Evidence map›Paper›PMID 32179746›Full record

ArticleTranslational psychiatry2020

Elevated serum chemokine CCL22 levels in first-episode psychosis: associations with symptoms, peripheral immune state and in vivo brain glial cell function.

Heikki Laurikainen, Arja Vuorela, Anna Toivonen, Linnea Reinert-Hartwall, Kalevi Trontti, Maija Lindgren, Jaakko Keinänen, Teemu Mäntylä, Janina Paju, Tuula Ilonen and 14 more

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 4 pooled it
0.9field-weighted citation impact, top 33% 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

16 citing papers in PubMed, 4 syntheses or guidelines pooled it, 26 citations in OpenAlex.

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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

24 authors at 4 institutions in 2 countries.

Heikki LaurikainenTurku PET Centre, University of Turku, Turku, Finland. heikki.laurikainen@utu.fi.
Arja VuorelaClinicum, University of Helsinki, Helsinki, Finland.
Anna ToivonenDepartment of Psychiatry, University of Turku and Turku University Hospital, Turku, Finland.
Linnea Reinert-HartwallResearch Program for Clinical and Molecular Metabolism, University of Helsinki, Helsinki, Finland.
Kalevi TronttiSleepWell Research Program, University of Helsinki, Helsinki, Finland.
Maija LindgrenFinnish Institute for Health and Welfare, Mental Health Unit, Helsinki, Finland.
Jaakko KeinänenFinnish Institute for Health and Welfare, Mental Health Unit, Helsinki, Finland.
Teemu MäntyläDepartment of Psychology and Logopedics, University of Helsinki, Helsinki, Finland.
Janina PajuDepartment of Psychiatry, University of Turku and Turku University Hospital, Turku, Finland.
Tuula IlonenDepartment of Psychiatry, University of Turku and Turku University Hospital, Turku, Finland.
Reetta-Liina ArmioTurku PET Centre, University of Turku, Turku, Finland.
Maija WaltaDepartment of Psychiatry, University of Turku and Turku University Hospital, Turku, Finland.
Jouni TuiskuTurku PET Centre, University of Turku, Turku, Finland.
Semi HelinTurku PET Centre, University of Turku, Turku, Finland.
Päivi MarjamäkiTurku PET Centre, University of Turku, Turku, Finland.
Iiris HovattaSleepWell Research Program, University of Helsinki, Helsinki, Finland.ORCID http://orcid.org/0000-0002-5990-7892
Sebastian ThermanFinnish Institute for Health and Welfare, Mental Health Unit, Helsinki, Finland.ORCID http://orcid.org/0000-0001-9407-4905
Outi VaaralaResearch Program for Clinical and Molecular Metabolism, University of Helsinki, Helsinki, Finland.
Outi LinnarantaDouglas Mental Health University Institute, Montreal, QC, Canada.ORCID http://orcid.org/0000-0002-0383-7215
Tuula KieseppäDepartment of Psychiatry, Helsinki University and Helsinki University Hospital, Helsinki, Finland.
Raimo K R SalokangasDepartment of Psychiatry, University of Turku and Turku University Hospital, Turku, Finland.
Jarno HonkanenResearch Program for Clinical and Molecular Metabolism, University of Helsinki, Helsinki, Finland.
Jarmo HietalaTurku PET Centre, University of Turku, Turku, Finland.
Jaana SuvisaariFinnish Institute for Health and Welfare, Mental Health Unit, Helsinki, Finland.ORCID http://orcid.org/0000-0001-7167-0990
University of Turku · FIUniversity of Helsinki · FIFinnish Institute for Health and Welfare · FIDouglas Mental Health University Institute · CA

Funding

Academy of Finland (Suomen Akatemia) 278155Academy of Finland (Suomen Akatemia) 278181Academy of Finland (Suomen Akatemia) 323035
6 · The paper itself

Abstract

Several lines of research support immune system dysregulation in psychotic disorders. However, it remains unclear whether the immunological marker alterations are stable and how they associate with brain glial cell function. This longitudinal study aimed at investigating whether peripheral immune functions are altered in the early phases of psychotic disorders, whether the changes are associated with core symptoms, remission, brain glial cell function, and whether they persist in a one-year follow-up. Two independent cohorts comprising in total of 129 first-episode psychosis (FEP) patients and 130 controls were assessed at baseline and at the one-year follow-up. Serum cyto-/chemokines were measured using a 38-plex Luminex assay. The FEP patients showed a marked increase in chemokine CCL22 levels both at baseline (p < 0.0001; Cohen's d = 0.70) and at the 12-month follow-up (p = 0.0007) compared to controls. The group difference remained significant (p = 0.0019) after accounting for relevant covariates including BMI, smoking, and antipsychotic medication. Elevated serum CCL22 levels were significantly associated with hallucinations (ρ = 0.20) and disorganization (ρ = 0.23), and with worse verbal performance (ρ = -0.23). Brain glial cell activity was indexed with positron emission tomography and the translocator protein radiotracer [

Indexed as

Psychotic DisordersBrainChemokine CCL22HumansLongitudinal StudiesNeurogliaCCL22 protein, humanChemokine CCL22

Identifiers

PMID32179746
PMCPMC7075957
OpenAlexW3011389959

What OpenQuestion holds

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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 OpenQuestion graph.