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Published on: April 25, 2014
Effects of Short-term High Dose Atorvastatin on Left Ventricular Remodeling in Patients with First Time Attack of
Zhi-Jian Liu1, Gao-Pin Hu1, Mei-Ying Fei1
1Department of Cardiology, the 210th Hospital of People's Liberation Army, Dalian, Liaoning 116021, China.
Insights
Short-term high-dose atorvastatin therapy for acute anterior myocardial infarction (AAMI) reduced inflammatory markers like hs-CRP, ET-1, and MMP-9. However, this intensive treatment did not significantly improve left ventricular remodeling compared to standard dosing.
Area of Science:
- Cardiology
- Pharmacology
- Biochemistry
Background:
- Acute anterior myocardial infarction (AAMI) is a critical cardiovascular event.
- Inflammatory markers and ventricular remodeling are key indicators of AAMI prognosis.
- Atorvastatin is a widely used statin for cardiovascular disease management.
Purpose of the Study:
- To evaluate the impact of short-term high-dose atorvastatin on inflammatory markers and left ventricular (LV) remodeling in AAMI patients.
- To compare intensive treatment (40mg then 20mg) versus standard treatment (20mg) of atorvastatin.
Main Methods:
- 103 AAMI patients undergoing percutaneous coronary intervention were randomized into intensive (IT) and standard (ST) atorvastatin groups.
- Plasma levels of hs-CRP, MDA, ET-1, MMP-2, and MMP-9 were measured at baseline and follow-up points.
- Echocardiography assessed LV remodeling (LVEDV, LVESV, LVEF) at baseline, 2 weeks, and 1 year.
Main Results:
- The IT group showed significantly lower levels of hs-CRP, ET-1, MMP-9, and pro-BNP at 1 week post-AAMI compared to the ST group.
- No significant differences were observed in the changes of LVEDV, LVESV, and LVEF at 1-year follow-up between the IT and ST groups.
- Malondialdehyde (MDA) levels were also measured but not explicitly detailed in the provided results summary.
Conclusions:
- Short-term high-dose atorvastatin therapy in AAMI patients leads to a reduction in specific inflammatory markers and endothelin-1.
- The observed reduction in inflammatory markers with intensive atorvastatin treatment does not translate to improved left ventricular remodeling at one year.
- Further research may be needed to elucidate the long-term clinical implications of these findings.
Abstract:
Objects The aim of this trial was to evaluate the effect of short-term high-dose atorvastatin therapy on levels of high-sensitivity C-reactive protein (hs-CRP), malonaldehyde (MDA), endothelin-1(ET-1), matrix metalloproteinases (MMPs), and left ventricular (LV) remodeling in patients with first time attack of acute anterior myocardial infarction (AAMI) .Methods A hundred and three patients with first time attack of AAMI who underwent successful primary percutaneous coronary intervention were randomized to receive atorvastatin 40 mg once daily for 1 week followed by 20 mg once daily (intensive treatment group, IT group, n=49), or atorvastatin 20 mg once daily (standard treatment group, ST group, n=54). Plasma levels of hs-CRP, MDA, ET-1, MMP-2 and MMP-9 were measured on admission, at 1 week, 2 weeks and 6 months follow up and compared between the IT group and ST group. Echocardiography was performed on admission, at 2 week, and 1 year follow up. The left ventricular end-diastolic volume (LVEDV), left ventricular end-systolic volume (LVESV) and left ventricular ejection fraction (LVEF) were measured at each echocardiographic examination and compared between the IT group and ST group.Results Plasma levels of hs-CRP (F=7.718, P=0.009), ET-1 (F=7.882, P=0.006), MMP-9 (F=4.834, P=0.028) and pro-BNP (F=4.603, P=0.032) were significantly lower at 1 week after initial onset of AAMI in the IT group compared with the ST group. The changes of LVEDV, LVESV, and LVEF at the 1 year follow-up from the admission did not differ between the IT group and the ST group (t=0.722, P=0.444; t=1.228, P=0.221; t=1.354, P=0.187, repectively).Conclusions Short-term high-dose atorvastatin treatment for AAMI was associated with lower hs-CRP, ET-1 and MMP-9 levels compared to the standard dose treatment. However, this beneficial effect is not likely to related to the left ventricular remodeling.
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