Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

Treatment with aripiprazole once-monthly injectable formulation is effective in improving symptoms and global functioning in schizophrenia with and without comorbid substance use – a post hoc analysis of the ReLiAM study

BMC Psychiatry volume 22, Article number: 773 (2022) Cite this article

Abstract

Background

ReLiAM, Real-Life Assessment of Abilify Maintena, was the first reported long-term prospective non-interventional study for patients with schizophrenia treated with aripiprazole once-monthly injectable formulation (AOM) under real-life conditions. ReLiAM’s primary aim was to evaluate the evolution of global functional status in patients treated with AOM for 12 months in Canada.

Methods

The objective of this post hoc analysis of the ReLiAM study is to investigate the treatment effects of real-life use of AOM over a 1-year period in the subgroup of patients with reported substance use compared with patients without substance use.

Results

The results of this post hoc analysis demonstrate that treatment with AOM for 12 months in patients with schizophrenia was comparably effective in improving global functioning in subgroups of patients with and without concomitant substance use.

Conclusions

These results support the use of AOM for the treatment of schizophrenia in patients with or without concomitant substance use.

Trial registration

ClinicalTrials.gov NCT02131415, first posted on May 6, 2014. Overall trial status: Terminated.

Peer Review reports

Background

Psychoactive substances are frequently used and often abused by patients with schizophrenia [1]. The incidence of substance use disorder (SUD) in patients with schizophrenia is high compared to the average rates of SUD in the general adult population [2]. Nearly half of patients with schizophrenia will develop a SUD in their lifetime, with the most frequently used substances being alcohol and cannabis, at approximately three times the rate of people without schizophrenia [3]. In a study of individuals with severe psychotic disorders, the risk of heavy alcohol use was four times greater compared to the general population [4]. A recent meta-analysis of patients with schizophrenia found a lifetime prevalence of alcohol and cannabis use of 24.3% and 26.2%, respectively [5]. Margolese et al. (2006) reported alcohol (35.6%) and cannabis (35.1%) as the most common primary substances of abuse in a 12-month prospective study of patients with comorbid schizophrenia-spectrum disorders and substance abuse [6]. Data suggest that genetic predisposition to schizophrenia is associated with substance use patterns later in life. In a prospective study, schizophrenia vulnerability was associated with stronger cannabis use during adolescence (age 16–20 years) [7], and previous reports on individuals at genetic risk for developing schizophrenia suggest that cannabis use is an independent risk factor for psychosis [8,9,10]. Ultimately, the co-occurrence of schizophrenia and SUD is associated with poorer clinical outcomes due to increased symptom severity, psychosocial instability, and treatment non-adherence [3].

The impact of treatment with oral aripiprazole in patients with schizophrenia and comorbid alcohol, cannabis, and stimulant use has been documented [11,12,13]. A switch from oral to long-acting injectable (LAI) antipsychotic medication is a common strategy to overcome non-adherence in patients with schizophrenia [14, 15]. Recent studies looked at the effect of LAI second-generation antipsychotic medications in various populations with comorbid substance use. Patients with schizophrenia and alcohol use disorder treated with LAI versus oral risperidone had significantly fewer heavy drinking days over time and fewer drinking days per week [16]. Furthermore, patients who took the LAI formulation had better overall treatment adherence. In patients with first-episode psychosis and SUD, a Canadian study found that first-line treatment with LAI compared to oral antipsychotics resulted in a significantly lower relapse rate (67.7% vs. 76.7%) and longer relapse-free survival time (694 vs. 447 days), as well as trends for reduced re-hospitalization rates (48.4% vs. 57.3%) and hospitalization-free survival time (813 vs. 619 days) [17].

ReLiAM, Real-Life Assessment of Abilify Maintena, was the first reported long-term prospective non-interventional study for patients with schizophrenia treated with aripiprazole once-monthly injectable formulation (AOM) under real-life conditions [18]. The primary aim of the ReLiAM study was to evaluate the evolution of global functional status in patients treated with AOM for 12 months in Canada. The primary and secondary outcome measures of global, social, and occupational functioning showed significant improvements with progress from serious to mild impairment in patients with schizophrenia treated with AOM over 1 year. In addition, the severity of illness was significantly reduced. Given the naturalistic design of the ReLiAM study, a subpopulation of patients enrolled had reported substance use. The objective of this post hoc analysis is to investigate the treatment effects of real-life use of AOM over a 1-year period in the subgroup of patients with reported substance use compared to patients without substance use.

Method

Design

This is a post hoc analysis of data from the ReLiAM study. The design of the ReLiAM study, which was a naturalistic, non-interventional, prospective cohort study, was previously described [18]. Briefly, the primary outcome of global functioning was assessed with the Global Assessment of Functioning Scale (GAF) at 3-month intervals for 1 year. The Social and Occupational Functioning Scale (SOFAS), the Clinical Global Impression-Severity Scale (CGI-S), and the Brief Psychiatric Rating Scale (BPRS) were used as secondary outcome measures. Adverse drug reactions (ADR) were also collected. This manuscript adheres to CONSORT guidelines.

Study participants

Patients were recruited to the ReLiAM study from 17 Canadian community- or hospital-based clinical settings, selected as a representative sample of practice of Canadian psychiatrists who treat patients with schizophrenia spectrum disorders [18]. One hundred and ninety-nine patients were enrolled in the study according to the following inclusion and exclusion criteria:

  • Inclusion criteria: Patients diagnosed with schizophrenia, at least mildly ill (CGI-S score of ≥ 3), age 18 years (19 for patients from British Columbia) or older, fluent in English and/or French, able to provide informed consent, and for whom the treating psychiatrist had decided, prior to and independently of enrolment in the study, to prescribe AOM for the treatment of schizophrenia.

  • Exclusion criteria: Patients who did not comprehend the informed consent, had contraindications to the use of AOM as specified in the Canadian Product Monograph, had previously received one or more doses of AOM, presented a significant suicidal risk as judged by the investigator, or pregnant or lactating females.

Of those 199 patients who met eligibility criteria, 30 were not included in the analyses due to missing information (1) or the lack of post-baseline assessment (29). Thus, 169 patients constituted the primary analysis population of the ReLiAM study. All patients that received at least 1 dose of AOM were included in the safety assessments.

This post hoc analysis reports on changes in primary and secondary outcomes for patients in the ReLiAM study who reported at baseline reported substance use at baseline compared to those who had reported no use. Substance users were defined as patients who, at the baseline visit, reported substance use in the previous 30 days. Non-users were patients who, at the baseline visit, reported no substance use in the previous 30 days. Substance use was based solely on self-report, and any use prior to the 30 days immediately preceding study enrollment was not captured. Heavy alcohol use was defined as ≥7 drinks per week for women and ≥14 drinks per week for men, reported at baseline. Non-heavy users of alcohol included non-users of alcohol. Heavy cannabis use referred to ≥7 marijuana cigarettes per week, reported at baseline, and non-heavy users of cannabis included non-users of cannabis.

Statistical analysis

Descriptive statistics were produced for all study variables including the mean and standard deviation (SD) for continuous scale variables and frequency distributions for categorical scale variables. All statistical tests were 2-sided and a p-value of 0.05 or less was considered significant.

Results

At baseline, 116 (68.6%) of the 169 eligible patients were active substance users (Table 1). The majority of substance users were male (77.6%). Substances reported by users included nicotine, alcohol, cannabis, and other substances (Table 2). Seventy-four (43.8%) patients used alcohol and 35 patients (20.7%) used cannabis at baseline. In patients who were users of the respective substances at baseline, there was no significant change in reported use of the substance during treatment with AOM.

Table 1 Baseline Demographics by Use of Any Substance (yes vs. no) primary analysis set
Full size table
Table 2 Substances Reported by Substance Users
Full size table

Primary outcome: GAF

Overall, improvements in GAF scores after AOM treatment for 12 months were not significantly different between users and non-users of substances, nor between groups of heavy users and non-users. The absolute increase in GAF scores from baseline to 12 months was 12.4 in users of any substances. This was not significantly different from the change in GAF scores observed in non-users of any substances (12.1 change from baseline to 12 months, P = 0.939) (Fig. 1A). More specifically, there was no difference in the absolute change in GAF scores from baseline to 12 months between alcohol users and non-users (12.3 vs. 12.3, P = 0.988) (Fig. 1B). Cannabis users had a global functioning score improvement of 14.3 from baseline to 12 months, which was not statistically different from non-users of cannabis (11.9, P = 0.543) (Fig. 1C).

Fig. 1
figure 1

Absolute Change from Baseline in Global Assessment of Functioning Scale (GAF) over Time in Substance Users and Non-Users. A Patients reporting any substance use at baseline. B Patients reporting alcohol use at baseline. C Patients reporting cannabis use at baseline

Full size image

Although the number of patients in the subgroups were limited, differences in the absolute change in GAF scores over 12 months were similar in both heavy cannabis users and non-heavy cannabis users (absolute change in GAF score from baseline to 12 months: 18.9 vs. 11.8, P = 0.222) (Supplemental Fig. 1A). Similar results were observed in heavy alcohol drinkers vs. non-heavy alcohol drinkers, even when considering baseline alcohol users only (absolute change in GAF score from baseline to 12 months: 15.0 vs. 12.1, P = 0.641) (Supplemental Fig 1B).

Secondary outcomes: SOFAS, CGI-S, BPRS

After AOM treatment for 12 months, there were no statistically significant differences in improvements in social and occupational functioning assessment scale (SOFAS) scores between users and non-users of any substance (respective mean changes from baseline in SOFAS scores were 9.8 vs. 11.9; P = 0.424) (Fig. 2A). Although a significant difference between alcohol users and non-users was observed at 3 months (3.7 vs. 9.7; P = 0.001), there was no difference in the mean change in SOFAS scores from baseline to 12 months between alcohol users and non-users (8.6 vs. 11.9, P = 0.159) (Fig. 2B). Amongst cannabis users and non-users at 12 months, there was no difference in change from baseline SOFAS scores (12.3 vs. 10.2, P = 0.501) (Fig. 2C).

Fig. 2
figure 2

Change in Social and Occupational Functioning Assessment Scale (SOFAS) over Time in Substance Users and Non-Users. A Patients reporting any substance use at baseline. B Patients reporting alcohol use at baseline. C Patients reporting cannabis use at baseline

Full size image

Similarly, CGI-S scores showed no difference in mean change from baseline to 12 months between users and non-users of any substance (-0.9 vs. -0.9, P = 0.9127) (Fig. 3A). There was also no significant difference in the mean change in CGI-S scores from baseline to 12 months between users and non-users of alcohol (-1.0 vs. -0.9, P = 0.6144) (Fig. 3B), or between users and non-users of cannabis (-1.1 vs. -0.9, P = 0.4655) (Fig. 3C).

Fig. 3
figure 3

Change in Clinical Global Impression Scale – Severity (CGI-S) over Time in Substance Users and Non-Users. A Patients reporting any substance use at baseline. B Patients reporting alcohol use at baseline. C Patients reporting cannabis use at baseline

Full size image

Decrease from baseline in BPRS total scores after AOM treatment for 12 months showed no significant difference between users and non-users of any substances (-9.9 vs. -11.6, P = 0.441) (Fig. 4A), between alcohol users and non-users (-10.5 vs. -10.4, P = 0.967) (Fig. 4B), or between cannabis users and non-users (11.7 vs. -10.2, P = 0.578) (Fig. 4C).

Fig. 4
figure 4

Change in Brief Psychiatric Rating Scale (BPRS) – Total Score over Time in Substance Users and Non-Users. A Patients reporting any substance use at baseline. B Patients reporting alcohol use at baseline. C Patients reporting cannabis use at baseline

Full size image

Adverse drug reactions

A total of 198 patients were evaluated in the safety analysis. Adverse drug reactions were primarily non-serious and mild and have been reported in detail in the primary publication [18]. However, in this post hoc analysis, the rate of occurrence of adverse events was notably higher amongst substance users vs. non-users (48.5% vs. 19.7%). This pattern was reflected across all safety parameters examined (Fig 5).

Fig. 5
figure 5

Adverse Drug Reactions by Substance Users and Non-Users

Full size image

Discussion

The results of this post hoc analysis of a real-world prospective cohort study show that treatment of schizophrenia with AOM for 12 months is as effective at improving global functioning in patients with concomitant substance use as in those without. Both groups demonstrated similar and significant improvements. It is important to make the distinction between patients in many studies cited herein who had formal diagnoses of SUD based on standardized criteria, and the patients in this post hoc analysis who simply self-reported use or non-use of substances.

Previous studies have reported on the impact of treatment with AOM in patients with psychosis and SUD. In a head-to-head comparison of AOM versus paliperidone LAI, quality of life and substance craving indicators improved in both groups, with greater effect in those treated with AOM [14]. More recently, a retrospective study by Szerman et al. (2020) reported on the efficacy and impact of AOM in patients with schizophrenia and comorbid substance use disorders [19]. The results showed that AOM reduced disease severity scores by >30% and significantly improved daily functioning in these patients. In this post hoc analysis, treatment with AOM also significantly improved outcomes in patients with reported substance use.

There are a few potential implications of the results of this post hoc analysis. A wide range of studies have demonstrated the association between substance use and poor medication adherence in patients with schizophrenia, leading to treatment discontinuation and relapse [20,21,22]. A systematic review of factors influencing medication adherence in individuals with schizophrenia identified substance abuse as a key driver of non-adherence [23]. In a Canadian cross-sectional survey of 207 psychiatric outpatients, those with a psychotic disorder and current substance use were more likely to be medication non-compliant than those with a single diagnosis of psychotic disorder (27.6% vs. 4.5%) [1]. LAI antipsychotic medications reduce adherence demands compared with daily oral antipsychotics and are a recommended treatment option for non-adherent patients [24]. A study of adherence with oral versus LAI antipsychotics in patients with early psychosis showed a significantly higher proportion of days with medication in the LAI formulation group than in those treated with oral antipsychotics (76% vs. 32%) [25]. This is important because effective early treatment with antipsychotic medication decreases relapse risk, leading to better outcomes [26]. A two-year cluster randomized clinical study showed that administration of a LAI medication (AOM) was associated with a delayed time to hospitalization [27]. Evidence from a systematic literature review supports the assertion that LAI antipsychotics are associated with enhanced adherence and reduced relapse rates, but the small number of available studies necessitate cautious interpretation of this result [28]. Real-world data of patients with schizophrenia showed significantly better medication adherence (33.9% vs. 25.5%) in patients receiving LAI antipsychotics compared to oral antipsychotic users [9]. The LAI group was also 20% less likely to discontinue their medication during the entire follow-up period [29]. In another real-world study comparing AOM with oral antipsychotics in patients with schizophrenia, individuals treated with AOM had significantly greater medication adherence and significantly longer time to treatment discontinuation [30]. In this post hoc analysis of patients with schizophrenia and concomitant substance use, we hypothesize that the LAI formulation appears to provide a key additional benefit in this patient population, reducing instability of treatment adherence related to substance use and leading to better outcomes. Furthermore, in real-life settings, lack of adherence to an injectable medication is more easily monitored by the healthcare team, resulting in timely interventions.

The results of this post hoc analysis also suggest potential benefits for illness severity and functional status, in that improved treatment adherence reduces the risk of relapse [23, 31, 32], thus improving the lifetime trajectory of schizophrenia. Generally, patients with schizophrenia and SUD have a higher rate of relapse due to poor adherence to treatment. Relapses disrupt remission and interfere with recovery. They are associated with re-hospitalization, treatment resistance, and loss of gains in function [33]. Subsequent episodes of relapse in a patient’s lifetime may render recovery more difficult due to disease progression and treatment refractoriness [34]. This is meaningful to clinicians because effective management of schizophrenia requires continuous long-term treatment. Therefore, treatment options that improve adherence should be prioritized regardless of whether patients will continue to use substances abuse or not. In addition, LAI’s have been shown to have small peak-to-trough fluctuations in drug levels which may increase their tolerability compared to oral therapeutics [35]. An increase in tolerability may in turn affect treatment adherence.

Finally, the observed lack of difference in global functioning between schizophrenia substance users and non-users may also reflect the level of patient deficits. Patients with schizophrenia who are also substance users may have fewer negative symptoms of schizophrenia, more social contacts, and better social-leisure functioning [36]. A meta-analysis highlighted the importance of intermediate factors such as the preferred substance used in understanding the contradictory cognitive capacities among substance-abusing patients with schizophrenia [37]. For example, preferential use of cannabis, as opposed to alcohol, by patients with schizophrenia and SUD was associated with higher scores for problem solving and reasoning, and visual memory. These cognitive features in patients with dual diagnosis may affect their capacity to be more structured and capable of the necessary socialization to go out to procure and use their substance.

Limitations

Limitations related to the design of the ReLiAM study were previously described [18]. Although real-world evidence is more aligned with daily clinical practice than randomized clinical trials, its interpretation poses challenges related to the lack of a control group, potential selection bias, and data quality management. While this post hoc analysis informs on outcomes related to the subgroup of substance users that were not captured by the primary analysis, these results are also subject to limitations inherent in post hoc analyses. Possible interpretations are mostly limited to users of alcohol and cannabis, as the number of patients using other substances was too low to make any meaningful comparisons. Finally, data could not be analyzed beyond 12 months of treatment due to the 12-month study duration of the original ReLiAM study.

Conclusion

This post hoc analysis of the real-world ReLiAM study demonstrates that treatment with AOM for 12 months in patients with schizophrenia was effective in improving global functioning in subgroups of patients with and without concomitant substance use. A lack of significant differences between substance users and non-users was also evident through multiple secondary endpoints measuring function and disease severity. Adverse events occurred more frequently in substance users vs. non-users; however, these were primarily non-serious and mild. These results support the use of AOM for the treatment of schizophrenia in patients with or without concomitant substance use. In light of evidence demonstrating improved adherence with AOM versus oral treatment in patients with comorbid schizophrenia and substance use, the AOM treatment paradigm may be particularly beneficial for this group of patients.

Availability of data and materials

For ethical reasons, to ensure the privacy of the patient-level data utilized in the current study, and for reasons related to data ownership by the sponsor, data cannot be made available. However, data could be made available upon request for the purpose of conducting meta-analytic review in future.

Abbreviations

ADR:

Adverse Drug Reactions

AOM:

Aripiprazole Once-monthly Injectable Formulation

BRPS:

Brief Psychiatric Rating Scale

CGI-S:

Clinical Global Impression Severity

GAF:

Global Assessment of Functioning Scale

LAI:

Long-Acting Injectable

ReLiAM:

Real-Life Assessment of Abilify Maintena

SD:

Standard Deviation

SOFAS:

Social and Occupational Functioning Assessment Scale

SUD:

Substance Use Disorder

References

  1. Margolese HC, Malchy L, Negrete JC, et al. Drug and alcohol use among patients with schizophrenia and related psychoses: levels and consequences. Schizophr Res. 2004;67(2–3):157-166.g.

    Article  Google Scholar 

  2. Volkow ND. Substance use disorders in schizophrenia – clinical implications of comorbidity. Schizophr Bull. 2009;35(3):469–72.

    Article  Google Scholar 

  3. Green AI, Drake RE, Brunette MF, et al. Schizophrenia and co-occurring substance abuse disorder. Am J Psychiatry. 2007;164(3):402–8.

    Article  Google Scholar 

  4. Hartz SM, Pato CN, Medeiros H, et al. Comorbidity of severe psychotic disorders with measures of substance use. JAMA Psychiat. 2014;71(3):248–54.

    Article  Google Scholar 

  5. Hunt GE, Large MM, Cleary M, et al. Prevalence of comorbid substance use in schizophrenia spectrum disorders in community and clinical settings, 1990–2017: systematic review and meta-analysis. Drug Alcohol Depend. 2018;191:234–58.

    Article  Google Scholar 

  6. Margolese HC, Negrete JC, Temmpier R, et al. A 12-month prospective follow-up study of patients with schizophrenia-spectrum disorders and substance abuse: changes in psychiatric symptoms and substance use. Schizophr Res. 2006;83(1):65–75.

    Article  Google Scholar 

  7. Hiemstra M, Nelemans S, Branje S, et al. Genetic vulnerability to schizophrenia is associated with cannabis use patterns during adolescence. Drug Alcohol Depend. 2018;190:143–50.

    Article  Google Scholar 

  8. Semple DM, McIntosh A, Lawrie SM. Cannabis as a risk factor for psychosis: systematic review. J Psychopharmacol. 2005;19(2):187–94.

    Article  Google Scholar 

  9. Moore THM, Zammit S, Lingford-Hughes A, et al. Cannabis use and risk of psychotic or affective mental health outcomes: a systematic review. Lancet. 2007;370(9584):319–28.

    Article  Google Scholar 

  10. Barnes TRE, Mutsatsa SH, Hutton SB, et al. Comorbid substance use and age at onset of schizophrenia. Br J Psychiatry. 2006;188:237–42.

    Article  Google Scholar 

  11. Warsi M, Sattar SP, Bhatia SC, Petty F. Aripiprazole reduces alcohol use. Can J Psychiatry. 2005;50(4):244.

    Article  Google Scholar 

  12. Beresford TP, Clapp L, Martin B, et al. Aripiprazole in schizophrenia with cocaine dependence: a pilot study. J Clin Psychopharmacol. 2005;25(4):363–6.

    Article  CAS  Google Scholar 

  13. Desseilles M, Mathot F, Desseilles M. Aripiprazole diminishes cannabis use in schizophrenia. J Neuropsychiatry Clin Neurosci. 2008;20(1):117–8.

    Article  Google Scholar 

  14. Cuomo I, Kotzalidis GD, de Persis S, et al. Head-to-head comparison of 1-year aripiprazole long-acting injectable (LAI) versus paliperidone LAI in comorbid psychosis and substance use disorder: impact on clinical status, substance craving, and quality of life. Neuropsychiatr Dis Treat. 2018;14:1645–56.

    Article  CAS  Google Scholar 

  15. Haddad PM, Brain C, Scott J. Non-adherence with antipsychotic medication in schizophrenia: challenges and management strategies. Patients Relat Outcome Meas. 2014;5:43–62.

    Article  Google Scholar 

  16. Green AI, Brunette MF, Dawson D, et al. Long-acting injectable vs. oral risperidone for schizophrenia and co-occurring alcohol use disorder: a randomized trial. J Clin Psychiatry. 2015;76(10):1359–65.

    Article  Google Scholar 

  17. Abdel-Baki A, Thibault D, Medrano S, et al. Long-acting antipsychotic medication as first-line treatment of first-episode psychosis with comorbid substance use disorder. Early Interv Psychiatry. 2020;14(1):69–79.

    Article  Google Scholar 

  18. Mustafa S, Bougie J, Miguelez M, et al. Real-life assessment of aripiprazole monthly (Abilify Maintena) in schizophrenia: a Canadian naturalistic non-interventional prospective cohort study. BMC Psychiatry. 2019;19:114. https://doi.org/10.1186/s12888-019-2103-x.

    Article  CAS  Google Scholar 

  19. Szerman N, Basurte-Villamor I, Vega P, et al. Once-monthly long-acting injectable aripiprazole for the treatment of patients with schizophrenia and co-occurring substance use disorders: a multicentre, observational study. Drugs - Real World Outcomes. 2020;7:75–83.

    Article  Google Scholar 

  20. Colizzi M, Carra E, Fraietta S, et al. Substance use, medication adherence and outcome one year following a first episode of psychosis. Schizophr Res. 2016;170(2–3):311–7.

    Article  Google Scholar 

  21. Perkins DO, Hongbin G, Weiden PJ, et al. Predictors of treatment discontinuation and medication nonadherence in patients recovering from a first episode of schizophrenia, schizophreniform disorder, or schizoaffective disorder: a randomized, double-blind, flexible-dose multicenter study. J Clin Psychiatry. 2008;69(1):106.

    Article  CAS  Google Scholar 

  22. Weiss KA, Smith TE, Hull JW, et al. Predictors of nonadherence in outpatients with schizophrenia and other psychotic disorders. Schizophr Bull. 2002;28(2):341–9.

    Article  Google Scholar 

  23. Higashi K, Medic G, Littlewood K, et al. Medication adherence in schizophrenia: factors influencing adherence and consequences of nonadherence, a systematic literature review. Ther Adv Psychopharmacol. 2013;3(4):200–18.

    Article  Google Scholar 

  24. Marcus SC, Zummo J, Pettit AR, et al. Antipsychotic adherence and rehospitalization in schizophrenia patients receiving oral versus long-acting injectable antipsychotics following hospital discharge. J Manag Care Spec Pharm. 2015;21(9):754–69.

    Google Scholar 

  25. Titus-Lay EN, Ansara ED, Isaacs AN, et al. Evaluation of adherence and persistence with oral versus long-acting injectable antipsychotics in patients with early psychosis. Mental Health Clinician. 2018;8(2):56–62.

    Article  Google Scholar 

  26. McGorry PD. Early intervention in psychotic disorders: beyond debate to solving problems. Br J Psychiatry. 2005;187(S48):S108–10.

    Article  Google Scholar 

  27. Kane JM. Effect of long-acting injectable antipsychotics vs usual care on time to first hospitalization n early-phase schizophrenia: A randomized clinical trial. JAMA Psychiat. 2020;77(12):1217–24.

    Article  Google Scholar 

  28. Coles A, Knezevic D, George TP, et al. Long-acting injectable antipsychotic treatment in schizophrenia and co-occurring substance use disorders: a systematic review. Front Psychiatry. 2021;12:808002. https://doi.org/10.3389/fpsyt.2021.808002.

    Article  Google Scholar 

  29. Greene M, Yan T, Chang E, et al. Medication adherence and discontinuation of long-acting injectable versus oral antipsychotics in patients with schizophrenia or bipolar disorder. J Med Econ. 2018;21(2):127–34.

    Article  Google Scholar 

  30. Yan T, Greene M, Chang E, et al. Medication adherence and discontinuation of aripiprazole once monthly 400 mg (AOM 400) versus oral antipsychotics in patients with schizophrenia or bipolar I disorder: a real-world study using US claims data. Adv Ther. 2018;35:1612–25.

    Article  CAS  Google Scholar 

  31. Alvarez-Jimenez M, Priede A, Hetrick SE, et al. Risk factors for relapse following treatment for first episode psychosis: a systematic review and meta-analysis of longitudinal studies. Schizophr Res. 2012;139(1–3):116–28.

    Article  CAS  Google Scholar 

  32. Lindenmayer JP, Liu-Seifert H, Kulkarni PM, et al. Medication nonadherence and treatment outcome in patients with schizophrenia or schizoaffective disorder with suboptimal prior response. J Clin Psychiatry. 2009;70(7):990–6.

    Article  CAS  Google Scholar 

  33. Kane JM. Improving patient outcomes in schizophrenia: Achieving remission, preventing relapse, and measuring success. J Clin Psychiatry. 2013;74(9):e18.

    Article  Google Scholar 

  34. Emsley R, Chiliza B, Asmal L. The evidence for illness progression after relapse in schizophrenia. Schizophr Res. 2013;148(1–3):117–21.

    Article  Google Scholar 

  35. Sheehan JJ, Reilly KR, Fu DJ, Alphs L. Comparison of the peak-to-trough fluctuation in plasma concentration of long-acting injectable antipsychotics and their oral equivalents. Innov Clin Neurosci. 2012;9(7–8):17–23.

    Google Scholar 

  36. Salyers MP, Mueser KT. Social functioning, psychopathology, and medication side effects in relation to substance use and abuse in schizophrenia. Schizophr Res. 2001;48(1):109–23.

    Article  CAS  Google Scholar 

  37. Potvin S, Joyal C, Pelletier J, et al. Contradictory cognitive capacities among substance-abusing patients with schizophrenia: a meta-analysis. Schizophr Res. 2008;100(1–3):242–51.

    Article  Google Scholar 

Download references

Acknowledgements

We would like to thank Dr. Oloruntoba Oluboka (University of Calgary) and Dr. Ofer Agid (University of Toronto) who provided consultation and advice on the design of the ReLiAM study. We would also like to thank the following principal investigators at the participating sites: Dr. Ranjith Chandrasena, Dr. Leandro Cortese, Dr. Lois Ligate, Dr. Marc André Roy, Dr. Heather Milliken, Dr. Alexander McIntyre, Dr. Jean-Pierre Melun, Dr. Rebecca Carriere, Dr. Adekunle Garba Ahmed, Dr. Thomas Raedler, Dr. Rajendra Harricharan, Dr. Roumen Milev, Dr. Ridha Joober, Dr. Sunny Johnson, Dr. Soma Ganesan, Dr. Ashok Malla, and Dr. Jean-François de La Sablionnière. We would also like to thank Kataka Medical Communication for medical writing, editorial and administrative assistance.

Funding

The ReliAM study was sponsored and funded by Otsuka Canada Pharmaceutical Inc and Lundbeck Canada Inc. Both organizations were involved in developing the study protocol, the collection, analysis, and interpretation of data and the review and approval of the manuscript.

Dr. Howard Margolese has received research grant support from AIFred, SyneuRx and the Montreal General Hospital Foundation; speaker/consultation fees from Abbvie, HLS Therapeutics, Lundbeck, Janssen, Otsuka, Sunovion and Teva. No stocks or employment.

Francois Therrien and Matthieu Boucher are full-time employees of Otsuka Canada Pharmaceutical Inc. Guerline Clerzius is a former full-time employee at Lundbeck Canada Inc.

Author information

Authors and Affiliations

  1. Schizophrenia Program, McGill University Health Centre, Montreal, QC, Canada

    Howard C. Margolese

  2. Department of Psychiatry, McGill University, Montreal, QC, Canada

    Howard C. Margolese

  3. MUHC, Allan Memorial Institute, 1025 Pine Ave W, Montreal, QC, H3A 1A1, Canada

    Howard C. Margolese

  4. Medical Affairs, Otsuka Canada Pharmaceutical Inc, St-Laurent, QC, Canada

    Matthieu Boucher & Francois Therrien

  5. Department of Pharmacology and Therapeutics, Faculty of Medicine and Health Sciences, McGill University, Montreal, QC, Canada

    Matthieu Boucher

  6. Lundbeck Canada Inc., St-Laurent, QC, Canada

    Guerline Clerzius

Authors
  1. Howard C. Margolese
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Matthieu Boucher
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Francois Therrien
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Guerline Clerzius
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

HCM, MB, FT and GC contributed to the interpretation of data provided through revisions to the manuscript at all stages. All authors approved the final manuscript.

Corresponding author

Correspondence to Howard C. Margolese.

Ethics declarations

Ethics approval and consent to participate

All patients signed an informed consent form before any study related procedures were performed for the ReLiAM study. Central Ethics approval was obtained from IRB Services, Aurora, Ontario, Canada. In addition, approval from local institutional ethics boards (University of Windsor, McGill University Health Centre, Institut Universitaire en Sante Mentale de Quebec, Capital Health, Ottawa Health Science Network, Royal Ottawa Health Care Group, University of Calgary, Western University, Queen’s University, Douglas Mental Health Institute, University of British Columbia) was obtained as required.

Consent for publication

Not applicable.

Competing interests

HCM has received research/grant support from the Montreal General Hospital Foundation, Aifred health, Lundbeck, Otsuka and SyneuRx; and has received honoraria as a paid speaker and/or consultant for AbbVie, HLS Therapeutics, Janssen, Lundbeck, Otsuka, Sunovion and Teva. MB is a full-time employee of Otsuka Canada Pharmaceutical Inc. and affiliate member of the Department of Pharmacology & Therapeutics, Faculty of Medicine and Health Sciences at McGill University, Montreal, Canada.

FT is a full-time employee of Otsuka Canada Pharmaceutical Inc.

GC was a full-time employee of Lundbeck Canada Inc at the time of this analysis.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Supplemental Figure 1.

Absolute Change from Baseline in Global Assessment of Functioning Scale GAF over Time in Heavy Substance Users and Non-Users of Substances. (A) Patients reporting heavy cannabis use at baseline. (B) Patients reporting heavy alcohol use at baseline.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Margolese, H.C., Boucher, M., Therrien, F. et al. Treatment with aripiprazole once-monthly injectable formulation is effective in improving symptoms and global functioning in schizophrenia with and without comorbid substance use – a post hoc analysis of the ReLiAM study. BMC Psychiatry 22, 773 (2022). https://doi.org/10.1186/s12888-022-04397-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12888-022-04397-x

Keywords

BMC Psychiatry

ISSN: 1471-244X

Contact us