Evidence map›Paper›PMID 30604052›Full record

ArticleEuropean archives of psychiatry and clinical neuroscience2020

Profiling of lipidomics before and after antipsychotic treatment in first-episode psychosis.

Liisa Leppik, Madis Parksepp, Sven Janno, Kati Koido, Liina Haring, Eero Vasar, Mihkel Zilmer

Abstract read
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In one paragraph

Article in European archives of psychiatry and clinical neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

36 citing papers in PubMed, 57 citations in OpenAlex.

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  17. LC-HRMS Lipidomic Fingerprints in Serbian Cohort of Schizophrenia Patients.International journal of molecular sciences · 2024
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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 2 institutions in 2 countries.

Liisa LeppikPsychiatry Clinic of Tartu University Hospital, 31 Raja Street, 50417, Tartu, Estonia. Liisa.Leppik@kliinikum.ee.ORCID http://orcid.org/0000-0002-8873-0627
Madis ParkseppPsychiatry Clinic of Tartu University Hospital, 31 Raja Street, 50417, Tartu, Estonia.
Sven JannoPsychiatry Clinic of Tartu University Hospital, 31 Raja Street, 50417, Tartu, Estonia.
Kati KoidoInstitute of Biomedicine and Translational Medicine, Centre of Excellence for Genomics and Translational Medicine, University of Tartu, 19 Ravila Street, 50411, Tartu, Estonia.
Liina HaringPsychiatry Clinic of Tartu University Hospital, 31 Raja Street, 50417, Tartu, Estonia.
Eero VasarInstitute of Biomedicine and Translational Medicine, Centre of Excellence for Genomics and Translational Medicine, University of Tartu, 19 Ravila Street, 50411, Tartu, Estonia.
Mihkel ZilmerInstitute of Biomedicine and Translational Medicine, Centre of Excellence for Genomics and Translational Medicine, University of Tartu, 19 Ravila Street, 50411, Tartu, Estonia.
Tartu University Hospital · EEUniversity of Tartu · EE

Funding

Estonian Research Foundation IUT 20-41Estonian Research Foundation IUT 20-42European Regional Development Fund 2014-2020.4.01.15-0012
6 · The paper itself

Abstract

Alterations in complex lipids may be involved in pathophysiology of schizophrenia spectrum disorders. Previously, we demonstrated importance of detecting lipid metabolism dysregulation by acylcarnitine (ACs) profile analysis in patients with first-episode psychosis (FEP). The aim of this study was to adopt lipidomics to identify serum glycerophospholipids (GPLs) and sphingomyelins (SMs) for describing FEP status before and after 7-month antipsychotic treatment. Using mass spectrometry and liquid chromatography technique, we profiled 105 individual lipids [14 lysophosphatidylcholines (LysoPCs), 76 phosphatidylcholines (PCs) and 15 SMs] in serum samples from 53 antipsychotic-naïve FEP patients, 44 of them were studied longitudinally and from 37 control subjects (CSs). Among the identified and quantified metabolites one LysoPC was elevated, and contrary the levels of 16 PCs as well as the level of one SM were significantly (p ≤ 0.0005) reduced in antipsychotic-naïve FEP patients compared to CSs. Comparison of serum lipids profiles of FEP patients before and after 7-month antipsychotic treatment revealed that 11 GPLs (2 LysoPCs, 9 PCs), and 2 SMs were found to be significantly changed (p ≤ 0.0005) in which GPLs were up-regulated, and SMs were down-regulated. However, no significant differences were noted when treated patient's serum lipid profiles were compared with CSs. Our findings suggest that complex lipid profile abnormalities are specifically associated with FEP and these discrepancies reflect two different disease-related pathways. Our findings provide insight into lipidomic information that may be used for monitoring FEP status and impact of the treatment in the early stage of the schizophrenia spectrum disorder.

Indexed as

LipidomicsAdolescentAdultAntipsychotic AgentsChromatography, LiquidFemaleGlycerophospholipidsHumansLongitudinal StudiesMaleMass SpectrometryPsychotic DisordersSchizophreniaSphingomyelinsYoung AdultAntipsychotic AgentsGlycerophospholipidsSphingomyelinsFirst-episode psychosisGlycerophospholipidsLipidomicsLysophosphatidylcholinesPhosphatidylcholinesSphingomyelins

Identifiers

PMID30604052
OpenAlexW2907155709

What OpenQuestion holds

Textmetadata
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.