Evidence map›Paper›PMID 36526431›Full record

ArticleNeurology2023

Association Between Orthostatic Hypotension and Dementia in Patients With Parkinson Disease and Multiple System Atrophy.

Iñigo Ruiz Barrio, Yasuo Miki, Zane T Jaunmuktane, Thomas Warner, Eduardo De Pablo-Fernandez

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 43 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 3 pooled it
6.1field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 3 syntheses or guidelines pooled it, 54 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Autonomic debate: symptoms are an optimal target for orthostatic hypotension screening and management. An argument in opposition.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2026
    Article
  5. Symptoms are an optimal target for orthostatic hypotension screening and management: an argument in favor.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2026
    Review
  6. Observational
  7. Early Autonomic Burden in Prodromal Parkinson's Disease Predicts Cognitive Impairment.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
  8. Review
  9. Predictive factors of global cognitive impairment in de novo Parkinson disease with normal cognition at baseline: a 10-year cohort study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Orthostatic hypotension in Parkinson's disease-More than just lightheadedness and fainting.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2025
    Article
  15. Enhanced visual illusions in Parkinson's disease with cardiovascular autonomic failure.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2025
    Article
  16. Article
  17. Review
  18. A reset on our reclined position-a call to prioritize neurogenic supine hypertension in the synucleinopathies.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2025
    Review
  19. Review
  20. Orthostatic Hypotension and Cognition in Lewy Body Disorders: On Promising Tides.Movement disorders : official journal of the Movement Disorder Society · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 3 countries.

Iñigo Ruiz BarrioFrom the Queen Square Brain Bank for Neurological Disorders, (I.R.B., Y.M., Z.T.J., T.W., E.d.P-F.), and Reta Lila Weston Institute of Neurological Studies (T.W., E.d.P-F.), Department of Clinical and Movement Neurosciences UCL Queen Square Institute of Neurology, London, United Kingdom; Movement Disorders Unit, (I.R.B.), Neurology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain; and Department of Neuropathology (Y.M.), Institute of Brain Science, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Yasuo MikiFrom the Queen Square Brain Bank for Neurological Disorders, (I.R.B., Y.M., Z.T.J., T.W., E.d.P-F.), and Reta Lila Weston Institute of Neurological Studies (T.W., E.d.P-F.), Department of Clinical and Movement Neurosciences UCL Queen Square Institute of Neurology, London, United Kingdom; Movement Disorders Unit, (I.R.B.), Neurology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain; and Department of Neuropathology (Y.M.), Institute of Brain Science, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Zane T JaunmuktaneFrom the Queen Square Brain Bank for Neurological Disorders, (I.R.B., Y.M., Z.T.J., T.W., E.d.P-F.), and Reta Lila Weston Institute of Neurological Studies (T.W., E.d.P-F.), Department of Clinical and Movement Neurosciences UCL Queen Square Institute of Neurology, London, United Kingdom; Movement Disorders Unit, (I.R.B.), Neurology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain; and Department of Neuropathology (Y.M.), Institute of Brain Science, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Thomas WarnerFrom the Queen Square Brain Bank for Neurological Disorders, (I.R.B., Y.M., Z.T.J., T.W., E.d.P-F.), and Reta Lila Weston Institute of Neurological Studies (T.W., E.d.P-F.), Department of Clinical and Movement Neurosciences UCL Queen Square Institute of Neurology, London, United Kingdom; Movement Disorders Unit, (I.R.B.), Neurology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain; and Department of Neuropathology (Y.M.), Institute of Brain Science, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Eduardo De Pablo-FernandezFrom the Queen Square Brain Bank for Neurological Disorders, (I.R.B., Y.M., Z.T.J., T.W., E.d.P-F.), and Reta Lila Weston Institute of Neurological Studies (T.W., E.d.P-F.), Department of Clinical and Movement Neurosciences UCL Queen Square Institute of Neurology, London, United Kingdom; Movement Disorders Unit, (I.R.B.), Neurology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain; and Department of Neuropathology (Y.M.), Institute of Brain Science, Hirosaki University Graduate School of Medicine, Hirosaki, Japan. eduardo.fernandez.13@ucl.ac.uk.
National Hospital for Neurology and Neurosurgery · GBHirosaki University · JPHospital de Sant Pau · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesOrthostatic hypotension (OH) increases dementia risk in patients with Parkinson disease (PD), although the underlying mechanisms and whether a similar association between OH and cognitive impairment exists in other synucleinopathies remain unknown. The aim is to evaluate the association between OH and dementia risk in patients with PD, and cognitive impairment risk in patients with multiple system atrophy (MSA), and to explore relevant clinical and neuropathologic factors to understand underlying pathogenic mechanisms.

methodsThis is a retrospective cohort study. Medical records throughout the entire disease course of consecutive patients with neuropathology-confirmed PD and MSA from the Queen Square Brain Bank were systematically reviewed. Time of onset and severity of OH-related symptoms were documented, and their association with other clinical and neuropathologic variables was evaluated. Dementia risk for patients with PD and cognitive impairment risk for patients with MSA were estimated using multivariable hazard regression.

resultsOne hundred thirty-two patients with PD and 137 with MSA were included. Patients with MSA developed OH more frequently, earlier in the disease course and with more severe symptoms. Cumulative dementia prevalence was higher in patients with PD. Multivariable adjusted regression models showed that early OH, but not its symptom severity, increased dementia risk in patients with PD by 14% per year (hazard ratio [HR] = 0.86; 95% CI, 0.80-0.93) and cognitive impairment risk in patients with MSA by 41% per year (HR = 0.59; 95% CI, 0.42-0.83). Early OH was not associated with increased α-synuclein, β-amyloid, tau, Alzheimer, or cerebrovascular pathologies. No significant associations were found between severity of OH symptoms and other clinical or neuropathologic variables. DISCUSSION: Early OH, but not its symptom severity, increases the risk of cognitive impairment in patients with PD and MSA. OH is not associated with more extensive Lewy, β-amyloid, tau, Alzheimer, or cerebrovascular pathologies. It is likely that OH contributes to cognitive impairment in patients with PD and MSA by hypoxia-induced nonspecific neurodegeneration. Further research should evaluate whether improving brain perfusion by treating OH may modify the risk of dementia in these conditions.

Indexed as

Alzheimer DiseaseHypotension, OrthostaticMultiple System AtrophyParkinson DiseaseDisease ProgressionHumansRetrospective Studies

Identifiers

PMID36526431
PMCPMC9990860
OpenAlexW4311821080

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.