The role of matrix metalloproteinases (MMPs) in routine cardiac operations including cardiopulmonary bypass (CPB) is still poorly explored. The purpose of this systematic review was to thoroughly summarize and discuss the existing knowledge of the MMP profile in cardiac surgery. All studies meeting the inclusion criteria (i.e., those reporting detailed data about MMP release during and after CPB) were selected after screening the literature published between July 1975 and August 2022. Fifteen trials that enrolled a total of 431 participants were included. MMP levels were found to be significantly correlated with CPB in all included studies. The gelatinases MMP-2 and MMP-9 were highly released in cardiac surgery with CPB. MMP-9 levels were found to be increased after CPB start and during the duration of CPB. Particularly, it is overexpressed both in the myocardial tissue and circulating in the bloodstream. Also, MMP-2 levels increased after CPB both in plasma and in myocardial tissue. MMP-7, MMP-8, and MMP-13 levels increased after CPB start and remained elevated up to 6 h later. Increased levels of MMPs were associated with adverse post-operative outcomes. Conversely, TIMP-1 decreased with CPB. Mechanical and pharmacological strategies were applied in two studies to analyze their effect on the inflammatory response to cardiac surgery and CPB and on postoperative outcomes. New targeted MMP inhibitor therapies could protect against systemic inflammatory response syndrome after CPB and should be the subject of future large prospective multicenter randomized clinical trials.

Metalloproteinases in cardiac surgery. A systematic review / Filiberto Serraino, Giuseppe; Jiritano, Federica; Costa, Davide; Ielapi, Nicola; Battaglia, Domenica; Marcello Bracale, Umberto; Mastroroberto, Pasquale; Andreucci, Michele; Serra, Raffaele. - In: BIOMOLECULES. - ISSN 2218-273X. - 13:1(2023), pp. 1-12. [10.3390/biom13010113]

Metalloproteinases in cardiac surgery. A systematic review

Nicola Ielapi;
2023

Abstract

The role of matrix metalloproteinases (MMPs) in routine cardiac operations including cardiopulmonary bypass (CPB) is still poorly explored. The purpose of this systematic review was to thoroughly summarize and discuss the existing knowledge of the MMP profile in cardiac surgery. All studies meeting the inclusion criteria (i.e., those reporting detailed data about MMP release during and after CPB) were selected after screening the literature published between July 1975 and August 2022. Fifteen trials that enrolled a total of 431 participants were included. MMP levels were found to be significantly correlated with CPB in all included studies. The gelatinases MMP-2 and MMP-9 were highly released in cardiac surgery with CPB. MMP-9 levels were found to be increased after CPB start and during the duration of CPB. Particularly, it is overexpressed both in the myocardial tissue and circulating in the bloodstream. Also, MMP-2 levels increased after CPB both in plasma and in myocardial tissue. MMP-7, MMP-8, and MMP-13 levels increased after CPB start and remained elevated up to 6 h later. Increased levels of MMPs were associated with adverse post-operative outcomes. Conversely, TIMP-1 decreased with CPB. Mechanical and pharmacological strategies were applied in two studies to analyze their effect on the inflammatory response to cardiac surgery and CPB and on postoperative outcomes. New targeted MMP inhibitor therapies could protect against systemic inflammatory response syndrome after CPB and should be the subject of future large prospective multicenter randomized clinical trials.
2023
matrix metalloproteinases; cardiopulmonary bypass; cardiac surgery; inflammation; sirs
01 Pubblicazione su rivista::01g Articolo di rassegna (Review)
Metalloproteinases in cardiac surgery. A systematic review / Filiberto Serraino, Giuseppe; Jiritano, Federica; Costa, Davide; Ielapi, Nicola; Battaglia, Domenica; Marcello Bracale, Umberto; Mastroroberto, Pasquale; Andreucci, Michele; Serra, Raffaele. - In: BIOMOLECULES. - ISSN 2218-273X. - 13:1(2023), pp. 1-12. [10.3390/biom13010113]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1665059
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