Key result
Metabolic syndrome was associated with a significantly larger infarct size after acute myocardial infarction compared to controls, indicated by higher median peak CK-MB (390 vs 287 ng/mL) and Wall Motion Score Index (2.91 vs 2.29).
Why the study?
Does the presence of metabolic syndrome increase infarct size in patients with acute myocardial infarction?
Observational (n=200)
No
Does the presence of metabolic syndrome increase infarct size in patients with acute myocardial infarction?
Absolute Event Rate: 390% vs 287%
p-value: p=<0.001
Metabolic syndrome is associated with significantly larger infarct size and worse regional wall motion abnormalities in patients presenting with a first acute myocardial infarction.
Larger post-AMI infarcts in metabolic syndrome patients warrant targeted secondary prevention; extends RCT evidence on metabolic risk modification of necrosis.
BACKGROUND: Infarct size is an important surrogate end point for early and late mortality after acute myocardial infarction. Despite the high prevalence of metabolic syndrome in patients with atherosclerotic diseases, adequate data are still lacking regarding the extent of myocardial necrosis after acute myocardial infarction in these patients. OBJECTIVES: In the present study we aimed to compare myocardial infarction size in patients with metabolic syndrome to those without metabolic syndrome using peak CK-MB and cardiac troponin I (cTnI) at 72 hours after the onset of symptoms. PATIENTS AND METHODS: One-hundred patients with metabolic syndrome (group I) and 100 control subjects without metabolic syndrome (group II) who experienced acute myocardial infarction were included in the study. Diagnosis of metabolic syndrome was based on the National Cholesterol Education Program Adult Treatment Panel III (NCEP ATP III) guidelines published in 2001. Myocardial infarction size was compared between the two groups of patients using peak CK-MB and cTnI level in 72 hours after the onset of symptoms. RESULTS: Peak CK-MB and cTnI in 72 hours were found to be significantly higher in patients with metabolic syndrome compared with control subjects (both P < 0.001). Patients with metabolic syndrome also had markedly higher wall motion abnormality at 72 hours after the onset of symptoms as assessed by echocardiographically-derived Wall Motion Score Index (WMSI) (P < 0.001). Moreover, statistically significant relationships were found between WMSI and peak CK-MB and also cTnI at 72 hours (Spearman's rho = 0.56, P < 0.001 and Spearman's rho = 0.5, P < 0.001; respectively). However, association between WMSI and left ventricular ejection fraction was insignificant (Spearman's rho = -0.05, P = 0.46). CONCLUSIONS: We showed that patients with metabolic syndrome have larger infarct size compared to control subjects.
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Chitsazan et al. (2015) conducted an observational in Acute myocardial infarction (n=200). Metabolic syndrome vs. Without metabolic syndrome was evaluated on Peak CK-MB level (ng/mL) (p=<0.001). Metabolic syndrome was associated with a significantly larger infarct size after acute myocardial infarction compared to controls, indicated by higher median peak CK-MB (390 vs 287 ng/mL) and Wall Motion Score Index (2.91 vs 2.29).
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