HEPATIC LIPASE AND LIPOPROTEIN-LIPASE ARE NOT MAJOR DETERMINANTS OF THE LOW-DENSITY-LIPOPROTEIN SUBCLASS PATTERN IN HUMAN-SUBJECTS WITH CORONARY HEART-DISEASE

被引:79
作者
JANSEN, H
HOP, W
VANTOL, A
BRUSCHKE, AVG
BIRKENHAGER, JC
机构
[1] ERASMUS UNIV ROTTERDAM,DEPT BIOCHEM,3000 DR ROTTERDAM,NETHERLANDS
[2] ERASMUS UNIV ROTTERDAM,DEPT EPIDEMIOL & BIOSTAT,3000 DR ROTTERDAM,NETHERLANDS
[3] INTERUNIV CARDIOL INST NETHERLANDS,UTRECHT,NETHERLANDS
关键词
LDL (SUBCLASS); HEPATIC LIPASE; LIPOPROTEIN LIPASE; CORONARY HEART DISEASE; INSULIN RESISTANCE;
D O I
10.1016/0021-9150(94)90140-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The influence of hepatic lipase (HL) and lipoprotein lipase (LPL) activity on the low density lipoprotein (LDL) subclass pattern was studied in a population of males with coronary heart disease and without severe hypercholesterolemia. LDL subclass patterns, lipases and plasma lipoproteins were determined in 326 patients. In part of the study population, fasting insulin and glucose levels were also determined. The LDL subclass pattern was determined by gradient gel electrophoresis (GGE) and classified according to Austin et al. (J. Am. Med. Assoc. 260 (1988) 1917 (predominantly large LDL = A-pattern, predominantly small LDL = B-pattern). An LDL subclass A-pattern was exhibited by 199 subjects; 108 exhibited a B-pattern. in 19 subjects no distinctive A- or B-pattern was present (A-pattern). Hepatic and lipoprotein activities differed significantly between patients with the A- or B-pattern. The median hepatic lipase activity was lower (384 vs. 417 mU/ml, P = 0.006), and the lipoprotein lipase activity higher (122 vs. 101 mU/ml, P = 0.001) in the A-pattern subjects than in the B-pattern subjects. In subjects with the A/B pattern the lipase activities were intermediate between the values in the A- and B-pattern subjects (HL 408 +/- 87 mU/ml, LPL 115 +/- 55 mU/ml). Plasma triglyceride, very low density lipoprotein (VLDL)-triglyceride, intermediate density lipoprotein (IDL)-triglyceride and LDL-triglyceride were higher in the patients with a B-pattern (+ 84%, +171%, +10% and +16%, respectively). Total plasma cholesterol was not different between A- and B-pattern subjects. VLDL- and IDL-cholesterol were higher in the B-pattern group (+174% and +66%, respectively), while LDL- and HDL-cholesterol were higher in the A-pattern group (+2 and +24%, respectively). In univariate analysis HL, LPL, plasma (and VLDL) triglyceride, HDL-cholesterol and IDL-cholesterol were each significantly associated with the LDL subclass pattern. In multivariate analysis plasma triglyceride (or VLDL-triglyceride) and HDL-cholesterol appeared to be independently associated with the LDL subclass pattern. No additional discriminative value of HL or LPL was found. Similar results were obtained if the patients with or without beta blocker were evaluated separately. An estimate of insulin resistance (EIR), calculated from plasma insulin and glucose in part of the study population (n = 145), was significantly higher in the subjects with a B-pattern than in those with an A-pattern (3.12 vs. 2.00, P < 0.003). EIR correlated, positively with plasma triglyceride (P < 0.0001), but not with HL or LPL. It is concluded that, although LPL and HL activities are related with the LDL subclass pattern, the lipases are not major determinants of the subclass pattern. In subjects in which insulin resistance is relatively high the LDL subclass B-pattern prevails, mainly due to a relatively high plasma triglyceride under these conditions.
引用
收藏
页码:45 / 54
页数:10
相关论文
共 44 条
[1]  
AUSTIN MA, 1988, AM J HUM GENET, V43, P838
[2]  
AUSTIN MA, 1988, JAMA-J AM MED ASSOC, V260, P1917
[3]  
AUSTIN MA, 1986, LANCET, V2, P592
[4]   LARGE BUOYANT LDL-LIKE PARTICLES IN HEPATIC LIPASE DEFICIENCY [J].
AUWERX, JH ;
MARZETTA, CA ;
HOKANSON, JE ;
BRUNZELL, JD .
ARTERIOSCLEROSIS, 1989, 9 (03) :319-325
[5]  
AVILA EM, 1978, ARTERY, V4, P36
[6]   THE ROLE OF INSULIN INSENSITIVITY AND HEPATIC LIPASE IN THE DYSLIPIDEMIA OF TYPE-2 DIABETES [J].
BAYNES, C ;
HENDERSON, AD ;
ANYAOKU, V ;
RICHMOND, W ;
HUGHES, CL ;
JOHNSTON, DG ;
ELKELES, RS .
DIABETIC MEDICINE, 1991, 8 (06) :560-566
[7]   METABOLIC CONSEQUENCES OF GENETIC-HETEROGENEITY OF LIPOPROTEIN COMPOSITION (LIPOPROTEIN HETEROGENEITY) [J].
BRUNZELL, JD ;
CHAIT, A ;
ALBERS, JJ ;
FOSTER, DM ;
FAILOR, RA ;
BIERMAN, EL .
AMERICAN HEART JOURNAL, 1987, 113 (02) :583-588
[8]   LOW-DENSITY-LIPOPROTEIN PARTICLE-SIZE AND CORONARY-ARTERY DISEASE [J].
CAMPOS, H ;
GENEST, JJ ;
BLIJLEVENS, E ;
MCNAMARA, JR ;
JENNER, JL ;
ORDOVAS, JM ;
WILSON, PWF ;
SCHAEFER, EJ .
ARTERIOSCLEROSIS AND THROMBOSIS, 1992, 12 (02) :187-195
[9]  
CHAPMAN MJ, 1988, J LIPID RES, V29, P442
[10]  
CROUSE JR, 1985, J LIPID RES, V26, P566