Clinical benefit of drugs targeting mitochondrial function as an adjunct to reperfusion in ST-segment elevation myocardial infarction: A meta-analysis of randomized clinical trials

被引:20
作者
Campo, Gianluca [1 ]
Pavasini, Rita [1 ]
Morciano, Giampaolo [2 ]
Lincoff, A. Michael [3 ]
Gibson, C. Michael [4 ]
Kitakaze, Masafumi [5 ]
Lonborg, Jacob [6 ]
Ahluwalia, Amrita [7 ]
Ishii, Hideki [8 ]
Frenneaux, Michael [9 ]
Ovize, Michel [10 ]
Galvani, Marcello [11 ]
Atar, Dan [12 ,13 ]
Ibanez, Borja [14 ,15 ]
Cerisano, Giampaolo [16 ]
Biscaglia, Simone [1 ]
Neil, Brandon J.
Asakura, Masanori [5 ]
Engstrom, Thomas [6 ]
Jones, Daniel A. [7 ]
Dawson, Dana [17 ]
Ferrari, Roberto [1 ,18 ]
Pinton, Paolo [2 ]
Ottani, Filippo [11 ]
机构
[1] Azienda Osped Univ Ferrara, Cardiol Unit, Cona, FE, Italy
[2] Univ Ferrara, Sect Pathol Oncol & Expt Biol, Dept Morphol Surg & Expt Med, Ferrara, Italy
[3] Cleveland Clin, Coordinating Ctr Clin Res C5Res, Cleveland, OH 44106 USA
[4] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Dept Med, PERFUSE Study Grp,Cardiovasc Div, Boston, MA USA
[5] Natl Cardiovasc Ctr, Cardiovasc Div Med, Suita, Osaka, Japan
[6] Rigshosp, Dept Cardiol, Copenhagen, Denmark
[7] Queen Mary Univ, Barts & London Med Sch, William Harvey Res Inst, Ctr Clin Pharmacol,Barts NIHR Cardiovasc Biomed R, London, England
[8] Nagoya Univ, Grad Sch Med, Dept Cardiol, Nagoya, Aichi, Japan
[9] Univ East Anglia, Norwich Med Sch, Norwich, Norfolk, England
[10] Clin Invest Ctr Lyon, Lyon, France
[11] Osped GB Morgagni, Unita Operat Cardiol, Forli, Italy
[12] Univ Oslo, Oslo Univ Hosp Ullevall, Dept Cardiol B, Oslo, Norway
[13] Univ Oslo, Fac Med, Oslo, Norway
[14] Ctr Nacl Invest Cardiovasc Carlos III CNIC, Madrid, Spain
[15] Fdn Jimenez Diaz Hosp, Inst Invest, Madrid, Spain
[16] Univ Florence, Careggi Hosp, Div Cardiol, Florence, Italy
[17] Univ Aberdeen, Sch Med & Dent, Aberdeen, Scotland
[18] ES Hlth Sci Fdn, Maria Cecilia Hosp, GVM Care & Res, Cotignola, Italy
关键词
Mitochondrial function; ST-segment elevation myocardial infarction; Primary percutaneous coronary intervention; Mortality; Reperfusion injury; CELLULAR BIOLOGY; POSITION PAPER; WORKING GROUP; PERMEABILITY TRANSITION; EUROPEAN-SOCIETY; NICORANDIL; INJURY; CARDIOPROTECTION; CYCLOSPORINE; IDENTITY;
D O I
10.1016/j.ijcard.2017.06.040
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: To perform a systematic review and meta-analysis of randomized clinical trials (RCT) comparing the effectiveness of drugs targeting mitochondrial function vs. placebo in patients with ST-segment elevation myocardial infarction (STEMI) undergoing mechanical coronary reperfusion. Methods: Inclusion criteria: RCTs enrolling STEMI patients treated with primary percutaneous coronary intervention (PCI) and comparing drugs targeting mitochondrial function vs. placebo. Odds ratios (OR) were computed from individual studies and pooled with random-effect meta-analysis. Results: Fifteen studies were identified involving 5680 patients. When compared with placebo, drugs targeting mitochondrial component/pathway were not associated with significant reduction of cardiovascular and all-cause mortality (OR 0.9, 95% CI 0.7-1.17 and OR 0.92, 95% CI 0.69-1.23, respectively). However, these agents significantly reduced hospital admission for heart failure (HF) (OR 0.64; 95% CI 0.45-0.92) and increased left ventricular ejection fraction (LVEF) (OR 1.44; 95% CI 1.15-1.82). After analysis for subgroups according to the mechanism of action, drugs with direct/selective action did not reduce any outcome. Conversely, those with indirect/unspecific action showed a significant effect on cardiovascular mortality (0.65, 95% CI 0.46-0.92), all cause mortality (OR 0.69, 95% CI 0.52-0.92), hospital readmission for HF (OR 0.41, 95% CI 0.28-0.6) and LVEF (OR 1.49, 95% CI 1.09-2.05). Conclusions: Administration of drugs targeting mitochondrial function in STEMI patients undergoing primary PCI appear to have no effect on mortality, but may reduce hospital readmission for HF. The drugs with a broad-spectrum mechanism of action seem to be more effective in reducing adverse events. (c) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:59 / 66
页数:8
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