Atomoxetine for the Treatment of Executive Dysfunction in Parkinson's Disease: A Pilot Open-Label Study

被引:98
作者
Marsh, Laura [1 ,2 ,3 ]
Biglan, Kevin [2 ]
Gerstenhaber, Melissa [1 ,3 ]
Williams, James R. [3 ,4 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Psychiat & Behav Sci, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurol & Neurol Sci, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ, Sch Med, Morris K Udall Parkinsons Dis Res Ctr Excellence, Baltimore, MD 21287 USA
[4] Johns Hopkins Univ, Sch Med, Dept Mental Hlth, Bloomberg Sch Publ Hlth, Baltimore, MD 21287 USA
关键词
executive dysfunction; Parkinson's disease; cognition; norepinephrine reuptake inhibition; atomoxetine; RESPONSE-INHIBITION; L-DOPA; ATTENTION; ADULTS; METHYLPHENIDATE; DEMENTIA; DEFICITS;
D O I
10.1002/mds.22307
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Executive dysfunction (ED) is a prominent and often disabling feature of cognitive impairment in Parkinson's disease (PD). Few studies have examined treatments. Given the role of noradrenergic pathology in ED, atomoxetine, a norepinephrine reuptake inhibitor indicated for attention deficit hyperactivity disorder (ADHD), may be a potential treatment for PD-related ED. Twelve patients with PD and disabling ED completed an 8-week pilot open-label, flexible dose (25-100 mg/day) trial or atomoxetine. On primary outcome measures, atomoxetine was associated with improved ED based on the Clinical Global Impression-Change Scale (75% positive response rate; 95% CI: 43-95%, P < 05) and behavioral measures of ED [Frontal Systems Behavior Scale (FrSBE) Executive Dysfunction and Connors Adult ADHD Rating Scale (CAARS) inattention/memory subscales]. Adverse effects included sleep and gastrointestinal disturbances and hypomania. Atomoxetine is tolerable in PD and may benefit clinical manifestations of ED, warranting further study in controlled trials. (C) 2008 Movement Disorder Society
引用
收藏
页码:277 / 282
页数:6
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