The composite autonomic symptom scale 31 is a useful screening tool for patients with Parkinsonism

Younsoo Kim, Jin Myoung Seok, Jongkyu Park, Kun-Hyun Kim, Ju-Hong Min, Jin Whan Cho, Suyeon Park, Hyun-Jin Kim, Byoung Joon Kim, Jinyoung Youn, Younsoo Kim, Jin Myoung Seok, Jongkyu Park, Kun-Hyun Kim, Ju-Hong Min, Jin Whan Cho, Suyeon Park, Hyun-Jin Kim, Byoung Joon Kim, Jinyoung Youn

Abstract

Differentiation of multiple system atrophy with predominant parkinsonism (MSA-P) and Parkinson's disease (PD) is important, but an effective tool for differentiation has not been identified. We investigated the efficacy of the composite autonomic symptom scale 31 (COMPASS 31) questionnaire as a tool for evaluating autonomic function in parkinsonism patients. In this study, we enrolled drug-naïve patients with MSA-P and PD, and administered the COMPASS-31 and an objective autonomic dysfunction test (AFT). Demographic and clinical data, including parkinsonism and autonomic dysfunction, were compared between the two groups. Additionally, we determined the optimal COMPASS 31 cut-off score to differentiate MSA-P from PD for use as a screening tool. In this study, 27 MSA-P patients and 41 PD patients were recruited. The total COMPASS 31 score was well correlated with the objective AFT results. When we compared the COMPASS 31 score between the two groups, MSA-P patients showed higher total scores and sub-scores in the orthostatic intolerance, gastrointestinal, and bladder domains compared with PD patients. Similarly, MSA-P patients had more abnormalities in expiration to inspiration ratio, Valsalva ratio and pressure recovery time than PD patients in objective AFT. With 13.25 as the cut-off score for diagnosis of MSA-P, the total COMPASS-31 score demonstrated high sensitivity (92.6%) and moderate specificity (51.2%) with an area under the curve of 0.765. Based on our results, the COMPASS 31 is an effective tool for evaluation of autonomic function in patients with parkinsonism. The COMPASS-31 could be used as a sensitive and convenient screening tool, especially for the differentiation between MSA-P and PD.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Fig 1. Comparison of COMPASS 31 scores…
Fig 1. Comparison of COMPASS 31 scores among the patients with PD and MSA-P.
The MSA-P patient group had higher total COMPASS 31 scores and higher sub-scores in the orthostatic intolerance, gastrointestinal, and bladder domains compared with PD patients. The error bars represent the standard error of mean. COMPASS 31, composite autonomic symptom scale 31 questionnaire; PD, Parkinson’s disease; MSA-P, multiple system atrophy with predominant parkinsonism. *p-value < 0.05.
Fig 2. ROC curve for COMPASS 31…
Fig 2. ROC curve for COMPASS 31 total score diagnostic performance.
With 13.25 as the cut-off score for differential diagnosis of MSA-P from PD, the total COMPASS 31 score demonstrated high sensitivity (92.6%) and moderate specificity (51.2%) with an area under the curve of 0.765. ROC, receiver operating characteristic; COMPASS 31, composite autonomic symptom scale 31 questionnaire; MSA-P, multiple system atrophy with predominant parkinsonism; PD, Parkinson’s disease.

References

    1. Gilman S, Wenning GK, Low PA, Brooks DJ, Mathias CJ, Trojanowski JQ, et al. Second consensus statement on the diagnosis of multiple system atrophy. Neurology. 2008;71(9):670–6. Epub 2008/08/30. doi: ; PubMed Central PMCID: PMCPmc2676993.
    1. Kim JS, Lee SH, Oh YS, Park JW, An JY, Park SK, et al. Cardiovascular Autonomic Dysfunction in Mild and Advanced Parkinson's Disease. Journal of movement disorders. 2016;9(2):97–103. doi: ; PubMed Central PMCID: PMC4886202.
    1. Kim JB, Kim BJ, Koh SB, Park KW. Autonomic dysfunction according to disease progression in Parkinson's disease. Parkinsonism & related disorders. 2014;20(3):303–7. doi: .
    1. Baschieri F, Calandra-Buonaura G, Doria A, Mastrolilli F, Palareti A, Barletta G, et al. Cardiovascular autonomic testing performed with a new integrated instrumental approach is useful in differentiating MSA-P from PD at an early stage. Parkinsonism & related disorders. 2015;21(5):477–82. doi: .
    1. Kimpinski K, Iodice V, Burton DD, Camilleri M, Mullan BP, Lipp A, et al. The role of autonomic testing in the differentiation of Parkinson's disease from multiple system atrophy. Journal of the neurological sciences. 2012;317(1–2):92–6. doi: ; PubMed Central PMCID: PMC3340456.
    1. Riley DE, Chelimsky TC. Autonomic nervous system testing may not distinguish multiple system atrophy from Parkinson's disease. Journal of neurology, neurosurgery, and psychiatry. 2003;74(1):56–60. ; PubMed Central PMCID: PMC1738185. doi:
    1. Lipp A, Sandroni P, Ahlskog E, Fealey RD, Kimpinski K, Iodice V, et al. Prospective Differentiation of Multiple System Atrophy From Parkinson Disease, With and Without Autonomic Failure. Arch Neurol. 2009;66(6):742–50. doi:
    1. Reimann M, Schmidt C, Herting B, Prieur S, Junghanns S, Schweitzer K, et al. Comprehensive autonomic assessment does not differentiate between Parkinson's disease, multiple system atrophy and progressive supranuclear palsy. Journal of neural transmission. 2010;117(1):69–76. doi: .
    1. Sletten DM, Suarez GA, Low PA, Mandrekar J, Singer W. COMPASS 31: a refined and abbreviated Composite Autonomic Symptom Score. Mayo Clinic proceedings. 2012;87(12):1196–201. doi: ; PubMed Central PMCID: PMC3541923.
    1. Cortez MM, Nagi Reddy SK, Goodman B, Carter JL, Wingerchuk DM. Autonomic symptom burden is associated with MS-related fatigue and quality of life. Multiple sclerosis and related disorders. 2015;4(3):258–63. doi: .
    1. Treister R, O'Neil K, Downs HM, Oaklander AL. Validation of the composite autonomic symptom scale 31 (COMPASS-31) in patients with and without small fiber polyneuropathy. European journal of neurology. 2015;22(7):1124–30. doi: ; PubMed Central PMCID: PMC4464987.
    1. Kang JH, Kim JK, Hong SH, Lee CH, Choi BY. Heart Rate Variability for Quantification of Autonomic Dysfunction in Fibromyalgia. Annals of rehabilitation medicine. 2016;40(2):301–9. doi: ; PubMed Central PMCID: PMC4855125.
    1. Chaudhuri KR, Schapira AH. Non-motor symptoms of Parkinson's disease: dopaminergic pathophysiology and treatment. Lancet Neurol. 2009;8(5):464–74. doi: .
    1. Hughes AJ, Daniel SE, Kilford L, Lees AJ. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. Journal of neurology, neurosurgery, and psychiatry. 1992;55(3):181–4. Epub 1992/03/01. ; PubMed Central PMCID: PMCPmc1014720.
    1. Hoehn MM, Yahr MD. Parkinsonism: onset, progression, and mortality. 1967. Neurology. 1998;50(2):318 and 16 pages following. .
    1. Vogel ER, Sandroni P, Low PA. Blood pressure recovery from Valsalva maneuver in patients with autonomic failure. Neurology. 2005;65(10):1533–7. doi: .
    1. Novak P. Quantitative autonomic testing. Journal of visualized experiments: JoVE. 2011;(53). doi: ; PubMed Central PMCID: PMC3196175.
    1. Chung EJ, Lee WY, Yoon WT, Kim BJ, Lee GH. MIBG scintigraphy for differentiating Parkinson's disease with autonomic dysfunction from Parkinsonism-predominant multiple system atrophy. Mov Disord. 2009;24(11):1650–5. doi: .
    1. Yokota T, Matsunaga T, Okiyama R, Hirose K, Tanabe H, Furukawa T, et al. Sympathetic skin response in patients with multiple sclerosis compared with patients with spinal cord transection and normal controls. Brain. 1991;114 (Pt 3):1381–94. .
    1. Low PA. Composite Autonomic Scoring Scale for Laboratory Quantification of Generalized Autonomic Failure. Mayo Clinic proceedings. 1993;68:748–52.

Source: PubMed

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