Skip to main content

Advertisement

Log in

Baseline prevalence and longitudinal assessment of autonomic dysfunction in early Parkinson’s disease

  • Neurology and Preclinical Neurological Studies - Original Article
  • Published:
Journal of Neural Transmission Aims and scope Submit manuscript

Abstract

Autonomic dysfunction (AutD) is common and debilitating in Parkinson’s disease (PD). Predictors of AutD are unclear, and data are limited on the biological relevance of AutD in PD. Here, we evaluated the baseline prevalence and 2-year longitudinal assessment of AutD in patients with de novo PD compared with healthy controls (HC). Moreover, we also assessed various variables that could predict longitudinal changes in AutD in early PD. Parkinson’s Progression Markers Initiative (PPMI) was utilized to evaluate untreated PD participants at baseline and HC. Autonomic function was assessed using the 25-item Scale for Outcomes in Parkinson’s Disease-Autonomic (SCOPA-AUT) score at baseline and 2 years. Clinical and biological variables were measured for their correlations with AuD for up to 2 years. Two hundred and ninety PD subjects and 170 HC were enrolled and followed for 2 years. SCOPA-AUT mean (SD) scores increased from baseline 8.49 ± 5.23 to 10.12 ± 5.77 at year 2 in PD subjects (p < 0.001) versus from 4.98 ± 3.34 to 5.03 ± 374 in HC (p = 0.496), with a significant difference between the groups (p < 0.001). Among them, 242 PD participants and 151 HC completed the SCOPA-AUT assessment, including sexual function. In the multivariate analysis, a higher baseline SCOPA-AUT score was associated with higher baseline MDS-UPDRS Part I scores (p < 0.001). Moreover, a longitudinal increase in autonomic function severity was associated with the white race (p = 0.010) at baseline. In contrast, there was no association with the CSF biomarkers. MDS-UPDRS Part I score may predict AuD in patients with early PD, which is correlated with nonmotor symptoms and race.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Availability of data and materials

The datasets generated during and/or analyzed during the current study are available from the corresponding author upon reasonable request.

References

  • Aliev G et al (2003) Role of vascular hypoperfusion-induced oxidative stress and mitochondria failure in the pathogenesis of Azheimer disease. Neurotox Res 5(7):491–504

    Article  PubMed  Google Scholar 

  • Arnao V et al (2015) In patient’s with Parkinson disease, autonomic symptoms are frequent and associated with other non-motor symptoms. Clin Auton Res 25(5):301–307

    Article  PubMed  Google Scholar 

  • Berg A et al (2022) Autonomic dysfunction in Parkinson’s disease: results from the Faroese Parkinson’s disease cohort. Neurosci Lett 785:136789

    Article  CAS  PubMed  Google Scholar 

  • Bostantjopoulou S et al (2016) Self-reported autonomic symptoms in Parkinson’s disease: properties of the SCOPA-AUT scale. Hippokratia 20(2):115–120

    CAS  PubMed  PubMed Central  Google Scholar 

  • Braak H et al (2003) Staging of brain pathology related to sporadic Parkinson’s disease. Neurobiol Aging 24(2):197–211

    Article  PubMed  Google Scholar 

  • Brockmann K et al (2011) GBA-associated PD presents with nonmotor characteristics. Neurology 77(3):276–280

    Article  CAS  PubMed  Google Scholar 

  • Chaudhuri KR, Schapira AH (2009) Non-motor symptoms of Parkinson’s disease: dopaminergic pathophysiology and treatment. Lancet Neurol 8(5):464–474

    Article  CAS  PubMed  Google Scholar 

  • Coon EA, Cutsforth-Gregory JK, Benarroch EE (2018) Neuropathology of autonomic dysfunction in synucleinopathies. Mov Disord 33(3):349–358

    Article  PubMed  Google Scholar 

  • Cui J et al (2021) Activities of daily living as a longitudinal moderator of the effect of autonomic dysfunction on anxiety and depression of Parkinson’s patients. Brain Behav 11(8):e2297

    Article  PubMed  PubMed Central  Google Scholar 

  • de la Torre JC (2000) Critically attained threshold of cerebral hypoperfusion: the CATCH hypothesis of Alzheimer’s pathogenesis. Neurobiol Aging 21(2):331–342

    Article  PubMed  Google Scholar 

  • De Pablo-Fernandez E et al (2017) Association of autonomic dysfunction with disease progression and survival in parkinson disease. JAMA Neurol 74(8):970–976

    Article  PubMed  PubMed Central  Google Scholar 

  • Forjaz MJ et al (2010) Assessing autonomic symptoms of Parkinson’s disease with the SCOPA-AUT: a new perspective from Rasch analysis. Eur J Neurol 17(2):273–279

    Article  CAS  PubMed  Google Scholar 

  • Gray WK, Wood BH, Walker RW (2009) Do autonomic function tests in people with Parkinson’s disease predict survival rates at 7 years follow-up? Mov Disord 24(16):2432–2434

    Article  PubMed  Google Scholar 

  • Hinkle JT et al (2018) Dopamine transporter availability reflects gastrointestinal dysautonomia in early Parkinson disease. Parkinsonism Relat Disord 55:8–14

    Article  PubMed  PubMed Central  Google Scholar 

  • Jankovic J (2008) Parkinson’s disease: clinical features and diagnosis. J Neurol Neurosurg Psychiatry 79(4):368–376

    Article  CAS  PubMed  Google Scholar 

  • Kendall PC et al (1976) The state-trait anxiety inventory: a systematic evaluation. J Consult Clin Psychol 44(3):406–412

    Article  CAS  PubMed  Google Scholar 

  • Khoo TK et al (2013) The spectrum of nonmotor symptoms in early Parkinson disease. Neurology 80(3):276–281

    Article  PubMed  PubMed Central  Google Scholar 

  • Kim JY et al (2017) Validation of the Korean version of the scale for outcomes in Parkinson’s disease-autonomic. J Mov Disord 10(1):29–34

    Article  PubMed  PubMed Central  Google Scholar 

  • Ledda C et al (2022) Burden of caregiving for cardiovascular dysautonomia in Parkinson’s disease. Clin Auton Res 32(6):455–461

    Article  PubMed  PubMed Central  Google Scholar 

  • Longardner K et al (2022) Differential impact of individual autonomic domains on clinical outcomes in Parkinson’s disease. J Neurol 269(10):5510–5520

    Article  PubMed  PubMed Central  Google Scholar 

  • Marek K et al (2011) The Parkinson Progression Marker Initiative (PPMI). Prog Neurobiol. 95(4):629–35

    Article  PubMed Central  Google Scholar 

  • Merola A et al (2016) Orthostatic hypotension in Parkinson’s disease: does it matter if asymptomatic? Parkinsonism Relat Disord 33:65–71

    Article  PubMed  Google Scholar 

  • Merola A et al (2018) Autonomic dysfunction in Parkinson’s disease: a prospective cohort study. Mov Disord 33(3):391–397

    Article  PubMed  Google Scholar 

  • Nasreddine ZS et al (2005) The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment. J Am Geriatr Soc 53(4):695–699

    Article  PubMed  Google Scholar 

  • Pazo JH, Belforte JE (2002) Basal ganglia and functions of the autonomic nervous system. Cell Mol Neurobiol 22(5–6):645–654

    Article  CAS  PubMed  Google Scholar 

  • Petrucci S et al (2020) GBA-related Parkinson’s disease: dissection of genotype-phenotype correlates in a large Italian cohort. Mov Disord 35(11):2106–2111

    Article  CAS  PubMed  Google Scholar 

  • Pilipovich AA et al (2022) Gastrointestinal dysfunction impact on life quality in a cohort of russian patients with Parkinson’s disease I-III H&Y stage. Parkinsons Dis 2022:1571801

    CAS  PubMed  PubMed Central  Google Scholar 

  • Pilotto A et al (2019) Orthostatic hypotension and REM sleep behaviour disorder: impact on clinical outcomes in α-synucleinopathies. J Neurol Neurosurg Psychiatry 90(11):1257–1263

    Article  PubMed  Google Scholar 

  • Pilotto A et al (2021) Association of orthostatic hypotension with cerebral atrophy in patients with Lewy body disorders. Neurology 97(8):e814–e824

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Sklerov M et al (2020) Longitudinal change in autonomic symptoms predicts activities of daily living and depression in Parkinson’s disease. Clin Auton Res 30(3):223–230

    Article  PubMed  Google Scholar 

  • Sklerov M et al (2022) Autonomic and depression symptoms in Parkinson’s disease: clinical evidence for overlapping physiology. J Parkinsons Dis 12(3):1059–1067

    Article  CAS  PubMed  Google Scholar 

  • Stanković I et al (2019) Longitudinal assessment of autonomic dysfunction in early Parkinson’s disease. Parkinsonism Relat Disord 66:74–79

    Article  PubMed  Google Scholar 

  • van Deursen DN et al (2020) Autonomic failure in Parkinson’s disease is associated with striatal dopamine deficiencies. J Neurol 267(7):1922–1930

    Article  PubMed  PubMed Central  Google Scholar 

  • Vichayanrat E et al (2021) Lower urinary tract dysfunction in Parkinsonian syndromes. Neurol Sci 42(10):4045–4054

    Article  PubMed  Google Scholar 

  • Visser M et al (2004) Assessment of autonomic dysfunction in Parkinson’s disease: the SCOPA-AUT. Mov Disord 19(11):1306–1312

    Article  PubMed  Google Scholar 

  • Winge K et al (2005) Relationship between nigrostriatal dopaminergic degeneration, urinary symptoms, and bladder control in Parkinson’s disease. Eur J Neurol 12(11):842–850

    Article  CAS  PubMed  Google Scholar 

  • Yeh TL et al (2006) Correlation between striatal dopamine D2/D3 receptor binding and cardiovascular activity in healthy subjects. Am J Hypertens 19(9):964–969

    Article  CAS  PubMed  Google Scholar 

  • Yu Z, Li Y, The Parkinson’s Progression Markers (2021) Association of autonomic symptoms with cerebrospinal fluid biomarkers in Parkinson disease and scans without evidence of dopaminergic deficit. Medicine (Baltimore). 100(7):e24837

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Zhou Z et al (2021) Characteristics of autonomic dysfunction in parkinson’s disease: a large chinese multicenter cohort study. Front Aging Neurosci 13:761044

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Funding

This study received no funding support.

Author information

Authors and Affiliations

Authors

Contributions

MY: conceived and designed the experiments. LY and HG: contributed significantly to the experiments, arranging data and performing data analyses. LY: wrote the draft manuscript. MY revised the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Min Ye.

Ethics declarations

Conflict of interest

The authors declare that they have no conflicts of interest.

Ethical approval and consent to participate

All patients provided their written, voluntarily informed consent. All procedures were carried out in accordance with the guidelines outlined in the Helsinki Declaration, and the Ethics Committee of the Affiliated Brain Hospital of Nanjing Medical University approved this study.

Consent for publication

Not applicable.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Yang, L., Gao, H. & Ye, M. Baseline prevalence and longitudinal assessment of autonomic dysfunction in early Parkinson’s disease. J Neural Transm 131, 127–139 (2024). https://doi.org/10.1007/s00702-023-02711-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00702-023-02711-9

Keywords

Navigation