Beta2-microglobulin removal by extracorporeal renal replacement therapies

被引:15
作者
Krieter, DH
Lemke, HD
Canaud, B
Wanner, C
机构
[1] Univ Wurzburg, Div Nephrol, Dept Med, D-97080 Wurzburg, Germany
[2] Univ Montpellier, Lapeyronie Hosp, Dept Nephrol, F-34059 Montpellier, France
[3] Membrana Res, Obernburg, Germany
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2005年 / 1753卷 / 01期
关键词
beta(2)-microglobulin; beta(2)-microglobulin removal; clinical haemodialysis; haemofiltration; haemodiafiltration;
D O I
10.1016/j.bbapap.2005.08.008
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
There is increasing evidence that end-stage renal disease patients with lower beta(2)-microglobulin plasma levels and patients on convective renal replacement therapy are at lower mortality risk. Therefore, an enhanced beta2-microglobulin removal by renal replacement procedures has to be regarded as a contribution to a more adequate dialysis therapy. In contrast to high-flux dialysis, low-flux hemodialysis is not qualified to eliminate substantial amounts of beta(2)-microglobulin. In hemodialysis using modem high-flux dialysis membranes, a beta(2)-microglobulin removal similar to that obtained in hemofiltration or hemodiafiltration can be achieved. Several of these high-flux membranes are protein-leaking, making them suitable only for hemodialysis due to a high albumin loss when used in more convective therapy procedures. On-line hemodiafiltration infusing large substitution fluid volumes represents the most efficient and innovative renal replacement therapy form. To maximize beta(2)-microglobulin removal, modifications of this procedure have been proposed. These modifications ensure safer operating conditions, such as mixed hemodiafiltration, or control albumin loss at maximum purification from beta(2)-microglobulin, such as mid-dilution hemodiafiltration, push/pull hemodiafiltration or programmed filtration. Whether these innovative hemodiafiltration options will become accepted in clinical routine use needs to be proven in future. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:146 / 153
页数:8
相关论文
共 67 条
[1]  
Ahrenholz PG, 2004, CLIN NEPHROL, V62, P21
[2]   On-line predilution hemofiltration versus ultrapure high-flux hemodialysis: A multicenter prospective study in 23 patients [J].
Altieri, P ;
Sorba, GB ;
Bolasco, PG ;
Bostrom, M ;
Asproni, E ;
Ferrara, R ;
Bolasco, F ;
Cossu, M ;
Cadinu, F ;
Cabiddu, GF ;
Casu, D ;
Ganadu, M ;
Passaghe, M ;
Pinna, M .
BLOOD PURIFICATION, 1997, 15 (03) :169-181
[3]  
[Anonymous], 2002, NEPHROL DIAL TRANSPL, DOI DOI 10.1093/NDT/17.SUPPL_7.21
[4]  
BAMMENS AK, 2004, J AM SOC NEPHROL, V15, pA632
[5]  
BERGSTROM J, 1987, LANCET, V1, P628
[6]   FAILURE OF A DAILY HEMOFILTRATION PROGRAM USING A HIGHLY PERMEABLE MEMBRANE TO RETURN BETA-2-MICROGLOBULIN CONCENTRATIONS TO NORMAL IN HEMODIALYSIS-PATIENTS [J].
CANAUD, B ;
ASSOUNGA, A ;
KERR, P ;
AZNAR, R ;
MION, C .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1992, 7 (09) :924-930
[7]  
Canaud B, 2003, J AM SOC NEPHROL, V14, p31A
[8]  
Cheung AK, 2002, J AM SOC NEPHROL, V13, p432A
[9]  
Clark WR, 2002, J AM SOC NEPHROL, V13, pS41
[10]  
DAVID S, 1989, NEPHROL DIAL TRANSPL, V4, P37