Evidence map›Paper›PMID 41540976›Full record

ArticleGenetics in medicine open2026

Impact of variants of uncertain significance on decision making about genetic testing for Hispanic males.

Jasmine Saunders, Veda N Giri, Susan Vadaparampil, Adrian Rivera, Tatiana Sanchez Nolasco, Mariana Rangel Camacho, Nataliya Byrne, Kellie Owens, Michele Santacatterina, Stacy Loeb

Abstract read
In one paragraph

Article in Genetics in medicine open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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

10 authors.

Jasmine SaundersDepartment of Urology, New York University Langone Health, New York, NY.
Veda N GiriDepartment of Internal Medicine, Section of Medical Oncology, Yale School of Medicine and Yale Cancer Center, New Haven, CT.
Susan VadaparampilDepartment of Health Outcomes and Behavior, Moffitt Cancer Center, Tampa, FL.
Adrian RiveraDepartment of Urology, New York University Langone Health, New York, NY.
Tatiana Sanchez NolascoDepartment of Urology, New York University Langone Health, New York, NY.
Mariana Rangel CamachoDepartment of Urology, New York University Langone Health, New York, NY.
Nataliya ByrneDepartment of Urology, New York University Langone Health, New York, NY.
Kellie OwensDepartment Population Health, New York University Langone Health, New York, NY.
Michele SantacatterinaDepartment Population Health, New York University Langone Health, New York, NY.
Stacy LoebDepartment of Urology, New York University Langone Health, New York, NY.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Underutilization of genetic testing among Hispanic males results in higher rates of variants of uncertain significance (VUS). We examined the impact of VUS on decision making and behavioral intentions. Methods: We conducted a nationwide survey of 807 US Hispanic males aged ≥40 in English and Spanish on perspectives about genetic testing results. Logistic regression was used to examine predictors of worry and behavior change with a hypothetical VUS result. Results: Over half of Hispanic male participants would still participate in genetic testing with a 1 in 5 chance of VUS. However, 36% were at least somewhat likely to regret testing and 49.9% would worry about cancer risk with VUS results. In addition, 56.3% were somewhat or very likely to change behavior due to a VUS, such as getting checked by the doctor more often or telling family members to get checked. Younger age and college education were associated with more worry and intended behavior change. Conclusion: Although many Hispanic males are interested in genetic testing despite the higher likelihood of VUS, potential consequences include decisional regret, anxiety, and even changes in behavior. Effective counseling and support are important for minoritized groups undergoing genetic evaluation to avoid the potential to exacerbate health disparities.

Indexed as

Genetic counselingGenetic testingHispanicVariants of uncertain significance

Identifiers

PMID41540976
PMCPMC12803809

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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.