4.7 Article

Gene expression study in monocytes: evidence of inflammatory dysregulation in early-onset obsessive-compulsive disorder

Journal

TRANSLATIONAL PSYCHIATRY
Volume 12, Issue 1, Pages -

Publisher

SPRINGERNATURE
DOI: 10.1038/s41398-022-01905-1

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Funding

  1. Alicia Koplowitz Foundation
  2. Ministerio de Economia y Competitividad, Instituto de Salud Carlos III, Fondo de Investigacion Sanitaria (FIS) [PI13/01767]
  3. Fondo Europeo de Desarrollo Regional (FEDER)Union Europea
  4. Agencia de Gestio d'Ajuts Universitaris i Recerca (AGAUR) of the Generalitat de Catalunya [2014 SGR 489, 2014 SGR 436, 2020 FI-SDUR 00327]

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In this study, we investigated the gene expression and immune dysfunction of monocytes in pediatric patients with OCD. We found that several immune processes were altered in the monocytes of OCD patients, both under basal conditions and after immune stimulation. Although qPCR analysis did not show significant differences, there were high correlations between gene expression levels and inflammatory markers.
Obsessive-compulsive disorder (OCD) has a complex etiology that seems to include immune dysfunction and alterations in circulating monocytes. To investigate the immune basis and the functional dysregulation of monocytes in this disease, we analyzed gene expression in the peripheral monocytes of pediatric patients with OCD (N = 102) compared to controls (N = 47). We examined gene expression in primary cultures of peripheral monocytes from participants, under basal conditions and under exposure to lipopolysaccharide (LPS) to stimulate immune response. Whole-genome expression was assessed in 8 patients and 8 controls. Differentially expressed genes were identified followed by protein-protein interaction network construction and functional annotation analysis to identify the genes and biological processes that are altered in the monocytes of OCD patients. We also explored the expression levels of selected genes in monocytes from the other participants using qPCR. Several changes in gene expression were observed in the monocytes of OCD patients, with several immune processes involved under basal conditions (antigen processing and presentation, regulation of immune system and leukocyte cell adhesion) and after LPS stimulation (immune and inflammatory response, cytokine production and leukocyte activation). Despite the qPCR analysis provided no significant differences between patients and controls, high correlations were observed between the expression levels of some of the genes and inflammatory markers (i.e., T helper 17 and regulatory T cell levels, total monocyte and proinflammatory monocyte subset levels, and the cytokine production by resting and stimulated monocytes) of the study participants. Our findings provide more evidence of the involvement of monocyte dysregulation in early-onset OCD, indicating a proinflammatory predisposition and an enhanced immune response to environmental triggers.

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