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Alpha-2-macroglobulin as a Promising Biological Marker of Endothelial Function

Aims: Alpha-2-macroglobulin (α(2)MG) is thought to be associated with inflammatory reactions and procoagulant properties that might cause ischemic stroke. Endothelial dysfunction plays an important role in atherosclerosis development and in the occurrence of cardiovascular events. In this study, we...

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Autores principales: Shimomura, Ryo, Nezu, Tomohisa, Hosomi, Naohisa, Aoki, Shiro, Sugimoto, Takamichi, Kinoshita, Naoto, Araki, Mutsuko, Takahashi, Tetsuya, Maruyama, Hirofumi, Matsumoto, Masayasu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japan Atherosclerosis Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5906188/
https://www.ncbi.nlm.nih.gov/pubmed/29093276
http://dx.doi.org/10.5551/jat.41335
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author Shimomura, Ryo
Nezu, Tomohisa
Hosomi, Naohisa
Aoki, Shiro
Sugimoto, Takamichi
Kinoshita, Naoto
Araki, Mutsuko
Takahashi, Tetsuya
Maruyama, Hirofumi
Matsumoto, Masayasu
author_facet Shimomura, Ryo
Nezu, Tomohisa
Hosomi, Naohisa
Aoki, Shiro
Sugimoto, Takamichi
Kinoshita, Naoto
Araki, Mutsuko
Takahashi, Tetsuya
Maruyama, Hirofumi
Matsumoto, Masayasu
author_sort Shimomura, Ryo
collection PubMed
description Aims: Alpha-2-macroglobulin (α(2)MG) is thought to be associated with inflammatory reactions and procoagulant properties that might cause ischemic stroke. Endothelial dysfunction plays an important role in atherosclerosis development and in the occurrence of cardiovascular events. In this study, we investigated whether serum α(2)MG levels, endothelial function, and endothelial progenitor cell (EPC) number were associated in patients with chronic stroke or cardiovascular risk factors. Methods: Patients with a history of stroke or any established cardiovascular risk factors were enrolled in this study (n = 102; 69 men, 70.1 ± 9.2 years). Endothelial function was assessed by flow-mediated dilation (FMD). EPC numbers (CD34+/CD133+) were measured using flow cytometry (n = 91). Serum α(2)MG levels were measured by nephelometry. Results: Patients in the highest tertile of serum α(2)MG levels were older (P = 0.019) and more frequently exhibited dyslipidemia (P = 0.021). Univariate-regression analysis revealed that increased α(2)MG levels were negatively associated with FMD values (r = −0.25; P = 0.010), whereas increased EPC numbers were positively associated (r = 0.21; P = 0.044). Multivariate-regression analysis adjusted for male gender, hypertension, and severe white-matter lesions showed that serum α(2)MG levels were independently associated with FMD values (standardized partial regression coefficient [β] −0.185; P = 0.033), although not significantly associated with EPC numbers. Conclusion: Serum α(2)MG levels might reflect endothelial dysfunction evaluated by FMD in patients with chronic stroke or cardiovascular risk factors.
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spelling pubmed-59061882018-04-19 Alpha-2-macroglobulin as a Promising Biological Marker of Endothelial Function Shimomura, Ryo Nezu, Tomohisa Hosomi, Naohisa Aoki, Shiro Sugimoto, Takamichi Kinoshita, Naoto Araki, Mutsuko Takahashi, Tetsuya Maruyama, Hirofumi Matsumoto, Masayasu J Atheroscler Thromb Original Article Aims: Alpha-2-macroglobulin (α(2)MG) is thought to be associated with inflammatory reactions and procoagulant properties that might cause ischemic stroke. Endothelial dysfunction plays an important role in atherosclerosis development and in the occurrence of cardiovascular events. In this study, we investigated whether serum α(2)MG levels, endothelial function, and endothelial progenitor cell (EPC) number were associated in patients with chronic stroke or cardiovascular risk factors. Methods: Patients with a history of stroke or any established cardiovascular risk factors were enrolled in this study (n = 102; 69 men, 70.1 ± 9.2 years). Endothelial function was assessed by flow-mediated dilation (FMD). EPC numbers (CD34+/CD133+) were measured using flow cytometry (n = 91). Serum α(2)MG levels were measured by nephelometry. Results: Patients in the highest tertile of serum α(2)MG levels were older (P = 0.019) and more frequently exhibited dyslipidemia (P = 0.021). Univariate-regression analysis revealed that increased α(2)MG levels were negatively associated with FMD values (r = −0.25; P = 0.010), whereas increased EPC numbers were positively associated (r = 0.21; P = 0.044). Multivariate-regression analysis adjusted for male gender, hypertension, and severe white-matter lesions showed that serum α(2)MG levels were independently associated with FMD values (standardized partial regression coefficient [β] −0.185; P = 0.033), although not significantly associated with EPC numbers. Conclusion: Serum α(2)MG levels might reflect endothelial dysfunction evaluated by FMD in patients with chronic stroke or cardiovascular risk factors. Japan Atherosclerosis Society 2018-04-01 /pmc/articles/PMC5906188/ /pubmed/29093276 http://dx.doi.org/10.5551/jat.41335 Text en 2018 Japan Atherosclerosis Society This article is distributed under the terms of the latest version of CC BY-NC-SA defined by the Creative Commons Attribution License.http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Original Article
Shimomura, Ryo
Nezu, Tomohisa
Hosomi, Naohisa
Aoki, Shiro
Sugimoto, Takamichi
Kinoshita, Naoto
Araki, Mutsuko
Takahashi, Tetsuya
Maruyama, Hirofumi
Matsumoto, Masayasu
Alpha-2-macroglobulin as a Promising Biological Marker of Endothelial Function
title Alpha-2-macroglobulin as a Promising Biological Marker of Endothelial Function
title_full Alpha-2-macroglobulin as a Promising Biological Marker of Endothelial Function
title_fullStr Alpha-2-macroglobulin as a Promising Biological Marker of Endothelial Function
title_full_unstemmed Alpha-2-macroglobulin as a Promising Biological Marker of Endothelial Function
title_short Alpha-2-macroglobulin as a Promising Biological Marker of Endothelial Function
title_sort alpha-2-macroglobulin as a promising biological marker of endothelial function
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5906188/
https://www.ncbi.nlm.nih.gov/pubmed/29093276
http://dx.doi.org/10.5551/jat.41335
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