Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2015 Jul 1.
Published in final edited form as: J Neurol. 2014 Jun 11;261(7):1439–1441. doi: 10.1007/s00415-014-7392-x

Internal Consistency of the University of Michigan RBD Questionnaire

Donald L Bliwise 1, Michael K Scullin 1, Stewart A Factor 1
PMCID: PMC4101050  NIHMSID: NIHMS603990  PMID: 24916829

The presence of REM Behavior Disorder (RBD) has been shown to predict later development of Parkinsonism, and several questionnaire approaches [13] have been devised to collect spouse/caregiver reported data on such dream enactment behavior. The University of Michigan RBD Questionnaire (UMRBDQ) was developed a number of years ago [1] and has seen only sporadic use. The scale is composed of seven items. Each item is scored on a proportional basis (range: 0.0 – 1.0) and a mean item score is computed, which constitutes the patient's total score. We report here data suggesting very high internal consistency of this short scale, its utility in differentiating the conditions across the synucleinopathic spectrum, and its sensitivity/specificity in distinguishing synucleinopathic conditions versus neurologically normal subjects.

Caregivers or spouses of 72 patients [55 idiopathic Parkinson's disease (IPD); 12 Dementia with Lewy Bodies (DLB); 5 idiopathic RBD (IRBD)] completed the UMRBDQ and were rated on Unified Parkinson's Disease Rating Scale (UPDRS) (motor subscale) by a movement disorders specialist. Controls (n = 15) were derived from a community-based movement disorders screening day; all were administered the UPDRS. Among controls, 7 self-completed the UMBDQ, but mean values did not differ from 8 with spouse-completion. All protocols were IRB-approved. Demographics and clinical information are shown in Table 1 and indicate that both IPD and DLB patients had significantly greater motor impairment relative to controls and IRBD. None of the controls and a very small number of IRBD received dopaminergic medications. Mean (standard deviation) levo-dopa and pergolide dose equivalence for the IPD patients was 320.1 (332.5) mg and 1.24 (1.56) mg, respectively. Mean (SD) UMRBDQ score was .34 (.25). Cronbach's alpha for the seven items on the UMRBDQ was .858, suggesting that all were highly reliable with each other, i.e., dream enactment could be encompassed as a single trait. Reported dream enactment varied across group (F = 149.66, df 3, 83, p < .001) (see Figure 1) with controls being significantly lower than IPD, DLB and IRBD and IRBD significantly higher than IPD. UMRBDQ score was associated with the patient's own reported experience of vivid dreaming (rho = .39, p < .001) and nightmares (rho = .35, p = .001) collected from a separate questionnaire given to the patients [4, 5]. After controlling for demographics, diagnosis, UPDRS score, years since diagnosis, levo-dopa equivalence and dopamine agonist equivalence, 24% of remaining variance (p < .001) in the UMRBDQ could be accounted for by the patient's own reports of vivid dreaming and nightmares. Use of a UMRBDQ cutpoint score of ≥ .30 resulted in relatively high specificity (80.0%) for differentiating controls from each of the three groups. Sensitivities were 49.1% for IPD (p = .044), 83.3% for DLB (p = .001) and 100% for IRBD (p = .002).

Table 1.

Demographic and clinical data across groups (A-D). Mean and standard deviations are shown. Significant (p < .05) pairwise comparisons are indicated under inferential statistics. Corrected p values were used when Levene's Test for Inequality of Variances was significant.

Healthy Controls (A) Idiopathic Parkinson's Disease (B) Dementia with Lewy bodies (C) REM Sleep Behavior Disorder (D) Inferential Statistics
Age 61.3 (12.1) 63.8 (9.0) 71.2 (7.1) 69.0 (11.3) F=3.05, p=.033; A<C, B<C
Sex (% Female) 66.7 30.9 8.3 20.0 X2=11.42, p=.009; A>B, A>C
UPDRS motor 1.7 (1.8) 19.2 (8.7) 23.1 (12.4) 4.2 (1.8) F=23.51, p<.001; A<B, A<C, A<D, B>D, C>D
Years Since Diagnosis N/A 5.5 (3.8) 3.0 (1.4) 5.9 (4.0) F=2.59, p=.083
L-dopa (% taking medication) 0 61.82 41.67 20.00 X2=19.77, p<.001; A<B, A<C
Dopamine agonist (% taking) 0 45.45 8.33 20.00 X2=15.27, p=.001; A<B, B>C

Figure 1.

Figure 1

Bar graph showing mean and standard deviation for UMRBDQ score for each of the 4 groups. Horizontal lines reflect statistically significant pairwise differences between groups. *** p<.001; ** p < .005

Assessment of dream enactment by history is a challenging task in the exam setting and may be enhanced by polysomnography [69], but standardized questionnaires such as the UMRBDQ are a quick way to appreciate this important and potentially prognostic sign. The high inter-item consistency suggests that perhaps even a single question might be of value. In situations where a caregiver/spouse may not be available, the patient's own report of their experiences may also represent an important corroborating source of data.

Footnotes

Disclosures: Bliwise (Consultant: New England Research Institute; Ferring Pharmaceuticals; Morehouse School of Medicine, Vantia Therapeutics, Georgia Institute of Technology); Scullin (None); Factor (Consultant: Merz, Chelsea, ADAMAS, Neurocrine, Lundbeck, Ceregene; Royalties: Demos, Blackwell Futura; Grants: Ceregene, TEVA, Ipsen, Allergan, Medtronics, Auspex, Genzyme, MJ Fox Foundation)

Conflicts of Interest: Bliwise (none); Scullin (none); Factor (none)

References

  • 1.Consens FB, Chervin RD, Koeppe RA, et al. Validation of a polysomnographic score for REM sleep behavior disorder. Sleep. 2005;28:993–7. doi: 10.1093/sleep/28.8.993. [DOI] [PubMed] [Google Scholar]
  • 2.Boeve BF, Molano JR, Ferman TJ, et al. Validation of the Mayo Sleep Questionnaire to screen for REM sleep behavior disorder in an aging and dementia cohort. Sleep Med. 2011;12:445–53. doi: 10.1016/j.sleep.2010.12.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Stiasny-Kolster K, Mayer G, Schafer S, et al. The REM sleep behavior disorder screening instrument—a new diagnostic instrument. Mov Disord. 2007;22:2386–93. doi: 10.1002/mds.21740. [DOI] [PubMed] [Google Scholar]
  • 4.Lee JH, Bliwise DL, Lebret-Bories E, et al. Dream-disturbed sleep in insomnia and narcolepsy. J Nerv Ment Dis. 1993;181:320–4. doi: 10.1097/00005053-199305000-00008. [DOI] [PubMed] [Google Scholar]
  • 5.Scullin MK, Harrison TL, Factor SA, Bliwise DL. A Neurodegenerative Disease Sleep Questionnaire: principal component analysis in Parkinson's disease. J Neurol Sci. 2014;336:243–6. doi: 10.1016/j.jns.2013.09.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Bliwise DL, Rye DB. Elevated phasic electromyographic metric (PEM) rates identify rapid eye movement behavior disorder patients on nights without behavioral abnormalities. Sleep. 2008;31:853–7. doi: 10.1093/sleep/31.6.853. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Ferri R, Franceschini C, Zucconi M, Vandi S, Poli F, Bruni O, Cipolli C, Montagna P, Plazzi G. Searching for a marker of REM sleep behavior disorder: submentalis muscle EMG amplitude analysis during sleep in patients with narcolepsy/cataplexy. Sleep. 2008;31:1409–17. [PMC free article] [PubMed] [Google Scholar]
  • 8.Frauscher B, Iranzo A, Hogl B, Casanova-Molla J, Salamero M, Gschliesser V, Tolosa E, Poewe W, Santamaria J. Quantification of electromyographic activity during REM sleep in multiple muscles in REM sleep behavior disorder. Sleep. 2008;31:724–31. doi: 10.1093/sleep/31.5.724. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Mayer G, Kesper K, Ploch T, Canisius S, Penzel T, Oertel W, Stiasny-Koslter K. Quantification of tonic and phasic muscle activity in REM sleep behavior disorder. J Clin Neurophysiol. 2008;25:48–55. doi: 10.1097/WNP.0b013e318162acd7. [DOI] [PubMed] [Google Scholar]

RESOURCES