MovDisordV3, Main, Exploration, bibRecord, 003215

Relative risk of spread of symptoms among the focal onset primary dystonias

Identifieur interne : 003215 ( Main/Exploration ); précédent : 003214; suivant : 003216

Relative risk of spread of symptoms among the focal onset primary dystonias

Auteurs : Elliott M. Weiss [États-Unis] ; Tamara Hershey [États-Unis] ; Morvarid Karimi [États-Unis] ; Brad Racette [États-Unis] ; Samer D. Tabbal [États-Unis] ; Jonathan W. Mink [États-Unis] ; Randal C. Paniello [États-Unis] ; Joel S. Perlmutter [États-Unis]

Source :

Movement Disorders [ 0885-3185 ] ; 2006-08.

RBID : ISTEX:65C1E5D214C07BFE688E24586D6CB95DCB067599

Descripteurs français

Pascal (Inist)
- Blépharospasme, Dystonie, Facteur risque, Pronostic, Système nerveux pathologie.

English descriptors

KwdEn :
- Adult, Blepharospasm, Disease Progression, Dystonia, Dystonia Musculorum Deformans (mortality), Dystonia Musculorum Deformans (physiopathology), Female, Humans, Male, Nervous system diseases, Organ Specificity, Prognosis, Retrospective Studies, Risk Factors, Risk factor, Survival Analysis, Time Factors, age at onset, blepharospasm, primary dystonia, prognosis, progression, site of onset.
MESH :
- mortality : Dystonia Musculorum Deformans.
- physiopathology : Dystonia Musculorum Deformans.
- Adult, Disease Progression, Female, Humans, Male, Organ Specificity, Retrospective Studies, Risk Factors, Survival Analysis, Time Factors.

Abstract

Adult‐onset primary torsion dystonia (PTD) may spread to multiple body parts, but the relative risk of spread by site of onset of dystonia has not been well characterized. We retrospectively identified 602 patients with PTD out of 1,500 dystonia patients in our electronic database and extracted age at onset, site of onset, family history, and spread. Survival analyses were performed for groups based on site of onset, and hazard ratios compared relative risk of spread across groups. Patients with adult‐onset blepharospasm were more likely to spread (31% past the head) than those with dystonia starting in the neck (9%), larynx (12%), or upper extremities (16%). Hazard ratios proved that the blepharospasm group had the greatest relative risk of spread. The rate of spread after onset varied significantly between the different groups. Most spread occurred in the first 1 to 2 years after onset of blepharospasm, whereas the risk of spread was relatively constant over time in cervical and laryngeal dystonia. Different sites of onset of PTD confer different risks of spread, important for clinical prognosis. Different risks of spread may provide clues about underlying pathogenesis of adult‐onset primary dystonias. © 2006 Movement Disorder Society

Url:

https://api.istex.fr/document/65C1E5D214C07BFE688E24586D6CB95DCB067599/fulltext/pdf

DOI: 10.1002/mds.20919

Affiliations:

Le document en format XML

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<term>Dystonia Musculorum Deformans (mortality)</term>
<term>Dystonia Musculorum Deformans (physiopathology)</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Nervous system diseases</term>
<term>Organ Specificity</term>
<term>Prognosis</term>
<term>Retrospective Studies</term>
<term>Risk Factors</term>
<term>Risk factor</term>
<term>Survival Analysis</term>
<term>Time Factors</term>
<term>age at onset</term>
<term>blepharospasm</term>
<term>primary dystonia</term>
<term>prognosis</term>
<term>progression</term>
<term>site of onset</term>
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<term>Disease Progression</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Organ Specificity</term>
<term>Retrospective Studies</term>
<term>Risk Factors</term>
<term>Survival Analysis</term>
<term>Time Factors</term>
</keywords>
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<term>Dystonie</term>
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<front><div type="abstract" xml:lang="en">Adult‐onset primary torsion dystonia (PTD) may spread to multiple body parts, but the relative risk of spread by site of onset of dystonia has not been well characterized. We retrospectively identified 602 patients with PTD out of 1,500 dystonia patients in our electronic database and extracted age at onset, site of onset, family history, and spread. Survival analyses were performed for groups based on site of onset, and hazard ratios compared relative risk of spread across groups. Patients with adult‐onset blepharospasm were more likely to spread (31% past the head) than those with dystonia starting in the neck (9%), larynx (12%), or upper extremities (16%). Hazard ratios proved that the blepharospasm group had the greatest relative risk of spread. The rate of spread after onset varied significantly between the different groups. Most spread occurred in the first 1 to 2 years after onset of blepharospasm, whereas the risk of spread was relatively constant over time in cervical and laryngeal dystonia. Different sites of onset of PTD confer different risks of spread, important for clinical prognosis. Different risks of spread may provide clues about underlying pathogenesis of adult‐onset primary dystonias. © 2006 Movement Disorder Society</div>
</front>
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<name sortKey="Perlmutter, Joel S" sort="Perlmutter, Joel S" uniqKey="Perlmutter J" first="Joel S." last="Perlmutter">Joel S. Perlmutter</name>
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Movement Disorders (revue)

Relative risk of spread of symptoms among the focal onset primary dystonias

Relative risk of spread of symptoms among the focal onset primary dystonias

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.