[123I]FP-CIT striatal binding in early Parkinson's disease patients with tremor vs. akinetic-rigid onset.

Ioannis U Isaias, Riccardo Benti, Roberto Cilia, Margherita Canesi, Giorgio Marotta, Paolo Gerundini, Gianni Pezzoli, Angelo Antonini
Author Information
  1. Ioannis U Isaias: Parkinson Institute, Istituti Clinici di Perfezionamento, Milan 20126, Italy.

Abstract

We performed [123I]FP-CIT/SPECT in 20 drug-naive Parkinson's disease (PD) patients, 10 with unilateral akinesia/rigidity at onset (arPD) and 10 with additional tremor-at-rest (tPD), to evaluate whether resting tremor at onset is associated with differences in striatal dopamine transporter binding. Patients of the two cohorts were matched for age, disease duration (<3 years) and severity of non-tremor motor symptoms; 31 healthy participants served as controls. Mean striatal dopamine transporter binding reduction in PD patients vs. controls was 42% for arPD and 50% for tPD; mean ipsilateral striatum and caudate nucleus uptake values were lower by 12 and 24%, respectively, in tPD than arPD. We conclude that widespread degeneration of the nigrostriatal dopaminergic pathway might be necessary for the development of parkinsonian tremor-at-rest.

MeSH Term

Aged
Corpus Striatum
Female
Humans
Image Processing, Computer-Assisted
Iodine Radioisotopes
Male
Middle Aged
Muscle Rigidity
Parkinson Disease
Tomography, Emission-Computed, Single-Photon
Tremor
Tropanes

Chemicals

Iodine Radioisotopes
Tropanes
2-carbomethoxy-8-(3-fluoropropyl)-3-(4-iodophenyl)tropane

Word Cloud

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