Literature DB >> 22742954

Prefrontal thickening in PD with levodopa-induced dyskinesias: new evidence from cortical thickness measurement.

Antonio Cerasa1, Maurizio Morelli, Antonio Augimeri, Maria Salsone, Fabiana Novellino, Maria Cecilia Gioia, Gennarina Arabia, Aldo Quattrone.   

Abstract

PURPOSE: Neurodegenerative processes in Parkinson's disease (PD) patients with levodopa-induced dyskinesias (LID) are still a matter of debate. Recently, we demonstrated that this clinical phenotype is associated with an abnormal gray matter increase in the prefrontal cortex when compared to PD without LID. This evidence was found by using voxel-based morphometry (VBM). However, VBM may not be the most appropriate procedure to assess cortical pathology, since its normalization/smoothing steps reduce the ability to anatomically characterize sulci and gyri. The aim of this study is to better delineate the LID-related anatomical abnormalities by using an advanced neuroimaging method that provides a direct and objective measure of the cortical morphology.
METHODS: Surface-based investigation of cortical mantle (cortical thickness) was carried out by using Freesurfer in two groups of treated PD patients with LID (no 29) and without LID (no 30), and one group of age- and sex-matched controls (no 24).
RESULTS: Cortical thickness analysis revealed a pronounced increase of thickness in the right inferior frontal sulcus in PD patients with LID with respect to PD patients without LID. DISCUSSION: The current study confirms our previous morphological findings on the role of the prefrontal cortex in the pathophysiology of LID and delineates with more precision the anatomical abnormalities characterizing this clinical phenotype.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22742954     DOI: 10.1016/j.parkreldis.2012.06.003

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN: 1353-8020            Impact factor:   4.891


  23 in total

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2.  Baseline cognitive profile is closely associated with long-term motor prognosis in newly diagnosed Parkinson's disease.

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3.  Transcranial Non-Invasive Brain Stimulation in Parkinson's Disease Patients with Dyskinesias. Where is the Optimal Target?

Authors:  Antonio Cerasa; Ignacio Obeso; Michele Dileone; Aldo Quattrone
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Review 4.  Impulse control disorders in Parkinson's disease.

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5.  BDNF rs6265 single-nucleotide polymorphism is involved in levodopa-induced dyskinesia in Parkinson's disease via its regulation of the cortical thickness of the left postcentral gyrus.

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6.  White matter connectivity networks predict levodopa-induced dyskinesia in Parkinson's disease.

Authors:  Jin Ho Jung; Yae Ji Kim; Seok Jong Chung; Han Soo Yoo; Yang Hyun Lee; Kyoungwon Baik; Seong Ho Jeong; Young Gun Lee; Hye Sun Lee; Byoung Seok Ye; Young H Sohn; Yong Jeong; Phil Hyu Lee
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7.  Gender-based analysis of cortical thickness and structural connectivity in Parkinson's disease.

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Review 8.  Advantages of Using Both Voxel- and Surface-based Morphometry in Cortical Morphology Analysis: A Review of Various Applications.

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9.  Morphometric changes in the reward system of Parkinson's disease patients with impulse control disorders.

Authors:  Clelia Pellicano; Flavia Niccolini; Kit Wu; Sean S O'Sullivan; Andrew D Lawrence; Andrew J Lees; Paola Piccini; Marios Politis
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10.  Excessive Sensitivity to Uncertain Visual Input in L-DOPA-Induced Dyskinesias in Parkinson's Disease: Further Implications for Cerebellar Involvement.

Authors:  James K R Stevenson; Chonho Lee; Bu-Sung Lee; Pouria Talebifard; Edna Ty; Kristina Aseeva; Meeko M K Oishi; Martin J McKeown
Journal:  Front Neurol       Date:  2014-02-04       Impact factor: 4.003

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