La maladie de Parkinson en France (serveur d'exploration)

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Experimental pain sensitivity in multiple system atrophy and Parkinson's disease at an early stage.

Identifieur interne : 000163 ( PubMed/Checkpoint ); précédent : 000162; suivant : 000164

Experimental pain sensitivity in multiple system atrophy and Parkinson's disease at an early stage.

Auteurs : V. Mylius [Allemagne] ; S. Pee [Allemagne] ; H. Pape [Allemagne] ; M. Teepker [Allemagne] ; M. Stamelou [Allemagne] ; K. Eggert [Allemagne] ; J-P Lefaucheur [France] ; W H Oertel [Allemagne] ; J C Möller [Allemagne]

Source :

RBID : pubmed:26914528

Abstract

Chronic spontaneous pain is a clinically relevant non-motor symptom in multiple system atrophy (MSA) and Parkinson's disease (PD). Experimental pain sensitivity, reflecting the mechanisms of nociception and pain perception leading to clinical pain, is known to be enhanced in both diseases at advanced stages. Also, this study aimed at investigating experimental pain sensitivity already at an early stage (i.e. symptom duration ≤5 years).

DOI: 10.1002/ejp.846
PubMed: 26914528


Affiliations:


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pubmed:26914528

Le document en format XML

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<div type="abstract" xml:lang="en">Chronic spontaneous pain is a clinically relevant non-motor symptom in multiple system atrophy (MSA) and Parkinson's disease (PD). Experimental pain sensitivity, reflecting the mechanisms of nociception and pain perception leading to clinical pain, is known to be enhanced in both diseases at advanced stages. Also, this study aimed at investigating experimental pain sensitivity already at an early stage (i.e. symptom duration ≤5 years).</div>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Chronic spontaneous pain is a clinically relevant non-motor symptom in multiple system atrophy (MSA) and Parkinson's disease (PD). Experimental pain sensitivity, reflecting the mechanisms of nociception and pain perception leading to clinical pain, is known to be enhanced in both diseases at advanced stages. Also, this study aimed at investigating experimental pain sensitivity already at an early stage (i.e. symptom duration ≤5 years).</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Experimental pain sensitivity was assessed by investigating the nociceptive flexion reflex (NFR, reflecting spinal nociception) and heat and electrical pain thresholds. 'Off-drug' MSA (n = 11) and PD (n = 14) patients selected at an early stage of the disease were compared to healthy controls (HC, n = 27). MSA patients had either parkinsonian (MSA-P, n = 5) or cerebellar (MSA-C, n = 6) subtypes.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Compared to HC, MSA patients had lower heat pain sensitivity, whereas PD patients had reduced NFR threshold. MSA and PD patients did not differ from HC regarding other variables. MSA-P and MSA-C patients did not differ, either.</AbstractText>
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   |texte=   Experimental pain sensitivity in multiple system atrophy and Parkinson's disease at an early stage.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/RBID.i   -Sk "pubmed:26914528" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd   \
       | NlmPubMed2Wicri -a ParkinsonFranceV1 

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