Literature DB >> 14998426

Factors affecting variability in distribution of tacrolimus in liver transplant recipients.

H Zahir1, G McCaughan, M Gleeson, R A Nand, A J McLachlan.   

Abstract

AIMS: Therapeutic drug monitoring (TDM) of tacrolimus is complicated by conflicting data on the correlation between tacrolimus trough blood concentrations and the incidence of rejection. The aim of this cross-sectional study was to investigate the blood distribution and protein binding of tacrolimus in liver transplant recipients to explore better predictors of clinical outcome.
METHODS: Blood and plasma distribution of 3H-dihydro-tacrolimus was investigated in 40 liver transplant recipients using Ficoll Paque and density gradient ultracentrifugation, respectively, and equilibrium dialysis to investigate plasma protein binding.
RESULTS: In blood tacrolimus was mainly associated with the erythrocyte fraction (83.2%, range 74.6-94.9%), followed by diluted plasma (16.1%, range 4.5-24.9%), and lymphocyte fraction (0.61%, range: 0.11-1.53%). In plasma, lipoprotein deficient serum fraction (54.2%, range 38.5-68.2%) was the main reservoir of tacrolimus. The unbound fraction of tacrolimus was found to be 0.47 +/- 0.18% (range 0.07-0.89%). The percentage of tacrolimus associated with the lymphocytes (0.8 +/- 0.4 vs 0.3 +/- 0.1%, P = 0.012) and estimated unbound concentration (0.42 +/- 0.21 ng l-1vs 0.24 +/- 0.08 ng l-1, P < 0.001) of tacrolimus were significantly different in stable transplant recipients and those experiencing rejection. Haematocrit and red blood cell count significantly influenced the percentage of tacrolimus associated with erythrocytes. The fraction unbound of tacrolimus was correlated with alpha1-acid glycoprotein and high density lipoprotein cholesterol concentrations.
CONCLUSIONS: Tacrolimus unbound concentration was observed to be lower in liver transplant recipients experiencing rejection and further study is required to evaluate its utility in the TDM of tacrolimus.

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Year:  2004        PMID: 14998426      PMCID: PMC1884454          DOI: 10.1046/j.1365-2125.2003.02008.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  27 in total

1.  Association of elevated FK 506 plasma levels with nephrotoxicity in liver-grafted patients.

Authors:  M Winkler; U Jost; B Ringe; G Gubernatis; K Wonigeit; R Pichlmayr
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2.  Whole blood and plasma levels of FK 506 after liver transplantation: correlation with toxicity.

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Journal:  Transplant Proc       Date:  1994-06       Impact factor: 1.066

3.  Plasma FK506 levels in patients with histopathologically documented renal allograft rejection.

Authors:  E Erden; V Warty; M Magnone; R Shapiro; J Demetris; P Randhawa
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Review 4.  Plasma protein binding and pharmacological response.

Authors:  P du Souich; J Verges; S Erill
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Review 5.  Tacrolimus: a new immunosuppressive agent.

Authors:  P A Kelly; G J Burckart; R Venkataramanan
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6.  Distribution characteristics of immunosuppressants FK506 and cyclosporin A in the blood compartment.

Authors:  K Takada; N Katayama; A Kiriyama; H Usuda
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Review 7.  Mode of action of tacrolimus (FK506): molecular and cellular mechanisms.

Authors:  A W Thomson; C A Bonham; A Zeevi
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Review 8.  Clinical pharmacokinetics of tacrolimus.

Authors:  R Venkataramanan; A Swaminathan; T Prasad; A Jain; S Zuckerman; V Warty; J McMichael; J Lever; G Burckart; T Starzl
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9.  Pharmacokinetics of tacrolimus in liver transplant patients.

Authors:  W J Jusko; W Piekoszewski; G B Klintmalm; M S Shaefer; M F Hebert; A A Piergies; C C Lee; P Schechter; Q A Mekki
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10.  Morphological characteristics of renal allografts showing renal dysfunction under FK 506 therapy: is graft biopsy available to reveal the morphological findings corresponding with FK 506 nephropathy? Japanese FK 506 Study Group.

Authors: 
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  26 in total

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Authors:  Itziar Oteo; John C Lukas; Nerea Leal; Elena Suarez; Andres Valdivieso; Mikel Gastaca; Jorge Ortiz de Urbina; Rosario Calvo
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3.  Explaining variability in ciclosporin exposure in adult kidney transplant recipients.

Authors:  Rogier R Press; Bart A Ploeger; Jan den Hartigh; T van der Straaten; Hans van Pelt; Meindert Danhof; Hans de Fijter; Henk-Jan Guchelaar
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Review 4.  Interpreting tacrolimus concentrations during pregnancy and postpartum.

Authors:  Mary F Hebert; Songmao Zheng; Karen Hays; Danny D Shen; Connie L Davis; Jason G Umans; Menachem Miodovnik; Kenneth E Thummel; Thomas R Easterling
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5.  Retrospective analysis of the correlation between tacrolimus concentrations measured in whole blood and variations of blood cell counts in patients undergoing allogeneic haematopoietic stem cell transplantation.

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6.  Determination of the most influential sources of variability in tacrolimus trough blood concentrations in adult liver transplant recipients: a bottom-up approach.

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7.  Tacrolimus placental transfer at delivery and neonatal exposure through breast milk.

Authors:  Songmao Zheng; Thomas R Easterling; Karen Hays; Jason G Umans; Menachem Miodovnik; Shannon Clark; Justina C Calamia; Kenneth E Thummel; Danny D Shen; Connie L Davis; Mary F Hebert
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8.  The Effect of Weight and CYP3A5 Genotype on the Population Pharmacokinetics of Tacrolimus in Stable Paediatric Renal Transplant Recipients.

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9.  ''Minimizing tacrolimus'' strategy and long-term survival after liver transplantation.

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10.  Pharmacokinetics of tacrolimus during pregnancy.

Authors:  Songmao Zheng; Thomas R Easterling; Jason G Umans; Menachem Miodovnik; Justina C Calamia; Kenneth E Thummel; Danny D Shen; Connie L Davis; Mary F Hebert
Journal:  Ther Drug Monit       Date:  2012-12       Impact factor: 3.681

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