Evidence map›Paper›PMID 41162596›Full record

ArticleNPJ digital medicine2025

Actigraphy-based detection of isolated REM sleep behavior disorder: multicenter validation across devices and populations.

Li Zhou, Andreas Brink-Kjaer, Katarina Gunter, Salonee Marwaha, Ambra Stefani, Birgit Högl, Michele T Hu, Emmanuel Mignot, Ankit Parekh, Qi Tang and 11 more

Abstract read
In one paragraph

Article in NPJ digital medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. A gradual and sustainable approach to diagnosing sleep and circadian disturbances in dementia.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Review
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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

21 authors.

Li Zhou *Department of Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Andreas Brink-Kjaer *Department of Health Technology, Denmark Technical University, Kongens Lyngby, Denmark.
Katarina GunterNuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, UK.
Salonee MarwahaDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York City, NY, USA.
Ambra StefaniDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Birgit HöglDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Michele T HuNuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, UK.
Emmanuel MignotDepartment of Psychiatry and Behavioral Sciences, Stanford Center for Sleep Sciences and Medicine, Stanford University, Redwood City, CA, USA.
Ankit ParekhDepartment of Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Qi TangDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Merve Aktan-SüzgünDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Bei HuangDepartment of Psychiatry, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR, China.
Shi TangDepartment of Psychiatry, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR, China.
Siyi GongDepartment of Psychiatry, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR, China.
Yuhua YangDepartment of Psychiatry, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR, China.
Xie ChenDepartment of Psychiatry, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR, China.
Jianzhang NiDepartment of Psychiatry, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR, China.
Ningning LiDepartment of Psychiatry, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR, China.
Zhixuan HeDepartment of Psychiatry, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR, China.
Yun Kwok WingDepartment of Psychiatry, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR, China.
Emmanuel DuringDepartment of Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA. emmanuel.during@mssm.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Scalable home-based detection of isolated REM sleep behavior disorder (iRBD) is essential for early care, prevention trials, and identifying candidates for neuroprotective interventions against synucleinopathies. We previously showed that high-resolution wrist actigraphy (Axivity AX6) could identify iRBD based on abnormal sleep (AUC of 0.916) and rest-activity-rhythms (RAR, AUC of 0.856) using machine learning. Here, we aimed to assess generalizability across: (1) other actigraphs using lower resolutions; (2) different populations. We tested the analysis pipeline directly in cohorts from the International RBD Study Group using: Axivity AX6 (50-100 Hz), Philips Actiwatch (60-second epoch), and MicroMini-Motionlogger (30-second epoch). The cohorts included a total of 352 iRBD and 258 non-RBD participants from 4 centers (Mount Sinai, Oxford, Hong Kong, and Innsbruck). Two conversion pipelines were created to map activity counts from Actiwatch and MicroMini-Motionlogger to AX6 from 14 volunteers co-wearing two devices. In addition to the actigraphy analysis, four synucleinopathy prodromes-RBD symptoms, hyposmia, constipation, orthostatic hypotension-were tested in a two-stage screening approach. The sleep model achieved AUCs of 0.838-0.865 across centers, and the RAR model 0.520-0.818. Screening based on prodromes followed by actigraphy achieved sensitivities, specificities, and positive predictive values (PPVs) of 59.4-78.3%, 84.1-98.2%, and 56.0-98.6% (RBD symptoms), 46.5%, 99.0%, and 98.9% (hyposmia), 25.8-43.3%, 95.5-98.8%, 96.3-98.0% (constipation), and 11.6-36.8%, 96.0-100%, and 96.2-100% (orthostatic hypotension), respectively. Resolution (high versus low) did not affect the performance. After adjusting for a real-world iRBD prevalence of 1.5%, the corresponding PPVs would range from 6.3% to 100.0% depending on the prodromes. This multicenter study shows that the original actigraphy-based detection model of iRBD using sleep features but not RAR features generalizes well across independent cohorts and devices. Combined with key prodromes of synucleinopathies, it could enable precise, scalable population-level screening.

Identifiers

PMID41162596
PMCPMC12572274

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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 OpenQuestion graph.