Evidence map›Paper›PMID 41810369›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Statistical uncertainty explains the poor agreement in polygenic scoring for type 2 diabetes.

Ravi Mandla, Xinzhe Li, Zhuozheng Shi, Sarah A Abramowitz, Sandra Lapinska, Penn Medicine Biobank, Michael G Levin, Scott M Damrauer, Bogdan Pasaniuc

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 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

9 authors.

Ravi MandlaGraduate Program in Genomics and Computational Biology, University of Pennsylvania.ORCID 0000-0002-0782-0138
Xinzhe LiGraduate Program in Genomics and Computational Biology, University of Pennsylvania.
Zhuozheng ShiGraduate Program in Genomics and Computational Biology, University of Pennsylvania.ORCID 0000-0002-9769-9027
Sarah A AbramowitzDepartment of Surgery, Perelman School of Medicine, University of Pennsylvania.
Sandra LapinskaGraduate Program in Genomics and Computational Biology, University of Pennsylvania.
Penn Medicine Biobank
Michael G LevinDivision of Cardiovascular Medicine, Department of Medicine, University of Pennsylvania Perelman School of Medicine.ORCID 0000-0002-9937-9932
Scott M DamrauerDepartment of Surgery, Perelman School of Medicine, University of Pennsylvania.ORCID 0000-0001-8009-1632
Bogdan PasaniucDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania.

Funding

Phenotypic Diversity in COVID-19UL1TR001878 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2016 to 2025
$102.4M
NCATS NIH HHS UL1 TR001878
6 · The paper itself

Abstract

Polygenic scores (PGS) have emerged as an important tool for genetic risk prediction in medicine to identify individuals at high-risk for disease. A major limitation in their implementation is the apparent disagreement among scores for the same individual decreasing their interpretability and utility in clinical settings. Here we show that the poor agreement across PGSes for type 2 diabetes (T2D) is fully explained by statistical uncertainty in PGS-based prediction; individual-level uncertainty estimates from a single PGS explain the variability across existing PGSes. We provide an approach for the selection of high-risk individuals that incorporates measures of uncertainty and show that individuals with high confidence based on their PGS uncertainty have higher risk agreement across existing PGS and are more likely to develop T2D than high-risk individuals based on only point estimates of PGS. Together, these findings shed light on the factors underlying a roadblock in PGS implementation and underscore the need to incorporate uncertainty in PGS-based predictions.

Identifiers

PMID41810369
PMCPMC12970363

What Socratic 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 Socratic graph.