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CORRECTION article

Front. Psychiatry, 04 August 2022
Sec. Sleep Disorders
Volume 13 - 2022 | https://doi.org/10.3389/fpsyt.2022.893816

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

This article is a correction to:

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

    1. Read original article
\nLindsay M. Melhuish Beaupre,Lindsay M. Melhuish Beaupre1,2Arun K. Tiwari,Arun K. Tiwari1,3Vanessa F. Gonalves,,Vanessa F. Gonçalves1,2,3Clement C. Zai,,,Clement C. Zai1,2,3,4Victoria S. Marshe,Victoria S. Marshe1,2Cathryn M. Lewis,Cathryn M. Lewis5,6Nicholas G. MartinNicholas G. Martin7Andrew M. McIntoshAndrew M. McIntosh8Mark J. AdamsMark J. Adams8Bernhard T. Baune,,Bernhard T. Baune9,10,11Doug F. LevinsonDoug F. Levinson12Dorret I. BoomsmaDorret I. Boomsma13Brenda W. J. H. PenninxBrenda W. J. H. Penninx14Gerome Breen,Gerome Breen5,15Steve HamiltonSteve Hamilton16Swapnil AwasthiSwapnil Awasthi17Stephan Ripke,,,Stephan Ripke17,18,19,20Lisa JonesLisa Jones21Ian JonesIan Jones22Enda M. ByrneEnda M. Byrne23Ian B. HickieIan B. Hickie24James P. PotashJames P. Potash25Jianxin ShiJianxin Shi26Myrna M. Weissman,Myrna M. Weissman27,28Yuri MilaneschiYuri Milaneschi14Stanley I. ShynStanley I. Shyn29Eco J. C. de GeusEco J. C. de Geus14Gonneke WillemsenGonneke Willemsen14Gregory M. Brown,Gregory M. Brown1,2James L. Kennedy,, James L. Kennedy1,2,3*Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium&#x; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium†
  • 1Molecular Brain Science Research Department, Centre for Addiction and Mental Health, Campbell Family Mental Health Research Institute, Toronto, ON, Canada
  • 2Institute of Medical Sciences, University of Toronto, Toronto, ON, Canada
  • 3Department of Psychiatry, University of Toronto, Toronto, ON, Canada
  • 4Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada
  • 5Social, Genetic and Developmental Psychiatry Centre, King's College London, London, United Kingdom
  • 6Department of Medical and Molecular Genetics, King's College London, London, United Kingdom
  • 7Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia
  • 8Division of Psychiatry, University of Edinburgh, Edinburgh, United Kingdom
  • 9Department of Psychiatry, University of Münster, Münster, Germany
  • 10Department of Psychiatry, Melbourne Medical School, University of Melbourne, Melbourne, VIC, Australia
  • 11Florey Institute of Neuroscience and Mental Health, University of Melbourne, Melbourne, VIC, Australia
  • 12Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, United States
  • 13Department of Biological Psychology, Amsterdam Public Health Research Institute, Vrije Universiteit, Amsterdam, Netherlands
  • 14Department of Psychiatry, Amsterdam Public Health and Amsterdam Neuroscience, Amsterdam UMC/Vrije Universiteit, Amsterdam, Netherlands
  • 15National Institute for Health Research (NIHR) Maudsley Biomedical Research Centre, King's College London, London, United Kingdom
  • 16The Permanente Medical Group, San Francisco, CA, United States
  • 17Department of Psychiatry and Psychotherapy, Universitäts Medizin Berlin Campus Charité Mitte, Berlin, Germany
  • 18Analytic and Translational Genetic Unit, Massachusetts General Hospital, Boston, MA, United States
  • 19Medical and Population Genetics, Broad Institute, Cambridge, MA, United States
  • 20Department of Psychiatry, Charité, Berlin, Germany
  • 21Psychological Medicine, University of Worcester, Worcester, United Kingdom
  • 22Medical Research Council (MRC) Centre for Neuropsychiatric Genetics and Genomics, Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, United Kingdom
  • 23Institute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia
  • 24Brain and Mind Centre, University of Sydney, Sydney, NSW, Australia
  • 25Psychiatry Department, University of Iowa, Iowa City, IA, United States
  • 26Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, United States
  • 27Psychiatry Department, Columbia University College of Physicians and Surgeons, New York, NY, United States
  • 28Division of Epidemiology, New York State Psychiatric Institute, New York, NY, United States
  • 29Washington Permanente Medical Group, Kaiser Permanente Washington Health Research Institute, Seattle, WA, United States

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

by Melhuish Beaupre, L. M., Tiwari, A. K., Gonçalves, V. F., Zai, C. C., Marshe, V. S., Lewis, C. M., Martin, N. G., McIntosh, A. M., Adams, M. J., Baune, B. T., Levinson, D. F., Boomsma, D. I., Penninx, B. W. J. H., Breen, G., Hamilton, S., Awasthi, S., Ripke, S., Jones, L., Jones, I., Byrne, E. M., Hickie, I. B., Potash, J. P., Shi, J., Weissman, M. M., Milaneschi, Y., Shyn, S. I., Geus, E. J. C. d., Willemsen, G., Brown, G. M., Kennedy, J. L., and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2021). Front. Psychiatry 12:734077. doi: 10.3389/fpsyt.2021.734077

In the original article, there was an error. The prevalence of hypersomnia in females and males was reversed, such that the prevalence of hypersomnia was reported as the prevalence of no hypersomnia for both sexes.

A correction has been made to Results, paragraph one:

“N = 4,583 (68%) of individuals were female in the insomnia sample and N = 4,358 (68%) in the hypersomnia sample. Of the females, 77.3% of reported insomnia while 22.7% do not; 68.1% of females reported hypersomnia while 31.9% did not. In males, 79% reported insomnia while 21% did not; 75% reported hypersomnia while 25% did not” has been corrected to “N = 4,583 (68%) of individuals were female in the insomnia sample and N = 4,358 (68%) in the hypersomnia sample. Of the females, 77.3% reported insomnia while 22.7% did not; 31.9% of females reported hypersomnia while 68.1% did not. In males, 79% reported insomnia while 21% did not; 25% reported hypersomnia while 75% did not.”

A correction has been made to Discussion, paragraph two:

“First, we found that the prevalence rates for insomnia are representative of the prevalence rates from other reports (8, 40). The prevalence of hypersomnia in our sample is slightly higher than others have reported (8, 40). Interestingly, the prevalence of insomnia between sexes was similar, but the prevalence of hypersomnia in males was 7% higher than in females. The direction of our hypersomnia results is in accordance with prior literature, which suggests depressed males are more likely to experience hypersomnia than depressed females. However, the study also suggests a more significant difference than observed in our results (41). However, their sample was significantly smaller (N < 500, which may explain the difference in prevalence rates)” has been corrected to “First, we found that the prevalence rates for insomnia were representative of the prevalence rates from other reports (8, 40). The prevalence of hypersomnia in our sample was slightly higher than others have reported (8, 40). Interestingly, the prevalence of insomnia between sexes was similar, but the prevalence of hypersomnia in females was 7% higher than in males. Our results are opposite to prior literature, that suggested depressed males are more likely to experience hypersomnia than depressed females (41). However, their sample was significantly smaller (N < 500), which may explain the difference in prevalence rates.”

In the original article, there were mistakes in the labelling of Supplementary Tables 1, 2 as published. Their labelling was reversed, such that Supplementary Table 1 was referred to as if it were Supplementary Table 2, and vice versa. The Supplementary Material labelling has been corrected.

In the original article, there was a mistake in the reference order for the citations included in Table 1. Twelve references [i.e., (20–32)] were incorrect. References 20–32 have been corrected and subsequently the full reference list and citations have been updated.

The authors apologize for these errors and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

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Keywords: sleep, major depressive disorder, insomnia, hypersomnia, polygenic risk

Citation: 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

Received: 10 March 2022; Accepted: 28 June 2022;
Published: 04 August 2022.

Edited and reviewed by: Mehmet Y. Agargün, Yuzuncu Yil University, Turkey

Copyright © 2022 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). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: James L. Kennedy, jim.kennedy@camh.ca

†Full list of Consortium members are present in the Supplementary Material

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