Title of article :
Cholesterol efflux from Fu5AH hepatoma cells induced by plasma of subjects with or without coronary artery disease and non-insulin-dependent diabetes: importance of LpA-I:A-II particles and phospholipid transfer protein
Author/Authors :
Mikko Syv?nne، نويسنده , , Graciela Castro، نويسنده , , Catherine Dengremont، نويسنده , , Catherine De Geitere، نويسنده , , Matti Jauhiainen، نويسنده , , Christian Ehnholm، نويسنده , , Silvia Michelagnoli، نويسنده , , Guido Franceschini، نويسنده , , Juhani Kahri، نويسنده , , Marja-Riitta Taskinen، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 1996
Abstract :
We measured the capacity of human plasma to induce cholesterol efflux from Fu5AH rat hepatoma cells in four groups of men with or without non-insulin-dependent diabetes mellitus (NIDDM) and coronary artery disease (CAD). Plasma from men with both NIDDM and CAD (n = 47) had the lowest efflux capacity (17.3 ± 3.6%) whereas healthy control subjects with neither diabetes nor CAD (n = 25) had the highest capacity (19.8 ± 3.4%). The groups with CAD but no diabetes (n = 44) and with NIDDM but no CAD (n = 35) had intermediate efflux values (18.5 ± 3.8 and 18.5 ± 3.9%, respectively). In a 2 × 2 factorial ANOVA, the differences were significant with respect to the presence of CAD (P = 0.038) and NIDDM (P = 0.041), with no interaction between the factors. The concentration of HDL particles containing apolipoprotein (apo) A-I but no apo A-II (LpA-I) was not related to efflux capacity in univariate or multivariate analyses. A multivariate regression analysis showed that when controlled for the presence of NIDDM and CAD, the concentration of particles containing both apo A-I and apo A-II (LpA-I:A-II) and plasma phospholipid transfer protein activity were both positively, independently, and significantly (P < 0.001) related to cholesterol efflux capacity.
Keywords :
Apolipoprotein-specific particles , High density lipoproteins , In vitro cholesterol efflux , Lecithin:cholesteryl acyltransferase , Lipid transfer proteins , reverse cholesterol transport
Journal title :
Atherosclerosis
Journal title :
Atherosclerosis