Key result
Hydrophilic statins show no difference in 1-year MACE compared to lipophilic statins after AMI.
Why the study?
A controversy exists about which statin is preferable for patients with acute myocardial infarction, and clinical impacts of different statins by lipophilicity have not been established.
Does the use of hydrophilic statins compared to lipophilic statins improve clinical outcomes in patients with acute myocardial infarction?
Cohort (n=1,124)
No
Does the use of hydrophilic statins compared to lipophilic statins improve clinical outcomes in patients with acute myocardial infarction?
In patients with acute myocardial infarction, the choice between hydrophilic and lipophilic statins does not significantly impact 1-year clinical outcomes, despite a potential short-term benefit with lipophilic statins.
Answers are grounded in this paper and cite their sources.
Statin hydrophilicity may not affect 1-year MACE in AMI; leaves open need for randomized confirmation.
BACKGROUND/AIMS: A controversy exists about which statin is preferable for patients with acute myocardial infarction (AMI), and clinical impacts of different statins according to lipophilicity have not been established. METHODS: The 1,124 patients with AMI included in the present study were divided into hydrophilic- and lipophilic-statin groups. In-hospital complications (defined as death, cardiogenic shock, ventricular arrhythmia, infection, bleeding, and renal insufficiency, and other fatal arrhythmias), major adverse cardiac events (MACE), all-cause death, re-myocardial infarction, re-percutaneous coronary intervention (re-PCI), and surgical revascularization were analyzed during a 1-year clinical follow-up. RESULTS: Baseline characteristics were similar between the two groups, and in-hospital complication rates showed no between-group differences (11.7% vs. 12.8%, p = 0.688). Although MACE at the 1- and 6-month clinical follow-ups occurred more in hydrophilic statin group I (1 month: 10.0% vs. 4.4%, p = 0.001; 6 month: 19.9% vs. 14.2%, p = 0.022), no significant difference in MACE was observed at the 1-year follow-up (21.5% vs. 17.9%, p = 0.172). Both statin groups showed similar efficacy for reducing serum lipid concentrations. A Cox-regression analysis showed that the use of a hydrophilic statin did not predict 1-year MACE, all-cause death, AMI, or re-PCI. CONCLUSIONS: Although short-term cardiovascular outcomes were better in the lipophilic-statin group, 1-year outcomes were similar in patients with AMI who were administered hydrophilic and lipophilic statins. In other words, the type of statin did not influence 1-year outcomes in patients with AMI.
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Kim et al. (2011) conducted a cohort in Acute Myocardial Infarction (n=1,124). Hydrophilic statin vs. Lipophilic statin was evaluated on 1-year major adverse cardiac events (MACE) (HR 1.29, 95% CI 0.93-1.80, p=0.122). Hydrophilic statins did not significantly differ from lipophilic statins in the 1-year risk of major adverse cardiac events among patients with acute myocardial infarction (adjusted HR 1.29).
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