Bright light therapy for depression in Parkinson disease

光疗法 帕金森病 萧条(经济学) 心情 医学 内科学 疾病 心理学 精神科 宏观经济学 经济
作者
Sonja Rutten,Chris Vriend,Jan H. Smit,Henk W. Berendse,Eus J.W. Van Someren,Adriaan W. Hoogendoorn,Jos W. R. Twisk,Ysbrand D. van der Werf,Odile A. van den Heuvel
出处
期刊:Neurology [Lippincott Williams & Wilkins]
卷期号:92 (11): e1145-e1156 被引量:77
标识
DOI:10.1212/wnl.0000000000007090
摘要

Objective

To assess the efficacy of bright light therapy (BLT) in reducing depressive symptoms in patients with Parkinson disease (PD) and major depressive disorder (MDD) compared to a control light.

Methods

In this double-blind controlled trial, we randomized patients with PD and MDD to treatment with BLT (±10,000 lux) or a control light (±200 lux). Participants were treated for 3 months, followed by a 6-month naturalistic follow-up. The primary outcome of the study was the Hamilton Depression Rating Scale (HDRS) score. Secondary outcomes were objective and subjective sleep measures and salivary melatonin and cortisol concentrations. Assessments were repeated halfway, at the end of treatment, and 1, 3, and 6 months after treatment. Data were analyzed with a linear mixed-model analysis.

Results

We enrolled 83 participants. HDRS scores decreased in both groups without a significant between-group difference at the end of treatment. Subjective sleep quality improved in both groups, with a larger improvement in the BLT group (B [SE] = 0.32 [0.16], p = 0.04). Total salivary cortisol secretion decreased in the BLT group, while it increased in the control group (B [SE] = −8.11 [3.93], p = 0.04).

Conclusion

BLT was not more effective in reducing depressive symptoms than a control light. Mood and subjective sleep improved in both groups. BLT was more effective in improving subjective sleep quality than control light, possibly through a BLT-induced decrease in cortisol levels.

ClinicalTrials.gov identifier:

NCT01604876.

Classification of evidence

This study provides Class I evidence that BLT is not superior to a control light device in reducing depressive symptoms in patients with PD with MDD.
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