Transient thrombopoietin peak after liver transplantation for end-stage liver disease

被引:21
作者
Faeh, M
Hauser, SP
Nydegger, UE [1 ]
机构
[1] Univ Hosp Bern, Dept Cardiovasc Surg, CH-3010 Bern, Switzerland
[2] Univ Hosp Bern, Cent Lab Haematol, CH-3010 Bern, Switzerland
关键词
TPO; platelet; orthotopic liver transplantation; thrombocytopenia; hypersplenism;
D O I
10.1046/j.1365-2141.2001.02567.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Knowledge about synthesis of thrombopoietin (TPO) by human liver cells is now well established and makes the study of TPO serum levels and interdependency with platelet concentrations important before and after liver transplantation. We followed these variables in 14 patients suffering from primary biliary cirrhosis (group A), 10 with hepatitis B (group B) and nine with hepatitis C (group C) infections, as well as 11 patients suffering from alcoholic cirrhosis (group D). In the pretransplant serum samples, TPO levels and platelet counts revealed median values (range) of 112.75 pg/ml (5.0-349.3) in group A, 67.8 pg/ml (14.8-249.9) in B, 68.6 pg/ml (31.4-147.3) in C and 57.9 pg/ml (25.2-264.2) in D for TPO, and 138 x 10(9)/l (36-243) in A, 48 x 10(9)/l (22-129) in B, 105 x 10(9)/l (32-176) in C and 109 x 10(9)/l (33-285) in D for platelets, the latter levels being abnormally reduced. Within 2-3 d of transplantation, the TPO levels started to increase to transient peaks of mostly 5-10 times baseline, which were followed by continuous correction of thrombocytopenia. Splenomegaly was identified to be an important co-factor of thrombocytopenia in groups A and D. We conclude that decreased TPO production in patients with end-stage liver diseases is reverted by orthotopic liver transplantation.
引用
收藏
页码:493 / 498
页数:6
相关论文
共 26 条
[2]  
BALLMAIER MJ, 1994, BLOOD, V84, pA214
[3]   Measurement of cytokines in clinical samples using immunoassays: Problems and pitfalls [J].
Banks, RE .
CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 2000, 37 (02) :131-182
[4]   STIMULATION OF MEGAKARYOCYTOPOIESIS AND THROMBOPOIESIS BY THE C-MPL LIGAND [J].
DESAUVAGE, FJ ;
HASS, PE ;
SPENCER, SD ;
MALLOY, BE ;
GURNEY, AL ;
SPENCER, SA ;
DARBONNE, WC ;
HENZEL, WJ ;
WONG, SC ;
KUANG, WJ ;
OLES, KJ ;
HULTGREN, B ;
SOLBERG, LA ;
GOEDDEL, DV ;
EATON, DL .
NATURE, 1994, 369 (6481) :533-538
[5]  
Folman CC, 1997, THROMB HAEMOSTASIS, V78, P1262
[6]   THROMBOKINETICS IN MAN [J].
HARKER, LA ;
FINCH, CA .
JOURNAL OF CLINICAL INVESTIGATION, 1969, 48 (06) :963-&
[7]  
KAJIWARA E, 1995, AM J GASTROENTEROL, V90, P962
[8]  
KATO N, 1996, GASTROENTEROLOGY, V110, pA1967
[9]   Thrombopoietin [J].
Kaushansky, K .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (11) :746-754
[10]   CLONING AND EXPRESSION OF MURINE THROMBOPOIETIN CDNA AND STIMULATION OF PLATELET PRODUCTION IN-VIVO [J].
LOK, S ;
KAUSHANSKY, K ;
HOLLY, RD ;
KUIJPER, JL ;
LOFTONDAY, CE ;
OORT, PJ ;
GRANT, FJ ;
HEIPEL, MD ;
BURKHEAD, SK ;
KRAMER, JM ;
BELL, LA ;
SPRECHER, CA ;
BLUMBERG, H ;
JOHNSON, R ;
PRUNKARD, D ;
CHING, AFT ;
MATHEWES, SL ;
BAILEY, MC ;
FORSTROM, JW ;
BUDDLE, MM ;
OSBORN, SG ;
EVANS, SJ ;
SHEPPARD, PO ;
PRESNELL, SR ;
OHARA, PJ ;
HAGEN, FS ;
ROTH, GJ ;
FOSTER, DC .
NATURE, 1994, 369 (6481) :565-568