Evidence map›Paper›PMID 42474300›Full record

ReviewJournal of Parkinson's disease2026

Return of genetic results to persons with Parkinson's disease: Blessing or foe?

Tamara Shiner, Roy N Alcalay

Abstract readReview
In one paragraph

Review in Journal of Parkinson's disease, 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

2 authors.

Tamara ShinerCognitive Neurology Unit, Neurological Institute, Tel-Aviv Medical Center, Tel-Aviv, Israel.ORCID 0000-0002-6368-9656
Roy N AlcalayGray Faculty of Medical & Health Sciences, Tel-Aviv University, Tel-Aviv, Israel.ORCID 0000-0002-5717-4875

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is increasingly understood as a biologically heterogeneous disorder, with genetic contributions ranging from high-penetrance monogenic variants to common polygenic risk. As testing becomes more accessible and clinically relevant, the key question has shifted from whether to test to whether -and how- to return results. Most PD associated variants confer probabilistic risk rather than deterministic outcomes, limiting individual-level prediction and complicating disclosure. Yet genetic findings may inform prognosis and increasingly determine eligibility for targeted therapies and clinical trials. Large-scale genetic studies show both feasibility, demand and utility with pathogenic variants identified in approximately 10-20% of patients. The ethical balance differs by context. In patients with established PD, results may provide insight and research access but require careful framing to avoid overinterpretation. In at-risk individuals, predictive testing offers limited clinical utility and can introduce psychological, familial, and insurance implications but can also allow informed family planning and participation in follow up and prevention trials. Current practice remains inconsistent, with major gaps in access to testing and counselling. Expanding disclosure without the appropriate infrastructure risks misinterpretation and widening disparities. We argue that return of genetic results in PD and at-risk individuals should be structured, and longitudinal. As clinical utility evolves, preparedness, will determine whether genetic testing becomes a part of standard care.

Indexed as

alpha-synucleincounselinggba1geneticslrrk2

Identifiers

PMID42474300
PMCPMC13443104

What Socratic holds

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LicenceCC BY-NC
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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 Socratic graph.