The dementia-associated APOE ε4 allele is not associated with rapid eye movement sleep behavior disorder
Articolo
Data di Pubblicazione:
2017
Citazione:
The dementia-associated APOE ε4 allele is not associated with rapid eye movement sleep behavior disorder / Gan-Or, Ziv; Montplaisir, Jacques Y.; Ross, Jay P.; Poirier, Judes; Warby, Simon C.; Arnulf, Isabelle; Strong, Stephanie; Dauvilliers, Yves; Leblond, Claire S.; Michele T. M., Hu; Högl, Birgit; Stefani, Ambra; Monaca, Christelle Charley; De Cock, Valérie Cochen; Boivin, Michel; Ferini-Strambi, Luigi; Plazzi, Giuseppe; Antelmi, Elena; Young, Peter; Heidbreder, Anna; Barber, Thomas R.; Evetts, Samuel G.; Rolinski, Michal; Dion, Patrick A.; Desautels, Alex; Gagnon, Jean-François; Dupré, Nicolas; Postuma, Ronald B.; Rouleau, Guy A.. - In: NEUROBIOLOGY OF AGING. - ISSN 0197-4580. - 49:(2017), pp. 218-218.e15. [10.1016/j.neurobiolaging.2016.10.002]
Abstract:
The present study aimed to examine whether the APOE ε4 allele, associated with dementia with Lewy bodies (DLB), and possibly with dementia in Parkinson's disease (PD), is also associated with idiopathic rapid eye movement sleep behavior disorder (RBD). Two single nucleotide polymorphisms, rs429358 and rs7412, were genotyped in RBD patients (n = 480) and in controls (n = 823). APOE ε4 allele frequency was 0.14 among RBD patients and 0.13 among controls (OR = 1.11, 95% CI: 0.88â1.40, p = 0.41). APOE ε4 allele frequencies were similar in those who converted to DLB (0.14) and those who converted to Parkinson's disease (0.12) or multiple system atrophy (0.14, p = 1.0). The APOE ε4 allele is neither a risk factor for RBD nor it is associated with conversion from RBD to DLB or other synucleinopathies.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
APOE; Dementia with Lewy bodies; Genetics; Parkinson's disease; REM sleep behavior disorder; Adolescent; Adult; Apolipoproteins E; Female; Gene Frequency; Humans; Lewy Body Disease; Male; Multiple System Atrophy; Parkinson Disease; REM Sleep Behavior Disorder; Risk Factors; Supranuclear Palsy, Progressive; Young Adult; Alleles; Genetic Association Studies; Polymorphism, Single Nucleotide; Neuroscience (all); Aging; Neurology (clinical); Developmental Biology; Geriatrics and Gerontology
Elenco autori:
Gan-Or, Ziv; Montplaisir, Jacques Y.; Ross, Jay P.; Poirier, Judes; Warby, Simon C.; Arnulf, Isabelle; Strong, Stephanie; Dauvilliers, Yves; Leblond, Claire S.; Michele T. M., Hu; Högl, Birgit; Stefani, Ambra; Monaca, Christelle Charley; De Cock, Valérie Cochen; Boivin, Michel; Ferini-Strambi, Luigi; Plazzi, Giuseppe; Antelmi, Elena; Young, Peter; Heidbreder, Anna; Barber, Thomas R.; Evetts, Samuel G.; Rolinski, Michal; Dion, Patrick A.; Desautels, Alex; Gagnon, Jean-François; Dupré, Nicolas; Postuma, Ronald B.; Rouleau, Guy A.
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