Can chronotype function as predictor of a persistent course of depressive and anxiety disorder?
•A later chronotype does not predict a persistent course of depressive disorder.•A later chronotype does also not predict a persistent course of anxiety disorder.•Results were similar for the two-year and four-year course.•Chronotype might not be useful for predicting a persistent course in clinical...
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Published in | Journal of affective disorders Vol. 242; pp. 159 - 164 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.01.2019
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Subjects | |
Online Access | Get full text |
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Summary: | •A later chronotype does not predict a persistent course of depressive disorder.•A later chronotype does also not predict a persistent course of anxiety disorder.•Results were similar for the two-year and four-year course.•Chronotype might not be useful for predicting a persistent course in clinical settings.
The role of chronotype, the individual timing of sleep/activity, has been studied in relation to depressive and anxiety disorders. A cross-sectional association between a depressive episode and evening-type has been identified. However, until now the predicting capacity of chronotype concerning persistence of psychiatric disorders remains unclear. Our aim is to examine whether a later chronotype in patients with a depressive and/or anxiety disorder can serve as a predictor of a persistent course.
A subsample of patients with a depressive and/or anxiety disorder diagnosis and chronotype data of the longitudinal Netherlands Study of Depression and Anxiety (NESDA) was used. Diagnosis of depressive and anxiety disorders (1-month DSM-IV based diagnosis) were determined at baseline (n = 505). From this group persistence was determined at 2-year (FU2) (persistent course: n = 248, non-persistent course: n = 208) and 4-year follow-up (FU4) (persistent course: n = 151, non-persistent course: n = 264). Chronotype was assessed at baseline with the Munich Chronotype Questionnaire.
A later chronotype did not predict a persistent course of depressive and/or anxiety disorder at FU2 (OR (95% CI) = 0.99 (0.83–1.19), P = 0.92) or at FU4 (OR (95% CI) = 0.94 (0.77–1.15), P = 0.57).
Persistence was defined as having a diagnosis of depressive and/or anxiety disorder at the two-year and four-year follow-up, patients may have remitted and relapsed between assessments.
Chronotype, measured as actual sleep timing, of patients with a depressive or anxiety disorder did not predict a persistent course which suggests it might be unsuitable as predictive tool in clinical settings. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0165-0327 1573-2517 |
DOI: | 10.1016/j.jad.2018.08.064 |