Evidence map›Paper›PMID 29317657›Full record

ArticleScientific reports2018

Blood plasma/IgG N-glycome biosignatures associated with major depressive disorder symptom severity and the antidepressant response.

Dong Ik Park, Jerko Štambuk, Genadij Razdorov, Maja Pučić-Baković, Daniel Martins-de-Souza, Gordan Lauc, Christoph W Turck

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

29 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. The Association of the Polymorphisms in theInternational journal of molecular sciences · 2023
    Article
  12. Article
  13. Review
  14. Article
  15. Post-translational Modifications in Brain Diseases: A Future for Biomarkers.Advances in experimental medicine and biology · 2022
    Article
  16. Review
  17. Review
  18. Article
  19. A Load to Find Clinically Useful Biomarkers for Depression.Advances in experimental medicine and biology · 2021
    Article
  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

7 authors at 4 institutions in 4 countries.

Dong Ik ParkMax Planck Institute of Psychiatry, Department of Translational Research in Psychiatry, 80804, Munich, Germany.
Jerko ŠtambukGenos Glycoscience Research Laboratory, Zagreb, Croatia.
Genadij RazdorovGenos Glycoscience Research Laboratory, Zagreb, Croatia.
Maja Pučić-BakovićGenos Glycoscience Research Laboratory, Zagreb, Croatia.ORCID http://orcid.org/0000-0003-0866-623X
Daniel Martins-de-SouzaInstitute of Biology, Department of Biochemistry and Tissue Biology, University of Campinas (UNICAMP), Campinas, Brazil.ORCID http://orcid.org/0000-0003-3595-5846
Gordan LaucGenos Glycoscience Research Laboratory, Zagreb, Croatia.
Christoph W TurckMax Planck Institute of Psychiatry, Department of Translational Research in Psychiatry, 80804, Munich, Germany. turck@psych.mpg.de.
Genos (Croatia) · HRMax Planck Institute of Psychiatry · DEUniversidade Estadual de Campinas (UNICAMP) · BRUniversity of Zagreb · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While N-linked glycosylation has been extensively studied in the context of inflammatory and metabolic disorders, its relationship with major depressive disorder (MDD) and antidepressant treatment response has not been investigated. In our exploratory study, we analysed N-glycan profiles in blood plasma samples collected from MDD patients (n = 18) and found gender-dependent correlations with severity of depressive symptoms prior to initiating antidepressant treatment. In addition, several N-glycosylation traits showed gender-dependent associations with clinical antidepressant response. Follow up proteomics analysis in peripheral blood mononuclear cells (PBMCs) collected from MDD patients (n = 20) identified baseline and post-antidepressant treatment pathway differences between responder and non-responder patients. Reactome data analysis further delineated potential biological reaction differences between responder and non-responder patients. Our preliminary results suggest that specific glycosylation traits are associated with depressive symptom severity and antidepressant response and may be of use as biomarkers.

Indexed as

Protein Processing, Post-TranslationalAdultAgedAntidepressive AgentsBiomarkersFemaleGlycosylationHumansImmunoglobulin GMajor Depressive DisorderMaleMiddle AgedMonocytesPolysaccharidesAntidepressive AgentsBiomarkersImmunoglobulin GPolysaccharides

Identifiers

PMID29317657
PMCPMC5760622
OpenAlexW2782012582

What OpenQuestion 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 OpenQuestion graph.