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Low Levels of Plasma Osteoglycin in Patients with Complex Coronary Lesions

Aim: Osteoglycin is one of proteoglycans that are biologically active components of vascular extracellular matrix. However, the role of osteoglycin in atherosclerosis remains unclear. Methods: We investigated plasma osteoglycin levels and the presence, severity, and lesion morphology of coronary art...

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Autores principales: Seki, Toshiki, Saita, Emi, Kishimoto, Yoshimi, Ibe, Susumu, Miyazaki, Yoshichika, Miura, Kotaro, Ohmori, Reiko, Ikegami, Yukinori, Kondo, Kazuo, Momiyama, Yukihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japan Atherosclerosis Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224206/
https://www.ncbi.nlm.nih.gov/pubmed/29503411
http://dx.doi.org/10.5551/jat.43059
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author Seki, Toshiki
Saita, Emi
Kishimoto, Yoshimi
Ibe, Susumu
Miyazaki, Yoshichika
Miura, Kotaro
Ohmori, Reiko
Ikegami, Yukinori
Kondo, Kazuo
Momiyama, Yukihiko
author_facet Seki, Toshiki
Saita, Emi
Kishimoto, Yoshimi
Ibe, Susumu
Miyazaki, Yoshichika
Miura, Kotaro
Ohmori, Reiko
Ikegami, Yukinori
Kondo, Kazuo
Momiyama, Yukihiko
author_sort Seki, Toshiki
collection PubMed
description Aim: Osteoglycin is one of proteoglycans that are biologically active components of vascular extracellular matrix. However, the role of osteoglycin in atherosclerosis remains unclear. Methods: We investigated plasma osteoglycin levels and the presence, severity, and lesion morphology of coronary artery disease (CAD) in 462 patients undergoing elective coronary angiography. Results: Of 462 patients, 245 had CAD. Osteoglycin levels were higher in patients with CAD than without CAD (median 29.7 vs. 25.0 ng/mL, P < 0.05). However, osteoglycin levels did not differ among patients with one-vessel, two-vessel, or three-vessel disease (30.8, 30.6, and 29.4 ng/mL, respectively) and did not correlate with the number of stenotic segments. Among 245 CAD patients, 41 had complex coronary lesions, and 70 had total occlusion, of whom 67 had good collateralization. Between 70 patients with occlusion and 175 without occlusion, osteoglycin levels did not differ (30.4 vs. 29.5 ng/mL). Notably, osteoglycin levels were lower in 41 patients with complex lesions than in 204 without such lesions (24.2 vs. 31.6 ng/mL, P < 0.02). In multivariate analysis, osteoglycin levels were an independent factor for complex lesion but not for CAD. Odds ratio for complex lesion was 0.80 (95%CI = 0.67–0.96) for each 10 ng/mL increase in osteoglycin levels (P < 0.02). Conclusion: Although plasma osteoglycin levels were high in patients with CAD, they did not correlate with the severity of CAD and were not an independent factor for CAD. Notably, osteoglycin levels were low in patients with complex lesions and were a factor for complex lesions, suggesting that osteoglycin plays a role in coronary plaque stabilization.
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spelling pubmed-62242062018-11-09 Low Levels of Plasma Osteoglycin in Patients with Complex Coronary Lesions Seki, Toshiki Saita, Emi Kishimoto, Yoshimi Ibe, Susumu Miyazaki, Yoshichika Miura, Kotaro Ohmori, Reiko Ikegami, Yukinori Kondo, Kazuo Momiyama, Yukihiko J Atheroscler Thromb Original Article Aim: Osteoglycin is one of proteoglycans that are biologically active components of vascular extracellular matrix. However, the role of osteoglycin in atherosclerosis remains unclear. Methods: We investigated plasma osteoglycin levels and the presence, severity, and lesion morphology of coronary artery disease (CAD) in 462 patients undergoing elective coronary angiography. Results: Of 462 patients, 245 had CAD. Osteoglycin levels were higher in patients with CAD than without CAD (median 29.7 vs. 25.0 ng/mL, P < 0.05). However, osteoglycin levels did not differ among patients with one-vessel, two-vessel, or three-vessel disease (30.8, 30.6, and 29.4 ng/mL, respectively) and did not correlate with the number of stenotic segments. Among 245 CAD patients, 41 had complex coronary lesions, and 70 had total occlusion, of whom 67 had good collateralization. Between 70 patients with occlusion and 175 without occlusion, osteoglycin levels did not differ (30.4 vs. 29.5 ng/mL). Notably, osteoglycin levels were lower in 41 patients with complex lesions than in 204 without such lesions (24.2 vs. 31.6 ng/mL, P < 0.02). In multivariate analysis, osteoglycin levels were an independent factor for complex lesion but not for CAD. Odds ratio for complex lesion was 0.80 (95%CI = 0.67–0.96) for each 10 ng/mL increase in osteoglycin levels (P < 0.02). Conclusion: Although plasma osteoglycin levels were high in patients with CAD, they did not correlate with the severity of CAD and were not an independent factor for CAD. Notably, osteoglycin levels were low in patients with complex lesions and were a factor for complex lesions, suggesting that osteoglycin plays a role in coronary plaque stabilization. Japan Atherosclerosis Society 2018-11-01 /pmc/articles/PMC6224206/ /pubmed/29503411 http://dx.doi.org/10.5551/jat.43059 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
Seki, Toshiki
Saita, Emi
Kishimoto, Yoshimi
Ibe, Susumu
Miyazaki, Yoshichika
Miura, Kotaro
Ohmori, Reiko
Ikegami, Yukinori
Kondo, Kazuo
Momiyama, Yukihiko
Low Levels of Plasma Osteoglycin in Patients with Complex Coronary Lesions
title Low Levels of Plasma Osteoglycin in Patients with Complex Coronary Lesions
title_full Low Levels of Plasma Osteoglycin in Patients with Complex Coronary Lesions
title_fullStr Low Levels of Plasma Osteoglycin in Patients with Complex Coronary Lesions
title_full_unstemmed Low Levels of Plasma Osteoglycin in Patients with Complex Coronary Lesions
title_short Low Levels of Plasma Osteoglycin in Patients with Complex Coronary Lesions
title_sort low levels of plasma osteoglycin in patients with complex coronary lesions
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224206/
https://www.ncbi.nlm.nih.gov/pubmed/29503411
http://dx.doi.org/10.5551/jat.43059
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