Efficacy and safety of a new whole-blood low-density lipoprotein apheresis system (Liposorber D) in severe hypercholesterolemia

被引:47
作者
Otto, C
Kern, P
Bambauer, R
Kallert, S
Schwandt, P
Parhofer, KG
机构
[1] Univ Hosp Munich, Med Dept Grosshadern 2, D-81377 Munich, Germany
[2] Franz von Prummer Klin, Bad Bruckenau, Germany
[3] Inst Blood Purificat, Homburg, Germany
[4] Arteriosclerosis Prevent Inst, Munich, Germany
关键词
low-density lipoprotein apheresis; whole-blood apheresis; hypercholesterolemia; low-density lipoprotein cholesterol; lipoprotein(a);
D O I
10.1111/j.1525-1594.2003.07200.x
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Low-density lipoprotein (LDL) apheresis is an extracorporeal modality to lower LDL cholesterol. While most of the devices eliminate LDL particles from plasma, a recently introduced whole-blood perfusion column (DALI) adsorbs lipoproteins directly from whole blood. We investigated the efficacy and safety of a new whole-blood LDL apheresis system (Liposorber D) in 10 patients with severe hypercholesterolemia in a multicenter trial. In 93 LDL aphereses, the mean reduction in LDL cholesterol and lipoprotein(a) was 62.2 +/- 11.5% and 55.6 +/- 16.9%, respectively (P < 0.01). If hemodilution during apheresis was considered, the reductions were 58.0 +/- 10.9 and 55.3 +/- 10.9%, respectively (P < 0.01), while high-density lipoprotein (HDL) cholesterol did not change significantly. Three mild episodes of hypocalcemia and two mild episodes of arterial hypotension were observed; however, LDL apheresis could be continued in each case. In conclusion, the new whole-blood LDL apheresis with Liposorber D is a safe, simple, and useful modality to reduce LDL cholesterol and lipoprotein(a) in cardiovascular high-risk patients.
引用
收藏
页码:1116 / 1122
页数:7
相关论文
共 26 条
[1]  
Bambauer R, 1997, Ther Apher, V1, P242, DOI 10.1111/j.1744-9987.1997.tb00145.x
[2]  
Bosch T, 1999, Ther Apher, V3, P209
[3]  
Collins R, 2002, LANCET, V360, P7, DOI 10.1016/S0140-6736(02)09327-3
[4]  
Dräger LJ, 1998, EUR J CLIN INVEST, V28, P994
[5]  
Jansen M, 2000, WIEN KLIN WOCHENSCHR, V112, P61
[6]   DIFFERENT EFFECTS OF 2 METHODS OF LOW-DENSITY-LIPOPROTEIN APHERESIS ON THE COAGULATION AND FIBRINOLYTIC SYSTEMS [J].
KNISEL, W ;
DINICUOLO, A ;
PFOHL, M ;
MULLER, H ;
RISLER, T ;
EGGSTEIN, M ;
SEIFRIED, E .
JOURNAL OF INTERNAL MEDICINE, 1993, 234 (05) :479-487
[7]   In vitro evaluation of dextran sulfate cellulose beads for whole blood infusion low-density lipoprotein-hemoperfusion [J].
Kobayashi, A ;
Nakatani, M ;
Furuyoshi, S ;
Tani, N .
THERAPEUTIC APHERESIS, 2002, 6 (05) :365-371
[8]   LIPOPROTEIN (A) INHIBITS THE GENERATION OF TRANSFORMING GROWTH-FACTOR-BETA - AN ENDOGENOUS INHIBITOR OF SMOOTH-MUSCLE CELL-MIGRATION [J].
KOJIMA, S ;
HARPEL, PC ;
RIFKIN, DB .
JOURNAL OF CELL BIOLOGY, 1991, 113 (06) :1439-1445
[9]   LDL-apheresis atherosclerosis regression study (LAARS) - Effect of aggressive versus conventional lipid lowering treatment on coronary atherosclerosis [J].
Kroon, AA ;
Aengevaeren, WRM ;
vanderWerf, T ;
Uijen, GJH ;
Reiber, JHC ;
Bruschke, AVG ;
Stalenhoef, AFH .
CIRCULATION, 1996, 93 (10) :1826-1835
[10]   Effect of statins on risk of coronary disease - A meta-analysis of randomized controlled trials [J].
LaRosa, JC ;
He, J ;
Vupputuri, S .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 282 (24) :2340-2346