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Decreased Serum Retinoic Acid May Predict Poor Outcome in Ischemic Stroke Patients

BACKGROUND AND AIMS: Decreased serum retinoic acid (RA) levels have been shown to be linked with increased mortality in cardiovascular diseases. This study aimed to investigate the relationship between serum RA and 3-month functional outcome after ischemic stroke. METHODS: Between January 2019 and S...

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Autores principales: Xu, Mengshi, Xu, Liang, Du, Huaping, Shan, Wanying, Feng, Jie, Zhai, Guojie, Yang, Xiuyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293911/
https://www.ncbi.nlm.nih.gov/pubmed/32606701
http://dx.doi.org/10.2147/NDT.S254591
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author Xu, Mengshi
Xu, Liang
Du, Huaping
Shan, Wanying
Feng, Jie
Zhai, Guojie
Yang, Xiuyan
author_facet Xu, Mengshi
Xu, Liang
Du, Huaping
Shan, Wanying
Feng, Jie
Zhai, Guojie
Yang, Xiuyan
author_sort Xu, Mengshi
collection PubMed
description BACKGROUND AND AIMS: Decreased serum retinoic acid (RA) levels have been shown to be linked with increased mortality in cardiovascular diseases. This study aimed to investigate the relationship between serum RA and 3-month functional outcome after ischemic stroke. METHODS: Between January 2019 and September 2019, we prospectively recruited ischemic stroke patients within 24 hrs of symptom onset. Serum RA levels were measured for all patients at admission. The primary outcome was defined as poor functional outcome (modified Rankin Scale 3–6) at 90 days. The secondary outcome was defined as early neurological deterioration (END), which is considered as an increase of ≥1 point in motor power or total National Institutes of Health Stroke Scale score of ≥2 points within 7 days. RESULTS: A total of 217 patients were included in the analysis. The median RA levels were 2.9 ng/mL. Ninety-four (43.3%) and 65 (30.0%) patients experienced 3-month poor outcome and END, respectively. After adjusted for potential confounders, decreased levels of serum RA were associated with a higher risk of poor outcome (P for trend = 0.001) and END (P for trend = 0.002). Adding RA quartile to the existing risk factors improved risk prediction for poor outcome [net reclassification improvement (NRI) = 42.6%, P = 0.001; integrated discrimination improvement (IDI) = 5.7%, P = 0.001] and END (NRI index = 45.4%, P = 0.001; IDI = 4.3%; P = 0.005). CONCLUSION: Low serum RA levels at baseline were associated with poor prognosis at 90 days after ischemic stroke, suggesting that RA may be a potential prognostic biomarker for ischemic stroke.
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spelling pubmed-72939112020-06-29 Decreased Serum Retinoic Acid May Predict Poor Outcome in Ischemic Stroke Patients Xu, Mengshi Xu, Liang Du, Huaping Shan, Wanying Feng, Jie Zhai, Guojie Yang, Xiuyan Neuropsychiatr Dis Treat Original Research BACKGROUND AND AIMS: Decreased serum retinoic acid (RA) levels have been shown to be linked with increased mortality in cardiovascular diseases. This study aimed to investigate the relationship between serum RA and 3-month functional outcome after ischemic stroke. METHODS: Between January 2019 and September 2019, we prospectively recruited ischemic stroke patients within 24 hrs of symptom onset. Serum RA levels were measured for all patients at admission. The primary outcome was defined as poor functional outcome (modified Rankin Scale 3–6) at 90 days. The secondary outcome was defined as early neurological deterioration (END), which is considered as an increase of ≥1 point in motor power or total National Institutes of Health Stroke Scale score of ≥2 points within 7 days. RESULTS: A total of 217 patients were included in the analysis. The median RA levels were 2.9 ng/mL. Ninety-four (43.3%) and 65 (30.0%) patients experienced 3-month poor outcome and END, respectively. After adjusted for potential confounders, decreased levels of serum RA were associated with a higher risk of poor outcome (P for trend = 0.001) and END (P for trend = 0.002). Adding RA quartile to the existing risk factors improved risk prediction for poor outcome [net reclassification improvement (NRI) = 42.6%, P = 0.001; integrated discrimination improvement (IDI) = 5.7%, P = 0.001] and END (NRI index = 45.4%, P = 0.001; IDI = 4.3%; P = 0.005). CONCLUSION: Low serum RA levels at baseline were associated with poor prognosis at 90 days after ischemic stroke, suggesting that RA may be a potential prognostic biomarker for ischemic stroke. Dove 2020-06-10 /pmc/articles/PMC7293911/ /pubmed/32606701 http://dx.doi.org/10.2147/NDT.S254591 Text en © 2020 Xu et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Xu, Mengshi
Xu, Liang
Du, Huaping
Shan, Wanying
Feng, Jie
Zhai, Guojie
Yang, Xiuyan
Decreased Serum Retinoic Acid May Predict Poor Outcome in Ischemic Stroke Patients
title Decreased Serum Retinoic Acid May Predict Poor Outcome in Ischemic Stroke Patients
title_full Decreased Serum Retinoic Acid May Predict Poor Outcome in Ischemic Stroke Patients
title_fullStr Decreased Serum Retinoic Acid May Predict Poor Outcome in Ischemic Stroke Patients
title_full_unstemmed Decreased Serum Retinoic Acid May Predict Poor Outcome in Ischemic Stroke Patients
title_short Decreased Serum Retinoic Acid May Predict Poor Outcome in Ischemic Stroke Patients
title_sort decreased serum retinoic acid may predict poor outcome in ischemic stroke patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293911/
https://www.ncbi.nlm.nih.gov/pubmed/32606701
http://dx.doi.org/10.2147/NDT.S254591
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