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基质金属蛋白酶在腹壁疝发病机制中的作用。

The role of matrix metalloproteinases in the pathogenesis of abdominal wall hernias.

机构信息

Krankenhaus Maria v. d. Aposteln Neuwerk, Mönchengladbach, Germany.

出版信息

Eur J Clin Invest. 2009 Nov;39(11):953-9. doi: 10.1111/j.1365-2362.2009.02199.x. Epub 2009 Jul 27.

Abstract

Surgical treatment of abdominal wall hernia has been based for many decades on observational evidence, as the disease physiopathology was ambiguous. The long-standing hypothesis of abnormal collagen metabolism as a causative factor of hernia disease seems to become substantiated by modern investigations, demonstrating a link between abnormal matrix metalloproteinase (MMP) expression and abdominal wall hernia. Current evidence suggests a strong correlation between MMP-2 and direct inguinal hernia, while the role of this MMP in indirect, incisional and recurrent hernias has not been completely elucidated yet. Furthermore, MMP-1 and MMP-13 seem to be implicated in the physiopathology of recurrent hernia, while limited data link MMP-1 also with incisional hernia formation. Despite the importance of MMP-9 in wound healing mechanisms, its role in hernia pathogenesis has not been adequately investigated. Future research is expected to decipher the complex physiopathological mechanisms of hernia development and provide a basis for potential therapeutic applications.

摘要

腹壁疝的外科治疗几十年来一直基于观察性证据,因为该病的病理生理学一直不明确。异常胶原代谢作为疝病发病因素的长期假说似乎得到了现代研究的证实,这些研究表明异常基质金属蛋白酶 (MMP) 表达与腹壁疝之间存在关联。目前的证据表明 MMP-2 与直接腹股沟疝之间存在很强的相关性,而这种 MMP 在间接疝、切口疝和复发性疝中的作用尚未完全阐明。此外,MMP-1 和 MMP-13 似乎与复发性疝的病理生理学有关,而有限的数据表明 MMP-1 也与切口疝的形成有关。尽管 MMP-9 在伤口愈合机制中很重要,但它在疝发病机制中的作用尚未得到充分研究。未来的研究有望破解疝发展的复杂病理生理学机制,并为潜在的治疗应用提供依据。

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