Mifepristone as a pharmacological intervention for stress‐induced alcohol craving: A human laboratory study

Author:

Haass‐Koffler Carolina L.1234ORCID,Magill Molly13,Cannella Nazzareno5ORCID,Brown Joshua C.6,Aoun Elie G.7,Cioe Patricia A.13,Sinha Rajita8ORCID,Swift Robert M.129,Ciccocioppo Roberto5ORCID,Leggio Lorenzo13101112ORCID

Affiliation:

1. Center for Alcohol and Addiction Studies Brown University Providence Rhode Island USA

2. Department of Psychiatry and Human Behavior, Warren Alpert Medical School Brown University Providence Rhode Island USA

3. Department of Behavioral and Social Sciences, School of Public Health Brown University Providence Rhode Island USA

4. Carney Institute for Brain Science Brown University Providence Rhode Island USA

5. School of Pharmacy, Pharmacology Unit University of Camerino Camerino Italy

6. Department of Psychiatry Harvard Medical School, McLean Hospital Belmont Massachusetts USA

7. Division of Law, Ethics and Psychiatry, Department of Psychiatry, College of Physicians and Surgeons Columbia University New York New York USA

8. Yale Stress Center, Department of Psychiatry, Department of Neuroscience, Yale School of Medicine Yale University New Haven Connecticut USA

9. Providence Veterans Affairs Medical Center Providence Rhode Island USA

10. Clinical Psychoneuroendocrinology and Neuropsychopharmacology Section, Translational Addiction Medicine Branch NIDA IRP and NIAAA DICBR Baltimore Maryland USA

11. Medication Development Program, National Institute on Drug Abuse Intramural Research Program National Institutes of Health Baltimore Maryland USA

12. Division of Addiction Medicine, Department of Medicine Johns Hopkins University School of Medicine Baltimore Maryland USA

Abstract

AbstractPreclinical and clinical work suggests that mifepristone may be a viable treatment for alcohol use disorder (AUD). This was a Phase 1/2, outpatient, cross‐over, randomized, double‐blind, placebo‐controlled trial with non‐treatment‐seeking individuals with AUD (N = 32). We assessed safety, alcohol craving and consumption, after 1‐week mifepristone 600 mg/day administration, in a human laboratory study comprised of a single oral yohimbine administration (32.4 mg), a cue‐reactivity procedure and alcohol self‐administration. Safety was monitored by adverse events and hemodynamic parameters, alcohol craving by alcohol craving questionnaire and cue‐induced saliva output. During the alcohol self‐administration, we assessed alcohol pharmacokinetics, subjective effects and consumption. Outcomes were assessed using Generalized Estimating Equations and mediation analysis. Mild‐moderate adverse events were reported in both conditions. There was no statistically significant difference between mifepristone and placebo in alcohol pharmacokinetics and subjective effects. Furthermore, blood pressure increased only in the placebo condition after the stress‐induced laboratory procedures. Mifepristone, compared to placebo, significantly reduced alcohol craving and increased cortisol levels. Mifepristone‐induced cortisol increase was not a mediator of alcohol craving. Mifepristone, compared to placebo, did not reduce alcohol consumption in the laboratory or in a naturalistic setting. This study successfully translated a developed preclinical procedure to a human laboratory study, confirming the safety of mifepristone in people with AUD and providing evidence to its role in reducing alcohol craving under stress procedures. The lack of effects on alcohol drinking may be related to the selection of non‐treatment seekers and suggests future treatment‐oriented trials should investigate mifepristone in people with AUD.

Funder

National Institute on Alcohol Abuse and Alcoholism

National Institute of General Medical Sciences

Publisher

Wiley

Subject

Psychiatry and Mental health,Pharmacology,Medicine (miscellaneous)

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