Stratifying drug treatment of cognitive impairments after traumatic brain injury using neuroimaging.
Adult
Brain
/ diagnostic imaging
Brain Injuries, Traumatic
/ complications
Central Nervous System Stimulants
/ therapeutic use
Cognitive Dysfunction
/ diagnostic imaging
Cross-Over Studies
Dopamine Plasma Membrane Transport Proteins
/ analysis
Double-Blind Method
Female
Humans
Male
Methylphenidate
/ therapeutic use
Middle Aged
Neuroimaging
/ methods
Tomography, Emission-Computed, Single-Photon
/ methods
Young Adult
cognitive enhancement
dopamine
methylphenidate
neuroimaging
traumatic brain injury
Journal
Brain : a journal of neurology
ISSN: 1460-2156
Titre abrégé: Brain
Pays: England
ID NLM: 0372537
Informations de publication
Date de publication:
01 08 2019
01 08 2019
Historique:
received:
10
09
2018
revised:
26
01
2019
accepted:
09
04
2019
pubmed:
15
6
2019
medline:
27
5
2020
entrez:
15
6
2019
Statut:
ppublish
Résumé
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 123I-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. 123I-ioflupane 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.
Identifiants
pubmed: 31199462
pii: 5519011
doi: 10.1093/brain/awz149
doi:
Substances chimiques
Central Nervous System Stimulants
0
Dopamine Plasma Membrane Transport Proteins
0
Methylphenidate
207ZZ9QZ49
Types de publication
Journal Article
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2367-2379Subventions
Organisme : Department of Health
ID : NIHR-RP-011-048
Pays : United Kingdom
Informations de copyright
© The Author(s) (2019). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oup.com.