Department of Cardiovascular Surgery, University Hospital Gießen and Marburg, Marburg, Germany.
Institute for Pathology, University Hospital Gießen and Marburg, Marburg, Germany.
J Card Surg. 2022 Jun;37(6):1613-1622. doi: 10.1111/jocs.16449. Epub 2022 Mar 28.
The pathogenesis of mitral valve insufficiency is not yet fully understood. Several studies stressed the role of matrix metalloproteinases (MMPs) in the emergence of valvular pathologies. The primary objective of the present study is to analyze the role of selected MMPs and their inhibitors in mitral valve insufficiency.
Eighty patients (33 female/47 male, mean age 67 years) underwent cardiopulmonary bypass surgery for mitral valve reconstruction between 2007 and 2015. All patients suffered from mitral insufficiency (MI) Stages iii and iv. When tissue resection was acquired specimens were taken immediately frozen and used for histological examination. Expression of MMP-1, MMP-9, tissue inhibitor of metalloproteinase (TIMP)-1, and TIMP-2 was examined immunohistochemically and distribution was analyzed in regard to preoperative clinical, echocardiographic, and histopathological findings.
A clear correlation between the MMP expression and the MI degree of severity could be shown. The expression of MMPs proved to be high in relation to mild insufficiencies and relatively weak in the case of severe ones. Additionally, the etiology of the MI was considered in the analysis and a significant difference in the expression of MMPs between the mitral valves with endocarditis and the ones featuring a degenerative disease could be shown. Within the group of valves with degenerative diseases, no significant difference could be established between the subgroups (myxoid and sclerosed valves).
The increased expression of MMPs and their inhibitors in mild insufficiencies could prove that the molecular changes in the valve precede the macroscopical and thus the echocardiographically diagnosable changes. Hence, new options for early diagnosis and therapy of MIs should be examined in further studies, respectively. Herein, the correlation of the MMP blood levels with MMP tissue expression should be addressed for surgical therapeutical decisions.
二尖瓣关闭不全的发病机制尚未完全阐明。有几项研究强调了基质金属蛋白酶(MMPs)在瓣膜病变中的作用。本研究的主要目的是分析选定的 MMPs 及其抑制剂在二尖瓣关闭不全中的作用。
2007 年至 2015 年间,80 例(33 名女性/47 名男性,平均年龄 67 岁)因二尖瓣重建而行心肺旁路手术的患者。所有患者均患有二尖瓣关闭不全(MI)III 期和 IV 期。当获取组织切除标本时,立即将其冷冻并用于组织学检查。免疫组织化学检查 MMP-1、MMP-9、金属蛋白酶组织抑制剂-1(TIMP-1)和 TIMP-2 的表达,并分析术前临床、超声心动图和组织病理学发现的分布情况。
MMP 表达与 MI 严重程度之间存在明显的相关性。MMP 的表达与轻度关闭不全呈高相关,与严重关闭不全呈弱相关。此外,在分析中考虑了 MI 的病因,结果表明,心内膜炎引起的二尖瓣与退行性疾病引起的二尖瓣之间的 MMP 表达存在显著差异。在退行性疾病组中,硬化型和黏液样瓣膜之间的 MMP 表达无显著差异。
在轻度关闭不全中 MMPs 及其抑制剂的表达增加表明,瓣膜的分子变化先于宏观和超声心动图可诊断的变化。因此,应在进一步的研究中分别检查用于早期诊断和治疗 MI 的新方法。在此,应针对手术治疗决策来研究 MMP 血液水平与 MMP 组织表达的相关性。