作者: D. Weintraub , S. Mavandadi , E. Mamikonyan , A. D. Siderowf , J. E. Duda
DOI: 10.1212/WNL.0B013E3181EBDD79
关键词: Psychiatry 、 Atomoxetine 、 Atomoxetine hydrochloride 、 Antidepressant 、 Randomized controlled trial 、 Effects of sleep deprivation on cognitive performance 、 Apathy 、 Mood 、 Internal medicine 、 Psychology 、 Anxiety
摘要: Objectives: Depression and antidepressant use, especially selective serotonin reuptake inhibitors (SSRIs), are common in Parkinson disease (PD). The objective of this clinical trial was to assess the efficacy atomoxetine, a norepinephrine inhibitor (SNRI), for treatment clinically significant depressive symptoms comorbid neuropsychiatric PD. Methods: A total 55 subjects with PD an Inventory Depressive Symptomatology–Clinician (IDS-C) score ≥22 were randomized 8 weeks atomoxetine or placebo (target dosage = 80 mg/day). response (>50% decrease IDS-C Clinical Global Impression–Improvement [CGI-I] 1 2) assessed using intention-to-treat modeling procedures. Secondary outcomes included global cognition, daytime sleepiness, anxiety, apathy, motor function. Results: There no between-groups differences priori–defined rates. Using more liberal criterion >40% IDS from baseline, there trend ( p 0.08) favoring atomoxetine. Patients receiving experienced significantly greater improvement cognition 0.003) sleepiness 0.001), well-tolerated. Conclusions: Atomoxetine not efficacious PD, but associated cognitive performance sleepiness. Larger studies SNRIs disorders mood, wakefulness appropriate. Classification evidence: This interventional study provides Class II evidence that mg/day) is improving depression