Relationship between cholesteryl ester transfer protein and LDL heterogeneity in familial hypercholesterolemia

被引:33
作者
Hogue, JC
Lamarche, B
Gaudet, D
Larivière, M
Tremblay, A
Bergeron, J
Lemieux, I
Després, JP
Gagné, C
Couture, P [1 ]
机构
[1] Univ Laval, Lipid Res Ctr, Quebec City, PQ, Canada
[2] Univ Laval, CHUL Res Ctr, Quebec City, PQ, Canada
[3] Univ Laval, Inst Nutraceut & Funct Foods, Quebec City, PQ, Canada
[4] Lipid Clin, Quebec City, PQ, Canada
[5] Ctr Hosp La Sagamie, Saguenay, PQ, Canada
[6] Univ Laval, Quebec Heart Inst, Laval, PQ, Canada
[7] Univ Laval, Laval Hosp, Res Ctr, Laval, PQ, Canada
关键词
atherosclerosis; enzyme-linked immunosorbent assay; low density lipoprotein size;
D O I
10.1194/jlr.M300420-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Small, dense LDL particles have been associated with an increased risk of coronary artery disease, and cholesteryl ester transfer protein (CETP) has been suggested to play a role in LDL particle remodeling. We examined the relationship between LDL heterogeneity and plasma CETP mass in familial hypercholesterolemia (FH). LDL particles were characterized by polyacrylamide gradient gel electrophoresis in a total of 259 FH heterozygotes and 208 nonFH controls. CETP mass was measured by enzyme-linked immunosorbent assay in a subgroup of 240 participants, which included 120 FH patients matched with 120 controls. As compared with controls, FH subjects had an 11% higher CETP mass. Moreover, LDL-peak particle diameter (LDL- PPD) was significantly smaller in FH heterozygotes than in controls (258.1 +/- 4.8 vs. 259.2 +/- 4.1 Angstrom; P = 0.01) after adjustment for covariates. There was also an inverse relationship between LDL-PPD and CETP mass (R = -0.15; P = 0.02), and this relationship was abolished by adjustment for the FH/control status, indicating that LDL-PPD changes in FH are mediated, at least in part, by an increase in plasma CETP mass concentrations. These results suggest that increased plasma CETP mass concentrations could lead to significant LDL particle remodeling in FH heterozygotes and could contribute to the pathogenesis of atherosclerosis.
引用
收藏
页码:1077 / 1083
页数:7
相关论文
共 39 条
[1]   LDL size distribution in relation to insulin sensitivity and lipoprotein pattern in young and healthy subjects [J].
Ambrosch, A ;
Muhlen, I ;
Kopf, D ;
Augustin, W ;
Dierkes, J ;
König, W ;
Luley, C ;
Lehnert, H .
DIABETES CARE, 1998, 21 (12) :2077-2084
[2]   Triglyceride, small, dense low-density lipoprotein, and the atherogenic lipoprotein phenotype. [J].
Austin M.A. .
Current Atherosclerosis Reports, 2000, 2 (3) :200-207
[3]   GENETICS OF LDL SUBCLASS PHENOTYPES IN WOMEN TWINS - CONCORDANCE, HERITABILITY, AND COMMINGLING ANALYSIS [J].
AUSTIN, MA ;
NEWMAN, B ;
SELBY, JV ;
EDWARDS, K ;
MAYER, EJ ;
KRAUSS, RM .
ARTERIOSCLEROSIS AND THROMBOSIS, 1993, 13 (05) :687-695
[4]   COMPOSITION OF LOW-DENSITY LIPOPROTEIN IN CHILDREN WITH HYPERLIPOPROTEINEMIA [J].
BAGNALL, TF ;
LLOYD, JK .
CLINICA CHIMICA ACTA, 1975, 59 (03) :271-276
[5]   Evidence for a major quantitative trait locus on chromosome 17q21 affecting low-density lipoprotein peak particle diameter [J].
Bossé, Y ;
Pérusse, L ;
Després, JP ;
Lamarche, B ;
Chagnon, YC ;
Rice, T ;
Rao, DC ;
Bouchard, C ;
Vohl, MC .
CIRCULATION, 2003, 107 (18) :2361-2368
[6]  
CARDIN AD, 1984, J BIOL CHEM, V259, P8522
[7]   Contribution of hepatic lipase, lipoprotein lipase, and cholesteryl ester transfer protein to LDL and HDL heterogeneity in healthy women [J].
Carr, MC ;
Ayyobi, AF ;
Murdoch, SJ ;
Deeb, SS ;
Brunzell, JD .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2002, 22 (04) :667-673
[8]  
Chung BH, 1998, ATHEROSCLEROSIS, V141, P209
[9]  
Couture P, 1998, HUM MUTAT, pS226
[10]   PLASMA TRIGLYCERIDE DETERMINES STRUCTURE-COMPOSITION IN LOW AND HIGH-DENSITY LIPOPROTEINS [J].
DECKELBAUM, RJ ;
GRANOT, E ;
OSCHRY, Y ;
ROSE, L ;
EISENBERG, S .
ARTERIOSCLEROSIS, 1984, 4 (03) :225-231