Clock gene influences on sleep quality and HPA axis in major depressive disorder
Year: 2025
Type: article
Study design: Observational Study
Abstract: BACKGROUND: Major Depressive Disorder (MDD) has been associated with disruptions in circadian rhythms and dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis. Circadian rhythms are regulated by "clock" genes, including BMAL1, which are also implicated in HPA axis function. This study aimed to examine the association between BMAL1 polymorphisms and sleep quality, their interactions with sex and MDD diagnosis, and their potential influence on HPA axis activity in MDD. METHODS: The sample included 84 patients with MDD and 120 healthy controls (HCs). Clinical and sociodemographic variables were assessed. HPA axis activity was measured using the cortisol awakening response (CAR) and diurnal cortisol slope. Six single nucleotide polymorphisms (SNPs) in the BMAL1 gene were analyzed. Multiple regression models were used, adjusting for relevant covariates. RESULTS: The BMAL1 SNP rs11022778 was significantly associated with sleep quality in the total sample. Interaction analyses revealed that this association was specific to individuals with MDD. Additionally, rs11022778 was significantly associated with both CAR and slope measures among MDD patients. CONCLUSIONS: These findings highlight the potential role of BMAL1 gene variants in modulating biological and clinical phenotypes related to circadian and stress regulation. The rs11022778 variant may contribute to altered sleep quality and HPA axis activity in MDD. Future research should consider such genetic markers to inform more personalized approaches to MDD treatment.
Source: Sleep Medicine
Institutions: Universitat Autònoma de Barcelona, Instituto de Salud Carlos III, Centro de Investigación Biomédica en Red de Salud Mental, Corporació Sanitària Parc Taulí, Institute of Research and Innovation Parc Tauli, Maresme Health Consortium, Institut Pere Mata, Institut de Recerca Biomèdica Catalunya Sud, Universitat Rovira i Virgili, Bellvitge University Hospital, Institut d'Investigació Biomédica de Bellvitge, Universitat de Barcelona, Complejo Hospitalario Universitario de Santiago, Instituto de Investigación Sanitaria de Santiago, Servicio Gallego de Salud, Universidade de Santiago de Compostela, Centre for Biomedical Network Research on Rare Diseases
Language: English
Subfield: Endocrine and Autonomic Systems
Field: Neuroscience
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $4,350
Awards: G1251285548, G2356201822, G3522678809, G4986797981, Estudio de la regulación de la expresión de Nrf2 en la depresión mayor mediante el análisis de cambios epigenéticos en el gen NFE2L2: asociación con la carga alostática y variables clínicas, G6771536215, G7604561293, Marcadores epigenéticos en depresión mayor: Efectos en fenotipos neurocognitivos, la evolución clínica y la resistencia terapéutica
OpenAlex ID: W4417435483
