Evidence map›Paper›PMID 33790752›Full record

ArticleFrontiers in human neuroscience2021

Individual Magnetoencephalography Response Profiles to Short-Duration L-Dopa in Parkinson's Disease.

Edgar Peña, Tareq M Mohammad, Fedaa Almohammed, Tahani AlOtaibi, Shahpar Nahrir, Sheraz Khan, Vahe Poghosyan, Matthew D Johnson, Jawad A Bajwa

Open access · goldAbstract read
In one paragraph

Article in Frontiers in human neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 2 pooled it
0.1field-weighted citation impact, top 56% 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

2 citing papers in PubMed, 2 syntheses or guidelines pooled it, 2 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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

9 authors at 3 institutions in 2 countries.

Edgar PeñaDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, United States.
Tareq M MohammadNational Neuroscience Nursing Administration, King Fahad Medical City, Riyadh, Saudi Arabia.
Fedaa AlmohammedDepartment of Neurophysiology, National Neuroscience Institute, King Fahad Medical City, Riyadh, Saudi Arabia.
Tahani AlOtaibiDepartment of Neurophysiology, National Neuroscience Institute, King Fahad Medical City, Riyadh, Saudi Arabia.
Shahpar NahrirDepartment of Neurology, National Neuroscience Institute, King Fahad Medical City, Riyadh, Saudi Arabia.
Sheraz KhanDepartment of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
Vahe PoghosyanDepartment of Neurophysiology, National Neuroscience Institute, King Fahad Medical City, Riyadh, Saudi Arabia.
Matthew D JohnsonDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, United States.
Jawad A BajwaDepartment of Neurology, National Neuroscience Institute, King Fahad Medical City, Riyadh, Saudi Arabia.
King Fahd Medical City · SAUniversity of Minnesota · USAthinoula A. Martinos Center for Biomedical Imaging · US

Funding

Pathophysiology-based approaches to deep brain stimulation for Parkinson's diseaseP50NS098573 · NINDS · UNIVERSITY OF MINNESOTA · PI JOHNSON, MATTHEW DOUGLAS · 2016 to 2020
$9.1M
Spatiotemporal Optimization of Deep Brain Stimulation for Parkinson's DiseaseR01NS094206 · NINDS · UNIVERSITY OF MINNESOTA · PI Matthew Douglas Johnson, THEODEN I NETOFF · 2016 to 2026
$5.6M
6 · The paper itself

Abstract

Clinical responses to dopamine replacement therapy for individuals with Parkinson's disease (PD) are often difficult to predict. We characterized changes in MDS-UPDRS motor factor scores resulting from a short-duration L-Dopa response (SDR), and investigated how the inter-subject clinical differences could be predicted from motor cortical magnetoencephalography (MEG). MDS-UPDRS motor factor scores and resting-state MEG recordings were collected during SDR from twenty individuals with a PD diagnosis. We used a novel subject-specific strategy based on linear support vector machines to quantify motor cortical oscillatory frequency profiles that best predicted medication state. Motor cortical profiles differed substantially across individuals and showed consistency across multiple data folds. There was a linear relationship between classification accuracy and SDR of lower limb bradykinesia, although this relationship did not persist after multiple comparison correction, suggesting that combinations of spectral power features alone are insufficient to predict clinical state. Factor score analysis of therapeutic response and novel subject-specific machine learning approaches based on subject-specific neuroimaging provide tools to predict outcomes of therapies for PD.

Indexed as

machine learningmagnetoencephalographymotor cortexParkinson’s diseaseshort duration L-Dopa response

Identifiers

PMID33790752
PMCPMC8005574
OpenAlexW3133696957

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.