Effects of trazodone versus cognitive behavioral therapy in the insomnia with short sleep duration phenotype: a preliminary study

被引:38
作者
Vgontzas, Alexandros N. [1 ]
Puzino, Kristina [1 ]
Fernandez-Mendoza, Julio [1 ]
Krishnamurthy, Venkatesh Basappa [1 ]
Basta, Maria [2 ]
Bixler, Edward O. [1 ]
机构
[1] Penn State Univ, Coll Med, Sleep Res & Treatment Ctr, Penn State Hlth Milton S Hershey Med Ctr, Hershey, PA 17033 USA
[2] Univ Crete, Univ Hosp Heraklion, Dept Psychiat, Iraklion, Crete, Greece
来源
JOURNAL OF CLINICAL SLEEP MEDICINE | 2020年 / 16卷 / 12期
关键词
insomnia; trazodone; cognitive-behavioral therapy for insomnia; total sleep time; cortisol; insomnia short sleep duration phenotype; PITUITARY-ADRENAL AXIS; PERSISTENT INSOMNIA; OLDER-ADULTS; DOUBLE-BLIND; EFFICACY; HYPERTENSION; DOXEPIN; TRIAL;
D O I
10.5664/jcsm.8740
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Objectives: The insomnia with objective short sleep duration phenotype is associated with increased risk for adverse health outcomes, physiological hyperarousal, and a blunted response to cognitive behavioral therapy for insomnia (CBT-I). Whether insomnia with objective short sleep duration responds better to pharmacological treatment compared to CBT-I has not been examined. Methods: Participants included 15 patients with chronic insomnia (86.7% female), aged 45.3 +/- 8.1 years. Eight patients were randomized to CBT-I and 7 to trazodone. Patients were examined with 2 weeks of actigraphy, salivary cortisol, and the insomnia severity index at 3 time points (pretreatment, 3-month posttreatment, and 6-month follow-up). Mixed between-within-subjects analysis of variance and univariate analysis of covariance were conducted to assess the impact of trazodone and CBT-I on patients' total sleep time, salivary cortisol, and insomnia severity index scores across the 3 time points. Results: Trazodone, but not CBT-I, significantly lengthened total sleep time (when measured with actigraphy) both at posttreatment (51.01 minutes vs -11.73 minutes; P =.051; Cohen's d = 1.383) and at follow-up (50.35 minutes vs -7.56 minutes; P =.012; Cohen's d = 1.725), respectively. In addition, trazodone, but not CBT-I, showed a clinically meaningful decrease in salivary cortisol from pretreatment to posttreatment (-36.07% vs -11.70%; Cohen's d = 0.793) and from pretreatment to follow-up (-21.37% vs -5.79%; Cohen's d = 0.284), respectively. Finally, therewere no differences on insomnia severity index scores between the trazodone and the CBT-I groups. Conclusions: The current preliminary, open-label, randomized trial suggests that trazodone, but not CBT-I, significantly improves objective sleep duration and reduces hypothalamic-pituitary-adrenal axis activation, suggesting a differential treatment response in the insomnia with objective short sleep duration phenotype. Clinical Trial Registration: Registry: ClinicalTrials.gov; Name: Study of Trazodone & Cognitive Behavioral Therapy to Treat Insomnia; URL: https:// clinicaltrials.gov/ct2/show/NCT01348542; Identifier: NCT01348542.
引用
收藏
页码:2009 / 2019
页数:11
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