Bipolar Disorder (BD) is a chronic psychiatric condition characterised by episodic
shifts between depressive and manic states. BD has a highly polygenic architecture,
which contributes to its substantial heritability and clinical variability. The disorder
also shares genetic susceptibility with schizophrenia and major depressive disorder
(MDD). Besides inherited risk, epigenetic processes—such as DNA methylation,
histone modifications, and noncoding RNAs—mediate gene–environment
interactions, influencing disease onset and progression. This review assesses the
potential of genetic and epigenetic markers to guide subtype-specific treatment in
BD, discusses present limitations, and proposes practical recommendations for
future research to support clinical implementation.
Keywords: bipolar disorder, genetic markers, epigenetics, psychiatric genomics,
biomarkers