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REM Sleep Behaviour Disorder in Multiple System Atrophy: From Prodromal to Progression of Disease
被引:17
|作者:
Giannini, Giulia
[1
,2
]
Provini, Federica
[1
,2
]
Cortelli, Pietro
[1
,2
]
Calandra-Buonaura, Giovanna
[1
,2
]
机构:
[1] IRCCS Ist Sci Neurol Bologna, Unita Operat Complessa UOC, Clin Neurol Rete Metropolitana NEUROMET, Bologna, Italy
[2] Univ Bologna Alma Mater Studiorum, Dept Biomed & NeuroMotor Sci DiBiNeM, Bologna, Italy
来源:
FRONTIERS IN NEUROLOGY
|
2021年
/
12卷
关键词:
disease progression;
sleep disorders;
phenoconversion;
prodromic phase;
review;
autonomic failure;
REM sleep behaviour disorder;
multiple system atrophy;
PURE AUTONOMIC FAILURE;
NEURODEGENERATIVE DISEASE;
PARKINSONS-DISEASE;
CLINICAL-FEATURES;
CONSENSUS STATEMENT;
DELAYED EMERGENCE;
EARLY MARKER;
MOVEMENT;
RISK;
STRIDOR;
D O I:
10.3389/fneur.2021.677213
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
A higher frequency of motor and breathing sleep-related disorders in multiple system atrophy (MSA) populations is reported. REM sleep behaviour disorder (RBD) is one of the most robust markers of an underlying alpha-synucleinopathy. Although a large corpus of literature documented the higher prevalence of RBD in MSA, few studies have systematically investigated the prevalence of RBD as mode of disease onset and its role in disease progression. Moreover, there has been increasing interest in phenoconversion into synucleinopathies of cohorts of patients with isolated RBD (iRBD). Finally, some studies investigated RBD as predictive factor of conversion in isolated autonomic failure, a synucleinopathy presenting with autonomic failure as the sole clinical manifestation that could convert to a manifest central nervous system synucleinopathy. As the field of neurodegenerative disorders moves increasingly towards developing disease-modifying therapies, detecting individuals in the prodromal stage of these synucleinopathies becomes crucial. The aims of this review are to summarise (1) the prevalence of RBD during the course of MSA and as presenting feature of MSA (iRBD), (2) the RBD features in MSA, (3) MSA progression and prognosis in the subgroup of patients with RBD predating disease onset, and (4) the prevalence of MSA conversion in iRBD cohorts. Moreover, we summarise previous results on the role of RBD in the context of isolated autonomic failure as marker of phenoconversion to other synucleinopathies and, in particular, to MSA.
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页数:10
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