Sex-based differences in psychiatric symptoms and opioid abstinence during buprenorphine/naloxone treatment in adolescents with opioid use disorders.


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:
02 2022
Historique:
received: 29 10 2020
revised: 29 12 2020
accepted: 25 05 2021
pubmed: 6 7 2021
medline: 22 3 2022
entrez: 5 7 2021
Statut: ppublish

Résumé

Recent studies indicate that sex-based differences exist in co-occurring psychiatric symptoms and disorders among individuals with opioid use disorders (OUD). Whether these associations are present in adolescent samples and change during OUD treatment is poorly understood. In the current study, we examined sex-based differences in psychiatric symptoms and relationships among sex, psychiatric symptoms, and opioid use outcomes in youth with OUD receiving buprenorphine/naloxone (Bup/Nal) and psychosocial treatment. The study randomly assigned one hundred and fifty-two youth (15-21 years old) diagnosed with OUD to either 12 weeks of treatment with Bup/Nal or up to 2 weeks of Bup/Nal detoxification with both treatment arms receiving weekly drug counseling as part of a multisite clinical trial (NIDA-CTN-0010). We compared psychiatric symptoms, assessed via the Youth Self Report (YSR) at baseline and week 12, across male and female OUD participants. The study used logistic regression models to identify sex and psychiatric symptom variables that were predictors of opioid positive urine (OPU) at week 12. Compared to males, females with OUD had higher mean psychiatric symptom scores at baseline across broad-band and narrow-band symptom domains. The study observed significant reductions in psychiatric symptom scores in both males and females during treatment, and by week 12, females only differed from males on anxious-depressive symptom scores. Females, in general, and youth of both sexes presenting to treatment with higher anxious depression scores were less likely to have a week-12 OPU. Clinically significant sex-based differences in psychiatric symptoms are present at baseline among youth with OUD receiving Bup/Nal-assisted treatment and mostly resolve during treatment.

Sections du résumé

BACKGROUND
Recent studies indicate that sex-based differences exist in co-occurring psychiatric symptoms and disorders among individuals with opioid use disorders (OUD). Whether these associations are present in adolescent samples and change during OUD treatment is poorly understood.
OBJECTIVES
In the current study, we examined sex-based differences in psychiatric symptoms and relationships among sex, psychiatric symptoms, and opioid use outcomes in youth with OUD receiving buprenorphine/naloxone (Bup/Nal) and psychosocial treatment.
METHODS
The study randomly assigned one hundred and fifty-two youth (15-21 years old) diagnosed with OUD to either 12 weeks of treatment with Bup/Nal or up to 2 weeks of Bup/Nal detoxification with both treatment arms receiving weekly drug counseling as part of a multisite clinical trial (NIDA-CTN-0010). We compared psychiatric symptoms, assessed via the Youth Self Report (YSR) at baseline and week 12, across male and female OUD participants. The study used logistic regression models to identify sex and psychiatric symptom variables that were predictors of opioid positive urine (OPU) at week 12.
RESULTS
Compared to males, females with OUD had higher mean psychiatric symptom scores at baseline across broad-band and narrow-band symptom domains. The study observed significant reductions in psychiatric symptom scores in both males and females during treatment, and by week 12, females only differed from males on anxious-depressive symptom scores. Females, in general, and youth of both sexes presenting to treatment with higher anxious depression scores were less likely to have a week-12 OPU.
CONCLUSIONS
Clinically significant sex-based differences in psychiatric symptoms are present at baseline among youth with OUD receiving Bup/Nal-assisted treatment and mostly resolve during treatment.

Identifiants

pubmed: 34218992
pii: S0740-5472(21)00221-X
doi: 10.1016/j.jsat.2021.108495
pii:
doi:

Substances chimiques

Analgesics, Opioid 0
Buprenorphine, Naloxone Drug Combination 0
Narcotic Antagonists 0
Buprenorphine 40D3SCR4GZ

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

108495

Subventions

Organisme : NIDA NIH HHS
ID : K12 DA000357
Pays : United States
Organisme : NIDA NIH HHS
ID : R34 DA050292
Pays : United States
Organisme : NIDA NIH HHS
ID : K12 DA000357
Pays : United States

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Christopher J Hammond (CJ)

Division of Child & Adolescent Psychiatry, Department of Psychiatry at Johns Hopkins University School of Medicine, United States of America; Behavioral Pharmacology Research Unit, Department of Psychiatry at Johns Hopkins University School of Medicine, United States of America. Electronic address: chammo20@jhmi.edu.

Grace Park (G)

Division of Child & Adolescent Psychiatry, Department of Psychiatry at Johns Hopkins University School of Medicine, United States of America.

Annabel Kady (A)

Division of Child & Adolescent Psychiatry, Department of Psychiatry at Johns Hopkins University School of Medicine, United States of America.

Krutika Rathod (K)

Division of Child & Adolescent Psychiatry, Department of Psychiatry at Johns Hopkins University School of Medicine, United States of America.

Naisa Rahman (N)

Division of Child & Adolescent Psychiatry, Department of Psychiatry at Johns Hopkins University School of Medicine, United States of America.

Carol Vidal (C)

Division of Child & Adolescent Psychiatry, Department of Psychiatry at Johns Hopkins University School of Medicine, United States of America.

Kevin Wenzel (K)

Mountain Manor Treatment Center, Maryland Treatment Centers, United States of America.

Marc Fishman (M)

Division of Child & Adolescent Psychiatry, Department of Psychiatry at Johns Hopkins University School of Medicine, United States of America; Mountain Manor Treatment Center, Maryland Treatment Centers, United States of America.

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Classifications MeSH