Evidence map›Paper›PMID 22584806›Full record

ArticleEuropean archives of psychiatry and clinical neuroscience2013

Chemokines in bipolar disorder: trait or state?

Izabela Guimarães Barbosa, Natália Pessoa Rocha, Moisés Evandro Bauer, Aline Silva de Miranda, Rodrigo Barreto Huguet, Helton José Reis, Patricia A Zunszain, Mark A Horowitz, Carmine M Pariante, Antônio Lúcio Teixeira

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in European archives of psychiatry and clinical neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 98 citations in OpenAlex.

  1. Pooled it
  2. Choroid plexus inflammation in bipolar disorder.Brain, behavior, and immunity · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Increased Serum Level of CCL5 in Children with Attention‑Deficit/Hyperactivity Disorder: First Results about Serum Chemokines.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2022
    Article
  13. Article
  14. Evaluating endophenotypes for bipolar disorder.International journal of bipolar disorders · 2021
    Review
  15. Review
  16. Review
  17. Review
  18. Neuroinflammation in Bipolar Depression.Frontiers in psychiatry · 2020
    Review
  19. The Role of Chemokines in the Pathophysiology of Major Depressive Disorder.International journal of molecular sciences · 2019
    Review
  20. Gene expression pattern ofJournal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2019
    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

10 authors at 3 institutions in 2 countries.

Izabela Guimarães BarbosaPrograma de Pós-Graduação em Neurociências, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Natália Pessoa Rocha
Moisés Evandro Bauer
Aline Silva de Miranda
Rodrigo Barreto Huguet
Helton José Reis
Patricia A Zunszain
Mark A Horowitz
Carmine M Pariante
Antônio Lúcio Teixeira
Universidade Federal de Minas Gerais · BRKing's College London · GBUniversidade Federal do Rio Grande · BR

Funding

Medical Research Council G108/603
6 · The paper itself

Abstract

Recent evidence has suggested that inflammatory and immune mechanisms may play a role in the pathophysiology of bipolar disorder (BD). Only a few studies have assessed the profile of chemokines, a family of chemotactic cytokines related to the recruitment of leukocytes, in BD. The objective of our study was to evaluate the plasma levels of chemokines in BD patients in different mood states in comparison with healthy controls. Seventy BD type I patients (35 in euthymia and 35 in mania), and 50 healthy controls matched by age, gender, and education level were enrolled in this study. All subjects were assessed by the Mini-International Neuropsychiatry Interview and the patients by the Young Mania Rating Scale and the Hamilton Depression Rating Scale. The plasma levels of CCL2, CCL3, CCL11, CCL24, CXCL8, and CXCL10 were measured by enzyme-linked immunosorbent assay. BD patients presented higher plasma levels of CCL11 (1.69-fold increase; p < 0.001), CCL24 (1.40-fold increase; p = 0.02), CXCL10 (1.45-fold increase; p < 0.001) and decreased plasma levels of CXCL8 (8.68-fold decrease p < 0.001). Logistic regression stressed the main effect of increased plasma levels of CXCL10 (OR = 1.009, 95 % CI = 1.000-1.018, p = 0.042) and CCL11 (OR = 1.002, 95 % CI = 1.001-1.003, p = 0.003) and decreased plasma levels of CXCL8 (OR = 0.995, 95 % CI = 0.990-0.999, p = 0.013) to BD. This study reinforces the view that BD is associated with an immune dysfunction.

Indexed as

AdultAffectBipolar DisorderCase-Control StudiesChemokinesDisease ProgressionEnzyme-Linked Immunosorbent AssayFemaleHumansInflammationLogistic ModelsMaleMiddle AgedChemokines

Identifiers

PMID22584806
OpenAlexW2094235026

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.