Evidence map›Paper›PMID 27845774›Full record

ArticleTranslational psychiatry2016

Serum metabolite profile associates with the development of metabolic co-morbidities in first-episode psychosis.

T Suvitaival, O Mantere, T Kieseppä, I Mattila, P Pöhö, T Hyötyläinen, J Suvisaari, M Orešič

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
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  9. Observational
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  15. Profiling of lipidomics before and after antipsychotic treatment in first-episode psychosis.European archives of psychiatry and clinical neuroscience · 2020
    Article
  16. Article
  17. Article
  18. Metabolomics Biomarkers for Precision Psychiatry.Advances in experimental medicine and biology · 2019
    Review
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  20. 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

8 authors at 6 institutions in 4 countries.

T SuvitaivalSteno Diabetes Center, Gentofte, Denmark.
O MantereMental Health Unit, National Institute for Health and Welfare, Helsinki, Finland.
T KieseppäMental Health Unit, National Institute for Health and Welfare, Helsinki, Finland.
I MattilaSteno Diabetes Center, Gentofte, Denmark.
P PöhöFaculty of Pharmacy, University of Helsinki, Helsinki, Finland.
T HyötyläinenSteno Diabetes Center, Gentofte, Denmark.
J SuvisaariMental Health Unit, National Institute for Health and Welfare, Helsinki, Finland.
M OrešičSteno Diabetes Center, Gentofte, Denmark.
Steno Diabetes Center · DKFinnish Institute for Health and Welfare · FIHelsinki University Hospital · FIMcGill University · CAÖrebro University · SEUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Psychotic patients are at high risk for developing obesity, metabolic syndrome and type 2 diabetes. These metabolic co-morbidities are hypothesized to be related to both treatment side effects as well as to metabolic changes occurring during the psychosis. Earlier metabolomics studies have shown that blood metabolite levels are predictive of insulin resistance and type 2 diabetes in the general population as well as sensitive to the effects of antipsychotics. In this study, we aimed to identify the metabolite profiles predicting future weight gain and other metabolic abnormalities in psychotic patients. We applied comprehensive metabolomics to investigate serum metabolite profiles in a prospective study setting in 36 first-episode psychosis patients during the first year of the antipsychotic treatment and 19 controls. While corroborating several earlier findings when comparing cases and controls and the effects of the antipsychotic medication, we also found that prospective weight gain in psychotic patients was associated with increased levels of triacylglycerols with low carbon number and double-bond count at baseline, that is, lipids known to be associated with increased liver fat. Our study suggests that metabolite profiles may be used to identify the psychotic patients most vulnerable to develop metabolic co-morbidities, and may point to a pharmacological approach to counteract the antipsychotic-induced weight gain.

Indexed as

MetabolomicsAdolescentAdultAntipsychotic AgentsCase-Control StudiesDiabetes Mellitus, Type 2FemaleFollow-Up StudiesHumansLipidsMaleMetabolic SyndromeObesityPsychiatric Status Rating ScalesPsychotic DisordersRisk AssessmentAntipsychotic AgentsLipidsTriglycerides

Identifiers

PMID27845774
PMCPMC5314133
OpenAlexW2554789790

What OpenQuestion holds

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Registered trials

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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.