The cardiovascular effects of erythropoietin

被引:216
作者
Smith, KJ
Bleyer, AJ
Little, WC
Sane, DC
机构
[1] Wake Forest Univ, Sch Med, Dept Internal Med, Cardiol Sect, Winston Salem, NC 27157 USA
[2] Wake Forest Univ, Sch Med, Dept Internal Med, Nephrol Sect, Winston Salem, NC 27157 USA
关键词
angiogenesis; endothelial function; platelets; renal function; thrombosis/embolism;
D O I
10.1016/S0008-6363(03)00468-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Erythropoietin is a hypoxia-induced hormone that is essential for normal erythropoiesis. The production of recombinant human erythropoietin (rHuEpo) has revolutionized the treatment of anemia associated with chronic renal failure and chemotherapy, and has been used as prophylaxis to prevent anemia after surgery. The erythropoietin receptor is widely distributed in the cardiovascular system, including endothelial cells, smooth muscle cells and cardiomyocytes. Epo has potentially beneficial effects on the endothelium, including anti-apoptotic, mitogenic and angiogenic activities. On the other hand, some reports suggest that rHuEpo may have pro-thrombotic or platelet-activating effects. Hypertension develops in 20-30% of renal patients treated with rHuEpo. Many patients with heart failure have anemia. Despite some potential adverse effects, early studies in heart failure patients with anemia suggest that rHuEpo therapy is safe and effective in reducing left ventricular hypertrophy, enhancing exercise performance and increasing ejection fraction. Further studies are warranted to define the role of rHuEpo in chronic heart failure and other cardiovascular settings. (C) 2003 European Society of Cardiology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:538 / 548
页数:11
相关论文
共 131 条
[31]   HEMATOCRIT, BLOOD-PRESSURE, AND HYPERTENSION - THE GUBBIO POPULATION STUDY [J].
CIRILLO, M ;
LAURENZI, M ;
TREVISAN, M ;
STAMLER, J .
HYPERTENSION, 1992, 20 (03) :319-326
[32]   Normalization of hematocrit in hemodialysis patients with cardiac disease does not increase blood pressure [J].
Conlon, PJ ;
Kovalik, E ;
Schumm, D ;
Minda, S ;
Schwab, SJ .
RENAL FAILURE, 2000, 22 (04) :435-444
[33]   Expression of erythropoietin by the human placenta [J].
Conrad, KP ;
Benyo, DF ;
WesterhausenLarsen, A ;
Miles, TM .
FASEB JOURNAL, 1996, 10 (07) :760-768
[34]   Efficacy of recombinant human erythropoietin in critically ill patients - A randomized controlled trial [J].
Corwin, HL ;
Gettinger, A ;
Pearl, RG ;
Fink, MP ;
Levy, MM ;
Shapiro, MJ ;
Corwin, MJ ;
Colton, T .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 288 (22) :2827-2835
[35]   Secular trends in recombinant erythropoietin therapy among the US hemodialysis population: 1990-1996 [J].
Cotter, DJ ;
Thamer, M ;
Kimmel, PL ;
Sadler, JH .
KIDNEY INTERNATIONAL, 1998, 54 (06) :2129-2139
[36]   Erythropoietin mRNA expression in human fetal and neonatal tissue [J].
Dame, C ;
Fahnenstich, H ;
Freitag, P ;
Hofmann, D ;
Abdul-Nour, T ;
Bartmann, P ;
Fandrey, J .
BLOOD, 1998, 92 (09) :3218-3225
[37]  
DeMarchi S, 1997, J AM SOC NEPHROL, V8, P1147
[38]  
Diaz-Ricart M, 1999, THROMB HAEMOSTASIS, V82, P1312
[39]   Erythropoietin-mediated neuroprotection involves cross-talk between Jak2 and NF-κB signalling cascades [J].
Digicaylioglu, M ;
Lipton, SA .
NATURE, 2001, 412 (6847) :641-647
[40]   Anaemia in end-stage renal disease: pathophysiological considerations [J].
Eckardt, KU .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2001, 16 :2-8