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  4. Dyslipidemias have a detrimental effect on left ventricular systolic function in patients with a first acute myocardial infarction
 
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Dyslipidemias have a detrimental effect on left ventricular systolic function in patients with a first acute myocardial infarction

Journal
American Journal of Cardiology
Journal Volume
81
Journal Issue
5
Pages
531-537
Date Issued
1998
Author(s)
TZUNG-DAU WANG  
CHAU-CHUNG WU  
WEN-JONE CHEN  
CHII-MING LEE  
MING-FONG CHEN  
Liau C.-S.
Sung F.-C.
Lee Y.-T.
DOI
10.1016/S0002-9149(97)00974-0
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/466318
Abstract
Several large-scale clinical trials have shown that lipid-lowering interventions are associated with reduced coronary events and mortality. However, whether dyslipidemias have a detrimental effect on the evolution of myocardial infarction (MI) is still unknown. To examine whether dyslipidemias can aggravate myocardial vulnerability following MI, 165 patients with a first MI were studied. All patients underwent measurements of serum lipid profiles 1 week and 3 months after MI, a radionuclide ventriculographic study, and a coronary angiographic study. The patients were divided into 3 groups according to their 3-month serum cholesterol levels (group 1, <200 mg/dl; group 2, 200 to 240 mg/dl; group 3, >240 mg/dl). Groups 1, 2, and 3 consisted of 66, 59, and 40 patients, respectively. Group 3 had a higher Gensini score than groups 1 and 2, although this was not statistically significant (p = 0.13). The postinfarct left ventricular ejection fraction (LVEF) was highest in group 1 (53 ± 13%), at mid level in group 2 (43 ± 14%), and lowest in group 3 (35 ± 11%) (p <0.0001). A significant negative correlation between 3-month low-density lipoprotein (LDL) cholesterol (r = - 0.55, p<0.0001) and the postinfarct LVEF was found. The product of peak creatine kinase (CK(MAX)) and time to CK(MAX) (p = 0.001), and patency of the infarct-related artery (p = 0.009), rather than variables of coronary atherosclerosis, were also independent predictors of the postinfarct LVEF. Increases in 1-week LDL cholesterol and decreases in 1-week high-density lipoprotein cholesterol were associated with a higher CK(MAX) and a lower patency rate of the infarct-related artery, respectively. This study revealed that dyslipidemias per se, especially LDL cholesterol, had a detrimental effect on the postinfarct LVEF; this effect might be independent of the atherogenic properties of dyslipidemias.
SDGs

[SDGs]SDG3

Other Subjects
creatine kinase; low density lipoprotein cholesterol; acute heart infarction; adult; aged; article; controlled study; coronary artery atherosclerosis; disease course; dyslipidemia; female; heart left ventricle failure; human; lipoprotein metabolism; major clinical study; male; priority journal; risk factor; Aged; Cholesterol, LDL; Coronary Angiography; Creatine Kinase; Female; Gated Blood-Pool Imaging; Humans; Hyperlipidemias; Linear Models; Male; Middle Aged; Myocardial Infarction; Stroke Volume; Systole; Vascular Patency; Ventricular Function, Left
Type
journal article

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