Evidence map›Paper›PMID 38015333›Full record

ArticleJournal of racial and ethnic health disparities2025

Genome-Wide Association Study of Gallstone Disease Identifies Novel Candidate Genomic Variants in a Latino Community of Southwest USA.

Amit Arora, Khadijah Jack, Ashok V Kumar, Mitesh Borad, Marlene E Girardo, Eleanna De Filippis, Ping Yang, Valentin Dinu

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Article in Journal of racial and ethnic health disparities, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.8field-weighted citation impact, top 13% of its field
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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Amit AroraCollege of Health Solutions, Arizona State University, Phoenix, AZ, 85004, USA. aarora50@asu.edu.ORCID 0009-0001-8841-0316
Khadijah JackCollege of Health Solutions, Arizona State University, Phoenix, AZ, 85004, USA.
Ashok V KumarDepartment of Quantitative Health Science, Mayo Clinic, Scottsdale, AZ, 85259, USA.
Mitesh BoradDivision of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ, 85259, USA.
Marlene E GirardoDepartment of Quantitative Health Science, Mayo Clinic, Scottsdale, AZ, 85259, USA.
Eleanna De FilippisDivision of Endocrinology, Mayo Clinic Arizona, Scottsdale, AZ, 85259, USA.
Ping YangDepartment of Quantitative Health Science, Mayo Clinic, Scottsdale, AZ, 85259, USA.
Valentin DinuCollege of Health Solutions, Arizona State University, Phoenix, AZ, 85004, USA.
Mayo Clinic in Arizona · USArizona State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gallstone disease (GSD) is a prevalent health condition that impacts many adults and is associated with presence of stones in gallbladder cavity that results in inflammation, pain, fever, nausea and vomiting. Several genome-wide association studies (GWAS) in the past have identified genes associated with GSD but only a few were focused on Latino population. To identify genetic risk factors for GSD in Latino population living in the Southwest USA we used self-reported clinical history, physical and lab measurements data in Sangre Por Salud (SPS) cohort and identified participants with and without diagnosis of GSD. We performed a GWAS on this phenotype using GSD cases matched to normal controls based on a tight criterion. We identified several novel loci associated with GSD as well as loci that were previously identified in past GWAS studies. The top 3 loci (MATN2, GPRIN3, GPC6) were strongly associated with GSD phenotype in our combined analysis and a sex stratified analysis results in females were closest to the overall results reflecting a general higher disease prevalence in females. The top identified variants in MATN2, GPRIN3, and GPC6 remain unchanged after local ancestry adjustment in SPS Latino population. Follow-up pathway enrichment analysis suggests enrichment of GO terms that are associated with immunological pathways; enzymatic processes in gallbladder, liver, and gastrointestinal tract; and GSD pathology. Our findings suggest an initial starting point towards better and deeper understanding of differences in gallstone disease pathology, biological mechanisms, and disease progression among Southwest US Latino population.

Indexed as

GallstonesGenome-Wide Association StudyHispanic or LatinoAdultAgedCase-Control StudiesFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedRisk FactorsSouthwestern United StatesBiobankCholelithiasisGall Stone DiseaseGenomewide Association StudyGWASHealth disparitiesHispanic populationsLatinosSangre Por Salud

Identifiers

PMID38015333
OpenAlexW4389082605

What OpenQuestion holds

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Registered trials

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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.