Introduction
Gambling disorder affects 0.4–2.4% of the population across the world and is linked to a variety of untoward outcomes such as high levels of comorbidities, disability, bankruptcy, and suicidality.Reference Hodgins, Stea and Grant 1 Gambling disorder is the first “behavioral addiction” to be recognized in the Diagnostic and Statistical Manual, Fifth Edition (DSM-5), 2 wherein it is listed in the category of “Substance-Related and Addictive Disorders.” This classification of gambling disorder alongside alcohol (and other substance) use disorders was driven by the recognition of high etiological, phenomenological, and comorbid overlap across these conditions.Reference Petry, Blanco and Auriacombe 3 As certain psychoactive substances such as alcohol can lead to addiction in some individuals, so too can certain behaviors—especially gambling.
A recent meta-analysis has indicated that frequency of alcohol use is a potential predisposing factor for gambling disorder, with small to medium effect sizes.Reference Dowling, Merkouris, Greenwood, Oldenhof, Toumbourou and Youssef 4 At the same time, however, complex bidirectional relationships are likely to exist. For example, gambling disorder leads to distress and functional impairment, which in turn may lead an individual to develop problematic alcohol use or an exacerbation of existing use. One major challenge in the alcohol use disorder literature per se is to differentiate any effects (or associations) due to current (or recent) alcohol use, from those attributable to a history of alcohol use disorder in itself.
Clinicians often suspect that a history of alcohol use disorder may be relevant to the presentation of gambling disorder and its response to treatment. For example, does the person’s lifetime history of alcohol use disorder indicate they are more prone to other addictions—or switching across them? Does the occurrence of lifetime alcohol use disorder mean that subsequent gambling disorder is harder to treat or presents differently (eg, with greater symptom severity)?
To address previously unanswered questions regarding lifetime alcohol use disorder and its relationship to gambling disorder, we aggregated data from previous clinical trials for gambling disorder, which excluded individuals with recent/current alcohol use disorder. Associations between lifetime (but not current) alcohol use disorder and other variables were characterized. Previous studies have found that adults with gambling disorder with current alcohol problems report greater gambling severityReference Petry 5 , Reference Welte, Barnes, Wieczorek and Tidwell 6 and are at an increased likelihood of relapse to gambling problems after treatment.Reference Hodgins and el-Guebaly 7 Similarly, a previous study consisting of 150 adults with gambling disorder found that those with a lifetime alcohol use disorder had worse lifetime gambling symptoms, exhibited more impairment in self-control, and greater resistance to externally motivated treatment approaches than gamblers without a lifetime alcohol use disorder history.Reference Lister, Milosevic and Ledgerwood 8 These studies, however, only examined lifetime alcohol problems that were also current and did not examine whether lifetime (but not current) alcohol use disorders had similar associations. Building upon this limited research, we hypothesized that lifetime alcohol use disorder would be associated with worse current gambling symptoms, family history of alcohol use disorder, male gender, and lesser clinical improvement in gambling from clinical trial participation. The findings from this study may provide needed research information as to the longer-term effects of alcohol use disorder on current gambling behavior and suggest important clinical information as to why some adults with gambling disorder are less successful in gambling treatment.
Methods
Participants
Data were aggregated from participants who attended clinical trials of pharmacotherapy or psychotherapy for gambling disorder at the University of Chicago and the University of Minnesota, USA. All diagnoses of gambling disorder were made by an experienced board-certified psychiatrist, using the criteria set forth by the Diagnostic and Statistical Manual, Fourth Edition (DSM-IV), 9 and the diagnoses were later confirmed to be consistent with the current requirements for gambling disorder using the DSM-5 criteria. 2 Diagnosis was made using a validated instrument (see later).
The exclusionary criteria for these studies are as follows: alcohol use disorder in the preceding 3 months (to eliminate the acute effects of alcohol use on symptom presentation and treatment response and allow for the examination of the more chronic effects of lifetime alcohol use disorder); history of psychotic or bipolar disorder (to ensure participant safety during a trial of medications that might destabilize psychotic or bipolar symptoms), any current (past 3 months) illicit drug use (to avoid the confounding effects of other drug use on symptom presentation and treatment outcome), or inability to provide informed consent. Data from multiple previously published clinical trials were included.Reference Kim, Grant, Adson and Shin 10 –Reference Grant, Odlaug and Chamberlain 16 Trials were from 8 weeks to 16 weeks in duration.
All study procedures were carried out in accordance with the Declaration of Helsinki. The Institutional Review Boards of the University of Minnesota and the University of Chicago approved the procedures and the accompanying consent forms. After all procedures were explained, all participants provided informed written consent.
Assessments
A semi-structured rater-administered questionnaire was used to collect detailed information on demographic and clinical features of gambling (eg, preferred types of gambling, amount of money lost, occurrence of gambling-related legal problems). A lifetime history of alcohol use disorder was assessed using the Structured Clinical Interview for DSM-IV Axis I Disorders (SCID-I).Reference First, Spitzer, Gibbon and Williams 17 All participants included in these trials were drawn from settings where multiple types of gambling (ie, both strategic and nonstrategic) are available. To determine the preferred form of gambling, as part of the semi-structured clinical interview, participants were asked which form of gambling they preferred. Strategic gambling was defined as games (eg, cards, sports, and dog/horse-race wagering) in which skill or knowledge may have some impact on outcomes.Reference Petry 18 Other games such as slots, lottery, and pull tabs require no skill, and consequently, these are categorized as “nonstrategic” gambling.
We undertook the family history method where the proband is asked about psychiatric and substance use problems in their first-degree relatives, despite its methodological limitations,Reference Andreasen, Endicott, Spitzer and Winokur 19 as this method aligns most closely with how family history is evaluated clinically. When a participant was unsure of a diagnosis, it was not included.
In addition, participants completed the following instruments:
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• Structured Clinical Interview for Gambling Disorder (SCI-GD) for diagnosis of gambling disorder.Reference Grant, Steinberg, Kim, Rounsaville and Potenza 20
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• SCID-I to identify mainstream psychiatric comorbidities.Reference First, Spitzer, Gibbon and Williams 17
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• Yale-Brown Obsessive-Compulsive Scale modified for Pathological Gambling (PG-YBOCS), a clinician-administered scale, to quantify symptom severity over the past 7 days.Reference Pallanti, DeCaria, Grant, Urpe and Hollander 21
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• Gambling Symptom Assessment Scale (GSAS), a self-report scale, to measure overall symptom severity for the past week.Reference Kim, Grant, Potenza, Blanco and Hollander 22
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• Hamilton Depression Rating Scale (HAM-D) to measure the severity of depressive symptoms.Reference Hamilton 23
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• Hamilton Anxiety Rating Scale (HAM-A) to measure the severity of anxiety symptoms.Reference Hamilton 24
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• Sheehan Disability Scale (SDS) to measure overall disability/functioning.Reference Sheehan, Harnett-Sheehan and Raj 25
Data analysis
The baseline demographic and clinical features of those who did and those who did not have lifetime alcohol use disorder were compared using analysis of variance for continuous variables or likelihood ratio chi-squares for categorical variables. To assist in the interpretation of significant results, we also reported Cohen’s D (for continuous variables) or relative risk (RR, for categorical variables). This being an exploratory study where we wished to avoid the risk of falsely assuming a variable was not important when it was (ie, to minimize the likelihood of false negatives), statistical significance was defined as p < 0.05 (we did however recognize the potential limitations this might pose, especially in terms of risk for type I errors in exploratory studies).
Results
Of the 621 participants in the clinical trials, 103 (16.6%) had lifetime but not current alcohol use disorder. The demographic characteristics of the two groups are shown in Table 1. Consistent with prior research (Petry et al., 2005), previous history of alcohol use disorder was significantly associated with male gender (RR = 1.42) and greater body weight (Cohen’s D = 0.27), but not with the other demographic variables that were examined.
Note: Statistical tests are analysis of variance except where indicated; LR = likelihood ratio chi-square test. Education level is a score reflecting the highest level of education obtained to date, ranging from 0 (did not complete initial basic schooling) to 5 (higher degree completed). For relationship data, presented as single versus not for simplicity for analysis carried out for full categories (eg, single, married, cohabiting, etc). Note that total cell sizes per group may differ due to missing data for some variables. * p < 0.05.
Table 2 shows the baseline clinical characteristics relating to gambling in each of the two groups. Lifetime alcohol use disorder was significantly associated with a higher occurrence of gambling-related legal problems (RR = 1.50), but not with the other gambling-related measures that were considered. In particular, and contrary to previous research,Reference Petry 5 , Reference Welte, Barnes, Wieczorek and Tidwell 6 lifetime alcohol use disorder was not associated with worse gambling symptom severity.
Note: Statistical tests are analysis of variance except where indicted; LR = likelihood ratio chi-square test; GSAS = Gambling Symptom Assessment Scale. Note that total cell sizes per group may differ due to missing data for some variables. * p < 0.05, ** p < 0.01.
The clinical features of the two groups for the other variables are shown in Table 3. Lifetime alcohol use disorder was significantly associated with previous psychiatric hospitalization (RR = 2.68) and with a family history of alcohol use disorder in at least one first-degree relative (RR = 1.46). It was not associated with the other clinical variables that were considered.
Note: Statistical tests are analysis of variance except where indicated; LR = likelihood ratio chi-square test; HAM-A = Hamilton Anxiety Rating Scale; HAM-D = Hamilton Depression Rating Scale. Note that total cell sizes per group may differ due to missing data for some variables. * p < 0.05.
Participants with a lifetime history of alcohol use disorder did not differ significantly from those without such a history in terms of subsequent clinical improvement observed during the clinical trials, either using a self-report (GSAS) (F = 2.487, p = 0.115) or a clinician-rated outcome measure (PG-YBOCS) (F = 0.107, p = 0.743), a finding that differs from previous suggestions that outcomes are worse for people with current alcohol use disorder.Reference Hodgins and el-Guebaly 7 , Reference Lister, Milosevic and Ledgerwood 8
Discussion
This study explored baseline and prospective clinical outcome variables associated with lifetime alcohol use disorder in a relatively large sample (N = 621) of people with gambling disorder who participated in clinical trials. The nature of the trials meant that current or recent (past 3 months) alcohol use disorder was exclusionary, enabling us to measure associations with lifetime alcohol use disorder without confounding influences related to current/recent alcohol problems.
On one level, it is perhaps surprising that the overall rate of lifetime alcohol use disorder was 16.6% in the current sample and not higher. The observed rate is lower than the US National Epidemiologic Survey on Alcohol and Related Conditions, which reported lifetime and past-year prevalence rates of alcohol use disorder of 30.3% and 8.5% in the general population.Reference Hasin and Grant 26 This could represent differences in the measures used to quantify lifetime alcohol use disorder in the different samples. Another possibility is that the current data analysis excluded people with current/recent alcohol use disorder because this was part of the requirements to participate in one of the composite clinical trials, and so one would expect lower rates of lifetime use disorder than may otherwise be found in gambling disorder in general. Thus, the relevance of this work is not so much the absolute rate of lifetime alcohol use disorder (contrary to population surveys), but rather the associations between lifetime alcohol use disorder and other variables in people with gambling disorder.
It was found that lifetime alcohol use disorder was linked to significantly higher gambling-related legal problems as well as male gender, previous psychiatric hospitalization, and higher weight (average weight of 202 pounds in history of alcohol use disorder vs 190.1 pounds in those without such history). Overall, these findings may suggest a profile of “impulsivity” in explaining the link between lifetime alcohol use disorder and current gambling disorder. A prior meta-analysis found that impulsivity was a predisposing factor for gambling disorder.Reference Dowling, Merkouris, Greenwood, Oldenhof, Toumbourou and Youssef 4 A tendency toward unduly hasty or reward-seeking acts may predispose to both gambling disorder and lifetime alcohol use disorder. Although the trials occurred partly before the rise of the online gambling phenomenon, impulsivity can also be prominent in young men who gamble online,Reference Ioannidis and Bowden-Jones 27 which may render this specific gambling phenotype (highly impulsive men with lifetime alcohol use disorder) even more relevant in current times. Another complementary perspective is that our sample of people who had lifetime alcohol use disorder may fit (to a larger degree as compared to the “control” sample) with the “type 3” gambling subtype, per Blaszczynski’s model, which tends to be linked to greater male gender, impulsivity, and greater tendency toward gambling to alleviate stress (and/or to provide meaning in life).Reference Steel and Blaszczynski 28
The link between lifetime alcohol use disorder and a family history of alcohol use disorder in first-degree relatives is perhaps to be expected. Not only would family history contribute to genetic vulnerability toward alcohol use disorder, but it is also well established that environment and family norms are important determinants of addiction propensity. This finding highlights the clinical importance of considering first-degree family history not only of gambling but also other related conditions in patient evaluations.
Contrary to our expectation, across the clinical trials, there was no evidence that people with a lifetime history of alcohol use disorder differed from those without such a history, in terms of symptom improvement associated with clinical trial participation. From the bench-to-bedside perspective, these findings suggest that, overall, lifetime alcohol use disorder may not impede treatment response in the absence of current/recent alcohol use disorder. This is also in line with recent work on online gambling treatment discontinuation predictors.Reference Palomäki, Lind, Heiskanen and Castrén 29 Of course, it may be that future treatments could be tailored to better help those with a lifetime of alcohol use disorder taking into account their different clinical profiles. Thus, the broader implications for treatment approaches might be to focus on the underlying “impulsivity” (the specific outlines of how to define and operationalize that may require further research) in terms of both psychological and pharmacological treatments. This could mean seeing lifetime alcohol use disorder as a vulnerability marker for a range of behavioral issues and focusing treatment on the cognitive domain of impulsivity as a more targeted and cost-effective approach.
While this is one of the first studies to explore variables associated with lifetime alcohol use disorder in clinical trials for gambling disorder, several limitations should be considered. Findings may not generalize to other settings, such as people who never seek treatment for gambling disorder. This being an opportunistic analysis of pooled data from previously conducted clinical trials, we were not able to analyze all measures that may be relevant in understanding the link between lifetime alcohol use disorder and current gambling disorder. In future work, it would be useful to collect a broader range of variables such as self-report and cognitive measures of impulsivity and compulsivity, antisocial tendencies, and aspects of upbringing and family norms. This type of future research might allow for more specific biological or psychological treatment targets (rather than a potentially vague diagnosis of “lifetime alcohol use disorder”) and open new avenues of investigation that could be beneficial.
Finally, this being a cross-sectional dataset, we cannot infer causality or directionality of effect.
Conclusions
In conclusion, clinical trials on participants with gambling disorder revealed that a lifetime history of alcohol use disorder was associated with male gender, greater gambling-related legal problems, higher previous psychiatric hospitalization, higher weight, and family history of alcohol use disorder in first-degree relative(s). Thus, even if patients do not have a current alcohol use problem, it is clinically relevant and important to inquire about lifetime problems since this can influence the clinical profile. At the same time, we did not find any evidence that lifetime alcohol use disorder was linked to worse outcomes from clinical trials, in terms of improvement in gambling symptom severity.
Author contribution
Conceptualization: K.I., S.R.C., J.E.G.; Formal analysis: K.I.; Investigation: K.I., S.R.C., J.E.G.; Methodology: K.I., S.R.C., J.E.G.; Writing – original draft: K.I., S.R.C., J.E.G.; Writing – review & editing: K.I., S.R.C., J.E.G.; Data curation: J.E.G.; Funding acquisition: J.E.G.; Project administration: J.E.G.
Financial support
There was no funding for this study.
Competing interest
Dr. Grant has received research grant support from NIDA, Janssen, and Biohaven Pharmaceuticals. He receives yearly compensation from Springer Publishing for acting as Editor-in-Chief of the Journal of Gambling Studies and has received royalties from Oxford University Press, American Psychiatric Publishing, Inc., Norton Press, and McGraw Hill. Dr. Ioannidis receives honoraria from Elsevier for editorial work. Dr. Chamberlain’s work is funded by the NHS. He receives honoraria from Elsevier for associate editor work.