REM sleep behavior disorder is related to striatal monoaminergic deficit in MSA

S. Gilman, R. A. Koeppe, R. D. Chervin, F. B. Consens, R. Little, H. An, L. Junck, M. Heumann

Research output: Contribution to journalArticlepeer-review

140 Citations (Scopus)

Abstract

Objective: To explore the neurochemical basis of REM sleep behavior disorder (RBD) in multiple-system atrophy (MSA). Methods: In 13 patients with probable MSA, nocturnal, laboratory-based polysomnography was used to rate the severity of REM atonia loss by the percentage of REM sleep with tonically increased electromyographic (EMG) activity and the percentage of REM sleep with phasic EMG bursts. PET with (+)-[11C]dihydrotetrabenazine ([11C]DTBZ) was employed to measure the density of striatal monoaminergic terminals and SPECT with (-)-5-[123I]iodobenzovesamicol ([123I]IBVM) to measure the density of thalamic cholinergic terminals. Data in the patient group were compared with data from 15 normal control subjects scanned with [11C]DTBZ and 12 with [123I]IBVM. Results: Age and gender distributions were similar in patient and normal control groups. The MSA subjects showed decreased mean [11C]DTBZ binding in the striatum (p < 0.0001) and decreased [123I]IBVM binding in the thalamus (p < 0.001). Moreover, in the MSA group, striatal [11C]DTBZ binding was inversely correlated with the severity of REM atonia loss (p = 0.003). Thalamic [123I] IBVM binding, however, was not correlated to the severity of REM atonia loss. Conclusion: Decreased nigrostriatal dopaminergic projections may contribute to RBD in MSA.

Original languageEnglish
Pages (from-to)29-34
Number of pages6
JournalNeurology
Volume61
Issue number1
DOIs
Publication statusPublished - 2003 Jul 8
Externally publishedYes

ASJC Scopus subject areas

  • Clinical Neurology

Fingerprint

Dive into the research topics of 'REM sleep behavior disorder is related to striatal monoaminergic deficit in MSA'. Together they form a unique fingerprint.

Cite this