萨摩亚人肥胖全基因组关联研究的初步血脂、脂蛋白和葡萄糖发现。

Samoa medical journal Pub Date : 2010-09-01
Nl Hawley, Hl Menard, G Agha, St McGarvey
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引用次数: 0

摘要

事实证明,萨摩亚人患肥胖症、糖尿病和心血管疾病等非传染性疾病的比率高得惊人。非传染性疾病负担高通常以人群中生物危险因素发生率高为特征,如血脂、脂蛋白和血糖水平升高。本报告描述了年龄在25-64岁的800名萨摩亚成年人(39%为男性,n=312)中这些生物风险因素的流行情况。11.5%的男性和10.0%的女性的总胆固醇水平较高。在研究的800人中,有617人(77.1%)的ldl -胆固醇水平过高。大量女性的高密度脂蛋白胆固醇水平过低(62.1%的女性与27.9%的男性相比),而高密度脂蛋白胆固醇可以预防心血管疾病的风险。男性显示出较高的甘油三酯平均水平,男性比女性被归类为心血管疾病风险增加的人群。相反,高血糖在女性中比男性更普遍(女性占12.5%,男性占7.7%)。这些生化结果支持了关于萨摩亚非传染性疾病负担高的报告。这种疾病负担不仅对个人有影响,而且对家庭和国民经济也有影响,因为医疗保健系统承受着越来越大的压力。这些疾病的初级预防战略必须是多方面的,应对非传染性疾病的多重决定因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PRELIMINARY BLOOD LIPID, LIPOPROTEIN AND GLUCOSE FINDINGS FROM THE GENOME-WIDE ASSOCIATION STUDY OF ADIPOSITY IN SAMOANS.

Samoans have been shown to exhibit alarmingly high rates of non-communicable disease such as obesity, diabetes and cardiovascular disease (CVD). A high NCD burden is usually characterized by high rates of biological risk factors within the population, such as elevated lipid, lipoprotein, and blood glucose levels. This report describes the prevalence of these biological risk factors in a population of 800 Samoan adults (39% male, n=312), aged 25-64 years. High levels of total cholesterol were found in 11.5% of men and 10.0% of women. Of the 800 individuals studied 617 (77.1%) had levels of LDL-cholesterol that were too high. A substantially greater proportion of women had levels of HDL-cholesterol, which is protective against CVD risk, that were too low (62.1% of women as compared to 27.9% of men). Men showed higher average levels of triglycerides, with more men than women being classified as having increased risk for CVD. High blood glucose was, conversely, more prevalent in women than men (12.5% of women, 7.7% of men). These biochemical findings support reports of a high NCD burden in Samoa. This disease burden has implications not only for the individual, but also the family and the national economy as the healthcare system is placed under increasing pressure. Primary prevention strategies for these diseases must be multifold, addressing the multiple determinants of NCDs.

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