Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Apr 14;7(1):37.
doi: 10.1038/s41531-021-00181-y.

Delayed orthostatic hypotension in Parkinson's disease

Affiliations

Delayed orthostatic hypotension in Parkinson's disease

Sang-Won Yoo et al. NPJ Parkinsons Dis. .

Abstract

Orthostatic hypotension (OH) is relatively common in the early stage of Parkinson's disease (PD). It is divided into delayed OH and classical OH. Classical OH in PD has been investigated widely, however, the clinical implications of delayed OH in PD have seldom been studied. The purpose of this study is to characterize delayed OH in PD. A total of 285 patients with early drug-naïve PD were enrolled and divided into three groups according to orthostatic change: no-OH, delayed OH, and classical OH. The disease severity in terms of motor, non-motor, and cognitive functions was assessed. The cortical thickness of 82 patients was analyzed with brain magnetic resonance imaging. The differences among groups and linear tendency in the order of no-OH, delayed OH, and classical OH were investigated. Seventy-seven patients were re-evaluated. Initial and follow-up evaluations were explored to discern any temporal effects of orthostasis on disease severity. Sixty-four (22.5%) patients were defined as having delayed OH and 117 (41.1%) had classical OH. Between-group comparisons revealed that classical OH had the worst outcomes in motor, non-motor, cognitive, and cortical thickness, compared to the other groups. No-OH and delayed OH did not differ significantly. Linear trends across the pre-ordered OH subtypes found that clinical parameters worsened along with the orthostatic challenge. Clinical scales deteriorated and the linear gradient was maintained during the follow-up period. This study suggests that delayed OH is a mild form of classical OH in PD. PD with delayed OH has milder disease severity and progression.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1. Enrolled patients study flow.
NMSS Non-Motor Symptoms Scale, PDQ-39 Parkinson’s Disease Quality of Life-39, OHQ Orthostatic Hypotension Questionnaire, MADRS Montgomery-Asberg Depression Rating Scale, RBDSQ REM Sleep Behavior Disorder Screening Questionnaire, UPDRS Unified Parkinson’s Disease Rating Scale, MMSE Mini-Mental Status Examination.
Fig. 2
Fig. 2. Temporal progression of cognitive and motor severities across the groups.
Error bars: standard error of the mean. UPDRS Unified Parkinson’s Disease Rating Scale, MMSE Mini-Mental Status Examination, OH orthostatic hypotension.

Similar articles

Cited by

References

    1. Jain S, Goldstein DS. Cardiovascular dysautonomia in Parkinson disease: from pathophysiology to pathogenesis. Neurobiol. Dis. 2012;46:572–580. doi: 10.1016/j.nbd.2011.10.025. - DOI - PMC - PubMed
    1. Pont‐Sunyer C, et al. The onset of nonmotor symptoms in Parkinson’s disease (The ONSET PD Study) Mov. Disord. 2015;30:229–237. doi: 10.1002/mds.26077. - DOI - PubMed
    1. Hiorth YH, Pedersen KF, Dalen I, Tysnes OB, Alves G. Orthostatic hypotension in Parkinson disease: a 7-year prospective population-based study. Neurology. 2019;93:e1526–e1534. doi: 10.1212/WNL.0000000000008314. - DOI - PubMed
    1. Kim JS, et al. Association of cognitive dysfunction with neurocirculatory abnormalities in early Parkinson disease. Neurology. 2012;79:1323–1331. doi: 10.1212/WNL.0b013e31826c1acd. - DOI - PMC - PubMed
    1. Anang JB, et al. Predictors of dementia in Parkinson disease: a prospective cohort study. Neurology. 2014;83:1253–1260. doi: 10.1212/WNL.0000000000000842. - DOI - PMC - PubMed

LinkOut - more resources