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Surrogate endpoints and emerging surrogate endpoints for risk reduction of cardiovascular disease.

机译:降低心血管疾病风险的替代终点和新兴替代终点。

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This article reviews surrogate endpoints and emerging biomarkers that were discussed at the annual "Cardiovascular Biomarkers and Surrogate Endpoints" symposium cosponsored by the US Food and Drug Administration (FDA) and the Montreal Heart Institute. The FDA's Center for Food Safety and Applied Nutrition (CFSAN) uses surrogate endpoints in its scientific review of a substance/disease relationship for a health claim. CFSAN currently recognizes three validated surrogate endpoints: blood pressure, blood total cholesterol, and blood low-density lipoprotein (LDL) concentration in its review of a health claim for cardiovascular disease (CVD). Numerous potential surrogate endpoints of CVD are being evaluated as the pathophysiology of heart disease is becoming better understood. However, these emerging biomarkers need to be validated as surrogate endpoints before they are used by CFSAN in the evaluation of a CVD health claim.
机译:本文回顾了由美国食品药品管理局(FDA)和蒙特利尔心脏研究所共同主办的年度“心血管生物标志物和替代终点”研讨会上讨论的替代终点和新兴生物标记。 FDA的食品安全与应用营养中心(CFSAN)在对物质/疾病关系进行健康审查的科学审查中使用了替代终点。 CFSAN在对心血管疾病(CVD)的健康声明进行审查时,目前识别出三个经过验证的替代终点:血压,血液总胆固醇和血液低密度脂蛋白(LDL)浓度。随着人们对心脏病的病理生理学的了解越来越多,正在评估许多潜在的CVD替代终点。但是,在CFSAN将其用于CVD健康声明评估之前,需要将这些新兴的生物标志物作为替代终点进行验证。

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