Suppr超能文献

血浆基质金属蛋白酶-28水平与钙化性主动脉瓣狭窄严重程度的相关性

Correlation Between Plasma Matrix Metalloproteinase-28 Levels and Severity of Calcific Aortic Valve Stenosis.

作者信息

Zhou Ke, Guo Ting, Xu Yawei, Guo Rong

机构信息

Department of Cardiology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China (mainland).

Department of Anesthesiology, Huashan Hospital, Fudan University, Shanghai, China (mainland).

出版信息

Med Sci Monit. 2020 Sep 20;26:e925260. doi: 10.12659/MSM.925260.

Abstract

BACKGROUND Calcific aortic valve disease is a common cardiovascular disorder worldwide. This study aimed to investigate the correlation between plasma matrix metalloproteinase-28 (MMP-28) levels and the severity of calcific aortic valve stenosis. MATERIAL AND METHODS Calcific aortic valve stenosis patients who were admitted to the heart center of our hospital between January 2016 and January 2019 to undergo surgery were successively enrolled in this study (55 males and 24 females with an average age of 58.5±9.6). Information on echocardiography, plasma MMP-28 levels, and other clinical data of the patients was retrospectively collected. RESULTS The average plasma MMP-28 level was 2.43±2.22 ng/mL (range, 0.22-8.27 ng/mL). Plasma MMP-28 levels in patients with mild (n=24), moderate (n=31), or severe (n=24) aortic valve stenosis were 0.74 (0.25-2.23), 1.46 (0.50-3.22), and 4.13 (1.54-6.18) ng/mL, respectively, indicating that the patients with severe aortic valve stenosis had significantly higher MMP-28 levels than the patients with moderate or mild aortic valve stenosis (both P<0.01). Regression analysis using the general linear model further revealed that plasma MMP-28 level was correlated with the peak blood flow velocity and mean pressure gradient of the transaortic valve, and the correlations were statistically significant (both P<0.01). CONCLUSIONS MMP-28 level is significantly elevated in severe cases of calcific aortic valve stenosis. Moreover, plasma MMP-28 levels are positively correlated with the mean pressure gradients and peak blood flow velocity of the transaortic valve.

摘要

背景

钙化性主动脉瓣疾病是全球常见的心血管疾病。本研究旨在探讨血浆基质金属蛋白酶-28(MMP-28)水平与钙化性主动脉瓣狭窄严重程度之间的相关性。

材料与方法

连续纳入2016年1月至2019年1月在我院心脏中心接受手术的钙化性主动脉瓣狭窄患者(55例男性和24例女性,平均年龄58.5±9.6岁)。回顾性收集患者的超声心动图、血浆MMP-28水平及其他临床资料。

结果

血浆MMP-28平均水平为2.43±2.22 ng/mL(范围0.22 - 8.27 ng/mL)。轻度(n = 24)、中度(n = 31)或重度(n = 24)主动脉瓣狭窄患者的血浆MMP-28水平分别为0.74(0.25 - 2.23)、1.46(0.50 - 3.22)和4.13(1.54 - 6.18)ng/mL,表明重度主动脉瓣狭窄患者的MMP-28水平显著高于中度或轻度主动脉瓣狭窄患者(均P < 0.01)。使用一般线性模型进行回归分析进一步显示,血浆MMP-28水平与经主动脉瓣的峰值血流速度和平均压力阶差相关,且相关性具有统计学意义(均P < 0.01)。

结论

在钙化性主动脉瓣狭窄严重病例中,MMP-28水平显著升高。此外,血浆MMP-28水平与经主动脉瓣的平均压力阶差和峰值血流速度呈正相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/feb5/7526340/396810f68eb0/medscimonit-26-e925260-g001.jpg

相似文献

3
Calcific aortic stenosis and its correlation with a novel inflammatory marker, the lymphocyte/monocyte ratio.
Rev Port Cardiol. 2016 Nov;35(11):573-578. doi: 10.1016/j.repc.2016.06.008. Epub 2016 Oct 1.
4
The relationship between neutrophil/lymphocyte ratio and calcific aortic stenosis.
Echocardiography. 2014 Oct;31(9):1031-5. doi: 10.1111/echo.12534. Epub 2014 Feb 14.
5
The relationship between severity of calcific aortic stenosis and serum uric acid levels.
Angiology. 2012 Nov;63(8):603-8. doi: 10.1177/0003319711433198. Epub 2012 Jan 18.
6
Association between plasma asymmetrical dimethylarginine activity and severity of aortic valve stenosis.
J Cardiovasc Med (Hagerstown). 2011 Feb;12(2):96-101. doi: 10.2459/JCM.0b013e32833cdcea.
7
A Role for MMP-10 (Matrix Metalloproteinase-10) in Calcific Aortic Valve Stenosis.
Arterioscler Thromb Vasc Biol. 2020 May;40(5):1370-1382. doi: 10.1161/ATVBAHA.120.314143. Epub 2020 Mar 19.
9
Multimodality and molecular imaging of matrix metalloproteinase activation in calcific aortic valve disease.
J Nucl Med. 2015 Jun;56(6):933-8. doi: 10.2967/jnumed.114.152355. Epub 2015 Apr 23.

引用本文的文献

2
Novel Circulating Biomarkers in Aortic Valve Stenosis.
Int J Mol Sci. 2025 Feb 22;26(5):1902. doi: 10.3390/ijms26051902.
3
Novel Biomarkers and Advanced Cardiac Imaging in Aortic Stenosis: Old and New.
Biomolecules. 2023 Nov 17;13(11):1661. doi: 10.3390/biom13111661.
4
Towards Personalized Therapy of Aortic Stenosis.
J Pers Med. 2021 Dec 3;11(12):1292. doi: 10.3390/jpm11121292.

本文引用的文献

1
Pathophysiology of Aortic Stenosis and Future Perspectives for Medical Therapy.
Cardiol Clin. 2020 Feb;38(1):1-12. doi: 10.1016/j.ccl.2019.09.010. Epub 2019 Nov 1.
2
Advances in transcatheter aortic valve replacement.
J Geriatr Cardiol. 2019 Sep;16(9):724-732. doi: 10.11909/j.issn.1671-5411.2019.09.002.
3
TAVI and the future of aortic valve replacement.
J Card Surg. 2019 Dec;34(12):1577-1590. doi: 10.1111/jocs.14226. Epub 2019 Oct 10.
6
Pathology of the Aortic Valve: Aortic Valve Stenosis/Aortic Regurgitation.
Curr Cardiol Rep. 2019 Jul 5;21(8):81. doi: 10.1007/s11886-019-1162-4.
7
Cellular Mechanisms of Valvular Thickening in Early and Intermediate Calcific Aortic Valve Disease.
Curr Cardiol Rev. 2018;14(4):264-271. doi: 10.2174/1573403X14666180820151325.
8
Comparison of Lipoprotein(a)-Levels in Patients ≥70 Years of Age With Versus Without Aortic Valve Stenosis.
Am J Cardiol. 2018 Aug 15;122(4):645-649. doi: 10.1016/j.amjcard.2018.04.046. Epub 2018 May 11.
9
Potential roles of circulating matrix metalloproteinase-28 (MMP-28) in patients with atrial fibrillation.
Life Sci. 2018 Jul 1;204:15-19. doi: 10.1016/j.lfs.2018.04.053. Epub 2018 May 2.
10
Matrix Metalloproteinases, Vascular Remodeling, and Vascular Disease.
Adv Pharmacol. 2018;81:241-330. doi: 10.1016/bs.apha.2017.08.002. Epub 2017 Sep 19.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验