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High Plasma Levels of Soluble Talin-1 in Patients with Coronary Artery Disease

AIMS: Talin-1 is a cytoskeletal protein that binds integrin, thereby leading to integrin activation and affecting focal adhesions. Recently, talin-1 expression was reported to be downregulated in human atherosclerotic plaques. However, blood levels of soluble talin-1 (sTalin-1) in patients with athe...

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Autores principales: Aoyama, Masayuki, Kishimoto, Yoshimi, Saita, Emi, Ikegami, Yukinori, Ohmori, Reiko, Nakamura, Masato, Kondo, Kazuo, Momiyama, Yukihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275969/
https://www.ncbi.nlm.nih.gov/pubmed/32566035
http://dx.doi.org/10.1155/2020/2479830
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author Aoyama, Masayuki
Kishimoto, Yoshimi
Saita, Emi
Ikegami, Yukinori
Ohmori, Reiko
Nakamura, Masato
Kondo, Kazuo
Momiyama, Yukihiko
author_facet Aoyama, Masayuki
Kishimoto, Yoshimi
Saita, Emi
Ikegami, Yukinori
Ohmori, Reiko
Nakamura, Masato
Kondo, Kazuo
Momiyama, Yukihiko
author_sort Aoyama, Masayuki
collection PubMed
description AIMS: Talin-1 is a cytoskeletal protein that binds integrin, thereby leading to integrin activation and affecting focal adhesions. Recently, talin-1 expression was reported to be downregulated in human atherosclerotic plaques. However, blood levels of soluble talin-1 (sTalin-1) in patients with atherosclerotic disease, such as coronary artery disease (CAD), have not been elucidated. METHODS: We measured plasma sTalin-1 levels in 349 patients undergoing elective coronary angiography. The severity of CAD was represented as the number of stenotic coronary vessels and segments. RESULTS: Of the 349 study patients, CAD was found in 194 patients, of whom 88 had 1-vessel disease (1-VD), 60 had 2-vessel disease (2-VD), and 46 had 3-vessel disease (3-VD). Plasma sTalin-1 levels were higher in 194 patients with CAD than in 155 without CAD (CAD(-) group) (median 0.30 vs. 0.23 ng/mL, P < 0.005). A stepwise increase in sTalin-1 levels was found depending on the number of >50% stenotic coronary vessels: 0.23 in CAD(-), 0.29 in 1-VD, 0.30 in 2-VD, and 0.32 ng/mL in 3-VD group, respectively, (P < 0.05). High sTalin-1 level (>0.28 ng/mL) was found in 36% of CAD(-), 51% of 1-VD, 53% of 2-VD, and 59% of 3-VD group (P < 0.025). sTalin-1 levels also correlated with the number of >50% stenotic segments (r = 0.14, P < 0.02). The multivariate analysis revealed that sTalin-1 levels were independently associated with CAD. The odds ratio for CAD was 1.83 (95%CI = 1.14 − 2.93) for high sTalin-1 level (>0.28 ng/mL) (P < 0.02). CONCLUSIONS: Plasma sTalin-1 levels in patients with CAD were found to be high and to be associated with the presence and severity of CAD, suggesting a role of sTalin-1 in the progression of coronary atherosclerosis.
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spelling pubmed-72759692020-06-18 High Plasma Levels of Soluble Talin-1 in Patients with Coronary Artery Disease Aoyama, Masayuki Kishimoto, Yoshimi Saita, Emi Ikegami, Yukinori Ohmori, Reiko Nakamura, Masato Kondo, Kazuo Momiyama, Yukihiko Dis Markers Research Article AIMS: Talin-1 is a cytoskeletal protein that binds integrin, thereby leading to integrin activation and affecting focal adhesions. Recently, talin-1 expression was reported to be downregulated in human atherosclerotic plaques. However, blood levels of soluble talin-1 (sTalin-1) in patients with atherosclerotic disease, such as coronary artery disease (CAD), have not been elucidated. METHODS: We measured plasma sTalin-1 levels in 349 patients undergoing elective coronary angiography. The severity of CAD was represented as the number of stenotic coronary vessels and segments. RESULTS: Of the 349 study patients, CAD was found in 194 patients, of whom 88 had 1-vessel disease (1-VD), 60 had 2-vessel disease (2-VD), and 46 had 3-vessel disease (3-VD). Plasma sTalin-1 levels were higher in 194 patients with CAD than in 155 without CAD (CAD(-) group) (median 0.30 vs. 0.23 ng/mL, P < 0.005). A stepwise increase in sTalin-1 levels was found depending on the number of >50% stenotic coronary vessels: 0.23 in CAD(-), 0.29 in 1-VD, 0.30 in 2-VD, and 0.32 ng/mL in 3-VD group, respectively, (P < 0.05). High sTalin-1 level (>0.28 ng/mL) was found in 36% of CAD(-), 51% of 1-VD, 53% of 2-VD, and 59% of 3-VD group (P < 0.025). sTalin-1 levels also correlated with the number of >50% stenotic segments (r = 0.14, P < 0.02). The multivariate analysis revealed that sTalin-1 levels were independently associated with CAD. The odds ratio for CAD was 1.83 (95%CI = 1.14 − 2.93) for high sTalin-1 level (>0.28 ng/mL) (P < 0.02). CONCLUSIONS: Plasma sTalin-1 levels in patients with CAD were found to be high and to be associated with the presence and severity of CAD, suggesting a role of sTalin-1 in the progression of coronary atherosclerosis. Hindawi 2020-05-29 /pmc/articles/PMC7275969/ /pubmed/32566035 http://dx.doi.org/10.1155/2020/2479830 Text en Copyright © 2020 Masayuki Aoyama et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Aoyama, Masayuki
Kishimoto, Yoshimi
Saita, Emi
Ikegami, Yukinori
Ohmori, Reiko
Nakamura, Masato
Kondo, Kazuo
Momiyama, Yukihiko
High Plasma Levels of Soluble Talin-1 in Patients with Coronary Artery Disease
title High Plasma Levels of Soluble Talin-1 in Patients with Coronary Artery Disease
title_full High Plasma Levels of Soluble Talin-1 in Patients with Coronary Artery Disease
title_fullStr High Plasma Levels of Soluble Talin-1 in Patients with Coronary Artery Disease
title_full_unstemmed High Plasma Levels of Soluble Talin-1 in Patients with Coronary Artery Disease
title_short High Plasma Levels of Soluble Talin-1 in Patients with Coronary Artery Disease
title_sort high plasma levels of soluble talin-1 in patients with coronary artery disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275969/
https://www.ncbi.nlm.nih.gov/pubmed/32566035
http://dx.doi.org/10.1155/2020/2479830
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