Evaluation of Metoprolol Pharmacokinetics in Patients Receiving Hi Flux Hemodialysis

University of Michigan8 enrolled

Overview

The current study will evaluate the plasma pharmacokinetics of metoprolol in a cohort of 8 adult volunteers who are receiving regular hemodialysis treatment (HD) 3 days a week for 4 hours each day and have been taking a total daily dose of 25-200 mg of metoprolol succinate for \>30 days as part of their usual care. Blood sampling will occur over 10 hours, with frequent sampling during HD and in the 4 hours after termination of HD treatment. The 8 subjects will all receive their prescribed dose (25-200 mg total daily dose) 2 hours prior to HD treatment. The pre-HD sample will also be sent for pharmacogenomics genotyping. Safety and pharmacodynamic assessments (blood pressure (BP) and heart rate (HR) assessments) will be performed throughout the study. Axiom Precision Medicine Research Array (Affymetrix, Santa Clara, CA) will be used to evaluate genotype of CYP2D6. CYP2D6 phenotype will be evaluated using the ratio of parent drug to metabolite. Non-compartmental analyses will be performed to compare maximum concentrations (Cmax), time to maximum concentration and area under the curve from time 0 to the last measurable sample (AUClast) between the two phases. Compartmental analyses will be performed to construct a model to explain time-dependent changes in metoprolol clearance. Monte Carlo simulations will be performed to compare metoprolol pharmacokinetic profiles on and off HD.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Hemodialysis Pharmacokinetics

Interventions

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Age \> 18 years 2. Indwelling tunneled catheter, AVF, AVG that is currently used for hemodialysis 3. Receiving in-center hemodialysis 3 days a week for 3-4.5 hours each treatment 4. Taking a total daily dose of 25-200 mg metoprolol succinate as prescribed by their physician 5. Hemoglobin ≥ 9.5 g/dL on most recent laboratory assessment prior to study Exclusion Criteria: 1. Any condition that would not allow for arm BP to be taken 2. Hemoglobin \< 9.5 g/dL on most recent lab prior to study 3. Patient is on a CYP2D6 inhibitor (most common in HD population amiodarone, bupropion, cinacalcet, diphenhydramine, fluoxetine, paroxetine)

Outcomes

Primary Outcomes

Plasma pharmacokinetics-Maximal Plasma Concentration

Characterize the pharmacokinetics of metoprolol and its metabolite, alpha-hydroxymetoprolol during and after HD