Postmortem transcriptional profiling reveals widespread increase in inflammation in schizophrenia: a comparison of prefrontal cortex, striatum, and hippocampus among matched tetrads of controls with subjects diagnosed with schizophrenia, bipolar or major depressive disorder

• Published in: Translational psychiatry Vol. 9; no. 1; p. 151
• Main Authors: Lanz, Thomas A., Reinhart, Veronica, Sheehan, Mark J., Rizzo, Stacey J. Sukoff, Bove, Susan E., James, Larry C., Volfson, Dmitri, Lewis, David A., Kleiman, Robin J.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 23.05.2019; Nature Publishing Group
• Subjects: 38/39; 38/61; 631/378/340; 692/699/476/1799; Animals; Antipsychotics; Autopsy; Behavioral Sciences; Biological Psychology; Bipolar disorder; Bipolar Disorder - genetics; Bipolar Disorder - immunology; Bipolar Disorder - metabolism; Brain; Corpus Striatum - immunology; Corpus Striatum - metabolism; Depressive Disorder, Major - genetics; Depressive Disorder, Major - immunology; Depressive Disorder, Major - metabolism; Gene Expression Profiling; Hippocampus - immunology; Hippocampus - metabolism; Humans; Inflammation; Inflammation - genetics; Inflammation - immunology; Inflammation - metabolism; Male; Medicine; Medicine & Public Health; Mental depression; Mental disorders; Neurosciences; Pharmacotherapy; Prefrontal Cortex - immunology; Prefrontal Cortex - metabolism; Psychiatry; Psychotropic drugs; Rats; Rats, Sprague-Dawley; Schizophrenia; Schizophrenia - genetics; Schizophrenia - immunology; Schizophrenia - metabolism
• DOI: 10.1038/s41398-019-0492-8
• ISSN: 2158-3188

Psychiatric disorders such as schizophrenia (SCZ), bipolar disorder (BD), and major depressive disorder (MDD) arise from complex interactions between genetic and environmental factors. Common genetic variants associated with multiple psychiatric disorders suggest that shared genetic architecture could contribute to divergent clinical syndromes. To evaluate shared transcriptional alterations across connected brain regions, Affymetrix microarrays were used to profile postmortem dorsolateral prefrontal cortex (DLPFC), hippocampus, and associative striatum from 19 well-matched tetrads of subjects with SCZ, BD, MDD, or unaffected controls. SCZ subjects showed a substantial burden of differentially expressed genes across all examined brain regions with the greatest effects in hippocampus, whereas BD and MDD showed less robust alterations. Pathway analysis of transcriptional profiles compared across diagnoses demonstrated commonly enriched pathways between all three disorders in hippocampus, significant overlap between SCZ and BD in DLPFC, but no significant overlap of enriched pathways between disorders in striatum. SCZ samples showed increased expression of transcripts associated with inflammation across all brain regions examined, which was not evident in BD or MDD, or in rat brain following chronic dosing with antipsychotic drugs. Several markers of inflammation were confirmed by RT-PCR in hippocampus, including S100A8/9, IL-6, MAFF, APOLD1, IFITM3, and BAG3. A cytokine ELISA panel showed significant increases in IL-2 and IL-12p70 protein content in hippocampal tissue collected from same SCZ subjects when compared to matched control subjects. These data suggest an overlapping subset of dysregulated pathways across psychiatric disorders; however, a widespread increase in inflammation appears to be a specific feature of the SCZ brain and is not likely to be attributable to chronic antipsychotic drug treatment.