Blood epigenome-wide association studies of suicide attempt in adults with bipolar disorder

• Published in: Translational psychiatry 2024-01, Vol.14 (1), p.70-10, Article 70
• Main Authors: Mirza, Salahudeen, Lima, Camila N. C., Del Favero-Campbell, Alexandra, Rubinstein, Alexandre, Topolski, Natasha, Cabrera-Mendoza, Brenda, Kovács, Emese H. C., Blumberg, Hilary P., Richards, Jenny Gringer, Williams, Aislinn J., Wemmie, John A., Magnotta, Vincent A., Fiedorowicz, Jess G., Gaine, Marie E., Walss-Bass, Consuelo, Quevedo, Joao, Soares, Jair C., Fries, Gabriel R.
• Format: Article
• Language: English
• Subjects: 38/61; 45/22; 45/43; 631/208/212/2166; 692/53/2423; Adult; Behavioral Sciences; Biological Psychology; Bipolar disorder; Bipolar Disorder - genetics; DNA Methylation; Epigenesis, Genetic; Epigenetics; Epigenome; Genome-Wide Association Study; Humans; Immune system; Medicine; Medicine & Public Health; Neurosciences; Pharmacotherapy; Psychiatry; Suicide, Attempted; Suicides & suicide attempts
• ISSN: 2158-3188; 2158-3188
• DOI: 10.1038/s41398-024-02760-y

Suicide attempt (SA) risk is elevated in individuals with bipolar disorder (BD), and DNA methylation patterns may serve as possible biomarkers of SA. We conducted epigenome-wide association studies (EWAS) of blood DNA methylation associated with BD and SA. DNA methylation was measured at >700,000 positions in a discovery cohort of n  = 84 adults with BD with a history of SA (BD/SA), n  = 79 adults with BD without history of SA (BD/non-SA), and n  = 76 non-psychiatric controls (CON). EWAS revealed six differentially methylated positions (DMPs) and seven differentially methylated regions (DMRs) between BD/SA and BD/non-SA, with multiple immune-related genes implicated. There were no epigenome-wide significant differences when BD/SA and BD/non-SA were each compared to CON, and patterns suggested that epigenetics differentiating BD/SA from BD/non-SA do not differentiate BD/non-SA from CON. Weighted gene co-methylation network analysis and trait enrichment analysis of the BD/SA vs. BD/non-SA contrast further corroborated immune system involvement, while gene ontology analysis implicated calcium signalling. In an independent replication cohort of n  = 48 BD/SA and n  = 47 BD/non-SA, fold changes at the discovery cohort’s significant sites showed moderate correlation across cohorts and agreement on direction. In both cohorts, classification accuracy for SA history among individuals with BD was highest when methylation at the significant CpG sites as well as information from clinical interviews were combined, with an AUC of 88.8% (CI = 83.8–93.8%) and 82.1% (CI = 73.6–90.5%) for the combined epigenetic-clinical classifier in the discovery and replication cohorts, respectively. Our results provide novel insight to the role of immune system functioning in SA and BD and also suggest that integrating information from multiple levels of analysis holds promise to improve risk assessment for SA in adults with BD.