La maladie de Parkinson au Canada (serveur d'exploration)

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Family history of idiopathic REM behavior disorder: a multicenter case-control study.

Identifieur interne : 000921 ( PubMed/Checkpoint ); précédent : 000920; suivant : 000922

Family history of idiopathic REM behavior disorder: a multicenter case-control study.

Auteurs : Yves Dauvilliers [France] ; Ronald B. Postuma ; Luigi Ferini-Strambi ; Isabelle Arnulf ; Birgit Högl ; Raffaele Manni ; Tomoyuki Miyamoto ; Wolfgang Oertel ; Maria Livia Fantini ; Monica Puligheddu ; Poul Jennum ; Karel Sonka ; Marco Zucconi ; Smeranda Leu-Semenescu ; Birgit Frauscher ; Michele Terzaghi ; Masayuki Miyamoto ; Marcus Unger ; Alex Desautels ; Christina Wolfson ; Amélie Pelletier ; Jacques Montplaisir

Source :

RBID : pubmed:23658378

English descriptors

Abstract

To compare the frequency of proxy-reported REM sleep behavior disorder (RBD) among relatives of patients with polysomnogram-diagnosed idiopathic RBD (iRBD) in comparison to controls using a large multicenter clinic-based cohort.

DOI: 10.1212/WNL.0b013e318296e967
PubMed: 23658378


Affiliations:


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


Links to Exploration step

pubmed:23658378

Le document en format XML

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<term>Humans</term>
<term>Male</term>
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<div type="abstract" xml:lang="en">To compare the frequency of proxy-reported REM sleep behavior disorder (RBD) among relatives of patients with polysomnogram-diagnosed idiopathic RBD (iRBD) in comparison to controls using a large multicenter clinic-based cohort.</div>
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<Day>11</Day>
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<Month>Jun</Month>
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<Title>Neurology</Title>
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<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">To compare the frequency of proxy-reported REM sleep behavior disorder (RBD) among relatives of patients with polysomnogram-diagnosed idiopathic RBD (iRBD) in comparison to controls using a large multicenter clinic-based cohort.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">A total of 316 patients with polysomnography-confirmed iRBD were recruited from 12 RBD study group centers, along with 316 controls matched on sex and age group. All subjects completed a self-administered questionnaire that collected proxy-reported information on family history of tremor, gait trouble, balance trouble, Parkinson disease, memory loss, and Alzheimer disease. The questionnaire also included a single question that asked about possible symptoms of RBD among first-degree relatives (siblings, parents, and children).</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">A positive family history of dream enactment was reported in 13.8% of iRBD cases compared to 4.8% of controls (odds ratio [OR] = 3.9, 95% confidence interval [CI] 2.0-7.7). ORs were increased for both siblings (OR = 6.1, 95% CI 2.1-18.1) and parents (OR = 3.2, 95% CI 1.4-7.8). We found no significant difference in sex, current age (65.3 ± 10.2 vs 66.9 ± 10.2 years), or age at self-reported RBD onset (55.2 ± 11.7 vs 56.6 ± 15.1 years) in possible familial vs sporadic iRBD. No differences were found in family history of tremor, walking and balance troubles, Parkinson disease, memory loss, or Alzheimer disease.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">We found increased odds of proxy-reported family history of presumed RBD among individuals with confirmed iRBD. This suggests the possibility of a genetic contribution to RBD.</AbstractText>
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