REM sleep behavior disorder, as assessed by questionnaire, in G2019S LRRK2 mutation PD and carriers

Background Rapid eye movement sleep behavior disorder occurs with idiopathic Parkinson's disease (PD) and often precedes PD. Its frequency in LRRK2‐PD and utility as a preclinical marker has not been established. Methods One hundred forty‐four idiopathic PD, 142 LRRK2 G2019S mutation PD, 117 no...

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Published inMovement disorders Vol. 30; no. 13; pp. 1834 - 1839
Main Authors Saunders-Pullman, Rachel, Alcalay, Roy N., Mirelman, Anat, Wang, Cuiling, Luciano, Marta San, Ortega, Roberto A., Glickman, Amanda, Raymond, Deborah, Mejia-Santana, Helen, Doan, Nancy, Johannes, Brooke, Yasinovsky, Kira, Ozelius, Laurie, Clark, Lorraine, Orr-Utreger, Avi, Marder, Karen, Giladi, Nir, Bressman, Susan B.
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.11.2015
Wiley Subscription Services, Inc
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Summary:Background Rapid eye movement sleep behavior disorder occurs with idiopathic Parkinson's disease (PD) and often precedes PD. Its frequency in LRRK2‐PD and utility as a preclinical marker has not been established. Methods One hundred forty‐four idiopathic PD, 142 LRRK2 G2019S mutation PD, 117 non‐manifesting carriers, 93 related noncarriers, and 40 healthy controls completed the Rapid eye movement sleep Behavior Disorder Screening Questionnaire. Results Cut scores were met by 30.6% idiopathic PD, 19.7% LRRK2‐PD, 6% nonmanifesting carriers, 20.4% related noncarriers, and 15% controls. The likelihood of abnormal scores was decreased in LRRK2‐PD versus idiopathic PD (odds ratio = 0.55, P = 0.03), nonmanifesting carriers versus related noncarriers (OR = 0.25, P < 0.01), and PD of less than 3 years' duration, 1 of 19 LRRK2‐PD versus 14 of 41 idiopathic PD (P < 0.05). Conclusions A lower frequency of abnormal questionnaire scores is seen in LRRK2‐PD, especially in early LRRK2‐PD, and in nonmanifesting carriers. Therefore, the Rapid eye movement sleep Behavior Disorder Questionnaire is unlikely to serve as a preclinical marker for phenoconversion to PD. © 2015 International Parkinson and Movement Disorder Society
Bibliography:Khan Foundation
The Tel Aviv Sourasky Medical Center Grant of Excellence
The Israel Science Foundation Heritage Legacy
istex:8575D01764D11FFCCD317278358DA60CCB84C6DA
ark:/67375/WNG-3CFR3Z5R-N
The Michael J Fox Foundation for Parkinson's Research
The National Institute of Health - No. K02-NS073836; No. R56NS036630; No. K02NS080915; No. NS050487; No. NS060113; No. UL1 TR000040; No. UL1 RR024156; No. NINDS 10628097
ArticleID:MDS26413
Full financial disclosures and author roles may be found in the online version of this article.
Nothing to report.
Relevant conflicts of interest/financial disclosures
Funding agencies
This study was funded by the Michael J Fox Foundation for Parkinson's Research, the National Institute of Health (through Grant Numbers K02‐NS073836, R56NS036630, K02NS080915, NS050487, NS060113, UL1 TR000040, UL1 RR024156 and NINDS 10628097) as well as by grants from the Tel Aviv Sourasky Medical Center Grant of Excellence, Khan Foundation, and the Israel Science Foundation Heritage Legacy. The funding sources had no involvement in the design, interpretation or writing of this manuscript.
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ISSN:0885-3185
1531-8257
DOI:10.1002/mds.26413