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心血管风险与代谢综合征。

Cardiovascular risk and the metabolic syndrome.

机构信息

Cardiovascular Research Group, Division of Cardiovascular and Endocrine Sciences, University of Manchester and Manchester Diabetes Centre, Manchester Royal Infirmary, Manchester, UK.

出版信息

Metab Syndr Relat Disord. 2006 Winter;4(4):252-60. doi: 10.1089/met.2006.4.252.

Abstract

Clustering of metabolic syndrome (MetS) components within individuals helps in the identification of subjects who are at increased risk for both cardiovascular disease (CVD) and diabetes. In this review we describe how the presence of MetS influences CVD risk. Our review focuses on published studies through May 2006 referring to incident CVD in relation to the National Cholesterol Education Program Adult Treatment Panel III (NCEP) definition of the MetS. We present data suggesting that the Framingham risk function is the most appropriate method for assessing CVD risk in subjects with or without MetS. We show how the CVD risk associated with MetS is influenced by the inclusion of subjects with diabetes and CVD at baseline, and by the development of diabetes during follow-up, and that this might explain why MetS may be a stronger risk factor for CVD in women than in men. We present data suggesting that CVD risk associated with MetS does not appear to be greater than the sum of its parts, and that adding CRP to MetS variables does not improve population CVD risk prediction. Lifestyle intervention and treatment of specific abnormal MetS components are appropriate until a better understanding of the pathogenesis of MetS is available. At such time we may be able to target the underlying causes of the syndrome and ultimately prevent the development of both CVD and diabetes.

摘要

代谢综合征(MetS)各组分在个体内的聚集有助于识别心血管疾病(CVD)和糖尿病风险增加的人群。本综述描述了 MetS 的存在如何影响 CVD 风险。我们的综述重点关注了截至 2006 年 5 月发表的文献,这些文献涉及与国家胆固醇教育计划成人治疗专家组第三版(NCEP)定义的 MetS 相关的新发 CVD。我们提供的数据表明,Framingham 风险函数是评估有或无 MetS 受试者 CVD 风险的最合适方法。我们展示了 MetS 相关的 CVD 风险如何受到基线时伴有糖尿病和 CVD 的受试者的影响,以及随访期间发生糖尿病的影响,这可能解释了为什么 MetS 可能是女性 CVD 风险的强于男性的危险因素。我们提供的数据表明,与 MetS 相关的 CVD 风险似乎并不大于其各组成部分的总和,并且将 CRP 添加到 MetS 变量中并不能改善人群 CVD 风险预测。在对 MetS 的发病机制有更好的了解之前,生活方式干预和特定异常 MetS 成分的治疗是合适的。届时,我们或许能够针对该综合征的根本原因,并最终预防 CVD 和糖尿病的发生。

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