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Genetic overlap between major depressive disorder and obstructive sleep apnea. | LitMetric

Genetic overlap between major depressive disorder and obstructive sleep apnea.

Front Psychiatry

Rehabilitation Medicine Department, The Affiliated Changsha Hospital of Xiangya School of Medicine, Central South University (The First Hospital of Changsha), Changsha, China.

Published: November 2024

AI Article Synopsis

  • - This study examines the genetic connections between major depressive disorder (MDD) and obstructive sleep apnea (OSA), two conditions that often occur together, by analyzing data from large genetic studies.
  • - Researchers found a significant genetic correlation between MDD and OSA, identified shared genetic markers (397 SNPs from 45 loci), and discovered 154 genes with roles in influencing both disorders.
  • - The analysis suggests that having MDD increases the risk of developing OSA, highlighting the potential shared mechanisms and genetic influences behind these two conditions.

Article Abstract

Objective: Observational studies have frequently shown a co-occurrence of psychiatric disorders and Obstructive sleep apnea (OSA), with major depressive disorder (MDD) being a prevalent psychiatric disorder. This study aims to investigate the genetic overlap between MDD and OSA to explore their underlying pathological mechanisms.

Methods: Leveraging the extensive and recent GWAS for OSA and MDD, we conducted genetic correlation analyses utilizing Linkage disequilibrium score regression (LDSC), re-evaluated their pleiotropic Single-nucleotide polymorphisms (SNP) with Cross-Phenotype Association (CPASSOC) and Colocalization (COLOC), investigated the overlap at the gene level using physical annotations and Multi-marker Analysis of GenoMic Annotation (MAGMA), and finally employed Mendelian randomization (MR) to assess potential causal relationships between the two disorders.

Results: Upon our investigation, we established that MDD and OSA exhibit high heritability (h2MDD=0.02, h2OSA=0.04) alongside a significant genetic correlation (rg=0.31, P= 1.42E-23). Utilizing CPASSOC, we identified 397 pleiotropic SNPs, associable with 45 loci, two of which share common genetic fragments with a pleiotropic role. Furthermore, the MAGMA study uncovered a total of 154 pleiotropic genes capable of influencing multiple brain regions. Lastly, leveraging MR analysis, we concluded that MDD heightens the risk of developing OSA (P=3. 10E-04, OR (95%CI):1.28(1.12~ 1.47)).

Conclusion: In summary, our study identified as a common gene between OSA and MDD and provided evidence that MDD causally contributes to the development of OSA. These insights enhance our understanding of the shared mechanisms underlying the comorbidity of these conditions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11574086PMC
http://dx.doi.org/10.3389/fpsyt.2024.1464396DOI Listing

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