Literature DB >> 21076373

Customized mycophenolate dosing based on measuring inosine-monophosphate dehydrogenase activity significantly improves patients' outcomes after renal transplantation.

Matthias C Raggi1, Stephanie B Siebert, Werner Steimer, Tibor Schuster, Manfred J Stangl, Dietmar K Abendroth.   

Abstract

BACKGROUND: Significant relationships have been reported between the uptake of mycophenolic acid (MPA) and the risk of acute rejection. In a prospective study after renal transplantation, we assessed the value of measuring inosine-monophosphate dehydrogenase (IMPDH) activity as a predictive indicator of an acute rejection episode in the initial postoperative period. PATIENTS AND METHODS: Fifty-two patients received 360 mg enteric-coated mycophenolate-sodium two times per day with concomitant tacrolimus/cyclosporine A, providing a total of 122 pharmacodynamic profiles. IMPDH activity was measured by a validated high-performance liquid chromatography method in four plasma samples collected at predose, 30 and 60 min, 2 and 4 hr, and preoperative, during weeks 1 and 2 and 3 months after transplantation. MPA concentrations were measured by mass spectrometry. Inhibition of IMPDH was correlated to the MPA values, MPA area under the curves, and predose levels of the different calcineurin inhibitors.
RESULTS: Comparing the two groups (group I: rejection; n=17; mean age 51±15 years vs. group II: no rejection; n=35; mean age 51±14 years), we found a significantly (P<0.001) lower inhibition of IMPDH in group I (26.5%±11% vs. 56.7%±18%) already in the first week after transplantation. There was no correlation of MPA values (6.85±4 vs. 4.1±3 mg/L; first week) nor with the calcineurin inhibitor trough blood levels. Area under the curves for MPA did not differ significantly. Furthermore, IMPDH activity was a reliable predictor of rejection episodes and inflammation.
CONCLUSION: The data suggest that measuring biologic response may be a more valuable indicator than traditional therapeutic drug monitoring of MPA. Patients at risk for rejection could be earlier identified, and the therapeutic potential of MPA will be optimized.

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Year:  2010        PMID: 21076373     DOI: 10.1097/TP.0b013e3182000027

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  10 in total

1.  Monitoring mycophenolate mofetil is necessary for the effective prophylaxis of acute GVHD after cord blood transplantation.

Authors:  Y Arai; T Kondo; T Kitano; M Hishizawa; K Yamashita; N Kadowaki; T Yamamoto; I Yano; K Matsubara; A Takaori-Kondo
Journal:  Bone Marrow Transplant       Date:  2014-11-10       Impact factor: 5.483

Review 2.  Maximum a posteriori Bayesian estimation of mycophenolic Acid area under the concentration-time curve: is this clinically useful for dosage prediction yet?

Authors:  Christine E Staatz; Susan E Tett
Journal:  Clin Pharmacokinet       Date:  2011-12-01       Impact factor: 6.447

3.  Peripheral Lymphocyte Response to Mycophenolic Acid In Vitro and Incidence of Cytomegalovirus Infection in Renal Transplantation.

Authors:  Kentaro Sugiyama; Hiroyasu Sasahara; Mahoto Tsukaguchi; Kazuya Isogai; Akira Toyama; Hiroshi Satoh; Kazuhide Saitoh; Yuki Nakagawa; Kota Takahashi; Sachiko Tanaka; Kenji Onda; Toshihiko Hirano
Journal:  Cell Med       Date:  2013-10-23

4.  The pharmacokinetics and pharmacodynamics of mycophenolate mofetil in younger and elderly renal transplant recipients.

Authors:  Jiang-Tao Tang; Brenda C de Winter; Dennis A Hesselink; Ferdi Sombogaard; Lan-Lan Wang; Teun van Gelder
Journal:  Br J Clin Pharmacol       Date:  2016-11-30       Impact factor: 4.335

Review 5.  Clinical pharmacokinetics and pharmacodynamics of mycophenolate in patients with autoimmune disease.

Authors:  Azrin N Abd Rahman; Susan E Tett; Christine E Staatz
Journal:  Clin Pharmacokinet       Date:  2013-05       Impact factor: 6.447

6.  Inosine monophosphate dehydrogenase expression and activity are significantly lower in kidney transplant recipients with diabetes mellitus.

Authors:  Miroslav Dostalek; Reginald Y Gohh; Fatemeh Akhlaghi
Journal:  Ther Drug Monit       Date:  2013-06       Impact factor: 3.681

7.  Population pharmacokinetic-pharmacodynamic modelling of mycophenolic acid in paediatric renal transplant recipients in the early post-transplant period.

Authors:  Min Dong; Tsuyoshi Fukuda; Shareen Cox; Marij T de Vries; David K Hooper; Jens Goebel; Alexander A Vinks
Journal:  Br J Clin Pharmacol       Date:  2014-11       Impact factor: 4.335

Review 8.  Optimizing Mycophenolic Acid Exposure in Kidney Transplant Recipients: Time for Target Concentration Intervention.

Authors:  David K Metz; Nick Holford; Joshua Y Kausman; Amanda Walker; Noel Cranswick; Christine E Staatz; Katherine A Barraclough; Francesco Ierino
Journal:  Transplantation       Date:  2019-10       Impact factor: 4.939

9.  Pharmacodynamic assessment of mycophenolic acid in resting and activated target cell population during the first year after renal transplantation.

Authors:  Rolf Anton Klaasen; Stein Bergan; Sara Bremer; Kristine Hole; Christine Berg Nordahl; Anders Mikal Andersen; Karsten Midtvedt; Morten Heier Skauby; Nils Tore Vethe
Journal:  Br J Clin Pharmacol       Date:  2020-02-16       Impact factor: 4.335

10.  Expression of IMPDH mRNA after mycophenolate administration in male volunteers.

Authors:  Sollip Kim; Woochang Lee; Sail Chun; Tae Hyun Um; Won-Ki Min
Journal:  Biomed Res Int       Date:  2014-07-01       Impact factor: 3.411

  10 in total

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