Peripheral blood E2F1 mRNA in depression and following electroconvulsive therapy.

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Authors

McGrory, Claire L
Ryan, Karen M
Kolshus, Erik
McLoughlin, Declan M

Issue Date

2018-10-24

Type

Clinical Trial
Journal Article
Research Support, Non-U.S. Gov't

Language

en

Keywords

Depression , E2F1 , Electroconvulsive therapy , Gene expression , Peripheral blood

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Abstract

The E2F transcription factors are a group of proteins that bind to the promotor region of the adenovirus E2 gene. E2F1, the first family member to be cloned, is linked to functions including cell proliferation and apoptosis, DNA repair, cell senescence and metabolism. We recently performed a deep sequencing study of micro-RNA changes in whole blood following ECT. Two micro-RNAs (miR-126-3p and miR-106a-5p) were identified and gene targeting analysis identified E2F1 as a shared target of these miRNAs. To our knowledge, no studies have examined E2F1 mRNA levels in patients with depression. Peripheral blood E2F1 mRNA levels were therefore examined in patients with depression, compared to healthy controls, and the effects of a course of ECT on peripheral blood E2F1 mRNA was investigated. Depressed patient and healthy control groups were balanced on the basis of age and sex. E2F1 mRNA levels were significantly lower in depressed patients in comparison to controls (p = .009) but did not change with ECT. There was no relationship between baseline E2F1 levels and depression severity, response to treatment, presence of psychosis or polarity of depression. There were no significant correlations between E2F1 levels and mood scores based on the HAM-D24. These results indicate that reduced peripheral blood E2F1 mRNA could be a trait feature of depression.

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Citation

McGrory, C. L., Ryan, K. M., Kolshus, E., & McLoughlin, D. M. (2019). Peripheral blood E2F1 mRNA in depression and following electroconvulsive therapy. Progress in neuro-psychopharmacology & biological psychiatry, 89, 380–385. https://doi.org/10.1016/j.pnpbp.2018.10.011

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Copyright © 2018 Elsevier Inc. All rights reserved.

Journal

Progress in neuro-psychopharmacology & biological psychiatry

Volume

89

Issue

PubMed ID

ISSN

1878-4216

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