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Circulation. 2013;128:1189-1197. R4 이태인 / Prof. 우종신
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Backgroud low HDL-C Until recently, low HDL-C was believed to be an important risk factor for residual risk among statin-treated patients The JUPITERtrial The JUPITER trial (Justification for the Use of statins in Prevention : an Intervention Trial Evaluating Rosuvastatin) On-treatment HDL-C was not predictive of residual risk : similar to apoA-I, TG, etc.
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not Chemically measured HDL-C may not fully capture HDL-related cardioprotection alternative indices of HDL → alternative indices of HDL : function, size, concentration of HDL particles Little is known about alternative HDL measures as determinants of residual risk after potent statin therapy
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Method (study population & laboratory measurement) The JUPITER trial 17,802 asymptomatic women ≥ 60years and men ≥ 50years without a previous history of CVD or DM ○ LDL-C < 130mg/dL, hsCRP ≥ 2mg/dL, TG < 500mg/dL Exclusion criteria ○ Previous or current use of lipid-lowering therapy Lipid profile : fasting sample HDL-C, TG, LDL-C, apoA-I Lipoprotein particle : NMR spectroscopy
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Method (outcomes) The primary end point A composite CVD end point, defined as first MI, stroke, hospitalization for unstable angina, arterial revasculization, or cardiovascular death
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Results (baseline chracteristics)
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Results (Changes with rosuvastatin)
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Results (Association with CVD Events)
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Results (Analyses combining HDL measures)
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Conclusions Under the potent statin therapy, HDL-P may be a better marker HDL-P may be a better marker of residual risk than chemically measured HDL-C or apoA-I
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