Biological tests for major depressive disorder that involve leukocyte gene expression assays

• Published in: Journal of psychiatric research Vol. 66-67; pp. 1 - 6
• Main Authors: Watanabe, Shin-ya, Iga, Jun-ichi, Ishii, Kazuo, Numata, Shusuke, Shimodera, Shinji, Fujita, Hirokazu, Ohmori, Tetsuro
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.07.2015
• Subjects: Adult; Biomarker; Depressive Disorder, Major - blood; Depressive Disorder, Major - diagnosis; Depressive Disorder, Major - genetics; Diagnostic test; Discriminant Analysis; Female; Gene Expression Profiling - methods; Healthy subjects; Humans; Leukocyte gene expression; Leukocytes - metabolism; Linear Models; Major depressive disorder; Male; Middle Aged; PCR array; Pilot Projects; Polymerase Chain Reaction; Psychiatry; RNA, Messenger - blood; Sensitivity and Specificity; Healthy subjects; Biomarker; Diagnostic test; Leukocyte gene expression; Major depressive disorder; PCR array
• ISSN: 0022-3956; 1879-1379; 1879-1379
• DOI: 10.1016/j.jpsychires.2015.03.004

Development of easy-to-use biological diagnostic tests for major depressive disorder (MDD) may facilitate MDD diagnosis and delivery of optimal treatment. Here, we examined leukocyte gene expression to develop a biological diagnostic test for MDD. 25 drug-naive MDD patients (MDDs) and 25 age- and sex-matched healthy subjects (Controls) participated in a pilot study. A subsequent replication study involved 20 MDDs and 18 Controls. We used custom-made PCR array plates to examine mRNA levels of 40 candidate genes in leukocyte samples to assess whether any combination of these genes could be used to differentiate MDDs from Controls based on expression profiles. Among 40 candidate genes, we identified a set of seven genes (PDGFC, SLC6A4, PDLIM5, ARHGAP24, PRNP, HDAC5, and IL1R2), each of which had expression levels that differed significantly between MDD and Control samples in the pilot study. To identify genes whose expression best differentiated between MDDs and Controls, a linear discriminant function was developed to discriminate between MDDs and Controls based on the standardized values of gene expression after Z-score transformation. Ultimately, five genes (PDGFC, SLC6A4, ARHGAP24, PRNP, and HDAC5) were selected for a multi-assay diagnostic test. In the pilot study, this diagnostic test demonstrated sensitivity and specificity of 80% and 92%, respectively. The replication study yielded nearly identical results, sensitivity of 85% and specificity of 89%. Using leukocyte gene expression profiles, we could differentiate MDDs from Controls with adequate sensitivity and specificity. Additional markers not yet identified might further improve the performance of this test. •Among 40 candidate genes, a set of 7 genes differed significanlty between MDD and Control samples in the pilot study.•A multi-assay test yielded sensitivity and specificity of over 80% each in differentiating patients with MDD from controls.•The gene expression profiles of peripheral leukocytes may be useful for clinical diagnostic test of MDD.