Evidence map›Paper›PMID 34111150›Full record

ArticlePloS one2021

P2RX7 gene variation mediates the effect of childhood adversity and recent stress on the severity of depressive symptoms.

Zsuliet Kristof, Nora Eszlari, Sara Sutori, Zsofia Gal, Dora Torok, Daniel Baksa, Peter Petschner, Beata Sperlagh, Ian M Anderson, John Francis William Deakin and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Embers of the Past: Early Childhood Traumas Interact with Variation inInternational 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

13 authors at 3 institutions in 2 countries.

Zsuliet KristofDoctoral School of Mental Health Sciences, Semmelweis University, Budapest, Hungary.
Nora EszlariFaculty of Pharmacy, Department of Pharmacodynamics, Semmelweis University, Budapest, Hungary.
Sara SutoriFaculty of Pharmacy, Department of Pharmacodynamics, Semmelweis University, Budapest, Hungary.ORCID 0000-0003-3468-0780
Zsofia GalFaculty of Pharmacy, Department of Pharmacodynamics, Semmelweis University, Budapest, Hungary.ORCID 0000-0002-9441-1497
Dora TorokFaculty of Pharmacy, Department of Pharmacodynamics, Semmelweis University, Budapest, Hungary.
Daniel BaksaFaculty of Pharmacy, Department of Pharmacodynamics, Semmelweis University, Budapest, Hungary.
Peter PetschnerFaculty of Pharmacy, Department of Pharmacodynamics, Semmelweis University, Budapest, Hungary.
Beata SperlaghLaboratory of Molecular Pharmacology, Institute of Experimental Medicine, Budapest, Hungary.
Ian M AndersonFaculty of Biological, Division of Neuroscience and Experimental Psychology, Neuroscience and Psychiatry Unit, School of Biological Sciences, Medical and Human Sciences, The University of Manchester and Manchester Academic Health Sciences Centre, Manchester, United Kingdom.
John Francis William DeakinFaculty of Biological, Division of Neuroscience and Experimental Psychology, Neuroscience and Psychiatry Unit, School of Biological Sciences, Medical and Human Sciences, The University of Manchester and Manchester Academic Health Sciences Centre, Manchester, United Kingdom.
Gabriella JuhaszFaculty of Pharmacy, Department of Pharmacodynamics, Semmelweis University, Budapest, Hungary.
Gyorgy BagdyFaculty of Pharmacy, Department of Pharmacodynamics, Semmelweis University, Budapest, Hungary.
Xenia GondaDepartment of Psychiatry and Psychotherapy, Semmelweis University, Budapest, Hungary.ORCID 0000-0001-9015-4203
Semmelweis University · HUManchester Academic Health Science Centre · GBHUN-REN Institute of Experimental Medicine · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The P2X purinoceptor 7 (P2RX7) mediates inflammatory microglial responses and is implicated in neuroimmune mechanisms of depression and neurodegenerative disorders. A number of studies suggest that psychosocial stress may precipitate depression through immune activation. Genetic association studies of P2RX7 variants with depression have been inconclusive. However, nearly all studies have focused on only one single-nucleotide polymorphism (SNP) and have not considered interaction with psychosocial stress. We investigated the effect of several variations in P2RX7 gene using a clumping method in interaction with early adversities and recent stress on depression severity. 1752 subjects provided information on childhood adversities, recent life events, and current depression severity. Participants were genotyped for 681 SNPs in the P2RX7 gene, 335 of them passed quality control and were entered into linear regression models followed by a clumping procedure for main effect and interactions. No significant main effect was observed. Rs74892325 emerged as a top SNP for interaction with childhood adversities and rs61953400 for interaction with recent life events. Our study is the first to investigate several variants in the P2RX7 gene and in interaction with two types of stress, extending our understanding of neuroinflammation in depression, and supporting that the majority of genes influence depression by enhancing sensitivity to stressors.

Indexed as

Genetic Predisposition to DiseaseGenetic VariationSeverity of Illness IndexAdolescentAdultAdverse Childhood ExperiencesChildComputer SimulationDepressionFemaleGenome, HumanHumansLinear ModelsMaleMiddle AgedPolymorphism, Single NucleotideP2RX7 protein, humanReceptors, Purinergic P2X7

Identifiers

PMID34111150
PMCPMC8191953
OpenAlexW3169814075

What OpenQuestion holds

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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.