Evidence map›Paper›PMID 19711335›Full record

Trial reportInternational journal of geriatric psychiatry2010

Treatment of subsyndromal depressive symptoms in middle-aged and older adults with schizophrenia: effect on functioning.

John Kasckow, Nicole Lanouette, Thomas Patterson, Ian Fellows, Shahrokh Golshan, Ellen Solorzano, Sidney Zisook

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in International journal of geriatric psychiatry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Antidepressants for people with both schizophrenia and depression.The Cochrane database of systematic reviews · 2002
    Pooled it
  3. Article
  4. Review
  5. Article
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

John KasckowVA Pittsburgh Health Care System MIRECC and Behavioral Health Service, 7180 Highland Dr., Pittsburgh, PA, USA. kasckowjw@upmc.edu
Nicole Lanouette
Thomas Patterson
Ian Fellows
Shahrokh Golshan
Ellen Solorzano
Sidney Zisook
University of California, San Diego · USUniversity of Pittsburgh Medical Center · USVA San Diego Healthcare System · US

Funding

Antidepressant Augmentation of Late Life SchizophreniaR01MH063798 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KASCKOW, JOHN W · 2001 to 2005
$1.7M
Citalopram Augmentation in Older Schizophrenia PatientsR01MH063931 · NIMH · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI ZISOOK, SIDNEY · 2001 to 2005
$1.6M
NIMH NIH HHS R01 MH063798NIMH NIH HHS R01 MH 063931NIMH NIH HHS R01 MH063931NIMH NIH HHS R01 MH6398
6 · The paper itself

Abstract

backgroundSubsyndromal symptoms of depression (SSD) in patients with schizophrenia are common and clinically important. SSRI's appear to be helpful in alleviating depressive symptoms in patients with schizophrenia who have SSD in patients age 40 and greater. It is not known whether SSRI's help improve functioning in this population. We hypothesized that treating this population with the SSRI citalopram would lead to improvements in social, mental and physical functioning as well as improvements in medication management and quality of life.

methodsParticipants were 198 adults > or = 40 years old with schizophrenia or schizoaffective disorder who met study criteria for subsyndromal depression based on having two or more of the nine DSM-IV symptoms of a major depressive episode, for at least 2 weeks, and a Hamilton depression rating scale (HAM-D 17) score > or = 8. Patients were randomly assigned to flexible-dose treatment with citalopram or placebo augmentation of their current antipsychotic medication(s) which was stable for 1 month. Subjects were assessed with the following functional scales at baseline and at the end of the 12-week trial: (1) social skills performance assessment (SSPA), (2) medication management ability assessment (MMAA), (3) mental and physical components of the medical outcomes study SF-12 Scale, and (4) the Heinrichs quality of life scale (QOLS). Analysis of covariance (ANCOVA) was used to compare differences between endpoint scores of the citalopram and placebo treated groups, controlling for site and baseline scores. ANCOVAs were also used to compare differences in the above endpoint scores in responders versus non-responders (responders = those with > 50% reduction in depressive symptoms).

resultsOverall, the citalopram group had significantly higher SSPA, mental functioning SF-12, and quality of life scale (QOLS) scores compared to the placebo group. There was no effect on MMAA or physical functioning SF-12 scores. Responders had significantly better endpoint mental SF-12 and QOLS scores compared to non-responders. Response to citalopram in terms of depressive symptoms mediated the effect of citalopram on mental functioning, but not on the quality of life.

conclusionsCitalopram augmentation of antipsychotic treatment in middle aged and older patients with schizophrenia and subsyndromal depression appears to improve social and mental health functioning as well as quality of life. Thus it is important for clinicians to monitor these aspects of functioning when treating this population of patients with schizophrenia with SSRI agents.

Indexed as

AgedAnalysis of VarianceAntipsychotic AgentsCitalopramDepressive DisorderFemaleHumansMaleMiddle AgedPsychiatric Status Rating ScalesQuality of LifeSchizophreniaSelective Serotonin Reuptake InhibitorsAntipsychotic AgentsCitalopramSelective Serotonin Reuptake Inhibitors

Identifiers

PMID19711335
PMCPMC3073368
OpenAlexW1966970697

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.