Evidence map›Paper›PMID 34934041›Full record

ArticleTranslational psychiatry2021

Gut microbiota, innate immune pathways, and inflammatory control mechanisms in patients with major depressive disorder.

Javier R Caso, Karina S MacDowell, Ana González-Pinto, Saínza García, Javier de Diego-Adeliño, Mar Carceller-Sindreu, Fernando Sarramea, Javier Caballero-Villarraso, Patricia Gracia-García, Concepción De la Cámara and 5 more

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 4 pooled it
4.3field-weighted citation impact, top 4% 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

67 citing papers in PubMed, 4 syntheses or guidelines pooled it, 94 citations in OpenAlex.

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7 more citing papers are in PubMed but not listed here.

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

15 authors at 6 institutions in 1 country.

Javier R Caso *Department of Pharmacology & Toxicology, Faculty of Medicine, Universidad Complutense de Madrid (UCM), Madrid, Spain.ORCID http://orcid.org/0000-0001-8622-749X
Karina S MacDowell *Department of Pharmacology & Toxicology, Faculty of Medicine, Universidad Complutense de Madrid (UCM), Madrid, Spain.
Ana González-PintoUniversity Hospital of Alava (HUA), University of the Basque Country (UPV/EHU), CIBERSAM, Vitoria-Gasteiz, Spain.
Saínza GarcíaUniversity Hospital of Alava (HUA), University of the Basque Country (UPV/EHU), CIBERSAM, Vitoria-Gasteiz, Spain.
Javier de Diego-AdeliñoDepartment of Psychiatry, Hospital de la Santa Creu i Sant Pau, Institut d'Investigació Biomèdica Sant Pau (IIB-Sant Pau), Universitat Autònoma de Barcelona (UAB), CIBERSAM, Barcelona, Spain.
Mar Carceller-SindreuDepartment of Psychiatry, Hospital de la Santa Creu i Sant Pau, Institut d'Investigació Biomèdica Sant Pau (IIB-Sant Pau), Universitat Autònoma de Barcelona (UAB), CIBERSAM, Barcelona, Spain.
Fernando SarrameaInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Unidad de Gestión Clínica de Salud Mental, Hospital Universitario Reina Sofía, CIBERSAM, Córdoba, Spain.
Javier Caballero-VillarrasoInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Unidad de Gestión Clínica de Salud Mental, Hospital Universitario Reina Sofía, CIBERSAM, Córdoba, Spain.ORCID http://orcid.org/0000-0003-0571-5147
Patricia Gracia-GarcíaServicio de Psiquiatría, Hospital Universitario Miguel Servet, Departamento de Medicina y Psiquiatría, Universidad de Zaragoza, CIBERSAM, Zaragoza, Spain.ORCID http://orcid.org/0000-0001-9822-6312
Concepción De la CámaraServicio de Psiquiatría, Hospital Clínico Universitario, Departamento de Medicina y Psiquiatría, Universidad de Zaragoza, CIBERSAM, Zaragoza, Spain.
Luis AgüeraPsychiatry Department, Hospital Universitario 12 de Octubre, UCM, CIBERSAM, Madrid, Spain.
María L Gómez-LusDepartment of Medicine-Microbiology Area, Faculty of Medicine, UCM, Madrid, Spain.
Claudio AlbaDepartment of Nutrition and Food Science, Faculty of Veterinary, UCM, Madrid, Spain.ORCID http://orcid.org/0000-0003-0620-0313
Juan M RodríguezDepartment of Nutrition and Food Science, Faculty of Veterinary, UCM, Madrid, Spain.
Juan C LezaDepartment of Pharmacology & Toxicology, Faculty of Medicine, Universidad Complutense de Madrid (UCM), Madrid, Spain. jcleza@med.ucm.es.ORCID http://orcid.org/0000-0002-9901-0094
Centro de Investigación Biomédica en Red de Salud Mental · ESUniversidad Complutense de Madrid · ESUniversidad de Zaragoza · ESUniversitat Autònoma de Barcelona · ESUniversity of the Basque Country · ESUnidades Centrales Científico-Técnicas · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although alterations in the gut microbiota have been linked to the pathophysiology of major depressive disorder (MDD), including through effects on the immune response, our understanding is deficient about the straight connection patterns among microbiota and MDD in patients. Male and female MDD patients were recruited: 46 patients with a current active MDD (a-MDD) and 22 in remission or with only mild symptoms (r-MDD). Forty-five healthy controls (HC) were also recruited. Psychopathological states were assessed, and fecal and blood samples were collected. Results indicated that the inducible nitric oxide synthase expression was higher in MDD patients compared with HC and the oxidative stress levels were greater in the a-MDD group. Furthermore, the lipopolysaccharide (an indirect marker of bacterial translocation) was higher in a-MDD patients compared with the other groups. Fecal samples did not cluster according to the presence or the absence of MDD. There were bacterial genera whose relative abundance was altered in MDD: Bilophila (2-fold) and Alistipes (1.5-fold) were higher, while Anaerostipes (1.5-fold) and Dialister (15-fold) were lower in MDD patients compared with HC. Patients with a-MDD presented higher relative abundance of Alistipes and Anaerostipes (1.5-fold) and a complete depletion of Dialister compared with HC. Patients with r-MDD presented higher abundance of Bilophila (2.5-fold) compared with HC. Thus, the abundance of bacterial genera and some immune pathways, both with potential implications in the pathophysiology of depression, appear to be altered in MDD, with the most noticeable changes occurring in patients with the worse clinical condition, the a-MDD group.

Indexed as

Gastrointestinal MicrobiomeMajor Depressive DisorderMicrobiotaFecesFemaleHumansImmunity, InnateMale

Identifiers

PMID34934041
PMCPMC8692500
OpenAlexW4200335610

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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.