确定年轻急性心肌梗死患者兄弟姐妹中血脂异常和脂蛋白异常的患病率。

A. Sharma, R. Nath, N. Pandit
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引用次数: 1

摘要

尽管有所有可用的理论假设,但没有研究确定年轻急性心肌梗死(MI)患者的兄弟姐妹中脂质和脂蛋白异常的患病率。这是第一次这样的研究。方法:采用病例-对照研究。对110例年轻急性心肌梗死患者的兄弟姐妹(A组)和50例健康年轻对照(B组)进行为期2年的研究。临床资料包括年龄、性别、吸烟、高血压、糖尿病、腹部肥胖和血脂异常。主要目的是研究血脂异常和脂蛋白异常的患病率。次要目的是研究年轻(<45岁)急性心肌梗死患者的兄弟姐妹中传统危险因素的患病率。结果:脂质谱分析发现,a组总胆固醇、甘油三酯、低密度脂蛋白、ApoB100、ApoB100: ApoA-1比值、脂蛋白(a)明显高于b组。常规危险因素研究发现,吸烟史、高血压、糖尿病、腰围增加在a组较b组更为普遍。与健康对照组相比,传统的动脉粥样硬化危险因素、脂质和脂蛋白异常在年轻急性心肌梗死患者的兄弟姐妹中更为普遍,这可能是年轻心肌梗死家族聚集的可能原因,强调了家族筛查的重要性。因此,在这些情况下,应加紧努力确定和改变可改变的危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
To determine the prevalence of dyslipidemia and lipoprotein abnormalities among siblings of young acute myocardial infarction patients.
Introduction: Despite all available theoretical assumptions, there is no study defining the prevalence of lipid and lipoprotein abnormalities among siblings of young acute myocardial infarction (MI) patients. This is the first such study. Methods: This was a case-control study. A total 110 siblings of young acute MI patients (Group A) and 50 healthy young controls (Group B) were studied for a duration of 2 years. Clinical profiles included age, sex, smoking, hypertension, diabetes mellitus, abdominal obesity and dyslipidemia for both cases and controls.The primary objective was to study the prevalence of dyslipidemia and lipoprotein abnormalities. The secondary objective was to study the prevalence of conventional risk factors among siblings of young (<45 years) acute MI patients. Results: On analyzing lipid profiles, it was found that total cholesterol, triglycerides, low-density lipoprotein, ApoB100, ApoB100: ApoA-1 ratio, and lipoprotein (a) were significantly raised in Group A in comparison to Group B. On studying conventional risk factors, it was observed that history of smoking, hypertension, diabetes mellitus, and increased waist circumference were more prevalent in Group A in comparison to Group B. Conclusion: Conventional atherosclerotic risk factors, lipid and lipoprotein abnormalities were significantly more prevalent in siblings of young acute MI patients in comparison to healthy controls and may be an answer to the possible cause of familial clustering in young MI emphasizing the importance of familial screening. Therefore, intensive efforts should be made to identify and alter modifiable risk factors in these cases.
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