• No results found

University of Groningen Rhythm & Blues Knapen, Stefan Erik

N/A
N/A
Protected

Academic year: 2021

Share "University of Groningen Rhythm & Blues Knapen, Stefan Erik"

Copied!
5
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

University of Groningen

Rhythm & Blues

Knapen, Stefan Erik

IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from it. Please check the document version below.

Document Version

Publisher's PDF, also known as Version of record

Publication date: 2019

Link to publication in University of Groningen/UMCG research database

Citation for published version (APA):

Knapen, S. E. (2019). Rhythm & Blues: Chronobiology in the pathophysiology and treatment of mood disorders. Rijksuniversiteit Groningen.

Copyright

Other than for strictly personal use, it is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license (like Creative Commons).

Take-down policy

If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim.

Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum.

(2)

Chapter 4

Letter to the editor:

Chronotype not associated

with non-remission,

but with current state?

S.E. Knapen1,2, S.J.M. Druiven1, Y. Meesters2 and H. Riese1

1. University of Groningen, University Medical Center Groningen, Department of Psy-chiatry, Interdisciplinary Center for Psychopathology and Emotion regulation (ICPE). Groningen, the Netherlands;

2. University of Groningen, University Medical Center Groningen, Department of Psy-chiatry, Research School of Behavioural and Cognitive Neurosciences (BCN), Gronin-gen, the Netherlands;

(3)

49

With great interest we read the paper by Chan and colleagues.(1) In their paper they showed the importance of studying chronotype, whether people are morning or eve-ning persons, in patients diagnosed with major depressive disorder (MDD). The number of citations to our esteemed colleagues’ paper (20 in 31 months according to a Scopus search in January 2017) shows the impact of the paper. However, when studying the cit-ing papers we noticed that over half of the citcit-ing papers misinterpreted the results and conclusions of the paper by Chan and colleagues.(1) We want to point out two terms, which were used in the paper, that may be related to the incorrectly interpreted causal-ity of the reported findings. Although incorrect citations are more common in research, these used terms might have unintentionally triggered some of the confusion.

First, Chan et al.(1) described a longitudinal cohort of patients diagnosed with current status of MDD (current episode in the past month) at inclusion in 2006 (T0). At T0, 419 MDD patients were included. This cohort was followed-up in 2010 (T1, n=371) and in 2011 (T2, n=253). At T2, diagnosis of MDD was confirmed, and severity of depression, eveningness and sleep-wake habits were assessed with valid instruments. For their publication data collected at T2 were tested (p911) to assess group differences in chro-notype. This makes the study a cross-sectional study, as they indeed stated in their Dis-cussion (p916). The statistical analysis used to test the relationship between evening-ness and MDD is a logistic regression analysis. The independent variable, eveningevening-ness, is described as a ‘risk-factor’ for depressive symptomatology (p915). This term implies a causal relationship, while this cannot be studied in their cross-sectional study. Mis-interpretation of this cross-sectional analysis in this longitudinal cohort is likely when the term risk factor is used, as we saw in citing papers.(2,3)

Second, another misinterpretation of the citing papers might be the result of the cat-egorisation of the MDD patients.(4,5) Prior analysis, patients were categorized into a ‘remission’ group and a ‘nonremission’ group. The patients in this latter group have a cut-off score of 8 or higher on the Hamilton Rating Scale for Depression and a current status of MDD according to the 1-month prevalence on the Mini-International Neuro-psychiatric Interview at T2 (note: independent of their depressive status at T1).(6,7) We agree with the definition of the remission group as all patients were depressed at T0 and remitted at T2. However, for the nonremission group the definition is lacking precision. It is unknown from the collected data whether this group also included pa-tients who were in remission at T1 and subsequently diagnosed with MDD at T2 and thus should be defined as suffering from a relapse. A more straightforward, or pure-ly descriptive way of labelling this group is ‘not-in-remission’ or, even more precisepure-ly ‘current depressive status according to the 1-month prevalence data’. Patients fulfilling the criteria of this latter definition are reported to be more evening type in the litera-ture before.(8) To define a better non-remission group, Chan and colleagues could have selected patients with a persisting depressive status (current depressive episode at T0, T1 and T2) as their non-remission group. This could decrease the sample size and negatively affect the power of the statistical analysis, although it likely creates more homogeneous groups, which may increase power. Albeit a subtle difference, we would like to point out that providing specific labels could make an important difference for the interpretability of the conclusions by the readers. In this case, it is important as the

(4)

term nonremission may unintentionally suggest that the authors studied the longitudi-nal course of depression.

The combination of the two terms (risk factor and nonremission) may unintentional-ly have implied a causal relationship between eveningness and the course of depres-sion, something that should not be concluded from Chan and colleagues’ paper. We are grateful Chan et al. increased the knowledge of the field by studying the influence of sleep problems on the association between eveningness and depression. However, whether there is a causal relationship between chronotype and the course of depres-sion remains unknown and a relevant subject for future research.

(5)

51

References

1. Chan JWY, Lam SP, Li SX, Yu MWM, Chan NY, Zhang J, et al. Eveningness and insomnia: inde-pendent risk factors of nonremission in major depressive disorder. Sleep. 2014;37(5):911–7. DOI: 10.5665/sleep.3658

2. Merikanto I, Kronholm E, Peltonen M, Laatikain-en T, VartiainLaatikain-en E, PartonLaatikain-en T. Circadian prefer-ence links to depression in general adult pop-ulation. J Affect Disord. 2015;188:143–8. DOI: 10.1016/j.jad.2015.08.061

3. Bei B, Ong JC, Rajaratnam SMW, Manber R. Chro-notype and improved sleep efficiency inde-pendently predict depressive symptom reduc-tion after group cognitive behavioral therapy for insomnia. J Clin Sleep Med. 2015;11(9):1021–7. 4. Kripke DF, Elliott JA, Welsh DK, Youngstedt SD. Photoperiodic and circadian bifurcation theo-ries of depression and mania. F1000Research. 2015;4(May):107. DOI: 10.12688/f1000re-search.6444.1

5. Melo MCA, Abreu RLC, Linhares Neto VB, de Bruin PFC, de Bruin VMS. Chronotype and cir-cadian rhythm in bipolar disorder: a systematic review. Sleep Med Rev. 2016; DOI: 10.1016/j. smrv.2016.06.007

6. Williams JBW, Link MJ, Rosenthal NE, Terman M. Structured Interview Guide for the Hamilton Depression Rating Scale—Seasonal Affective Disorder Version (SIGH-SAD). New York, New York State Psychiatr Inst. 1988;

7. Sheehan D V, Lecrubier Y, Sheehan KH, Amorim P, Janavs J, Weiller E, et al. The Mini-Internation-al Neuropsychiatric Interview (MINI): the devel-opment and validation of a structured diagnos-tic psychiatric interview for DSM-IV and ICD-10. J Clin Psychiatry. 1998;59:22–33.

8. Antypa N, Vogelzangs N, Meesters Y, Schoevers RA, Penninx BWJH. Chronotype associations with depression and anxiety in a large cohort study. Depress Anxiety. 2016 Jan;33(1):75–83.

Referenties

GERELATEERDE DOCUMENTEN

From this study, we conclude patients do not show more circadian rhythm problems compared to healthy controls in the euthymic phase, demonstrating that patients are able to maintain

With this in mind, continuous sleep measurement in patients with bipolar disorder could help to prevent full-blown episodes by early signalling of changes in these patterns.

In conclusion, we showed a novel method to study the temporal order of changes in symptomatology related to mood episodes and showed that patients suffer from sleep disturbances

Sex also affected the group differences in fractal pat- terns at larger time scales, i.e., female patients and siblings had more random activity fluctuations at >2h as quantified

In a database of studies with either 1 week or 2 weeks of light therapy we retrospec- tively analysed the relationship between expectations of patients on therapy response with

In the three studies which compared different methods of light therapy no significant differences be- tween light conditions were observed: study 1, main effect “condition” F(2,49)

Furthermore, we showed that for a sub diagnosis of major depressive disorder, seasonal affective disorder, light therapy is very effective, and only has to be administered for a

In de studies naar de bipolaire stoornis was het corrigeren voor medicatiegebruik nagenoeg onmogelijk, omdat patiënten veel verschillende types medicatie, met