Examining Lurasidone Efficacy in Patients with Schizophrenia Spectrum Illness and Concurrent Alcohol and Substance Use Disorder: A Prospective, Multicentric, Real-World Investigation

Author:

Cavallotto Clara1ORCID,Chiappini Stefania2ORCID,Mosca Alessio1ORCID,d’Andrea Giacomo1ORCID,Di Carlo Francesco1ORCID,Piro Tommaso1,Susini Ottavia1,Stefanelli Giulia1,Di Cesare Andrea3,Ricci Valerio4ORCID,Pepe Maria5,Dattoli Luigi1,Di Nicola Marco5ORCID,Pettorruso Mauro1ORCID,Martinotti Giovanni1ORCID

Affiliation:

1. Department of Neurosciences, Imaging and Clinical Sciences, “G. D’Annunzio” University, 66100 Chieti, Italy

2. School of Medicine, UniCamillus International Medical School University, 00131 Rome, Italy

3. Department of Mental Health, ASL 02 Lanciano-Vasto-Chieti, 66100 Chieti, Italy

4. Department of Psychiatry, “San Luigi Gonzaga” Hospital, University of Turin, 10124 Turin, Italy

5. University Policlinic Foundation “A. Gemelli” IRCSS-Catholic University of the Sacred Heart, Largo Agostino Gemelli, 8, 00136 Rome, Italy

Abstract

Background: Dual disorders (DD) entail the coexistence of a substance use disorder (SUD) and another mental health condition, often within psychotic and affective disorders. This study aims to evaluate lurasidone, an innovative atypical antipsychotic, in individuals diagnosed with schizophrenia spectrum disorder and concurrent comorbidities of alcohol use disorder/substance use disorder (AUD/SUD). Methods: A cohort of 23 subjects diagnosed with schizophrenia spectrum disorder and comorbid AUD/SUD underwent psychometric assessments at baseline (T0) and one-month (T1) post-lurasidone initiation. Results: Lurasidone exhibited significant reductions in psychopathological burden, evidenced by decreased total PANSS scores (Z = 2.574, p = 0.011). Positive symptoms, substance craving (VAS Craving; Z = 3.202, p = 0.001), and aggressivity (MOAS scale; Z = 2.000, p = 0.050) were notably reduced. Clinical Global Impression (CGI) scores significantly improved (Z = 2.934, p = 0.003). Quality of life enhancements were observed in SF-36 subscales (energy, emotional well-being, and social functioning) (p < 0.05) and Q-LES-Q-SF scale (Z = −2.341, p = 0.021). A safety analysis indicated lurasidone’s good tolerability, with only 8.7% reporting discontinuation due to side effects. Conclusions: This study offers initial evidence supporting lurasidone’s efficacy and safety in dual diagnoses, highlighting positive effects on psychopathology, substance craving, and quality of life. These findings emphasize the need for tailored, comprehensive treatment strategies in managing the complexities of this patient population.

Publisher

MDPI AG

Reference67 articles.

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3. Atypical Antipsychotic Drugs in Dual Disorders: Current Evidence for Clinical Practice;Martinotti;Curr. Pharm. Des.,2022

4. EMCDDA (2023). European Drug Report 2023: Trends and Developments.

5. Bahji, A. (2024). Navigating the Complex Intersection of Substance Use and Psychiatric Disorders: A Comprehensive Review. J. Clin. Med., 13.

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