The effects of three different LDL-apheresis methods on the plasma concentrations of E-selectin, VCAM-1, and ICAM-1

被引:38
作者
Empen, K [1 ]
Otto, C [1 ]
Brödl, UC [1 ]
Parhofer, KG [1 ]
机构
[1] Univ Munich, Dept Med 2, D-81366 Munich, Germany
关键词
direct absorption; dextran sulfate; heparin precipitation; fibrinogen; adhesion molecules;
D O I
10.1002/jca.10010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Plasma concentrations of cellular adhesion molecules are associated with atherosclerotic diseases and major cardiovascular risk factors, It was shown that LDL-apheresis with dextran sulfate lowers the levels of E-selectin and ICAM-1 in patients with familial hypercholesterolemia. The effects of different LDL-apheresis methods have not been studied yet. Cholesterol, triglycerides, LDL cholesterol, HDL cholesterol, fibrinogen, and the adhesion molecules E-selectin, VCAM-1, and ICAM-1 were measured in 20 patients with coronary heart disease and severe hyperlipoproteinemia immediately before and after regular LDL-apheresis. Treatment was performed by different apheresis methods (direct ab sorption, DA, n = 6; dextran sulfate adsorption, DS, n = 7; heparin precipitation. HP, n = 7). Rebound data of adhesion molecule levels were obtained from 2 patients of each group. Lipids were reduced similarly in all groups, The concentrations of all adhesion molecules were lowered during apheresis. The reduction of E-selcetin (-31 +/- 7 vs. -6 +/- 5 and -6 +/- 5%, respectively, P < 0.001) was most prominent in the patients treated by heparin precipitation. Depending on the method of LDL-apheresis, the concentrations of VCAM-1 and E-selectin in the outlets of the LDL-apheresis columns were significantly lower compared to the concentration in the inlets. Plasma concentrations of adhesion molecules increased to their pro-apheresis values with n 2 to 4 days following LDL-apheresis. The reductions of adhesion molecule levels observed during LDL-apheresis are at least partly due to adsorption to the LDL-apheresis column. The extent of absorption depends on the principle of extracorporeal LDL elimination.
引用
收藏
页码:38 / 43
页数:6
相关论文
共 18 条
[1]   Elevated concentrations of soluble E-selectin and vascular cell adhesion molecule-1 in NIDDM -: Effect of intensive insulin treatment [J].
Albertini, JP ;
Valensi, P ;
Lormeau, B ;
Aurousseau, MH ;
Ferrière, F ;
Attali, JR ;
Gattegno, L .
DIABETES CARE, 1998, 21 (06) :1008-1013
[2]  
BLANN AD, 1994, THROMB HAEMOSTASIS, V72, P151
[3]   THE EXPRESSION OF THE ADHESION MOLECULES ICAM-1, VCAM-1, PECAM, AND E-SELECTIN IN HUMAN ATHEROSCLEROSIS [J].
DAVIES, MJ ;
GORDON, JL ;
GEARING, AJH ;
PIGOTT, R ;
WOOLF, N ;
KATZ, D ;
KYRIAKOPOULOS, A .
JOURNAL OF PATHOLOGY, 1993, 171 (03) :223-229
[4]   CIRCULATING ADHESION MOLECULES IN DISEASE [J].
GEARING, AJH ;
NEWMAN, W .
IMMUNOLOGY TODAY, 1993, 14 (10) :506-512
[5]   Levels of soluble cell adhesion molecules in patients with dyslipidemia [J].
Hackman, A ;
Abe, Y ;
Insull, W ;
Pownall, H ;
Smith, L ;
Dunn, K ;
Gotto, AM ;
Ballantyne, CM .
CIRCULATION, 1996, 93 (07) :1334-1338
[6]  
Hwang SJ, 1997, CIRCULATION, V96, P4219
[7]   CELL-ADHESION MOLECULES IN CORONARY-ARTERY DISEASE [J].
JANG, YS ;
LINCOFF, AM ;
PLOW, EF ;
TOPOL, EJ .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1994, 24 (07) :1591-1601
[8]   Vascular effects of estrogen and vitamin E therapies in postmenopausal women [J].
Koh, KK ;
Blum, A ;
Hathaway, L ;
Mincemoyer, R ;
Csako, G ;
Waclawiw, MA ;
Panza, JA ;
Cannon, RO .
CIRCULATION, 1999, 100 (18) :1851-1857
[9]   Value of serum-soluble intercellular adhesion molecule-1 for the noninvasive risk assessment of transplant coronary artery disease, posttransplant ischemic events, and cardiac graft failure [J].
Labarrere, CA ;
Nelson, DR ;
Miller, SJ ;
Nieto, JM ;
Conner, JA ;
Pitts, DE ;
Kirlin, PC ;
Halbrook, HG .
CIRCULATION, 2000, 102 (13) :1549-1555
[10]   Circulating adhesion molecules in humans - Role of hyperglycemia and hyperinsulinemia [J].
Marfella, R ;
Esposito, K ;
Giunta, R ;
Coppola, G ;
De Angelis, L ;
Farzati, B ;
Paolisso, G ;
Giugliano, D .
CIRCULATION, 2000, 101 (19) :2247-2251