Evidence map›Paper›PMID 42499378›Full record

ArticleFrontiers in human neuroscience2026

An application of weighted support vector machines to individualized second-line therapy selection after levodopa in Parkinson's disease.

Cuong T Pham, Ruth B Schneider, Charles S Venuto, Greta Smith, Zachary P Brehm, Michael P McDermott, Ashkan Ertefaie

Abstract read
In one paragraph

Article in Frontiers in human neuroscience, 2026. 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

7 authors.

Cuong T PhamDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, NY, United States.
Ruth B SchneiderCenter for Health and Technology, University of Rochester, Rochester, NY, United States.
Charles S VenutoCenter for Health and Technology, University of Rochester, Rochester, NY, United States.
Greta SmithCenter for Health and Technology, University of Rochester, Rochester, NY, United States.
Zachary P BrehmDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, NY, United States.
Michael P McDermottDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, NY, United States.
Ashkan ErtefaieDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, NY, United States.

Funding

Advancing Personalized Medicine in PD Using Harmonized Multi-Site Clinical DataR33NS120240 · NINDS · UNIVERSITY OF ROCHESTER · PI ERTEFAIE, ASHKAN, MCDERMOTT, MICHAEL P · 2022 to 2024
$1.7M
Advancing personalized medicine in PD using harmonized multi-site clinical dataR61NS120240 · NINDS · UNIVERSITY OF ROCHESTER · PI ERTEFAIE, ASHKAN, MCDERMOTT, MICHAEL P · 2020 to 2021
$1.1M
NINDS NIH HHS R33 NS120240NINDS NIH HHS R61 NS120240
6 · The paper itself

Abstract

Parkinson's disease (PD) is a progressive neurological disorder characterized by motor symptoms, with treatment responses varying widely across patients. To address the growing need for individualized treatment strategies, this paper introduces a practical framework for constructing optimal individualized treatment strategies using weighted support vector machines (SVMs). We construct an optimal rule as a function of patients' clinical profiles and demographics using two methods: Outcome-Weighted Learning (OWL), which assumes no unmeasured confounders, and Instrumental Variable Outcome-Weighted Learning (IV-OWL), which accounts for potential unmeasured confounders. To illustrate the application of these methods, we use harmonized and curated clinical data from the NET-PD LS1 and PRECEPT/POSTCEPT studies to estimate the optimal second-line therapy decision rule for supplementing levodopa with either monoamine oxidase B (MAO-B) inhibitors or dopamine receptor agonists (DRA) based on patient characteristics. As an illustrative application, we analyzed two cohorts of patients who initiated second-line therapy within 90 and 180 days of baseline, with sample sizes of 84 and 121, respectively. Although the estimated improvements were not statistically significant, likely due in part to the small sample sizes, the learned IV-OWL rule showed improvement in annualized UPDRS III change compared with the observed treatment strategy and other static treatment strategies. This case study demonstrates the feasibility of applying weighted support vector machines to individualized second-line therapy selection in PD and illustrates the potential value of instrumental variable-based methods in addressing unmeasured confounders.

Indexed as

instrumental variable (IV) approachmachine learningoutcome weighted learningParkinson’s diseasepersonalized medicinesupport vector machine

Identifiers

PMID42499378
PMCPMC13396011

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.