11 research outputs found

    Candidate genetic analysis of plasma high-density lipoprotein-cholesterol and severity of coronary atherosclerosis

    Get PDF
    <p>Abstract</p> <p>Background</p> <p>Plasma level of high-density lipoprotein-cholesterol (HDL-C), a heritable trait, is an important determinant of susceptibility to atherosclerosis. Non-synonymous and regulatory single nucleotide polymorphisms (SNPs) in genes implicated in HDL-C synthesis and metabolism are likely to influence plasma HDL-C, apolipoprotein A-I (apo A-I) levels and severity of coronary atherosclerosis.</p> <p>Methods</p> <p>We genotyped 784 unrelated Caucasian individuals from two sets of populations (Lipoprotein and Coronary Atherosclerosis Study- LCAS, N = 333 and TexGen, N = 451) for 94 SNPs in 42 candidate genes by 5' nuclease assays. We tested the distribution of the phenotypes by the Shapiro-Wilk normality test. We used Box-Cox regression to analyze associations of the non-normally distributed phenotypes (plasma HDL-C and apo A-I levels) with the genotypes. We included sex, age, body mass index (BMI), diabetes mellitus (DM), and cigarette smoking as covariates. We calculated the q values as indicators of the false positive discovery rate (FDR).</p> <p>Results</p> <p>Plasma HDL-C levels were associated with sex (higher in females), BMI (inversely), smoking (lower in smokers), DM (lower in those with DM) and SNPs in <it>APOA5, APOC2</it>, <it>CETP, LPL </it>and <it>LIPC </it>(each q ≤0.01). Likewise, plasma apo A-I levels, available in the LCAS subset, were associated with SNPs in <it>CETP</it>, <it>APOA5</it>, and <it>APOC2 </it>as well as with BMI, sex and age (all q values ≤0.03). The <it>APOA5 </it>variant S19W was also associated with minimal lumen diameter (MLD) of coronary atherosclerotic lesions, a quantitative index of severity of coronary atherosclerosis (q = 0.018); mean number of coronary artery occlusions (p = 0.034) at the baseline and progression of coronary atherosclerosis, as indicated by the loss of MLD.</p> <p>Conclusion</p> <p>Putatively functional variants of <it>APOA2</it>, <it>APOA5, APOC2</it>, <it>CETP, LPL</it>, <it>LIPC </it>and <it>SOAT2 </it>are independent genetic determinants of plasma HDL-C levels. The non-synonymous S19W SNP in <it>APOA5 </it>is also an independent determinant of plasma apo A-I level, severity of coronary atherosclerosis and its progression.</p

    A compact high-speed (31,5) parallel counter circuit based on capacitive threshold-logic gates

    No full text

    The effect of scolicidal solutions on the biliary tracts (An experimental study in rats) SKOLISIDAL AJANLARIN SAFRA YOLLARI UZERINE ETKISI (DENEYSEL CALISMA)

    No full text
    Several cases of sclerosing cholangitis have been reported after surgical treatment of hepatic hydatid disease. In these patients, hypertonic saline of formaldehyde solutions had been given into the cysts. In our country, 3% hydrogen peroxide has been frequently injected into the cyst as a scolicidal agent and there have been no reported case of sclerosing cholangitis. In this experimental study, we showed that injection of 20% hypertonic saline solution, 2% formaldehyde solution, 3% hydrogen peroxide solution and 10% hydrogen peroxide solution into the biliary tract in rats caused lesions of the biliary epithelium. As compared with 20% hypertonic saline solution, 2% formaldehyde solution and 3% H2O2 resulted in more severe lesions in the biliary epithelium and in addition, induced the development of periductal fibrosis and pseudocirrhosis. This experimental study confirms the deleterious effect of all scolicidal solutions to the biliary epithelium and the liver
    corecore