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Randomized Controlled Trial
. 2021 Jun;238(6):1671-1686.
doi: 10.1007/s00213-021-05802-1. Epub 2021 Feb 26.

The acute effects of alcohol on state rumination in the laboratory

Affiliations
Randomized Controlled Trial

The acute effects of alcohol on state rumination in the laboratory

O Merve Mollaahmetoglu et al. Psychopharmacology (Berl). 2021 Jun.

Abstract

Rationale: Rumination is a repetitive, negative, self-focused thinking style associated with various forms of psychopathology. Recent studies suggest that rumination increases craving for alcohol and predicts harmful drinking and alcohol-related problems. However, the acute effects of alcohol on rumination have not been previously studied. It is proposed that alcohol may reduce ruminative thinking through decreasing negative mood.

Objectives: In the present study, we aimed to test the previously unexplored effects of acute alcohol consumption on rumination in a hazardous drinking population.

Methods: We conducted a randomised placebo-controlled laboratory study to examine the effect of low (0.4 g kg-1) and high doses (0.8 g kg-1) of alcohol on state rumination compared to placebo. Participants completed a rumination induction task prior to receiving drinks. We then measured state rumination and mood at repeated time points; 30 min, 60 min and 90 min post-drinks consumption.

Results: We found a significant decrease in state rumination in the low-dose alcohol group compared to placebo at 30 min post-alcohol consumption, but no difference was observed between the high-dose alcohol and placebo groups. Mediation analysis provided evidence for an indirect effect of alcohol on state rumination through concurrent changes in negative mood.

Conclusions: These findings suggest that acute alcohol consumption can regulate negative mood and concurrently rumination, providing preliminary evidence for the role of rumination in alcohol use disorders. Rumination may be a treatment target in alcohol use disorders.

Keywords: Alcohol use disorders; Depression; Negative affect; Rumination.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Fig. 1
Fig. 1
Study procedures with approximate timings
Fig. 2
Fig. 2
Mean BRAC (mg l−1) across time of testing and alcohol administration group. There were significant (*p < 0.05) group differences in BRAC at all time points except at baseline. Error bars represent standard error of the mean. Thirty-one participants contributed to placebo group, 30 to low-dose alcohol group and 29 to high-dose alcohol group
Fig. 3
Fig. 3
Mean state rumination about an unresolved problem over time and groups (low- and high-dose alcohol conditions collapsed together). There was a significant difference in state rumination between the placebo and the low-dose alcohol group at 30 min post-alcohol administration (*p < 0.05). Error bars represent standard error of the mean. 31 participants contributed to placebo group, 30 to low-dose alcohol group and 29 to high-dose alcohol group
Fig. 4
Fig. 4
Mean state rumination measured using BSRI total scores over time and groups. Time*Condition interaction was not statistically significant. Error bars represent standard error of the mean. Respectively, 30 and 29 participants contributed data to low-dose and high-dose alcohol groups, and 31 contributed data to placebo group
Fig. 5
Fig. 5
Mediation model demonstrating the indirect effect of alcohol dose on rumination by change in negative affect ratings. Significant effects are denoted by an asterisk

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