The rewarding effects of alcohol after bariatric surgery: do they change and are they associated with pharmacokinetic changes?


Journal

Surgery for obesity and related diseases : official journal of the American Society for Bariatric Surgery
ISSN: 1878-7533
Titre abrégé: Surg Obes Relat Dis
Pays: United States
ID NLM: 101233161

Informations de publication

Date de publication:
Feb 2022
Historique:
received: 07 05 2021
revised: 23 07 2021
accepted: 16 08 2021
pubmed: 30 9 2021
medline: 29 3 2022
entrez: 29 9 2021
Statut: ppublish

Résumé

Research shows that surgery patients who have undergone Roux-en-Y gastric bypass (RYGB) are at increased risk for an alcohol use disorder (AUD). However, the mechanisms through which this increased risk is incurred are poorly understood. A host of variables have been proposed as potentially causal in developing AUDs, but empirical examination of many of these variables in human samples is lacking. Our objective was to examine the extent to which alcohol pharmacokinetics (PK), the rewarding effects of alcohol, and the relationship between these variables change from before to after weight loss surgery. Large healthcare facility in the Midwest United States METHODS: Thirty-four participants completed assessments before and 1 year after RYGB. They completed laboratory sessions and provided data on the PK of alcohol and the extent to which alcohol was reinforcing to them at each timepoint. Findings show that the PK effects of alcohol (P < .01) and how rewarding alcohol was reported to be (P < .01) changed from before to 1 year after weight loss surgery. Further, statistically significant increases in the association between these variables were witnessed from before to 1 year after surgery (P < .01). These results implicate changes (from before surgery to one year after) in the reinforcing and PK effects of alcohol as possible mechanisms for increased risk of alcohol use disorder following Roux-en-Y gastric bypass surgery.

Sections du résumé

BACKGROUND BACKGROUND
Research shows that surgery patients who have undergone Roux-en-Y gastric bypass (RYGB) are at increased risk for an alcohol use disorder (AUD). However, the mechanisms through which this increased risk is incurred are poorly understood. A host of variables have been proposed as potentially causal in developing AUDs, but empirical examination of many of these variables in human samples is lacking.
OBJECTIVES OBJECTIVE
Our objective was to examine the extent to which alcohol pharmacokinetics (PK), the rewarding effects of alcohol, and the relationship between these variables change from before to after weight loss surgery.
SETTING METHODS
Large healthcare facility in the Midwest United States METHODS: Thirty-four participants completed assessments before and 1 year after RYGB. They completed laboratory sessions and provided data on the PK of alcohol and the extent to which alcohol was reinforcing to them at each timepoint.
RESULTS RESULTS
Findings show that the PK effects of alcohol (P < .01) and how rewarding alcohol was reported to be (P < .01) changed from before to 1 year after weight loss surgery. Further, statistically significant increases in the association between these variables were witnessed from before to 1 year after surgery (P < .01).
CONCLUSION CONCLUSIONS
These results implicate changes (from before surgery to one year after) in the reinforcing and PK effects of alcohol as possible mechanisms for increased risk of alcohol use disorder following Roux-en-Y gastric bypass surgery.

Identifiants

pubmed: 34583891
pii: S1550-7289(21)00410-X
doi: 10.1016/j.soard.2021.08.011
pmc: PMC8792168
mid: NIHMS1738025
pii:
doi:

Substances chimiques

Ethanol 3K9958V90M

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

190-195

Subventions

Organisme : NIGMS NIH HHS
ID : P30 GM114748
Pays : United States
Organisme : NIAAA NIH HHS
ID : R01 AA022336
Pays : United States

Informations de copyright

Copyright © 2022 American Society for Bariatric Surgery. Published by Elsevier Inc. All rights reserved.

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Auteurs

Scott G Engel (SG)

Sanford Center for Bio-behavioral Research, Sanford Research, Fargo, North Dakota; University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota. Electronic address: scott.engel@sanfordhealth.org.

Lauren M Schaefer (LM)

Sanford Center for Bio-behavioral Research, Sanford Research, Fargo, North Dakota; University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota.

Gail A Kerver (GA)

Sanford Center for Bio-behavioral Research, Sanford Research, Fargo, North Dakota; University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota.

Lynnette M Leone (LM)

Sanford Center for Bio-behavioral Research, Sanford Research, Fargo, North Dakota.

Greg Smith (G)

Department of Psychology, University of Kentucky, Lexington, Kentucky.

James E Mitchell (JE)

Sanford Center for Bio-behavioral Research, Sanford Research, Fargo, North Dakota; University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota.

John Gunstad (J)

Department of Psychology, Kent State University, Kent, Ohio.

Ross D Crosby (RD)

Sanford Center for Bio-behavioral Research, Sanford Research, Fargo, North Dakota; University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota.

Kristine Steffen (K)

Sanford Center for Bio-behavioral Research, Sanford Research, Fargo, North Dakota; Department of Pharmaceutical Sciences, North Dakota State University, Fargo, North Dakota.

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