4.6 Article

Network outcome analysis identifies difficulty initiating sleep as a primary target for prevention of depression: a 6-year prospective study

期刊

SLEEP
卷 43, 期 5, 页码 -

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/sleep/zsz288

关键词

insomnia; major depressive disorder; prevention; network outcome analysis; multivariate analysis

资金

  1. European Research Council [ERC-ADG-2014-671084-INSOMNIA]
  2. VU University
  3. Geestkracht Program of the Netherlands Organisation for Health Research and Development (ZonMw) [10-000-1002]
  4. VU University Medical Center
  5. GGZ in Geest
  6. Leiden University Medical Center
  7. Leiden University
  8. GGZ Rivierduinen
  9. University Medical Center Groningen
  10. University of Groningen
  11. Lentis
  12. GGZ Friesland
  13. GGZ Drenthe
  14. Rob Giel Onderzoekscentrum

向作者/读者索取更多资源

Study Objectives: Major depressive disorder (MDD) is the leading cause of disability worldwide. Its high recurrence rate calls for prevention of first-onset MDD. Although meta-analysis suggested insomnia as the strongest modifiable risk factor, previous studies insufficiently addressed that insomnia might also occur as a residual symptom of unassessed prior depression, or as a comorbid complaint secondary to other depression risks. Methods: In total, 768 participants from the Netherlands Study of Depression and Anxiety who were free from current and lifetime MDD were followed-up for four repeated assessments, spanning 6 years in total. We performed separate Cox proportional hazard analyses to evaluate whether baseline insomnia severity, short-sleep duration, and individual insomnia complaints prospectively predicted first-onset MDD during follow-up. The novel method of network outcome analysis (NOA) allowed us to sort out whether there is any direct predictive value of individual insomnia complaints among several other complaints that are associated with insomnia. Results: Over 6-year follow-up, 141 (18.4%) were diagnosed with first-onset MDD. Insomnia severity but not sleep duration predicted first-onset MDD (HR = 1.11, 95% CI: 1.07-1.15), and this was driven solely by the insomnia complaint difficulty initiating sleep (DIS) (HR = 1.10, 95% CI: 1.04-1.16). NOA likewise identified DIS only to directly predict first-onset MDD, independent of four other associated depression complaints. Conclusions: We showed prospectively that DIS is a risk factor for first-onset MDD. Among the different other insomnia symptoms, the specific treatment of DIS might be the most sensible target to combat the global burden of depression through prevention.

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