Evidence map›Paper›PMID 27552816›Full record

ArticleEuropean archives of psychiatry and clinical neuroscience2017

The emerging role of the FKBP5 gene polymorphisms in vulnerability-stress model of schizophrenia: further evidence from a Serbian population.

Marina Mihaljevic, Katarina Zeljic, Ivan Soldatovic, Sanja Andric, Tijana Mirjanic, Alexander Richards, Kiran Mantripragada, Tatjana Pekmezovic, Ivana Novakovic, Nadja P Maric

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Article in European archives of psychiatry and clinical neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

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  8. The Moderating Role of theJournal of clinical medicine · 2022
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  11. The Impact of theBrain sciences · 2021
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  12. Adverse Childhood Experiences and Methylation of theJournal of clinical medicine · 2020
    Article
  13. Review
  14. Article
  15. Hsp90 and FKBP51: complex regulators of psychiatric diseases.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    Review
  16. Article
  17. Review
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 4 institutions in 2 countries.

Marina MihaljevicClinic for Psychiatry, Clinical Centre of Serbia, Pasterova 2, Belgrade, 11000, Serbia. mihaljevicm@yahoo.com.ORCID http://orcid.org/0000-0003-3415-8706
Katarina ZeljicGenetics and Evolution Department, Faculty of Biology, University of Belgarde, Studentski trg 3, Belgrade, 11000, Serbia.
Ivan SoldatovicFaculty of Medicine, Institute for Biostatistics, Medical Informatics and Researches in Medicine, University of Belgrade, Dr Subotica 15, Belgrade, 11000, Serbia.
Sanja AndricClinic for Psychiatry, Clinical Centre of Serbia, Pasterova 2, Belgrade, 11000, Serbia.
Tijana MirjanicSpecial Hospital for Psychiatric Disorders Kovin, Cara Lazara 253, Kovin, 26220, Serbia.
Alexander RichardsMRC Centre for Neuropsychiatric Genetics and Genomics, Institute of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, CF24 4HQ, Wales, UK.
Kiran MantripragadaMRC Centre for Neuropsychiatric Genetics and Genomics, Institute of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, CF24 4HQ, Wales, UK.
Tatjana PekmezovicFaculty of Medicine, Institute of Epidemiology, University of Belgrade, Visegradska 26, Belgrade, 11000, Serbia.
Ivana NovakovicFaculty of Medicine, Institute of Human Genetics, University of Belgrade, Visegradska 26, Belgrade, 11000, Serbia.
Nadja P MaricClinic for Psychiatry, Clinical Centre of Serbia, Pasterova 2, Belgrade, 11000, Serbia.
University of Belgrade · RSCardiff University · GBCentar za Promociju Nauke · RSCenter for Health, Exercise and Sport Sciences · RS

Funding

Ministarstvo Prosvete, Nauke i Tehnološkog Razvoja III 41029
6 · The paper itself

Abstract

Increased reactivity to stress is observed in patients with schizophrenia spectrum disorders and their healthy siblings in comparison with the general population. Additionally, higher levels of neuroticism, as a proposed psychological measure of stress sensitivity, increase the risk of schizophrenia. HPA axis dysregulation is one of the possible mechanisms related to the vulnerability-stress model of schizophrenia, and recent studies revealed a possible role of the functional genetic variants of FK506-binding protein 51 (FKBP5) gene which modulate activity of HPA axis. The purpose of the present study was to investigate impact of FKBP5 on schizophrenia in Serbian patients and to explore relationship between genetic variants and neuroticism by using the case-sibling-control design. In 158 subjects, we measured psychotic experiences, childhood trauma and neuroticism. Nine single-nucleotide polymorphisms (rs9295158, rs3800373, rs9740080, rs737054, rs6926133, rs9380529, rs9394314, rs2766533 and rs12200498) were genotyped. The genetic influence was modeled using logistic regression, and the relationship between genetic variants and neuroticism was assessed by linear mixed model. Our results revealed genetic main effect of FKBP5 risk alleles (A allele of rs9296158 and T allele of rs3800373) and AGTC "risk" haplotype combination (rs9296158, rs3800373, rs9470080 and rs737054, respectively) on schizophrenia, particularly when childhood trauma was set as a confounding factor. We confirmed strong relationship between neuroticism and psychotic experiences in patients and siblings and further showed relationship between higher levels of neuroticism and FKBP5 risk variants suggesting potential link between biological and psychosocial risk factors. Our data support previous findings that trauma exposure shapes FKBP5 impact on schizophrenia.

Indexed as

Adult Survivors of Child Adverse EventsGene-Environment InteractionNeuroticismSiblingsAdultCase-Control StudiesDisease SusceptibilityFemaleHumansMaleModels, TheoreticalPolymorphism, Single NucleotidePsychotic DisordersRisk FactorsSchizophreniaSerbiaTacrolimus Binding Protein 5Tacrolimus Binding ProteinsFKBP5 genetic variantsHaplotypesHealthy siblingsNeuroticismSchizophrenia

Identifiers

PMID27552816
OpenAlexW2512786904

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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.