Divergent transcriptomic profiles in depressed individuals with hyper- and hypophagia implicating inflammatory status.
Torsten KlengelShu DanJulia HallLaura M HolsenPublished in: Research square (2023)
Major Depressive Disorder (MDD) is a heterogenous and etiologically complex disease encompassing a broad spectrum of psychopathology, presumably arising from distinct pathophysiological mechanisms. Divergent appetitive phenotypes including Hyperphagic MDD (characterized by an increased appetite) and Hypophagic MDD (characterized by a decrease in appetite) are important clinical characteristics that are closely related to comorbidities, including cardiometabolic disorders. Prior evidence supports the notion that hyperphagia is associated with atypical depression, decreased stress-hormone signaling, a pro-inflammatory status, hypersomnia, and poorer clinical outcomes. Yet, our understanding of the underlying mechanisms of Hyperphagic and Hypophagic MDD is limited, and knowledge of associated biological correlates of these endophenotypes remain fragmented. We performed an exploratory study on peripheral blood RNA profiling using bulk RNAseq in unmedicated individuals with Hyperphagic and Hypophagic MDD (n=8 and n=13, respectively) and discovered individual genes and gene pathways associated with appetitive phenotypes. In addition, we used the Maastricht Acute Stress Task to uncover stress-related transcriptomic profiles in Hyper- and Hypophagic MDD.
Keyphrases
- major depressive disorder
- bipolar disorder
- peripheral blood
- single cell
- genome wide
- weight loss
- healthcare
- rna seq
- oxidative stress
- stress induced
- liver failure
- depressive symptoms
- body weight
- dna methylation
- copy number
- gene expression
- genome wide identification
- heat stress
- sleep quality
- intensive care unit
- hepatitis b virus