Citation

Arnaldi D, Antelmi E, St Louis EK, Postuma RB, Arnulf I. Sleep Med. Rev. 2016; ePub(ePub): ePub.

Affiliation

Sleep Disorder Unit, Pitie-Salpetriere Hospital, APHP, Pierre and Marie Curie University, Paris, France. Electronic address: isabelle.arnulf@aphp.fr.

Copyright

(Copyright © 2016, Saunders, Publisher Elsevier Publishing)

DOI

10.1016/j.smrv.2016.11.002

PMID

28082168

Abstract

Most people with idiopathic REM sleep behavior disorder (iRBD) have an underlying synucleinopathy, mainly Parkinson's disease (PD) or dementia with Lewy bodies, with median conversion time of 4-9 y from iRBD diagnosis and of 11-16 y from symptom onset. Subtle signs and imaging tests indicate concomitant neurodegeneration in widespread brain areas. Risk factor studies suggest that iRBD patients may have prior head injury, occupational farming, pesticide exposure, low education level and possibly more frequent family history of dream-enactment behavior (but not of PD), plus unexpected risk factors (smoking, ischemic heart disease and inhaled corticosteroid use). Unlike PD, caffeine and smoking appear not to have a protective role. Prior depression and antidepressant use may be early neurodegenerative signs rather than exclusively causative factors. Age, hyposmia, impaired color vision, abnormal dopaminergic imaging, mild cognitive impairment and possibly sleepiness, may identify patients at greater risk of more rapid conversion. The consensus is to generally disclose the neurodegenerative risk to patients (with the caveat that phenoconversion and its temporal course remain uncertain in individuals without "soft neurodegenerative signs" and those under 50 y of age), to suggest a healthy lifestyle and to take part in prospective cohort studies in anticipation of eventual neuroprotective trials.

Copyright © 2016 Elsevier Ltd. All rights reserved.

Language: en

Keywords

Dementia; Dopamine; Exercise; Hyposmia; Lifestyle; Neurodegeneration; Parkinsonism; REM sleep behavior disorder; Synucleinopathy