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dc.contributor.authorGoff, Donald C.
dc.contributor.authorFan, Xiaoduo
dc.date2022-08-11T08:09:52.000
dc.date.accessioned2022-08-23T16:46:39Z
dc.date.available2022-08-23T16:46:39Z
dc.date.issued2019-01-29
dc.date.submitted2019-02-28
dc.identifier.citation<p>Schizophr Res. 2019 Jan 29. pii: S0920-9964(19)30018-0. doi: 10.1016/j.schres.2019.01.028. [Epub ahead of print]. <a href="https://doi.org/10.1016/j.schres.2019.01.028">Link to article on publisher's site</a></p>
dc.identifier.issn0920-9964 (Linking)
dc.identifier.doi10.1016/j.schres.2019.01.028
dc.identifier.pmid30709746
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40922
dc.description<p>Full author list omitted for brevity. For the full list of authors, see article.</p>
dc.description.abstractAntidepressants are frequently prescribed in first episode schizophrenia (FES) patients for negative symptoms or for subsyndromal depressive symptoms, but therapeutic benefit has not been established, despite evidence of efficacy in later-stage schizophrenia. We conducted a 52 week, placebo-controlled add-on trial of citalopram in patients with FES who did not meet criteria for major depression to determine whether maintenance therapy with citalopram would improve outcomes by preventing or improving negative and depressive symptoms. Primary outcomes were negative symptoms measured by the Scale for Assessment of Negative Symptoms and depressive symptoms measured by the Calgary Depression Scale for Schizophrenia; both were analyzed by an intent-to-treat, mixed effects, area-under-the-curve analysis to assess the cumulative effects of symptom improvement and symptom prevention over a one-year period. Ninety-five patients were randomized and 52 (54%) completed the trial. Negative symptoms were reduced with citalopram compared to placebo (p=.04); the effect size of citalopram versus placebo was 0.32 for participants with a duration of untreated psychosis (DUP) of < 18 weeks (median split) and 0.52 with a DUP > 18 weeks. Rates of new-onset depression did not differ between groups; improvement in depressive symptoms was greater with placebo than citalopram (p=.02). Sexual side effects were more common with citalopram, but overall treatment-emergent side effects were not increased compared to placebo. In conclusion, citalopram may reduce levels of negative symptoms, particularly in patients with longer DUP, but we found no evidence of benefit for subsyndromal depressive symptoms.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=30709746&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1016/j.schres.2019.01.028
dc.rights© 2019 The Authors. Published by Elsevier B.V. under http://creativecommons.org/licenses/by-nc-nd/4.0/.
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectcitalopram
dc.subjectantidepressants
dc.subjectschizophrenia
dc.subjectMental and Social Health
dc.subjectMental Disorders
dc.subjectPharmaceutical Preparations
dc.subjectPsychiatry
dc.subjectPsychiatry and Psychology
dc.subjectTherapeutics
dc.titleCitalopram in first episode schizophrenia: The DECIFER trial
dc.typeJournal Article
dc.source.journaltitleSchizophrenia research
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4733&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3721
dc.identifier.contextkey13921328
refterms.dateFOA2022-08-23T16:46:39Z
html.description.abstract<p>Antidepressants are frequently prescribed in first episode schizophrenia (FES) patients for negative symptoms or for subsyndromal depressive symptoms, but therapeutic benefit has not been established, despite evidence of efficacy in later-stage schizophrenia. We conducted a 52 week, placebo-controlled add-on trial of citalopram in patients with FES who did not meet criteria for major depression to determine whether maintenance therapy with citalopram would improve outcomes by preventing or improving negative and depressive symptoms. Primary outcomes were negative symptoms measured by the Scale for Assessment of Negative Symptoms and depressive symptoms measured by the Calgary Depression Scale for Schizophrenia; both were analyzed by an intent-to-treat, mixed effects, area-under-the-curve analysis to assess the cumulative effects of symptom improvement and symptom prevention over a one-year period. Ninety-five patients were randomized and 52 (54%) completed the trial. Negative symptoms were reduced with citalopram compared to placebo (p=.04); the effect size of citalopram versus placebo was 0.32 for participants with a duration of untreated psychosis (DUP) of < 18 weeks (median split) and 0.52 with a DUP > 18 weeks. Rates of new-onset depression did not differ between groups; improvement in depressive symptoms was greater with placebo than citalopram (p=.02). Sexual side effects were more common with citalopram, but overall treatment-emergent side effects were not increased compared to placebo. In conclusion, citalopram may reduce levels of negative symptoms, particularly in patients with longer DUP, but we found no evidence of benefit for subsyndromal depressive symptoms.</p>
dc.identifier.submissionpathoapubs/3721
dc.contributor.departmentDepartment of Psychiatry


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© 2019 The Authors. Published by Elsevier B.V. under http://creativecommons.org/licenses/by-nc-nd/4.0/.
Except where otherwise noted, this item's license is described as © 2019 The Authors. Published by Elsevier B.V. under http://creativecommons.org/licenses/by-nc-nd/4.0/.