Arteriosclerosis Thrombosis and Vascular Biology · 2010 · 84 citations · 34 references
Life SciencesBiochemistryEndocrinologyLipid BiochemistryProtein BiochemistryProteomicsInsulin ResistanceLipidomicsLipoprotein AnalysisLipoprotein MetabolismMetabolic SyndromeTargeted ProteomicsHigh-density Lipoprotein MetabolismIsotope Dilution Mass SpectrometryLipid Profile AnalysisLipoprotein Composition AnalysisLipoprotein Subfraction ProfilingTargeted Proteomics QuantificationTriglyceride-rich LipoproteinsVery Low-density Lipoprotein Metabolism
OBJECTIVE: To determine whether obesity and insulin resistance associate with changes in the protein content of high-density lipoprotein (HDL) in 2 different groups of men by using targeted proteomics. METHODS AND RESULTS: Insulin resistance and obesity are hallmarks of type 2 diabetes mellitus and the metabolic syndrome, which confer an increased risk of cardiovascular disease. Recent studies suggest that the protein cargo of HDL makes important contributions to the lipoprotein's cardioprotective effects. In a discovery study, we used isotope dilution mass spectrometry to quantify the relative concentrations of 5 proteins previously implicated in HDL's cardioprotective effects in 3 groups of healthy subjects: lean insulin-sensitive, lean insulin-resistant, and obese insulin-resistant individuals. We validated our findings in a different group of subjects. The clusterin concentration in HDL strongly and negatively associated with insulin resistance and body mass index in both populations. HDL clusterin levels were lower in subjects with low HDL and high triglycerides, key components of the metabolic syndrome. There was an inverse correlation between clusterin levels in HDL and very-low-density lipoprotein/low-density lipoprotein. CONCLUSIONS: Clusterin levels in HDL are lower in men with reduced insulin sensitivity, higher body mass index, and an unfavorable lipid profile. Our observations raise the possibility that clusterin depletion contributes to the loss of HDL's cardioprotective properties.
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Robert H. Eckel, KGMM Alberti, Scott M. Grundy et al. · The Lancet · 2010 · 6.3K citations
Targeting C-reactive protein for the treatment of cardiovascular disease
Mark B. Pepys, Gideon M. Hirschfield, Glenys A. Tennent et al. · Nature · 2006 · 676 citations · Full text
Medicine, Cardiology, Pharmacology +14