Literature DB >> 34341493

Effectiveness of spironolactone dispensation in reducing weekly alcohol use: a retrospective high-dimensional propensity score-matched cohort study.

Vanessa A Palzes1, Mehdi Farokhnia2,3, Andrea H Kline-Simon4, Joseph Elson5, Stacy Sterling4, Lorenzo Leggio2,6,7,8,9, Constance Weisner4,10, Felicia W Chi4.   

Abstract

There is a need to increase the armamentarium of pharmacotherapies for alcohol use disorder (AUD). Recent research suggests that mineralocorticoid receptor (MR) antagonism via spironolactone may represent a novel pharmacological treatment for AUD. We conducted a pharmacoepidemiologic retrospective cohort study (June 1, 2014 to May 31, 2018) to examine whether spironolactone dispensation (≥90 continuous days), for any indication, is associated with changes in weekly alcohol use about 6 months later. We compared 523 spironolactone-treated adults and 2305 untreated adults, matched on high-dimensional propensity scores created from a set of predefined (sociodemographic and health characteristics, diagnoses, and service utilization) and empirical electronic health record-derived covariates. The sample was 57% female and 27% non-White with a mean age of 59.2 years (SD = 19.3). Treated patients reduced their weekly alcohol use by 3.50 drinks (95% CI = -4.22, -2.79), while untreated patients reduced by 2.74 drinks (95% CI = -3.22, -2.26), yielding a significant difference of 0.76 fewer drinks (95% CI = -1.43, -0.11). Among those who drank >7 drinks/week at baseline, treated patients, compared to untreated patients, reported a greater reduction in weekly alcohol use by 4.18 drinks (95% CI = -5.38, -2.97), while there was no significant difference among those who drank less. There was a significant dose-response relationship between spironolactone dosage and change in drinks/week. Pending additional evidence on its safety and efficacy in individuals with AUD, spironolactone (and MR blockade, at large) may hold promise as a pharmacotherapy for AUD.
© 2021. The Author(s), under exclusive licence to American College of Neuropsychopharmacology.

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Year:  2021        PMID: 34341493      PMCID: PMC8505557          DOI: 10.1038/s41386-021-01117-z

Source DB:  PubMed          Journal:  Neuropsychopharmacology        ISSN: 0893-133X            Impact factor:   7.853


  1 in total

1.  Prescription opioid registry protocol in an integrated health system.

Authors:  G Thomas Ray; Amber L Bahorik; Paul C VanVeldhuisen; Constance M Weisner; Andrea L Rubinstein; Cynthia I Campbell
Journal:  Am J Manag Care       Date:  2017-05-01       Impact factor: 2.229

  1 in total
  1 in total

1.  Spironolactone as a potential new pharmacotherapy for alcohol use disorder: convergent evidence from rodent and human studies.

Authors:  Mehdi Farokhnia; Christopher T Rentsch; Vicky Chuong; M Adrienne McGinn; Sophie K Elvig; Eliza A Douglass; Luis A Gonzalez; Jenna E Sanfilippo; Renata C N Marchette; Brendan J Tunstall; David A Fiellin; George F Koob; Amy C Justice; Lorenzo Leggio; Leandro F Vendruscolo
Journal:  Mol Psychiatry       Date:  2022-09-20       Impact factor: 13.437

  1 in total

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