Underrepresentation of diverse populations and clinical characterization in opioid agonist treatment research: A systematic review of the neurocognitive effects of buprenorphine and methadone treatment.


Journal

Journal of substance abuse treatment
ISSN: 1873-6483
Titre abrégé: J Subst Abuse Treat
Pays: United States
ID NLM: 8500909

Informations de publication

Date de publication:
04 2022
Historique:
received: 26 03 2021
revised: 27 08 2021
accepted: 05 10 2021
pubmed: 4 12 2021
medline: 22 3 2022
entrez: 3 12 2021
Statut: ppublish

Résumé

The relative neurocognitive effects of the two most common opioid agonist treatments (OAT; buprenorphine and methadone) for opioid use disorder (OUD) are poorly understood. The aim of this systematic review is to examine the neurocognitive effects of OAT (buprenorphine and methadone) and the clinical and sociodemographic characteristics of study samples. The research team queried PubMed, PsycINFO and Cochrane Reviews for articles (01/1980-01/2020) with terms related to neurocognitive testing in adults (age ≥ 18) prescribed OAT. The team extracted neurocognitive data and grouped them by domain (e.g., executive functioning, learning/memory), and assessed study quality. The search retrieved 2341 abstracts, the team reviewed 278 full articles, and 32 met inclusion criteria. Of these, 31 were observational designs and one was an experimental design. Healthy controls performed better across neurocognitive domains than OAT-treated persons (buprenorphine or methadone). Compared to those with active OUD, OAT-treated persons had better neurocognition in various domains. However, in seven studies comparing buprenorphine- and methadone-treated persons, buprenorphine was associated with better neurocognition than was methadone, with moderate to large effect sizes in executive functioning, attention/working memory, and learning/memory. Additionally, OAT research underreports clinical characteristics and underrepresents Black and Latinx adults, as well as women. Findings suggest that compared to active opioid use, both buprenorphine and methadone treatment are associated with better neurocognitive functioning, but buprenorphine is associated with better executive functioning, attention/working memory, and learning/memory. These findings should be interpreted with caution given widespread methodological heterogeneity, and limited representation of ethnoracially diverse adults and women. Rigorous longitudinal comparisons with more diverse, better characterized samples will help to inform treatment and policy recommendations for persons with OUD.

Identifiants

pubmed: 34857427
pii: S0740-5472(21)00370-6
doi: 10.1016/j.jsat.2021.108644
pii:
doi:

Substances chimiques

Analgesics, Opioid 0
Buprenorphine 40D3SCR4GZ
Methadone UC6VBE7V1Z

Types de publication

Journal Article Research Support, N.I.H., Extramural Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

108644

Subventions

Organisme : NIDA NIH HHS
ID : P20 DA026149
Pays : United States
Organisme : NIDA NIH HHS
ID : R25 DA023021
Pays : United States

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Auteurs

Monica Rivera Mindt (MR)

Fordham University, Department of Psychology, USA; Icahn School of Medicine at Mount Sinai, Department of Neurology, USA. Electronic address: riveramindt@fordham.edu.

Kelly Coulehan (K)

Stony Brook Medicine, Department of Neurology, USA. Electronic address: kelly.coulehan@stonybrookmedicine.edu.

Maral Aghvinian (M)

Fordham University, Department of Psychology, USA; Icahn School of Medicine at Mount Sinai, Department of Neurology, USA. Electronic address: maghvinian@fordham.edu.

Travis M Scott (TM)

VA Palo Alto Health Care System, Sierra Pacific Mental Illness Research Education Clinical Center, USA; Stanford School of Medicine, Department of Psychiatry and Behavioral Sciences, USA. Electronic address: tshivleyscott@fordham.edu.

James Patrick Olsen (JP)

North Shore University Hospital, Department of Neurology, USA. Electronic address: jolsen10@fordham.edu.

Chinazo O Cunningham (CO)

Albert Einstein College of Medicine and Montefiore Medical Center, Department of Medicine, USA. Electronic address: chinazo.cunningham@einsteinmed.org.

Franchesca Arias (F)

The Aging Brain Center, Hebrew SeniorLife, USA; Harvard Medical School, Beth Israel Deaconess Medical Center, Department of Cognitive Neurology, USA. Electronic address: franchescaarias@hsl.harvard.edu.

Julia H Arnsten (JH)

Albert Einstein College of Medicine and Montefiore Medical Center, Department of Medicine, USA. Electronic address: jarnsten@montefiore.org.

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Classifications MeSH