Stratifying drug treatment of cognitive impairments after traumatic brain injury using neuroimaging

被引:39
作者
Jenkins, Peter O. [1 ]
De Simoni, Sara [1 ]
Bourke, Niall J. [1 ]
Fleminger, Jessica [1 ]
Scott, Gregory [1 ]
Towey, David J. [2 ]
Svensson, William [2 ]
Khan, Sameer [2 ]
Patel, Maneesh C. [3 ]
Greenwood, Richard [4 ]
Friedland, Daniel [1 ]
Hampshire, Adam [1 ]
Cole, James H. [1 ]
Sharp, David J. [1 ,5 ]
机构
[1] Imperial Coll London, Hammersmith Hosp, Div Brain Sci, Computat Cognit & Clin Neuroimaging Lab, London, England
[2] Imperial Coll Healthcare NHS Trust, Charing Cross Hosp, Dept Nucl Med, London, England
[3] Imperial Coll Healthcare NHS Trust, Charing Cross Hosp, Imaging Dept, London, England
[4] UCL, Inst Neurol, Div Clin Neurol, London, England
[5] United Kingdom UK Dementia Res Inst, 6th Floor,UCL Maple House Tottenham Court Rd, London W1T 7NF, England
基金
美国国家卫生研究院;
关键词
traumatic brain injury; methylphenidate; dopamine; neuroimaging; cognitive enhancement; DOPAMINE TRANSPORTERS; ATTENTION DEFICITS; METHYLPHENIDATE; SCALE; NEUROTRANSMISSION; I-123-BETA-CIT; INCREASES; NETWORK; SYSTEM; SPECT;
D O I
10.1093/brain/awz149
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cognitive impairment is common following traumatic brain injury. Dopaminergic drugs can enhance cognition after traumatic brain injury, but individual responses are highly variable. This may be due to variability in dopaminergic damage between patients. We investigate whether measuring dopamine transporter levels using I-123-ioflupane single-photon emission computed tomography (SPECT) predicts response to methylphenidate, a stimulant with dopaminergic effects. Forty patients with moderate-severe traumatic brain injury and cognitive impairments completed a randomized, double-blind, placebo-controlled, crossover study. (123)Iioflupane SPECT, MRI and neuropsychological testing were performed. Patients received 0.3 mg/kg of methylphenidate or placebo twice a day in 2-week blocks. Subjects received neuropsychological assessment after each block and completed daily home cognitive testing during the trial. The primary outcome measure was change in choice reaction time produced by methylphenidate and its relationship to stratification of patients into groups with normal and low dopamine transporter binding in the caudate. Overall, traumatic brain injury patients showed slow information processing speed. Patients with low caudate dopamine transporter binding showed improvement in response times with methylphenidate compared to placebo [median change = -16 ms; 95% confidence interval (CI): -28 to -3 ms; P = 0.02]. This represents a 27% improvement in the slowing produced by traumatic brain injury. Patients with normal dopamine transporter binding did not improve. Daily home-based choice reaction time results supported this: the low dopamine transporter group improved (median change -19 ms; 95% CI: -23 to -7 ms; P = 0.002) with no change in the normal dopamine transporter group (P = 0.50). The low dopamine transporter group also improved on self-reported and caregiver apathy assessments (P = 0.03 and P = 0.02, respectively). Both groups reported improvements in fatigue (P = 0.03 and P = 0.007). The cognitive effects of methylphenidate after traumatic brain injury were only seen in patients with low caudate dopamine transporter levels. This shows that identifying patients with a hypodopaminergic state after traumatic brain injury can help stratify the choice of cognitive enhancing therapy.
引用
收藏
页码:2367 / 2379
页数:13
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