Aciksari Gonul, Demir Bulent, Uygun Turgut, Gedikbasi Asuman, Kutlu Orkide, Atici Adem, Baycan Omer Faruk, Kocak Mehmet, Kul Seref
Department of Cardiology, Istanbul Medeniyet University Goztepe Training and Research Hospital, Istanbul, Turkey.
Department of Cardiology, Bakirkoy Dr. Sadi Konuk Training and Research Hospital, Istanbul, Turkey.
North Clin Istanb. 2020 Aug 17;7(5):471-477. doi: 10.14744/nci.2020.09086. eCollection 2020.
Although the underlying mechanism is not yet fully understood, Cardiac Syndrome X (CSX) is defined as microvascular dysfunction. Prolidase plays a role in collagen synthesis. Increased serum prolidase activity (SPA) has been shown to correlate with collagen turnover. Augmented collagen turn-over may be associated with vascular fibrosis and microvascular dysfunction. In this study, we assessed whether there was a correlation between CXS and prolidase activity.
This case-control study included 45 consecutive CSX patients (mean age 50.7±6.5 years, 27 women) and 40 healthy controls (mean age 51.2±6.5 years, 25 women). Prolidase activity was determined with the Human Xaa-Pro Dipeptidase/Prolidase enzyme-linked immunosorbent assay kit (Cusabio Biotech Co. Ltd, China).
Mean prolidase activity was 898.8±639.1 mU/mL in the CSX group and 434.1±289.8 mU/mL in the control group (p<0.001). In ROC analysis, it was found that the SPA value above 350 mU/mL sympathizes with the diagnosis of CSX.
Increased SPA in CXS patients may play an essential role in the pathophysiology of CSX, leading to augmented oxidative stress and vascular fibrosis, endothelial dysfunction, and increased microvascular resistance.
尽管潜在机制尚未完全明确,但心脏X综合征(CSX)被定义为微血管功能障碍。脯氨酰寡肽酶在胶原蛋白合成中起作用。血清脯氨酰寡肽酶活性(SPA)升高已被证明与胶原蛋白周转相关。胶原蛋白周转增加可能与血管纤维化和微血管功能障碍有关。在本研究中,我们评估了CSX与脯氨酰寡肽酶活性之间是否存在相关性。
本病例对照研究纳入了45例连续的CSX患者(平均年龄50.7±6.5岁,27例女性)和40例健康对照者(平均年龄51.2±6.5岁,25例女性)。使用人Xaa-Pro二肽酶/脯氨酰寡肽酶酶联免疫吸附测定试剂盒(中国武汉优宝生物科技有限公司)测定脯氨酰寡肽酶活性。
CSX组的平均脯氨酰寡肽酶活性为898.8±639.1 mU/mL,对照组为434.1±289.8 mU/mL(p<0.001)。在ROC分析中,发现SPA值高于350 mU/mL支持CSX的诊断。
CSX患者中升高的SPA可能在CSX的病理生理学中起重要作用,导致氧化应激增强、血管纤维化、内皮功能障碍和微血管阻力增加。