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May 24, 2011; 76 (21) Articles

Adenosine 2A receptor availability in dyskinetic and nondyskinetic patients with Parkinson disease

A.F. Ramlackhansingh, S.K. Bose, I. Ahmed, F.E. Turkheimer, N. Pavese, D.J. Brooks
First published May 23, 2011, DOI: https://doi.org/10.1212/WNL.0b013e31821ccce4
A.F. Ramlackhansingh
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S.K. Bose
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I. Ahmed
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F.E. Turkheimer
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N. Pavese
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D.J. Brooks
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Citation
Adenosine 2A receptor availability in dyskinetic and nondyskinetic patients with Parkinson disease
A.F. Ramlackhansingh, S.K. Bose, I. Ahmed, F.E. Turkheimer, N. Pavese, D.J. Brooks
Neurology May 2011, 76 (21) 1811-1816; DOI: 10.1212/WNL.0b013e31821ccce4

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Abstract

Objective: To investigate striatal adenosine A2A receptor availability in patients with Parkinson disease (PD) with and without levodopa-induced dyskinesias (LIDs). While providing effective relief from the motor symptoms of PD, chronic levodopa use is associated with development of LIDs. A2A receptors are expressed on the bodies of indirect pathway medium spiny striatal neurons and on dopamine terminals and play a role in modulating dopamine transmission. A2A antagonists have antiparkinsonian activity by boosting levodopa efficacy. We aimed to study A2A receptor availability in patients with PD with and without LIDs using PET and [11C]SCH442416, an A2A antagonist.

Methods: Six patients with PD with and 6 without LIDs were studied withdrawn 12 hours from medication. Their PET findings were compared with 6 age-matched healthy controls. Using spectral analysis, [11C]SCH442416 regional volumes of distribution (VT) were computed for the caudate, putamen, and thalamus and binding potentials (BPND) reflecting the ratio of specific:nonspecific uptake were compared between groups.

Results: A2A binding in the caudate and putamen of subjects with PD with LIDs was far higher (p = 0.026 and p = 0.036, respectively) than that of subjects with PD without LIDs, which lay within the control range. Thalamic A2A availability was similar for all 3 groups.

Conclusion: Patients with PD with LIDs show increased A2A receptor availability in the striatum. This finding is compatible with altered adenosine transmission playing a role in LIDs and provides a rationale for a trial of A2A receptor agents in the treatment of these motor complications.

Footnotes

  • Study funding: Supported by the Parkinsons Disease Society UK.

  • ANCOVA
    analysis of covariance
    GPe
    external pallidum
    GPi
    globus pallidus interna
    H&Y
    Hoehn &Yahr
    LED
    levodopa effective dose
    LEU
    levodopa equivalent unit
    LID
    levodopa-induced dyskinesia
    MPTP
    1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine
    PD
    Parkinson disease
    PPE
    preproenkephalin
    ROI
    region of interest
    SNpr
    substantia nigra pars reticulata
    UPDRS
    Unified Parkinson's Disease Rating Scale.

  • Received September 23, 2010.
  • Accepted February 10, 2011.
  • Copyright © 2011 by AAN Enterprises, Inc.
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