Research Topics
| Tsuyoshi FukudaSummaryAffiliation: Cincinnati Children's Hospital Medical Center Country: USA Publications
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Detail Information
Publications
UGT1A9, UGT2B7, and MRP2 genotypes can predict mycophenolic acid pharmacokinetic variability in pediatric kidney transplant recipientsTsuyoshi Fukuda
Division of Clinical Pharmacology, Cincinnati Children s Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio 45229 3039, USA
Ther Drug Monit 34:671-9. 2012..Here, the combined contribution of these genetic variants to MPA pharmacokinetic variability was investigated in pediatric renal transplant recipients who were on mycophenolic mofetil maintenance therapy...
Nonsteroidal anti-inflammatory drugs may reduce enterohepatic recirculation of mycophenolic acid in patients with childhood-onset systemic lupus erythematosusTsuyoshi Fukuda
Division of Clinical Pharmacology and Pediatric Pharmacology Research Unit, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio 45229 3039, USA
Ther Drug Monit 33:658-62. 2011..Here, we evaluated the effects of this potential drug-transporter interaction on MPA-PK in a cohort of patients with childhood-onset systemic lupus erythematosus on mycophenolate mofetil therapy...
Inosine monophosphate dehydrogenase (IMPDH) activity as a pharmacodynamic biomarker of mycophenolic acid effects in pediatric kidney transplant recipientsTsuyoshi Fukuda
Division of Clinical Pharmacology and Pediatric Pharmacology Research Unit, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio, USA
J Clin Pharmacol 51:309-20. 2011..Because IMPDH inhibition is well correlated to MPA concentration, pretransplant IMPDH activity may serve as an early marker to guide the initial level of MPA exposure required in a pediatric population...
Development of population PK model with enterohepatic circulation for mycophenolic acid in patients with childhood-onset systemic lupus erythematosusCatherine M T Sherwin
Division of Clinical Pharmacology, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio 45229 3039, USA
Br J Clin Pharmacol 73:727-40. 2012..This study aimed to develop a population pharmacokinetic (PK) enterohepatic recycling model for MPA in patients with childhood-onset systemic lupus erythematosus (cSLE)...
Pharmacokinetics and pharmacodynamics of mycophenolic acid and their relation to response to therapy of childhood-onset systemic lupus erythematosusAnna Carmela P Sagcal-Gironella
Division of Rheumatology, Cincinnati Children s Hospital Medical Center, Cincinnati, OH 45229 3039, USA
Semin Arthritis Rheum 40:307-13. 2011..The objectives of this study were to (1) characterize the pharmacokinetics (MPA-PK) and pharmacodynamics (MPA-PD) of MPA and (2) explore the relationship between MPA-PK and cSLE disease activity...
Risk of tacrolimus toxicity in CYP3A5 nonexpressors treated with intravenous nicardipine after kidney transplantationDavid K Hooper
Division of Nephrology and Hypertension, Cincinnati Children s Hospital Medical Center, Cincinnati, OH, USA
Transplantation 93:806-12. 2012....
The evolution of population pharmacokinetic models to describe the enterohepatic recycling of mycophenolic acid in solid organ transplantation and autoimmune diseaseCatherine M T Sherwin
Division of Clinical Pharmacology, Cincinnati Childrens Hospital Medical Center, Cincinnati, Ohio 45229 3039, USA
Clin Pharmacokinet 50:1-24. 2011..Already published population pharmacokinetic models will be examined, and the evolution of these models away from empirical approaches to more mechanism-based models will be discussed...
Morphine clearance in children: does race or genetics matter?Senthilkumar Sadhasivam
Department of Anesthesia, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio, USA
J Opioid Manag 8:217-26. 2012....
