value remained unclear. The aim of this study was to investigate the association between plasma ANGPTL‐4 concentrations and prognosis of ischemic stroke. METHODS: Base...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7951112/ https://www.ncbi.nlm.nih.gov/pubmed/33616301 http://dx.doi.org/10.1002/acn3.51319 |
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author | Zheng, Xiaowei Shen, Suwen Wang, Aili Zhu, Zhengbao Peng, Yanbo Peng, Hao Zhong, Chongke Guo, Daoxia Xu, Tan Chen, Jing Ju, Zhong Geng, Deqin Zhang, Yonghong He, Jiang |
author_facet | Zheng, Xiaowei Shen, Suwen Wang, Aili Zhu, Zhengbao Peng, Yanbo Peng, Hao Zhong, Chongke Guo, Daoxia Xu, Tan Chen, Jing Ju, Zhong Geng, Deqin Zhang, Yonghong He, Jiang |
author_sort | Zheng, Xiaowei |
collection | PubMed |
description | AIMS: Angiopoietin‐like protein 4 (ANGPTL‐4) had been reported to be associated with the risk of ischemic stroke, but its prognostic value remained unclear. The aim of this study was to investigate the association between plasma ANGPTL‐4 concentrations and prognosis of ischemic stroke. METHODS: Baseline plasma ANGPTL‐4 concentrations were measured in 3379 acute ischemic stroke patients. The primary outcome was a combination of death or major disability (modified Rankin Scale score, ≥3) at 3 months after ischemic stroke. RESULTS: At 3 months after ischemic stroke, 850 (26.16%) participants experienced major disability or died (750 major disabilities and 100 deaths). After adjusting for important covariates, odds ratios for the highest tertile of plasma ANGPTL‐4 concentrations were 1.59 (1.22–2.06) for primary outcome, 1.53 (1.18–1.97) for major disability, and 2.03 (1.03–4.00) for death when compared with the lowest tertile of plasma ANGPTL‐4 concentrations. For 1‐SD increase in log‐ANGPTL‐4 concentrations (0.44 ng/mL), the adjusted odds ratios were 1.24 (1.11–1.38), 1.14 (1.03–1.27), and 1.72 (1.32–2.23), respectively. Adding ANGPTL‐4 to a model containing conventional risk factors improved risk prediction for composite outcome of death and major disability. CONCLUSION: Higher plasma ANGPTL‐4 concentration was associated with poor prognosis in acute ischemic stroke patients, suggesting that ANGPTL‐4 might be a prognostic marker for ischemic stroke. |
format | Online Article Text |
id | pubmed-7951112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79511122021-03-17 Angiopoietin‐like protein 4 and clinical outcomes in ischemic stroke patients Zheng, Xiaowei Shen, Suwen Wang, Aili Zhu, Zhengbao Peng, Yanbo Peng, Hao Zhong, Chongke Guo, Daoxia Xu, Tan Chen, Jing Ju, Zhong Geng, Deqin Zhang, Yonghong He, Jiang Ann Clin Transl Neurol Research Articles AIMS: Angiopoietin‐like protein 4 (ANGPTL‐4) had been reported to be associated with the risk of ischemic stroke, but its prognostic value remained unclear. The aim of this study was to investigate the association between plasma ANGPTL‐4 concentrations and prognosis of ischemic stroke. METHODS: Baseline plasma ANGPTL‐4 concentrations were measured in 3379 acute ischemic stroke patients. The primary outcome was a combination of death or major disability (modified Rankin Scale score, ≥3) at 3 months after ischemic stroke. RESULTS: At 3 months after ischemic stroke, 850 (26.16%) participants experienced major disability or died (750 major disabilities and 100 deaths). After adjusting for important covariates, odds ratios for the highest tertile of plasma ANGPTL‐4 concentrations were 1.59 (1.22–2.06) for primary outcome, 1.53 (1.18–1.97) for major disability, and 2.03 (1.03–4.00) for death when compared with the lowest tertile of plasma ANGPTL‐4 concentrations. For 1‐SD increase in log‐ANGPTL‐4 concentrations (0.44 ng/mL), the adjusted odds ratios were 1.24 (1.11–1.38), 1.14 (1.03–1.27), and 1.72 (1.32–2.23), respectively. Adding ANGPTL‐4 to a model containing conventional risk factors improved risk prediction for composite outcome of death and major disability. CONCLUSION: Higher plasma ANGPTL‐4 concentration was associated with poor prognosis in acute ischemic stroke patients, suggesting that ANGPTL‐4 might be a prognostic marker for ischemic stroke. John Wiley and Sons Inc. 2021-02-22 /pmc/articles/PMC7951112/ /pubmed/33616301 http://dx.doi.org/10.1002/acn3.51319 Text en © 2021 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Zheng, Xiaowei Shen, Suwen Wang, Aili Zhu, Zhengbao Peng, Yanbo Peng, Hao Zhong, Chongke Guo, Daoxia Xu, Tan Chen, Jing Ju, Zhong Geng, Deqin Zhang, Yonghong He, Jiang Angiopoietin‐like protein 4 and clinical outcomes in ischemic stroke patients |
title | Angiopoietin‐like protein 4 and clinical outcomes in ischemic stroke patients |
title_full | Angiopoietin‐like protein 4 and clinical outcomes in ischemic stroke patients |
title_fullStr | Angiopoietin‐like protein 4 and clinical outcomes in ischemic stroke patients |
title_full_unstemmed | Angiopoietin‐like protein 4 and clinical outcomes in ischemic stroke patients |
title_short | Angiopoietin‐like protein 4 and clinical outcomes in ischemic stroke patients |
title_sort | angiopoietin‐like protein 4 and clinical outcomes in ischemic stroke patients |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7951112/ https://www.ncbi.nlm.nih.gov/pubmed/33616301 http://dx.doi.org/10.1002/acn3.51319 |
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