Evidence map›Paper›PMID 31323113›Full record

Trial reportActa psychiatrica Scandinavica2019

Phenotypic factors associated with amisulpride-induced weight gain in first-episode psychosis patients (from the OPTiMiSE cohort).

R Pandit, D Cianci, S E Ter Hark, I Winter-van Rossum, B H Ebdrup, B V Broberg, M P Garcia-Portilla, J Bobes, C H Vinkers, R S Kahn and 3 more

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Acta psychiatrica Scandinavica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Real-World Analysis of Antipsychotic Drugs' Effect on Weight Gain: An EHR Application.AMIA ... Annual Symposium proceedings. AMIA Symposium · 2023
    Article
  5. Article
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

13 authors at 6 institutions in 4 countries.

R PanditDepartment of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
D CianciDepartment of Biostatistics and Research Support, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, University of Utrecht, Utrecht, the Netherlands.
S E Ter HarkDepartment of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
I Winter-van RossumDepartment of Psychiatry, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
B H EbdrupCentre for Neuropsychiatric Schizophrenia Research, CNSR & Centre for Clinical Intervention and Neuropsychiatric Schizophrenia Research, CINS, Mental Health Centre Glostrup, Copenhagen University Hospital, Glostrup, Denmark.ORCID 0000-0002-2590-5055
B V BrobergCentre for Neuropsychiatric Schizophrenia Research, CNSR & Centre for Clinical Intervention and Neuropsychiatric Schizophrenia Research, CINS, Mental Health Centre Glostrup, Copenhagen University Hospital, Glostrup, Denmark.
M P Garcia-PortillaDepartment of Psychiatry and CIBERSAM, University of Oviedo, Oviedo, Spain.ORCID 0000-0003-3643-1622
J BobesDepartment of Psychiatry and CIBERSAM, University of Oviedo, Oviedo, Spain.
C H VinkersDepartment of Psychiatry, Amsterdam UMC (location VUmc), Amsterdam, the Netherlands.
R S KahnDepartment of Psychiatry, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
S GuloksuzDepartment of Psychiatry and Neuropsychology, School for Mental Health, Neuroscience Maastricht University Medical Center, Maastricht, the Netherlands.
A D R HuitemaDepartment of Pharmacy Pharmacology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
J J LuykxDepartment of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID 0000-0002-6439-2774
Utrecht University · NLUniversidad de Oviedo · ESAmsterdam Neuroscience · NLGlostrup Hospital · DKMaastricht University Medical Centre · NLUniversity of Copenhagen · DK

Funding

European Commission HEALTH-F2-2010-242114
6 · The paper itself

Abstract

objectiveAntipsychotic-induced weight gain (AiWG) is a debilitating adverse effect of most antipsychotics. First-episode psychosis patients are particularly vulnerable to the detrimental consequences of AiWG. Amisulpride has good efficacy and tolerability. We here aimed to identify the phenotypic factors associated with amisulpride-induced weight gain in first-episode psychosis patients.

methodData were collected from the Optimization of Treatment and Management of Schizophrenia in Europe trial. Multivariable regression models with various phenotypic variables (N = 305) were performed with absolute AiWG and clinically relevant AiWG (≥7% AiWG) as outcomes.

resultsFour weeks of amisulpride treatment increased body weight from 69.7 to 72.4 kg (P < 0.001). In the regression model of absolute AiWG, unemployment (β = 0.94, P = 0.016), younger age (β = -0.07, P = 0.031) and absence of current comorbid major depression disorder (β = -1.61, P = 0.034) were positively associated with absolute AiWG. In the regression model of clinically relevant AiWG, unemployment (OR = 2.83, P = 0.001), schizophreniform disorder (OR = 2.00, P = 0.025) and low baseline weight (OR = 0.97, P = 0.032) increased the likelihood of clinically relevant AiWG.

conclusionsClinicians prescribing amisulpride should consider the relatively high susceptibility to AiWG in unemployed first-episode patients with psychosis, in particular young subjects with a diagnosis of schizophreniform disorder. We advise to carefully monitor these patients and, when needed, implement weight-reducing strategies.

Indexed as

AdultAge FactorsAmisulprideAntipsychotic AgentsCohort StudiesEuropeFemaleHumansMalePhenotypePsychotic DisordersSchizophreniaUnemploymentWeight GainYoung AdultAmisulprideAntipsychotic Agentsamisulprideantipsychoticpsychosisschizophreniaweight gain

Identifiers

PMID31323113
PMCPMC6771865
OpenAlexW2963761736

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.