Pharmacogenomics-guided policy in opioid use disorder (OUD) management: An ethnically-diverse case-based approach

Introduction: Opioid use disorder (OUD) is characterized by a problematic pattern of opioid use leading to clinically-significant impairment or distress. Opioid agonist treatment is an integral component of OUD management, and buprenorphine is often utilized in OUD management due to strong clinical...

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Main Authors: Earl B. Ettienne, Edwin Chapman, Mary Maneno, Adaku Ofoegbu, Bradford Wilson, Beverlyn Settles-Reaves, Melissa Clarke, Georgia Dunston, Kevin Rosenblatt
Format: Article
Language:English
Published: Elsevier 2017-12-01
Series:Addictive Behaviors Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2352853217300111
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spelling doaj-5800feab6ecd42a0bc5fc9e4621dc3542020-11-24T22:54:29ZengElsevierAddictive Behaviors Reports2352-85322017-12-016814Pharmacogenomics-guided policy in opioid use disorder (OUD) management: An ethnically-diverse case-based approachEarl B. Ettienne0Edwin Chapman1Mary Maneno2Adaku Ofoegbu3Bradford Wilson4Beverlyn Settles-Reaves5Melissa Clarke6Georgia Dunston7Kevin Rosenblatt8Howard University College of Pharmacy, 2300 4th St NW, Washington, DC 20059, United States; Corresponding author at: Department of Clinical & Administrative Science, Howard University College of Pharmacy, 2300 4th St. NW, Annex III â Suite 119, Washington, DC 20059, United States.Department of Psychiatry & Behavioral Health Sciences, Howard University Hospital, 2041 Georgia Avenue, NW, Suite 5B01, Washington, DC 20060, United StatesHoward University College of Pharmacy, 2300 4th St NW, Washington, DC 20059, United StatesHoward University College of Pharmacy, 2300 4th St NW, Washington, DC 20059, United StatesNational Human Genome Center at Howard University, 2041 Georgia Ave. NW, Washington, DC 20060, United StatesHoward University Department of Community and Family Medicine, Towers Building, Suite 3600, 2041 Georgia Ave NW, Washington, DC 20060, United StatesNational Human Genome Center at Howard University, 2041 Georgia Ave. NW, Washington, DC 20060, United StatesNational Human Genome Center at Howard University, 2041 Georgia Ave. NW, Washington, DC 20060, United StatesConsultative Genomics, PLLC, 5909 West Loop South, Suite 310, Bellaire, TX 77401, United StatesIntroduction: Opioid use disorder (OUD) is characterized by a problematic pattern of opioid use leading to clinically-significant impairment or distress. Opioid agonist treatment is an integral component of OUD management, and buprenorphine is often utilized in OUD management due to strong clinical evidence for efficacy. However, interindividual genetic differences in buprenorphine metabolism may result in variable treatment response, leaving some patients undertreated and at increased risk for relapse. Clinical pharmacogenomics studies the effect that inherited genetic variations have on drug response. Our objective is to demonstrate the impact of pharmacogenetic testing on OUD management outcomes. Methods: We analyzed a patient who reported discomfort at daily buprenorphine dose of 24mg, which was a mandated daily maximum by the pharmacy benefits manager. Regular urine screenings were conducted to detect the presence of unauthorized substances, and pharmacogenetic testing was used to determine the appropriate dose of buprenorphine for OUD management. Results: At the 24mg buprenorphine daily dose, the patient had multiple relapses with unauthorized substances. Pharmacogenetic testing revealed that the patient exhibited a cytochrome P450 3A4 ultrarapid metabolizer phenotype, which necessitated a higher than recommended daily dose of buprenorphine (32mg) for adequate OUD management. The patient exhibited a reduction in the number of relapses on the pharmacogenetic-based dose recommendation compared to standard dosing. Conclusion: Pharmacogenomic testing as clinical decision support helped to individualize OUD management. Collaboration by key stakeholders is essential to establishing pharmacogenetic testing as standard of care in OUD management. Keywords: Opioid use disorder, Opioid agonist treatment, Buprenorphine, Pharmacogenomics, Policyhttp://www.sciencedirect.com/science/article/pii/S2352853217300111
collection DOAJ
language English
format Article
sources DOAJ
author Earl B. Ettienne
Edwin Chapman
Mary Maneno
Adaku Ofoegbu
Bradford Wilson
Beverlyn Settles-Reaves
Melissa Clarke
Georgia Dunston
Kevin Rosenblatt
spellingShingle Earl B. Ettienne
Edwin Chapman
Mary Maneno
Adaku Ofoegbu
Bradford Wilson
Beverlyn Settles-Reaves
Melissa Clarke
Georgia Dunston
Kevin Rosenblatt
Pharmacogenomics-guided policy in opioid use disorder (OUD) management: An ethnically-diverse case-based approach
Addictive Behaviors Reports
author_facet Earl B. Ettienne
Edwin Chapman
Mary Maneno
Adaku Ofoegbu
Bradford Wilson
Beverlyn Settles-Reaves
Melissa Clarke
Georgia Dunston
Kevin Rosenblatt
author_sort Earl B. Ettienne
title Pharmacogenomics-guided policy in opioid use disorder (OUD) management: An ethnically-diverse case-based approach
title_short Pharmacogenomics-guided policy in opioid use disorder (OUD) management: An ethnically-diverse case-based approach
title_full Pharmacogenomics-guided policy in opioid use disorder (OUD) management: An ethnically-diverse case-based approach
title_fullStr Pharmacogenomics-guided policy in opioid use disorder (OUD) management: An ethnically-diverse case-based approach
title_full_unstemmed Pharmacogenomics-guided policy in opioid use disorder (OUD) management: An ethnically-diverse case-based approach
title_sort pharmacogenomics-guided policy in opioid use disorder (oud) management: an ethnically-diverse case-based approach
publisher Elsevier
series Addictive Behaviors Reports
issn 2352-8532
publishDate 2017-12-01
description Introduction: Opioid use disorder (OUD) is characterized by a problematic pattern of opioid use leading to clinically-significant impairment or distress. Opioid agonist treatment is an integral component of OUD management, and buprenorphine is often utilized in OUD management due to strong clinical evidence for efficacy. However, interindividual genetic differences in buprenorphine metabolism may result in variable treatment response, leaving some patients undertreated and at increased risk for relapse. Clinical pharmacogenomics studies the effect that inherited genetic variations have on drug response. Our objective is to demonstrate the impact of pharmacogenetic testing on OUD management outcomes. Methods: We analyzed a patient who reported discomfort at daily buprenorphine dose of 24mg, which was a mandated daily maximum by the pharmacy benefits manager. Regular urine screenings were conducted to detect the presence of unauthorized substances, and pharmacogenetic testing was used to determine the appropriate dose of buprenorphine for OUD management. Results: At the 24mg buprenorphine daily dose, the patient had multiple relapses with unauthorized substances. Pharmacogenetic testing revealed that the patient exhibited a cytochrome P450 3A4 ultrarapid metabolizer phenotype, which necessitated a higher than recommended daily dose of buprenorphine (32mg) for adequate OUD management. The patient exhibited a reduction in the number of relapses on the pharmacogenetic-based dose recommendation compared to standard dosing. Conclusion: Pharmacogenomic testing as clinical decision support helped to individualize OUD management. Collaboration by key stakeholders is essential to establishing pharmacogenetic testing as standard of care in OUD management. Keywords: Opioid use disorder, Opioid agonist treatment, Buprenorphine, Pharmacogenomics, Policy
url http://www.sciencedirect.com/science/article/pii/S2352853217300111
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