BDNF gene Val66Met polymorphisms as a predictor for clinical presentation in schizophrenia - recent findings.

BDNF gene polymorphism genotyping neurotrophins schizophrenia

Journal

Frontiers in psychiatry
ISSN: 1664-0640
Titre abrégé: Front Psychiatry
Pays: Switzerland
ID NLM: 101545006

Informations de publication

Date de publication:
2023
Historique:
received: 03 06 2023
accepted: 25 09 2023
medline: 27 10 2023
pubmed: 27 10 2023
entrez: 27 10 2023
Statut: epublish

Résumé

Schizophrenia is a highly heritable, severe psychiatric disorder that involves dysfunctions in thinking, emotions, and behavior, with a profound impact on a person's ability to function normally in their daily life. Research efforts continue to focus on elucidating possible genetic underlying mechanisms of the disorder. Although the genetic loci identified to date to be significantly associated with schizophrenia risk do not represent disease-causing factors, each one of them could be seen as a possible incremental contributor. Considering the importance of finding new and more efficient pharmacological approaches to target the complex symptomatology of this disorder, in this scoping review, we are focusing on the most recent findings in studies aiming to elucidate the contribution of one of the genetic factors involved - the BDNF gene Val66Met polymorphisms. Here we performed a systematic search in Pubmed, Embase, and Web of Science databases with the search terms: (BDNF gene polymorphism) AND (schizophrenia) for articles published in the last 5 years. To be selected for this review, articles had to report on studies where genotyping for the BDNF Val66Met polymorphism was performed in participants diagnosed with schizophrenia (or schizophrenia spectrum disorders or first-episode psychosis). The search provided 35 results from Pubmed, 134 results from Embase, and 118 results from the Web of Science database. Twenty-two articles were selected to be included in this review, all reporting on studies where an implication of the BDNF Val66Met polymorphisms in the disorder's pathophysiology was sought to be elucidated. These studies looked at BDNF gene Val66Met polymorphism variants, their interactions with other genes of interest, and different facets of the illness. The Met/Met genotype was found to be associated with higher PANSS positive scores. Furthermore, Met/Met homozygous individuals appear to present with worse cognitive function and lower levels of serum BDNF. In the Val/Val genotype carriers, increased BDNF levels were found to correlate with weight gain under Risperidone treatment. However, due to heterogeneous results, the diversity in study populations and studies' small sample sizes, generalizations cannot be made. Our findings emphasize the need for further research dedicated to clarifying the role of gene polymorphisms in antipsychotic treatment to enhance specificity and efficacy in the treatment of schizophrenia.

Identifiants

pubmed: 37886115
doi: 10.3389/fpsyt.2023.1234220
pmc: PMC10598753
doi:

Types de publication

Systematic Review

Langues

eng

Pagination

1234220

Informations de copyright

Copyright © 2023 Farcas, Hindmarch and Iftene.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Adriana Farcas (A)

Centre for Neuroscience Studies, Queen's University, Kingston, ON, Canada.
Providence Care Hospital, Kingston, ON, Canada.

Charles Hindmarch (C)

Department of Biomedical and Molecular Sciences, Queen's University, Kingston, ON, Canada.
Department of Medicine, Queen's University, Kingston, ON, Canada.
Queen's Cardiopulmonary Unit, Translational Institute of Medicine, Queen's University, Kingston, ON, Canada.

Felicia Iftene (F)

Centre for Neuroscience Studies, Queen's University, Kingston, ON, Canada.
Providence Care Hospital, Kingston, ON, Canada.

Classifications MeSH