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Elevated Serum Amyloid A Is Associated With Cognitive Impairment in Ischemic Stroke Patients

BACKGROUND AND PURPOSE: The impact of serum amyloid A on cognitive impairment after ischemic stroke is unclear. We aimed to investigate the association between serum amyloid A (SAA) levels and post-stroke cognitive impairment (PSCI) at 3 months after ischemic stroke. METHODS: One hundred and ninety-...

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Autores principales: Zhang, Yun, Feng, Yue, Zuo, Jiacai, Shi, Jian, Zhang, Shanshan, Yang, Yao, Xie, Shu, Chen, Zhonglun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8801533/
https://www.ncbi.nlm.nih.gov/pubmed/35111127
http://dx.doi.org/10.3389/fneur.2021.789204
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author Zhang, Yun
Feng, Yue
Zuo, Jiacai
Shi, Jian
Zhang, Shanshan
Yang, Yao
Xie, Shu
Chen, Zhonglun
author_facet Zhang, Yun
Feng, Yue
Zuo, Jiacai
Shi, Jian
Zhang, Shanshan
Yang, Yao
Xie, Shu
Chen, Zhonglun
author_sort Zhang, Yun
collection PubMed
description BACKGROUND AND PURPOSE: The impact of serum amyloid A on cognitive impairment after ischemic stroke is unclear. We aimed to investigate the association between serum amyloid A (SAA) levels and post-stroke cognitive impairment (PSCI) at 3 months after ischemic stroke. METHODS: One hundred and ninety-eight patients were enrolled prospectively from June 2020 to April 2021. The SAA concentrations were measured using a commercially available enzyme-linked immunosorbent assay kit after admission. Cognitive function was assessed using the Montreal Cognitive Assessment score at 3 months after the symptom onset. We defined a Montreal Cognitive Assessment score <25 as cognitive impairment. RESULTS: During 3-month follow-up, 80 patients (40.4%) were diagnosed as having PSCI. As compared with patients with cognitively normal ischemic stroke, those with PSCI were older, more likely to have diabetes and white matter lesions, and had a higher baseline National Institutes of Health stroke score and SAA levels. After adjustment for age, the National Institutes of Health stroke score and other covariates, the OR for the highest quartile of SAA compared with the lowest quartile was 5.72 (95% CI, 2.17–15.04, P = 0.001) for PSCI. Also, ordinal logistic regression analysis showed that higher SAA concentrations were associated with increased risk of PSCI severity (OR, 4.31; 95% CI, 1.81–10.33, P = 0.001). Similar results were found when the SAA levels were analyzed as a continuous variable. CONCLUSIONS: This present study demonstrated that increased SAA levels might be associated with PSCI at 3 months after ischemic stroke.
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spelling pubmed-88015332022-02-01 Elevated Serum Amyloid A Is Associated With Cognitive Impairment in Ischemic Stroke Patients Zhang, Yun Feng, Yue Zuo, Jiacai Shi, Jian Zhang, Shanshan Yang, Yao Xie, Shu Chen, Zhonglun Front Neurol Neurology BACKGROUND AND PURPOSE: The impact of serum amyloid A on cognitive impairment after ischemic stroke is unclear. We aimed to investigate the association between serum amyloid A (SAA) levels and post-stroke cognitive impairment (PSCI) at 3 months after ischemic stroke. METHODS: One hundred and ninety-eight patients were enrolled prospectively from June 2020 to April 2021. The SAA concentrations were measured using a commercially available enzyme-linked immunosorbent assay kit after admission. Cognitive function was assessed using the Montreal Cognitive Assessment score at 3 months after the symptom onset. We defined a Montreal Cognitive Assessment score <25 as cognitive impairment. RESULTS: During 3-month follow-up, 80 patients (40.4%) were diagnosed as having PSCI. As compared with patients with cognitively normal ischemic stroke, those with PSCI were older, more likely to have diabetes and white matter lesions, and had a higher baseline National Institutes of Health stroke score and SAA levels. After adjustment for age, the National Institutes of Health stroke score and other covariates, the OR for the highest quartile of SAA compared with the lowest quartile was 5.72 (95% CI, 2.17–15.04, P = 0.001) for PSCI. Also, ordinal logistic regression analysis showed that higher SAA concentrations were associated with increased risk of PSCI severity (OR, 4.31; 95% CI, 1.81–10.33, P = 0.001). Similar results were found when the SAA levels were analyzed as a continuous variable. CONCLUSIONS: This present study demonstrated that increased SAA levels might be associated with PSCI at 3 months after ischemic stroke. Frontiers Media S.A. 2022-01-17 /pmc/articles/PMC8801533/ /pubmed/35111127 http://dx.doi.org/10.3389/fneur.2021.789204 Text en Copyright © 2022 Zhang, Feng, Zuo, Shi, Zhang, Yang, Xie and Chen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Zhang, Yun
Feng, Yue
Zuo, Jiacai
Shi, Jian
Zhang, Shanshan
Yang, Yao
Xie, Shu
Chen, Zhonglun
Elevated Serum Amyloid A Is Associated With Cognitive Impairment in Ischemic Stroke Patients
title Elevated Serum Amyloid A Is Associated With Cognitive Impairment in Ischemic Stroke Patients
title_full Elevated Serum Amyloid A Is Associated With Cognitive Impairment in Ischemic Stroke Patients
title_fullStr Elevated Serum Amyloid A Is Associated With Cognitive Impairment in Ischemic Stroke Patients
title_full_unstemmed Elevated Serum Amyloid A Is Associated With Cognitive Impairment in Ischemic Stroke Patients
title_short Elevated Serum Amyloid A Is Associated With Cognitive Impairment in Ischemic Stroke Patients
title_sort elevated serum amyloid a is associated with cognitive impairment in ischemic stroke patients
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8801533/
https://www.ncbi.nlm.nih.gov/pubmed/35111127
http://dx.doi.org/10.3389/fneur.2021.789204
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