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Potential Genetic Overlap Between Insomnia and Sleep Symptoms in Major Depressive Disorder: A Polygenic Risk Score Analysis

Melhuish Beaupre, L., Tiwari, A., Gonçalves, V., Zai, C., Marshe, V., Lewis, C., Martin, N., McIntosh, A., Adams, M., Baune, B., Levinson, D., Boomsma, D., Penninx, B., Breen, G., Hamilton, S., Awasthi, S., Ripke, S., Jones, Lisa ORCID: https://orcid.org/0000-0002-5122-8334, Jones, I., Byrne, E., Hickie, I., Potash, J., Shi, J., Weissman, M., Milaneschi, Y., Shyn, S., de Geus, E., Willemsen, G., Brown, G. and Kennedy, J. (2021) Potential Genetic Overlap Between Insomnia and Sleep Symptoms in Major Depressive Disorder: A Polygenic Risk Score Analysis. Frontiers in Psychiatry, 12 (734077). p. 2118. ISSN Online: 1664-0640

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Abstract

Background: The prevalence of insomnia and hypersomnia in depressed individuals is substantially higher than that found in the general population. Unfortunately, these concurrent sleep problems can have profound effects on the disease course. Although the full biology of sleep remains to be elucidated, a recent genome-wide association (GWAS) of insomnia, and other sleep traits in over 1 million individuals was recently published and provides many promising hits for genetics of insomnia in a population-based sample.

Methods: Using data from the largest available GWAS of insomnia and other sleep traits, we sought to test if sleep variable PRS scores derived from population-based studies predicted sleep variables in samples of depressed cases [Psychiatric Genomics Consortium - Major Depressive Disorder subjects (PGC MDD)]. A leave-one-out analysis was performed to determine the effects that each individual study had on our results.

Results: The only significant finding was for insomnia, where p-value threshold, p = 0.05 was associated with insomnia in our PGC MDD sample (R2 = 1.75−3, p = 0.006).

Conclusion: Our results reveal that <1% of variance is explained by the variants that cover the two significant p-value thresholds, which is in line with the fact that depression and insomnia are both polygenic disorders. To the best of our knowledge, this is the first study to investigate genetic overlap between the general population and a depression sample for insomnia, which has important treatment implications, such as leading to novel drug targets in future research efforts.

Item Type: Article
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A correction has been applied to this article in:

Corrigendum: Potential genetic overlap between insomnia and sleep symptoms in major depressive disorder: A polygenic risk score analysis

This document is attached to this entry as Supplemental Material and can be cited as:

Melhuish Beaupre LM, Tiwari AK, Gonçalves VF, Zai CC, Marshe VS, Lewis CM, Martin NG, McIntosh AM, Adams MJ, Baune BT, Levinson DF, Boomsma DI, Penninx BWJH, Breen G, Hamilton S, Awasthi S, Ripke S, Jones L, Jones I, Byrne EM, Hickie IB, Potash JP, Shi J, Weissman MM, Milaneschi Y, Shyn SI, Geus EJCd, Willemsen G, Brown GM, Kennedy JL and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2022) Corrigendum: Potential genetic overlap between insomnia and sleep symptoms in major depressive disorder: A polygenic risk score analysis. Front. Psychiatry 13:893816. doi: 10.3389/fpsyt.2022.893816 Published: 04 August 2022.

Uncontrolled Discrete Keywords: sleep, major depressive disorder, insomnia,, hypersomnia,, polygenic risk
Subjects: R Medicine > RC Internal medicine > RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry
Divisions: College of Health, Life and Environmental Sciences > School of Allied Health and Community
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Copyright Info: Copyright © 2021 Melhuish Beaupre, Tiwari, Gonçalves, Zai, Marshe, Lewis, Martin, McIntosh, Adams, Baune, Levinson, Boomsma, Penninx, Breen, Hamilton, Awasthi, Ripke, Jones, Jones, Byrne, Hickie, Potash, Shi, Weissman, Milaneschi, Shyn, Geus, Willemsen, Brown, Kennedy and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).
Depositing User: Katherine Gordon-Smith
Date Deposited: 22 Dec 2021 17:53
Last Modified: 21 May 2024 12:58
URI: https://eprints.worc.ac.uk/id/eprint/11582

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