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血脂异常与冠心病的二级预防

Dyslipidemias and the secondary prevention of coronary heart disease.

作者信息

Rosenson R S, Frauenheim W A, Tangney C C

机构信息

Department of Medicine, Rush University Chicago, Illinois.

出版信息

Dis Mon. 1994 Aug;40(8):369-464. doi: 10.1016/0011-5029(94)90027-2.

DOI:10.1016/0011-5029(94)90027-2
PMID:8050340
Abstract

Dyslipidemias in patients with coronary heart disease confer a greater risk of ischemic cardiac events than comparable dyslipidemias in people free of disease. A major dyslipidemia can be diagnosed in more than 80% of patients with established premature coronary heart disease. These dyslipidemias constitute not only elevations of low-density lipoprotein cholesterol (hypercholesterolemia) but also indicate abnormalities in the metabolism of triglyceride-rich lipoproteins, high-density lipoproteins, and lipoprotein(a). Clinical trials have demonstrated that therapy to lower low-density lipoprotein levels can delay angiographic progression of coronary stenoses and reduce recurrent cardiac event rates. These clinical benefits from low-density lipoprotein cholesterol lowering may occur as early as 6 to 12 months after initiation of therapy. Intervention strategies for dyslipidemias are directed toward lowering the low-density lipoprotein cholesterol fraction to 90 to 100 mg/dl. This approach begins with dietary modification, weight loss, smoking cessation, and aerobic exercise. Patients with hypercholesterolemia refractory to nonpharmacologic intervention require lipid-lowering agents. The choice of lipid-lowering medications is influenced by concomitant abnormalities of lipoprotein metabolism, such as hypertriglyceridemia or hypoalphalipoproteinemia. Treatment of primary dyslipidemias other than hypercholesterolemia may be warranted in the presence of other cardiac risk factors; however, a broader spectrum of clinical trial data is needed to support or refute this contention.

摘要

与无冠心病的人群中类似的血脂异常相比,冠心病患者的血脂异常会带来更高的缺血性心脏事件风险。在已确诊的早发性冠心病患者中,超过80%可诊断出主要血脂异常。这些血脂异常不仅表现为低密度脂蛋白胆固醇升高(高胆固醇血症),还表明富含甘油三酯的脂蛋白、高密度脂蛋白和脂蛋白(a)的代谢存在异常。临床试验表明,降低低密度脂蛋白水平的治疗可延缓冠状动脉狭窄的血管造影进展,并降低心脏事件复发率。这些降低低密度脂蛋白胆固醇带来的临床益处可能在治疗开始后的6至12个月就会出现。血脂异常的干预策略旨在将低密度脂蛋白胆固醇水平降至90至100mg/dl。这种方法首先从饮食调整、减肥、戒烟和有氧运动开始。对非药物干预难治的高胆固醇血症患者需要使用降脂药物。降脂药物的选择受脂蛋白代谢的伴随异常影响,如高甘油三酯血症或低α脂蛋白血症。在存在其他心脏危险因素的情况下,可能需要对除高胆固醇血症以外的原发性血脂异常进行治疗;然而,需要更广泛的临床试验数据来支持或反驳这一观点。

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