Evidence map›Paper›PMID 41312798›Full record

ArticlePharmacotherapy2026

Constructing a Personalized Treatment Rule for Initial Therapy in Early Parkinson's Disease.

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

Abstract read
In one paragraph

Article in Pharmacotherapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Zachary P BrehmDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, New York, USA.ORCID 0000-0001-7351-3526
Ruth B SchneiderCenter for Health and Technology, University of Rochester, Rochester, New York, USA.ORCID 0000-0001-8094-4041
Charles S VenutoCenter for Health and Technology, University of Rochester, Rochester, New York, USA.ORCID 0000-0002-2394-9513
Greta SmithCenter for Health and Technology, University of Rochester, Rochester, New York, USA.ORCID 0000-0003-0993-4136
Cuong Tuan PhamDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, New York, USA.ORCID 0000-0003-2781-5990
Michael P McDermottDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, New York, USA.ORCID 0000-0001-7443-9145
Ashkan ErtefaieDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, New York, USA.ORCID 0000-0003-2611-9512

Funding

Statistical methods to characterize causal mechanisms by which air pollution affects the recurrence of cardiovascular eventsR01ES034021 · NIEHS · UNIVERSITY OF ROCHESTER · PI Francesca Dominici, Ashkan Ertefaie · 2023 to 2026
$2.5M
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
NIDA NIH HHSNIEHS NIH HHS R01 ES034021NINDS NIH HHS R33 NS120240NINDS NIH HHS R61 NS120240
6 · The paper itself

Abstract

backgroundDopaminergic therapies such as levodopa and dopamine receptor agonists (DRA) improve motor function in people with Parkinson's disease. These therapies are also linked to the advent of motor complications such as dyskinesias and wearing-off episodes.

objectivesWe illustrate a method that creates a personalized treatment rule that takes patient-specific information and provides a recommended first-line therapy for Parkinson's disease that will provide the best mean improvement in motor function while constraining the probability of a motor complication within the first 2 years of therapy below a level mutually deemed to be the maximum acceptable risk by the patient and clinician.

methodsWe apply a machine learning technique that simultaneously optimizes for benefit and risk outcomes to a harmonized clinical dataset based on the CALM-PD and STEADY-PD III randomized clinical trials. This generates a decision rule for allocating patients to levodopa or a DRA, based on a specified risk threshold. We evaluate the individualized decision rule by comparing the mean benefit and risk outcomes under the decision rule to the mean outcomes from policies that assign all patients to either levodopa or a DRA.

resultsThe optimal decision rule improves the mean change from baseline in MDS-UPDRS (Movement Disorder Society Unified Parkinson's Disease Rating Scale) motor (Part 3) score compared to assigning all patients to a DRA and provides a smaller mean probability of motor complications than assigning all patients to levodopa. More data are required to further develop and validate this decision rule.

conclusionsAn optimal decision rule can provide improved data adaptive treatment decisions that balance benefit and risk outcomes given a maximum acceptable risk.

Indexed as

Antiparkinson AgentsClinical Decision RulesDopamine AgonistsLevodopaParkinson DiseasePrecision MedicineHumansMachine LearningRandomized Controlled Trials as TopicAntiparkinson AgentsDopamine AgonistsLevodopabenefit–riskmachine learningParkinson's diseasepersonalized treatment

Identifiers

PMID41312798
PMCPMC12824558

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.