Plasma distribution of apoA-IV in patients with coronary artery disease and healthy controls

被引:37
作者
Ezeh, B
Haiman, M
Alber, HF
Kunz, B
Paulweber, B
Lingenhel, A
Kraft, HG
Weidinger, F
Pachinger, O
Dieplinger, H
Kronenberg, F
机构
[1] Univ Innsbruck, Inst Med Biol & Human Genet, A-6020 Innsbruck, Austria
[2] Univ Innsbruck Hosp, Dept Cardiol, A-6020 Innsbruck, Austria
[3] Landeskrankenhaus, Dept Internal Med, Salzburg, Austria
[4] GSF Natl Res Ctr Environm & Hlth, Inst Epidemiol, Neuherberg, Germany
[5] Vitateq Biotechnol GmbH, Innsbruck, Austria
关键词
apolipoprotein A-IV; lipoprotein A-I : pA-IV; LpA-IV; lipid-free apoA-IV; antiatherogenic;
D O I
10.1194/jlr.M300060-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
Recent studies showed lower apolipoprotein A-IV (apoA-IV) plasma concentrations in patients with coronary artery disease (CAD). The actual distribution of the anti-atherogenic apoA-IV in human plasma, however, is discussed controversially and it was never investigated in CAD patients. We therefore developed a gentle technique to separate the various apoA-IV containing plasma fractions. Using a combination of precipitation of all lipoproteins with 40% phosphotungstic acid and 4 MgCl2, as well as immunoprecipitation of all apoA-I-containing particles with an anti-apoA-I antibody, we obtained three fractions of apoA IV: lipid-free apoA-IV (about 4% of toga apoA-IV), apoA-IV associated with apoA-I (LpA-I:A-IV, 125), and apoA-I-unbound but lipoprotein-containing apoA-IV (LpA-IV, 84%). We compared these three apoA-IV fractions between 52 patients with a history of CAD and 52 age- and sex-matched healthy controls. Patients had significantly lower apoA-IV levels when compared to controls (10.28 +/- 3.67 mg/dl vs. 11.85 +/- 2.82 mg/dl, P = 0.029), but no major differences for the three plasma apoA-IV fractions. We conclude that our gentle separation method reveals a different distribution of apoA-IV than in many earlier studies. No major differences exist in the apoA-IV plasma distribution pattern between CAD patients and controls. jlr Therefore, the antiatherogenic effect of apoA IV has to be explained by other functional properties of apoA IV (e.g., the antioxidative characteristics).
引用
收藏
页码:1523 / 1529
页数:7
相关论文
共 40 条
[1]   Subpopulations of high density lipoproteins in homozygous and heterozygous Tangier disease [J].
Asztalos, BF ;
Brousseau, ME ;
McNamara, JR ;
Horvath, KV ;
Roheim, PS ;
Schaefer, EJ .
ATHEROSCLEROSIS, 2001, 156 (01) :217-225
[2]   AN OPTIMIZED METHOD FOR MEASURING LECITHIN - CHOLESTEROL ACYLTRANSFERASE ACTIVITY, INDEPENDENT OF THE CONCENTRATION AND QUALITY OF THE PHYSIOLOGICAL SUBSTRATE [J].
BARTHOLOME, M ;
NIEDMANN, D ;
WIELAND, H ;
SEIDEL, D .
BIOCHIMICA ET BIOPHYSICA ACTA, 1981, 664 (02) :327-334
[3]   APOLIPOPROTEIN HOMOLOG OF RAT APOLIPOPROTEIN A-IV IN HUMAN-PLASMA - ISOLATION AND PARTIAL CHARACTERIZATION [J].
BEISIEGEL, U ;
UTERMANN, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1979, 93 (03) :601-608
[4]  
BISGAIER CL, 1985, J LIPID RES, V26, P11
[5]  
BISGAIER CL, 1987, J LIPID RES, V28, P693
[6]  
Böttcher A, 2000, J LIPID RES, V41, P905
[7]   ACTIVATION OF LECITHIN - CHOLESTEROL ACYLTRANSFERASE BY APOLIPOPROTEIN-E-2, APOLIPOPROTEIN-E-3, AND A-IV ISOLATED FROM HUMAN-PLASMA [J].
CHEN, CH ;
ALBERS, JJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 836 (03) :279-285
[8]   Reduced aortic lesions and elevated high density lipoprotein levels in transgenic mice overexpressing mouse apolipoprotein A-IV [J].
Cohen, RD ;
Castellani, LW ;
Qiao, JH ;
VanLenten, BJ ;
Lusis, AJ ;
Reue, K .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (08) :1906-1916
[9]  
DALLINGATHIE GM, 1985, J LIPID RES, V26, P970
[10]   PLASMA APOLIPOPROTEIN-A-IV METABOLISM IN PATIENTS WITH CHRONIC RENAL-DISEASE [J].
DIEPLINGER, H ;
LOBENTANZ, EM ;
KONIG, P ;
GRAF, H ;
SANDHOLZER, C ;
MATTHYS, E ;
ROSSENEU, M ;
UTERMANN, G .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1992, 22 (03) :166-174