2017
DOI: 10.1016/j.ijcard.2017.06.054
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Diagnostic and prognostic value of miR-1 and miR-29b on adverse ventricular remodeling after acute myocardial infarction – The SITAGRAMI-miR analysis

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Cited by 61 publications
(50 citation statements)
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“…In order to observe the progress of disease, it is significant to discover a biological marker used to predict the adverse events for CHD patients. As the accurate biomarkers of prognosis being of increasing clinical value, more studies [3,4] evaluating their validity of prognostic value have been performed. Currently, a metabolite called trimethylamine-N-oxide (TMAO) has recently shown association with the incidence of major adverse cardiac events (MACE) in patients with CHD [5][6][7][8][9][10][11].…”
Section: Introductionmentioning
confidence: 99%
“…In order to observe the progress of disease, it is significant to discover a biological marker used to predict the adverse events for CHD patients. As the accurate biomarkers of prognosis being of increasing clinical value, more studies [3,4] evaluating their validity of prognostic value have been performed. Currently, a metabolite called trimethylamine-N-oxide (TMAO) has recently shown association with the incidence of major adverse cardiac events (MACE) in patients with CHD [5][6][7][8][9][10][11].…”
Section: Introductionmentioning
confidence: 99%
“…The AUC value of post-AMI heart failure was 0.764, which was an independent predictor of heart failure after AMI [92]. Circulating miR-1 and miR-29b levels were correlated with changes in infarct volume of MRI indicators, and miR-29b levels were closely correlated with changes in left ventricular end-diastolic volume of MRI indicators [93], so increased circulating miR-1 levels could also predict the occurrence of heart failure after AMI [94].…”
Section: Micrornas As a Prognostic Marker For Acsmentioning
confidence: 86%
“…Altered expression of miRNAs (miR-499, miR-636, miR-380, miR-133a, miR-17, miR-21, miR-29b, miR-192, miR-194, miR-499, miR-1915, miR-34a, miR-423, miR-328, miR-134, miR-1254, miR-1, miR-181c, miR-208b, miR-566, miR-7-1, miR-92a, miR-455-3p, miR-126, miR-423-5p, miR-636, miR-486, and miR-1291 were upregulated, whereas miR-197, miR-106, and miR-223 were downregulated) have been detected in serum/plasma of patients with acute myocardial infarction and have been used as new biomarkers for predicting major adverse cardiovascular events in past studies (26). Clinical studies, including miRNAs that had both diagnostic and prognostic significance in the setting of acute myocardial infarction, are shown in Table 1 (49)(50)(51)(52)(53)(54)(55)(56). Coskunpinar et al (57) reported an increase of miR-221-3p in subjects with acute myocardial infarction, which were correlated with ejection fraction (inversely), troponin, and risk scores.…”
Section: Mirna and Acute Myocardial Infarctionmentioning
confidence: 99%