AI Article Synopsis

  • The study examines the potential link between MAOA gene polymorphisms and major depressive disorder (MDD), particularly focusing on differences between males and females.
  • While they found no significant associations in males, a connection was noted in females between specific MAOA polymorphisms and severe MDD.
  • Overall, the results indicate that MAOA polymorphisms likely do not have a major role in causing MDD or its subtypes, though there's a suggestion for further investigation in specific subgroups and different ethnic populations.

Article Abstract

It has been proposed that an MAOA abnormality may be an important factor in the development of major depressive disorder (MDD). Various polymorphisms of the MAOA gene have been investigated for possible associations with mood disorders, but results have been inconsistent. The goal of the present study was to investigate whether polymorphisms of the MAOA gene are associated with MDD or alternatively with different clinical subgroups of MDD. A total of 590 Han Chinese subjects in Taiwan (312 controls and 278 MDD patients) were recruited. Among the males, there were no associations with MAOA polymorphisms. Among the females, an association was found between MAOA polymorphisms and severe MDD (P=0.041 for uVNTR and 0.017 for EcoRV (rs1137070), respectively). However, in analyses of haplotype frequencies and multiple logistic regression, MAOA polymorphisms were not associated with either MDD or its subgroups. The results suggest that MAOA polymorphisms do not play a major role in the pathogenesis of MDD or its subgroups. However, a potential role for a minor association with some specific subgroups and with different ethnic samples needs to be explored further.

Download full-text PDF

Source
http://dx.doi.org/10.1080/15622970701816506DOI Listing

Publication Analysis

Top Keywords

maoa polymorphisms
20
maoa
8
clinical subgroups
8
major depressive
8
han chinese
8
polymorphisms maoa
8
maoa gene
8
associated mdd
8
mdd subgroups
8
polymorphisms
7

Similar Publications

Type A monoamine oxidase; its unique role in mood, behavior and neurodegeneration.

J Neural Transm (Vienna)

December 2024

Clinical Neurochemistry, Department of Psychiatry, Psychosomatics and Psychotherapy, University Hospital Würzburg, Würzburg, Germany.

Monoamine oxidase catalyzes oxidative deamination of monoamine transmitters and plays a critical role in the pathogenesis of neuropsychiatric diseases. Monoamine oxidase is classified into type A and B (MAO-A, MAO-B) according to the substrate specificity and sensitivity to inhibitors. The isoenzymes are different proteins coded by different genes localized on the X-chromosome, but they have identical intron-exon organization, similar protein structure and enzymatic mechanism and are considered to be derived from the same ancestral gene.

View Article and Find Full Text PDF

Pediatric autoimmune neuropsychiatric disorders associated with or without streptococcal and other bacterial infections (PANDAS/CANS) are emerging as a featured pediatric disorder. Although there is some controversy regarding treatment approaches, especially related to the behavioral sequelae, we have hypothesized in other published work that it is characterized by the rapid onset of Reward Deficiency Syndrome (RDS) in children. We propose utilizing a multi-systems biological approach involving the coupling of genetic addiction risk testing and pro-dopamine regulation (KB220/POLYGEN) to help induce "dopamine homeostasis" in patients with PANDAS, especially those with known DNA-induced hypodopaminergia.

View Article and Find Full Text PDF

The Monoamine Oxidase-A () EcoRV polymorphism (rs1137070) is a unique synonymous mutation (c.1409 T > C) within the gene, which plays a crucial role in gene expression and function. This study aimed to explore the relationship between the mouse rs1137070 genotype and differences in gene expression.

View Article and Find Full Text PDF

Betel quid (BQ) use disorder (BUD) is prevalent in many Asian countries, impacting approximately 600 million people. We conducted a randomized clinical trial to analyze the impact of MAOA genetic variations on the severity of BQ craving. This was measured using criteria and the Yale-Brown Obsessive-Compulsive Scale modified for betel quid use (Y-BOCS-BQ).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!