Evidence map›Paper›PMID 41550025›Full record

ArticleMovement disorders clinical practice2026

Genetic and Pathological Testing Attitudes for Parkinson's Disease in At-Risk Relatives.

Tal Weil, Anat Mirelman, Roy N Alcalay, Nurit Omer, Penina Ponger, Avner Thaler

Abstract read
In one paragraph

Article in Movement disorders clinical practice, 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

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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

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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. Review
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Tal WeilGray Faculty of Medical & Health Sciences, Tel-Aviv University, Tel-Aviv, Israel.ORCID https://orcid.org/0009-0002-1964-4503
Anat MirelmanGray Faculty of Medical & Health Sciences, Tel-Aviv University, Tel-Aviv, Israel.
Roy N AlcalayGray Faculty of Medical & Health Sciences, Tel-Aviv University, Tel-Aviv, Israel.
Nurit OmerNeurological Institute, Tel-Aviv Medical Center, Tel-Aviv, Israel.
Penina PongerNeurological Institute, Tel-Aviv Medical Center, Tel-Aviv, Israel.
Avner ThalerGray Faculty of Medical & Health Sciences, Tel-Aviv University, Tel-Aviv, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundParkinson's disease (PD) is increasingly recognized as a neurodegenerative disorder with a broad clinical spectrum and diverse biomarkers enabling early detection. α-synuclein seed amplification assays (SAA) and genetic testing now allow identification of PD pathology in asymptomatic individuals. As preventive strategies remain unavailable, it is important to understand at-risk individuals' attitudes toward disclosure of genetic and biomarker information.

objectivesTo examine awareness, emotional responses, and behavioral intentions among first-degree relatives of PD patients who underwent genetic testing and counseling.

methodsA cross-sectional questionnaire was administered to first-degree relatives tested and counseled at Tel Aviv Sourasky Medical Center. The survey assessed recall of testing and results, adequacy of information, emotional reactions, willingness to undergo biological testing (blood vs. lumbar puncture), and readiness to modify lifestyle following positive biomarker results.

resultsAmong 240 non-manifesting relatives (NMNC = 145; LRRK2 = 40; GBA1 = 49; dual = 6; 72% response), the mean interval from testing to survey was 5.3 ± 2.4 years. Despite prior counseling, only 70.3% recalled being tested and 66.5% remembered results. About half felt adequately informed about PD (50.9%) and their genetic status (53.7%). Willingness for blood testing was high (86.6%) but lower for lumbar puncture (41.5%). Mutation carriers reported greater distress, while 87.6% indicated readiness to adopt lifestyle changes if results were positive.

conclusionsFirst-degree relatives favored minimally invasive testing and showed strong motivation for lifestyle adaptation. Limited recall of results highlights the need for improved communication and ongoing counseling in preventive neurology.

Indexed as

FamilyGenetic Predisposition to DiseaseGenetic TestingParkinson DiseaseAdultAgedCross-Sectional StudiesFemaleHumansLeucine-Rich Repeat Serine-Threonine Protein Kinase-2MaleMiddle AgedSurveys and QuestionnairesLeucine-Rich Repeat Serine-Threonine Protein Kinase-2LRRK2 protein, humanat‐risk relativesgenetic testingParkinson's diseasepathological testingα‐Synuclein (SAA)

Identifiers

PMID41550025
PMCPMC13338983

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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.