The efficacy and heterogeneity of antipsychotic response in schizophrenia: A meta-analysis.


Journal

Molecular psychiatry
ISSN: 1476-5578
Titre abrégé: Mol Psychiatry
Pays: England
ID NLM: 9607835

Informations de publication

Date de publication:
04 2021
Historique:
received: 26 03 2019
accepted: 24 06 2019
revised: 05 06 2019
pubmed: 1 9 2019
medline: 15 5 2021
entrez: 1 9 2019
Statut: ppublish

Résumé

The response to antipsychotic treatment in schizophrenia appears to vary, and as such it has been proposed that different subtypes of schizophrenia exist, defined by treatment-response. This has not been formally examined using meta-analysis. Randomised controlled trials comparing placebo and antipsychotics in acute treatment of schizophrenia listed in PubMed, EMBASE and PsycINFO from inception until 30 November 2018 were examined. Relative variability of symptomatic improvement in antipsychotic-treated individuals compared to placebo-treated individuals was quantified using coefficient of variation ratio (CVR). Mean difference in symptom change was quantified using Hedges' g. In addition, individual patient data from two clinical trials was examined in terms of both the distribution of total symptom change, and the variability of individual symptoms and symptom factors. In total, 11,006 articles were identified. Sixty six met inclusion criteria, reporting on 17,202 patients. Compared with placebo, antipsychotic-treated patients demonstrated greater total symptom improvement (g = 0.47, p < 0.001) and reduced variability in symptomatic improvement for total (CVR = 0.86, p < 0.001), positive (CVR = 0.89, p < 0.001), and negative symptoms (CVR = 0.86, p = 0.001). Lower variability in antipsychotic-response relative to placebo was associated with studies published earlier (z = 3.98, p < 0.001), younger patients (z = 3.07, p = 0.002), higher dose treatments (z = -2.62, p = 0.009), and greater mean-difference in symptom-change (z = -5.70, p < 0.001). In the individual patient dataset (N = 522 patients), antipsychotic treated patients did not show significantly increased variability for any individual symptom, and there was no evidence of a bimodal distribution of response. Compared to placebo, antipsychotic treatment shows greater improvement and lower variability of change in total, positive and negative symptoms. This is contrary to the hypothesis that there is a subtype of antipsychotic non-responsive schizophrenia. Instead our findings, provide evidence for a relatively homogeneous effect of antipsychotic treatment in improving symptoms of schizophrenia.

Identifiants

pubmed: 31471576
doi: 10.1038/s41380-019-0502-5
pii: 10.1038/s41380-019-0502-5
pmc: PMC7610422
mid: EMS83518
doi:

Substances chimiques

Antipsychotic Agents 0

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1310-1320

Subventions

Organisme : Wellcome Trust
ID : 200102
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/L022176/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_U120097115
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC-A656-5QD30
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/N027078/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/N026063/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 094849
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0700995
Pays : United Kingdom
Organisme : Wellcome Trust
Pays : United Kingdom

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Auteurs

Robert A McCutcheon (RA)

Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, Kings College London, De Crespigny Park, London, SE5 8AF, UK.
Psychiatric Imaging Group, MRC London Institute of Medical Sciences, Hammersmith Hospital, London, W12 0NN, UK.
Institute of Clinical Sciences, Faculty of Medicine, Imperial College London, London, W12 0NN, UK.
South London and Maudsley NHS Foundation Trust, London, UK.

Toby Pillinger (T)

Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, Kings College London, De Crespigny Park, London, SE5 8AF, UK.
Psychiatric Imaging Group, MRC London Institute of Medical Sciences, Hammersmith Hospital, London, W12 0NN, UK.
Institute of Clinical Sciences, Faculty of Medicine, Imperial College London, London, W12 0NN, UK.
South London and Maudsley NHS Foundation Trust, London, UK.

Yuya Mizuno (Y)

Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, Kings College London, De Crespigny Park, London, SE5 8AF, UK.
Psychiatric Imaging Group, MRC London Institute of Medical Sciences, Hammersmith Hospital, London, W12 0NN, UK.
Institute of Clinical Sciences, Faculty of Medicine, Imperial College London, London, W12 0NN, UK.
South London and Maudsley NHS Foundation Trust, London, UK.
Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, 160-8582, Japan.

Adam Montgomery (A)

South London and Maudsley NHS Foundation Trust, London, UK.

Haridha Pandian (H)

South London and Maudsley NHS Foundation Trust, London, UK.

Luke Vano (L)

South London and Maudsley NHS Foundation Trust, London, UK.

Tiago Reis Marques (TR)

Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, Kings College London, De Crespigny Park, London, SE5 8AF, UK.
Psychiatric Imaging Group, MRC London Institute of Medical Sciences, Hammersmith Hospital, London, W12 0NN, UK.
Institute of Clinical Sciences, Faculty of Medicine, Imperial College London, London, W12 0NN, UK.
South London and Maudsley NHS Foundation Trust, London, UK.

Oliver D Howes (OD)

Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, Kings College London, De Crespigny Park, London, SE5 8AF, UK. oliver.howes@kcl.ac.uk.
Psychiatric Imaging Group, MRC London Institute of Medical Sciences, Hammersmith Hospital, London, W12 0NN, UK. oliver.howes@kcl.ac.uk.
Institute of Clinical Sciences, Faculty of Medicine, Imperial College London, London, W12 0NN, UK. oliver.howes@kcl.ac.uk.
South London and Maudsley NHS Foundation Trust, London, UK. oliver.howes@kcl.ac.uk.

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