Serveur d'exploration sur la maladie de Parkinson

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Enlarged hyperechogenic substantia nigra is related to motor performance and olfaction in the elderly

Identifieur interne : 000729 ( Main/Exploration ); précédent : 000728; suivant : 000730

Enlarged hyperechogenic substantia nigra is related to motor performance and olfaction in the elderly

Auteurs : Daniela Berg [Allemagne] ; Klaus Seppi [Autriche] ; Inga Liepelt [Allemagne] ; Katherine Schweitzer [Allemagne] ; Frank Wollenweber [Allemagne] ; Björn Wolf [Allemagne] ; Ulrich Dillmann [Allemagne] ; Heike Stockner [Autriche] ; Jana Godau [Allemagne] ; Stefan Kiechl [Autriche] ; Alexandra Gaenslen [Allemagne] ; Johann Willeit [Autriche] ; Adriana Di Santo [Allemagne] ; Walter Maetzler [Allemagne] ; Thomas Gasser [Allemagne] ; Werner Poewe [Autriche] ; Stefanie Behnke [Allemagne]

Source :

RBID : ISTEX:C0E03284366772921F8428DB8687CCB8ED938200

English descriptors

Abstract

Enlarged substantia nigra hyperechogenicity (SN+) assessed by transcranial sonography (TCS) may be associated with Parkinson's disease (PD) risk markers such as impaired motor performance and hyposmia. The aim of this multicenter cross‐sectional study was to define the association between SN+ and these risk markers in a large population older than 50 years without the diagnosis of PD. In three centers (Tuebingen, Homburg, and Innsbruck), 1,839 individuals were examined. The echostatus of the SN was assessed by TCS, motor performance by the Unified Parkinson's Disease Rating Scale (UPDRS) motor score, and olfactory function with Sniffin' Sticks. From the 1,603 subjects included in the analysis, 16.2% were SN+, 23.0% scored above zero in the UPDRS motor section, and 28.0% were hyposmic as defined by less than 75% correctly classified Sniffin' Sticks. SN+ was associated with a UPDRS motor score above zero (OR 1.45, 95% CI 1.08–1.96) and with a lower odor identification capability (OR 1.48, 95% CI 1.12–1.96). The combination of these two features (OR 1.98, 95% CI 1.25–3.15) and UPDRS motor scores ≥3 lead to higher OR. It is concluded that SN+, impaired motor performance, and hyposmia are frequently observed in the elderly and in isolation are unspecific and of limited use to predict a subject's risk for PD. Whether the association of SN+ with both impaired motor performance and hyposmia as seen in this study predicts an increased risk for the development of PD needs to be evaluated in the follow‐up investigations. © 2010 Movement Disorder Society

Url:
DOI: 10.1002/mds.23114


Affiliations:


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Le document en format XML

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<div type="abstract" xml:lang="en">Enlarged substantia nigra hyperechogenicity (SN+) assessed by transcranial sonography (TCS) may be associated with Parkinson's disease (PD) risk markers such as impaired motor performance and hyposmia. The aim of this multicenter cross‐sectional study was to define the association between SN+ and these risk markers in a large population older than 50 years without the diagnosis of PD. In three centers (Tuebingen, Homburg, and Innsbruck), 1,839 individuals were examined. The echostatus of the SN was assessed by TCS, motor performance by the Unified Parkinson's Disease Rating Scale (UPDRS) motor score, and olfactory function with Sniffin' Sticks. From the 1,603 subjects included in the analysis, 16.2% were SN+, 23.0% scored above zero in the UPDRS motor section, and 28.0% were hyposmic as defined by less than 75% correctly classified Sniffin' Sticks. SN+ was associated with a UPDRS motor score above zero (OR 1.45, 95% CI 1.08–1.96) and with a lower odor identification capability (OR 1.48, 95% CI 1.12–1.96). The combination of these two features (OR 1.98, 95% CI 1.25–3.15) and UPDRS motor scores ≥3 lead to higher OR. It is concluded that SN+, impaired motor performance, and hyposmia are frequently observed in the elderly and in isolation are unspecific and of limited use to predict a subject's risk for PD. Whether the association of SN+ with both impaired motor performance and hyposmia as seen in this study predicts an increased risk for the development of PD needs to be evaluated in the follow‐up investigations. © 2010 Movement Disorder Society</div>
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