TY - JOUR
T1 - Underlying Mechanisms Involved in Gambling Disorder Severity: A Pathway Analysis Considering Genetic, Psychosocial, and Clinical Variables
AU - Gómez-Peña, Mónica
AU - Etxandi, Mikel
AU - Gené, Manel
AU - Barrot, Carme
AU - Granero, Roser
AU - Moragas, Laura
AU - Ramoz, Nicolas
AU - Baenas, Isabel
AU - Jiménez-Murcia, Susana
AU - Solé-Morata, Neus
AU - Gorwood, Philip
AU - Fernández-Aranda, Fernando
N1 - Publisher Copyright:
© 2023 by the authors.
PY - 2023/1/13
Y1 - 2023/1/13
N2 - Gambling Disorder (GD) has a complex etiology that involves biological and environmental aspects. From a genetic perspective, neurotrophic factors (NTFs) polymorphisms have been associated with the risk of developing GD. The aim of this study was to assess the underlying mechanisms implicated in GD severity by considering the direct and mediational relationship between different variables including genetic, psychological, socio-demographic, and clinical factors. To do so, we used genetic variants that were significantly associated with an increased risk for GD and evaluated its relationship with GD severity through pathway analysis. We found that the interaction between these genetic variants and other different biopsychological features predicted a higher severity of GD. On the one hand, the presence of haplotype block 2, interrelated with haplotype block 3, was linked to a more dysfunctional personality profile and a worse psychopathological state, which, in turn, had a direct link with GD severity. On the other hand, having rs3763614 predicted higher general psychopathology and therefore, higher GD severity. The current study described the presence of complex interactions between biopsychosocial variables previously associated with the etiopathogenesis and severity of GD, while also supporting the involvement of genetic variants from the NTF family.
AB - Gambling Disorder (GD) has a complex etiology that involves biological and environmental aspects. From a genetic perspective, neurotrophic factors (NTFs) polymorphisms have been associated with the risk of developing GD. The aim of this study was to assess the underlying mechanisms implicated in GD severity by considering the direct and mediational relationship between different variables including genetic, psychological, socio-demographic, and clinical factors. To do so, we used genetic variants that were significantly associated with an increased risk for GD and evaluated its relationship with GD severity through pathway analysis. We found that the interaction between these genetic variants and other different biopsychological features predicted a higher severity of GD. On the one hand, the presence of haplotype block 2, interrelated with haplotype block 3, was linked to a more dysfunctional personality profile and a worse psychopathological state, which, in turn, had a direct link with GD severity. On the other hand, having rs3763614 predicted higher general psychopathology and therefore, higher GD severity. The current study described the presence of complex interactions between biopsychosocial variables previously associated with the etiopathogenesis and severity of GD, while also supporting the involvement of genetic variants from the NTF family.
KW - severity
KW - socio-demographics
KW - psychopathology
KW - personality traits
KW - neurotrophic genes
KW - gambling disorder
UR - https://www.scopus.com/pages/publications/85146753834
UR - https://www.mendeley.com/catalogue/89d0db17-cf0e-3d83-8fec-e8cc65068974/
UR - https://ddd.uab.cat/record/270874
U2 - 10.3390/nu15020418
DO - 10.3390/nu15020418
M3 - Article
C2 - 36678289
SN - 2072-6643
VL - 15
SP - 418
JO - Nutrients
JF - Nutrients
IS - 2
M1 - 418
ER -