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Tolerability of vortioxetine compared to selective serotonin reuptake inhibitors in older adults with major depressive disorder (VESPA): a randomised, assessor-blinded and statistician-blinded, multicentre, superiority trial.
Ostuzzi, Giovanni; Gastaldon, Chiara; Tettamanti, Mauro; Cartabia, Massimo; Monti, Igor; Aguglia, Andrea; Aguglia, Eugenio; Bartoli, Francesco; Callegari, Camilla; Canozzi, Andrea; Carbone, Elvira Anna; Carrà, Giuseppe; Caruso, Rosangela; Cavallotti, Simone; Chiappini, Stefania; Colasante, Fabrizio; Compri, Beatrice; D'Agostino, Armando; De Fazio, Pasquale; de Filippis, Renato; Gari, Matteo; Ielmini, Marta; Ingrosso, Gianmarco; Mammarella, Silvia; Martinotti, Giovanni; Rodolico, Alessandro; Roncone, Rita; Sterzi, Enrico; Tarsitani, Lorenzo; Tiberto, Elisa; Todini, Liliana; Amaddeo, Francesco; D'Avanzo, Barbara; Barbato, Angelo; Barbui, Corrado.
Affiliation
  • Ostuzzi G; Department of Neuroscience, Biomedicine and Movement Sciences, Section of Psychiatry, University of Verona, Verona, Italy.
  • Gastaldon C; Department of Neuroscience, Biomedicine and Movement Sciences, Section of Psychiatry, University of Verona, Verona, Italy.
  • Tettamanti M; Institute for Social and Preventive Medicine, University of Bern, Bern, Switzerland.
  • Cartabia M; Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milano, Italy.
  • Monti I; Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milano, Italy.
  • Aguglia A; Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milano, Italy.
  • Aguglia E; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), Section of Psychiatry, University of Genoa, Genoa, Italy.
  • Bartoli F; IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
  • Callegari C; Department of Clinical and Experimental Medicine, Institute of Psychiatry, University of Catania, Catania, Italy.
  • Canozzi A; Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
  • Carbone EA; Department of Medicine and Surgery, Section of Psychiatry, University of Insubria, Varese, Italy.
  • Carrà G; Department of Neuroscience, Biomedicine and Movement Sciences, Section of Psychiatry, University of Verona, Verona, Italy.
  • Caruso R; Psychiatry Unit, Department of Health Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.
  • Cavallotti S; Psychiatry Unit, Department of Medical and Surgical Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.
  • Chiappini S; Outpatient Clinic for Clinical Research and Treatment of Eating Disorders, University Hospital Renato Dulbecco, Catanzaro, Italy.
  • Colasante F; Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
  • Compri B; Department of Neuroscience and Rehabilitation, Institute of Psychiatry, University of Ferrara, Ferrara, Italy.
  • D'Agostino A; University Hospital Psychiatry Unit, Integrated Department of Mental Health and Addictive Behavior, University S. Anna Hospital and Health Trust, Ferrara, Italy.
  • De Fazio P; Department of Mental Health and Addiction, ASST Santi Paolo e Carlo, Milan, Italy.
  • de Filippis R; Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.
  • Gari M; Department of Neurosciences, Imaging and Clinical Sciences, University "G. D'Annunzio", Chieti, Italy.
  • Ielmini M; Department of Neuroscience, Biomedicine and Movement Sciences, Section of Psychiatry, University of Verona, Verona, Italy.
  • Ingrosso G; Santa Chiara Hospital, Verona, Italy.
  • Mammarella S; Department of Neuroscience, Biomedicine and Movement Sciences, Section of Psychiatry, University of Verona, Verona, Italy.
  • Martinotti G; Department of Mental Health and Addiction, ASST Santi Paolo e Carlo, Milan, Italy.
  • Rodolico A; Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.
  • Roncone R; Psychiatry Unit, Department of Health Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.
  • Sterzi E; Psychiatry Unit, Department of Medical and Surgical Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.
  • Tarsitani L; Outpatient Clinic for Clinical Research and Treatment of Eating Disorders, University Hospital Renato Dulbecco, Catanzaro, Italy.
  • Tiberto E; Psychiatry Unit, Department of Health Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.
  • Todini L; Psychiatry Unit, Department of Medical and Surgical Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.
  • Amaddeo F; Outpatient Clinic for Clinical Research and Treatment of Eating Disorders, University Hospital Renato Dulbecco, Catanzaro, Italy.
  • D'Avanzo B; IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
  • Barbato A; Department of Mental Health and Addiction, ASST Santi Paolo e Carlo, Milan, Italy.
  • Barbui C; Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.
EClinicalMedicine ; 69: 102491, 2024 Mar.
Article in En | MEDLINE | ID: mdl-38384338
ABSTRACT

Background:

Major depressive disorder (MDD) is prevalent and disabling among older adults. Standing on its tolerability profile, vortioxetine might be a promising alternative to selective serotonin reuptake inhibitors (SSRIs) in such a vulnerable population.

Methods:

We conducted a randomised, assessor- and statistician-blinded, superiority trial including older adults with MDD. The study was conducted between 02/02/2019 and 02/22/2023 in 11 Italian Psychiatric Services. Participants were randomised to vortioxetine or one of the SSRIs, selected according to common practice. Treatment discontinuation due to adverse events after six months was the primary outcome, for which we aimed to detect a 12% difference in favour of vortioxetine. The study was registered in the online repository clinicaltrials.gov (NCT03779789).

Findings:

The intention-to-treat population included 179 individuals randomised to vortioxetine and 178 to SSRIs. Mean age was 73.7 years (standard deviation 6.1), and 264 participants (69%) were female. Of those on vortioxetine, 78 (44%) discontinued the treatment due to adverse events at six months, compared to 59 (33%) of those on SSRIs (odds ratio 1.56; 95% confidence interval 1.01-2.39). Adjusted and per-protocol analyses confirmed point estimates in favour of SSRIs, but without a significant difference. With the exception of the unadjusted survival analysis showing SSRIs to outperform vortioxetine, secondary outcomes provided results consistent with a lack of substantial safety and tolerability differences between the two arms. Overall, no significant differences emerged in terms of response rates, depressive symptoms and quality of life, while SSRIs outperformed vortioxetine in terms of cognitive performance.

Interpretation:

As opposed to what was previously hypothesised, vortioxetine did not show a better tolerability profile compared to SSRIs in older adults with MDD in this study. Additionally, hypothetical advantages of vortioxetine on depression-related cognitive symptoms might be questioned. The study's statistical power and highly pragmatic design allow for generalisability to real-world practice.

Funding:

The study was funded by the Italian Medicines Agency within the "2016 Call for Independent Drug Research".
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: EClinicalMedicine Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: EClinicalMedicine Year: 2024 Document type: Article Affiliation country: