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• W2613403740 endingPage "346" @default.
• W2613403740 startingPage "337" @default.
• W2613403740 abstract "Purpose of review The atheroprotective properties of HDL are supported by epidemiological and preclinical research. However, the results of interventional trials paradoxically indicate that drugs increasing HDL-cholesterol (HDL-C) do not reduce coronary artery disease (CAD) risk. Moreover, Mendelian randomization studies have shown no effect of HDL-C-modifying variants on CAD outcome. Thus, the protective effects of HDL particles are more governed by their functional status than their cholesterol content. In this context, any successful clinical exploitation of HDL will depend on the identification of HDL-related biomarkers, better than HDL-C level, for assessing cardiovascular risk and monitoring responses to treatment. Recent findings Recent studies have enlightened the role of ecto-F 1 -ATPase as a cell surface receptor for apoA-I, the major apolipoprotein of HDL, involved in the important metabolic and vascular atheroprotective functions of HDL. In the light of these findings, the clinical relevance of ecto-F 1 -ATPase in humans has recently been supported by the identification of serum F 1 -ATPase inhibitor (IF1) as an independent determinant of HDL-C, CAD risk and cardiovascular mortality in CAD patients. Summary Serum IF1 measurement might be used as a novel HDL-related biomarker to better stratify risk in high-risk populations or to determine pharmacotherapy." @default.
• W2613403740 created "2017-05-19" @default.
• W2613403740 creator A5007687025 @default.
• W2613403740 creator A5017946579 @default.
• W2613403740 creator A5028270946 @default.
• W2613403740 creator A5034871287 @default.
• W2613403740 creator A5070833091 @default.
• W2613403740 date "2017-08-01" @default.
• W2613403740 modified "2023-09-30" @default.
• W2613403740 title "Serum inhibitory factor 1, high-density lipoprotein and cardiovascular diseases" @default.
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