Cortical thinning in patients with REM sleep behavior disorder is associated with clinical progression.
Neurodegenerative diseases
Predictive markers
Journal
NPJ Parkinson's disease
ISSN: 2373-8057
Titre abrégé: NPJ Parkinsons Dis
Pays: United States
ID NLM: 101675390
Informations de publication
Date de publication:
2019
2019
Historique:
received:
08
10
2018
accepted:
11
04
2019
entrez:
10
5
2019
pubmed:
10
5
2019
medline:
10
5
2019
Statut:
epublish
Résumé
The aim of this study is to determine whether structural MRI measures are associated with clinical impairment and progression to a Lewy body disease in patients with idiopathic REM sleep behavior disorder (iRBD). Twenty-seven patients with iRBD in addition to patients with de novo PD and healthy controls were included from the Parkinson's Progression Markers Initiative. Patients with iRBD were followed for up to 3 years. Clinical and MRI measures were compared across groups and the association between clinical features and structural MRI was assessed in iRBD patients. Cox regression analyses were applied to identify risk factors for progressing to a Lewy body disease in iRBD. Our results showed that, at baseline, iRBD patients showed parietal and occipital cortical thinning, compared to controls. They also showed worse motor and non-motor abilities, some of which correlated with motor, frontal or temporal cortical thinning. At follow-up, six (22%) iRBD patients were diagnosed with a Lewy body disorder. These patients showed cortical thinning in frontal, occipital and parietal areas compared to iRBD non-converters. Cortical thinning was a significant predictor for future development of a Lewy body disorder (HR: 0.784; 95% CI: 0.640-0.960; p = 0.02). We conclude that cortical thinning is associated with worse motor and non-motor abilities, and predicts conversion to a Lewy body disorder in iRBD, suggesting it could be used to select candidates for clinical trials to delay the onset of neurodegenerative disease.
Identifiants
pubmed: 31069252
doi: 10.1038/s41531-019-0079-3
pii: 79
pmc: PMC6499806
doi:
Types de publication
Journal Article
Langues
eng
Pagination
7Déclaration de conflit d'intérêts
The authors declare no competing interests.
Références
J Cogn Neurosci. 2000 Jan;12(1):1-47
pubmed: 10769304
Proc Natl Acad Sci U S A. 2000 Sep 26;97(20):11050-5
pubmed: 10984517
Neuron. 2002 Jan 31;33(3):341-55
pubmed: 11832223
Neuroimage. 2004 Oct;23(2):724-38
pubmed: 15488422
J Am Geriatr Soc. 2005 Apr;53(4):695-9
pubmed: 15817019
Lancet Neurol. 2006 Jul;5(7):572-7
pubmed: 16781987
Brain. 2007 Feb;130(Pt 2):450-6
pubmed: 17235126
Mov Disord. 2007 Dec;22(16):2386-93
pubmed: 17894337
Sleep. 1991 Dec;14(6):540-5
pubmed: 1798888
Prog Neurobiol. 2011 Dec;95(4):629-35
pubmed: 21930184
Mov Disord. 2012 May;27(6):677-89
pubmed: 22447623
Ann Neurol. 2012 Nov;72(5):635-47
pubmed: 22941893
Parkinsonism Relat Disord. 2013 Nov;19(11):970-4
pubmed: 23867866
Front Neuroinform. 2014 Jan 06;7:49
pubmed: 24432000
PLoS One. 2014 Jan 23;9(1):e86624
pubmed: 24466177
Brain. 2014 Apr;137(Pt 4):1120-9
pubmed: 24613932
Mov Disord. 2015 Apr 15;30(5):680-7
pubmed: 24676967
Neurology. 2014 Jun 3;82(22):2017-25
pubmed: 24808018
Am J Geriatr Psychiatry. 2015 Jan;23(1):38-46
pubmed: 25218360
Brain. 2014 Dec;137(Pt 12):3122-8
pubmed: 25338949
Ann Neurol. 2015 May;77(5):830-9
pubmed: 25767079
Hum Brain Mapp. 2015 Aug;36(8):2980-95
pubmed: 25950288
JAMA Neurol. 2015 Aug;72(8):863-73
pubmed: 26076039
Neurodegener Dis. 2015;15(5):294-300
pubmed: 26202063
Lancet Neurol. 2016 Apr;15(4):405-19
pubmed: 26971662
Sci Rep. 2016 Jun 01;6:26782
pubmed: 27245317
Neurology. 2017 Apr 18;88(16):1486-1487
pubmed: 28330957
Brain. 2017 Jul 1;140(7):1959-1976
pubmed: 28549077
Cereb Cortex. 2018 Feb 1;28(2):658-671
pubmed: 28591814
Ann Neurol. 2017 Sep;82(3):419-428
pubmed: 28833467
Neurology. 2018 May 15;90(20):e1759-e1770
pubmed: 29669906
Lancet Neurol. 2018 Jul;17(7):629-640
pubmed: 29914708
Neurology. 1967 May;17(5):427-42
pubmed: 6067254
Arch Neurol. 1978 Jun;35(6):364-7
pubmed: 655909
Laryngoscope. 1984 Feb;94(2 Pt 1):176-8
pubmed: 6694486