Evidence map›Paper›PMID 40463563›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Characterizing Parkinson's Disease Clinical and Biomarker Interactions in REM Sleep Behavior Disorder.

Vijaya L Reddy, Samantha Esposito, Erika Renkl, Amine Benyakoub, Kara Mead, Camalene Chrysostoum, Sapna Patel, John P Seibyl, Yuan Huang, Brian B Koo and 1 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Vijaya L ReddyDepartment of Neurology, Yale School of Medicine, New Haven CT 06511.ORCID 0009-0003-0954-4549
Samantha EspositoDepartment of Neurology, Yale School of Medicine, New Haven CT 06511.ORCID 0009-0001-8496-3917
Erika RenklDepartment of Neurology, Yale School of Medicine, New Haven CT 06511.ORCID 0009-0007-3528-9464
Amine BenyakoubDepartment of Radiology, Yale School of Medicine, New Haven, CT 06510.
Kara MeadDepartment of Neurology, Yale School of Medicine, New Haven CT 06511.ORCID 0000-0002-1166-1125
Camalene ChrysostoumDepartment of Neurology, Yale School of Medicine, New Haven CT 06511.
Sapna PatelDepartment of Neurology, Yale School of Medicine, New Haven CT 06511.
John P SeibylDepartment of Neurology, Yale School of Medicine, New Haven CT 06511.ORCID 0000-0002-4917-5413
Yuan HuangDepartment of Biostatistics, Yale School of Public Health 06511.ORCID 0000-0002-7005-1319
Brian B KooDepartment of Neurology, Yale School of Medicine, New Haven CT 06511.ORCID 0000-0003-1229-0247
Jesse M CedarbaumDepartment of Neurology, Yale School of Medicine, New Haven CT 06511.ORCID 0000-0002-5146-8784

Funding

Twenty-four hour patterns of light and activity and Alzheimer's Disease and Related Dementia: interplay with multi-omics biomarkers and AD pathogenesis pathwaysR01AG063946 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Qian Xiao · 2020 to 2026
$3.3M
NIA NIH HHS R01 AG063946
6 · The paper itself

Abstract

Background: REM Sleep Behavior Disorder (RBD), marked by dream enactment due to loss of REM-related muscle atonia, is a prominent prodromal indicator of synucleinopathies, particularly Parkinson's Disease (PD). Objectives: This study aimed to investigate the interplay among key PD biomarkers- α-synuclein seed amplification assay (SAA), hyposmia, and dopamine transporter (DaT) SPECT imaging - in individuals with RBD. Additionally, we evaluated how phenoconversion events and Movement Disorder Society (MDS)-Prodromal PD probability scores relate to clinical symptoms and biomarker profiles in an incident RBD population. Methods: Participants with polysomnographically-confirmed RBD underwent comprehensive clinical and biomarker assessments. They were grouped along three non-exclusive biomarker-based axes (hyposmic vs. normosmic, SAA positive vs. SAA negative, and DaT positive vs. intermediate vs. negative) and two clinical outcome-based axes (high vs. intermediate/low MDS-Prodromal PD probability; phenoconverters vs. non-phenoconverters). Within each category, performance on various clinical assessments, the presence of other biomarkers, and clinical outcomes were evaluated. Results: Hyposmia was associated with reductions in striatal DaT binding and α-syn SAA positivity. MDS Prodromal PD Probability Scores, which incorporate DaT and olfactory function, predicted SAA positivity and phenoconversion. DaT positivity was much more common (80%) among phenoconverters (RBD-PC), than non-phenoconverters (10%). No significant motor or non-motor symptom differences were observed between the two groups at baseline, likely due to the small sample size. Conclusions: α-syn SAA positivity, DaT positivity, and hyposmia are highly associated with each other. MDS Prodromal PD Probability scores may be useful predictors of near-term progression, and thus as stratification factors in clinical research study design.

Indexed as

BiomarkersParkinson’s diseaseREM Sleep Behavior Disorder

Identifiers

PMID40463563
PMCPMC12132163

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

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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 Socratic graph.