The role of childhood adversities, FKBP5, BDNF, NRN1, and generalized self-efficacy in suicide attempts in alcohol-dependent patients.


Journal

Pharmacological reports : PR
ISSN: 2299-5684
Titre abrégé: Pharmacol Rep
Pays: Switzerland
ID NLM: 101234999

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 29 01 2019
accepted: 30 12 2019
revised: 18 10 2019
pubmed: 12 3 2020
medline: 13 4 2021
entrez: 12 3 2020
Statut: ppublish

Résumé

Alcohol-dependent (AD) patients report higher number of adverse childhood experiences (ACEs), develop poor social skills, and have a higher rate of suicide attempts than the general population. We hypothesize that the association between ACEs and lifetime suicide attempts in AD patients is mediated by generalized self-efficacy and selected functional single nucleotide polymorphisms (SNPs) in genes involved in the stress response and neuroplasticity, including: FKBP5 rs1360780, BDNF rs6265, and NRN1 rs1475157. 176 AD patients and 127 healthy controls self-reported ACEs with the ACE Study questionnaire and three additional questions that inquired about ACE categories of acute stress; generalized self-efficacy-with the Generalized Self-Efficacy Scale. Genotyping for the three analysed SNPs was performed according to the manufacturer's standard PCR protocol. Hypotheses were tested with bivariate analyses, multiple regression model, and mediation models. Higher levels of generalized self-efficacy were associated with a blunted effect of ACEs on the risk of suicide attempts. The prevalence of the three analyzed SNPs genotypes and alleles did not differ between AD patients with a positive vs. negative lifetime history of suicide attempt and was not associated with GSES scoring. Generalized self-efficacy should be considered as a target for psychotherapeutic interventions aimed at reducing the risk of suicide attempts in AD patients who were exposed to childhood victimization. The negative results concerning the hypothesized role of the three analysed SNPs should be carefully interpreted due to the relatively small study sample, but represent a theoretical foundation for further research studies with larger study samples.

Sections du résumé

BACKGROUND BACKGROUND
Alcohol-dependent (AD) patients report higher number of adverse childhood experiences (ACEs), develop poor social skills, and have a higher rate of suicide attempts than the general population. We hypothesize that the association between ACEs and lifetime suicide attempts in AD patients is mediated by generalized self-efficacy and selected functional single nucleotide polymorphisms (SNPs) in genes involved in the stress response and neuroplasticity, including: FKBP5 rs1360780, BDNF rs6265, and NRN1 rs1475157.
METHODS METHODS
176 AD patients and 127 healthy controls self-reported ACEs with the ACE Study questionnaire and three additional questions that inquired about ACE categories of acute stress; generalized self-efficacy-with the Generalized Self-Efficacy Scale. Genotyping for the three analysed SNPs was performed according to the manufacturer's standard PCR protocol. Hypotheses were tested with bivariate analyses, multiple regression model, and mediation models.
RESULTS RESULTS
Higher levels of generalized self-efficacy were associated with a blunted effect of ACEs on the risk of suicide attempts. The prevalence of the three analyzed SNPs genotypes and alleles did not differ between AD patients with a positive vs. negative lifetime history of suicide attempt and was not associated with GSES scoring.
CONCLUSIONS CONCLUSIONS
Generalized self-efficacy should be considered as a target for psychotherapeutic interventions aimed at reducing the risk of suicide attempts in AD patients who were exposed to childhood victimization. The negative results concerning the hypothesized role of the three analysed SNPs should be carefully interpreted due to the relatively small study sample, but represent a theoretical foundation for further research studies with larger study samples.

Identifiants

pubmed: 32157595
doi: 10.1007/s43440-020-00080-8
pii: 10.1007/s43440-020-00080-8
pmc: PMC8217039
doi:

Substances chimiques

Brain-Derived Neurotrophic Factor 0
GPI-Linked Proteins 0
NRN1 protein, human 0
Neuropeptides 0
BDNF protein, human 7171WSG8A2
Tacrolimus Binding Proteins EC 5.2.1.-
tacrolimus binding protein 5 EC 5.2.1.8

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

730-743

Commentaires et corrections

Type : ErratumIn

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Auteurs

Dominika Berent (D)

Masovian Regional Psychiatric Hospital Drewnica, Ząbki, Poland. dominikaberent@poczta.fm.

Bożena Szymańska (B)

Central Scientific Laboratory, Medical University of Lodz, Lodz, Poland.

Dominika Kulczycka-Wojdala (D)

Central Scientific Laboratory, Medical University of Lodz, Lodz, Poland.

Marian Macander (M)

Aviation Patophysiology and Safety Flight Department, Military Institute of Aviation Medicine, Warsaw, Poland.

Zofia Pawłowska (Z)

Central Scientific Laboratory, Medical University of Lodz, Lodz, Poland.

Marcin Wojnar (M)

Department of Psychiatry, Medical University of Warsaw, Warsaw, Poland.
Department of Psychiatry, University of Michigan, Ann Arbor, MI, USA.

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Classifications MeSH