Evidence map›Paper›PMID 40894172›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Quantifying lifetime risk for 1,401 infectious diseases across the diabetes spectrum using a Bayesian approach.

Boomer B Olsen, Martin Tristani-Firouzi, Karen Eilbeck, Mark Yandell, Edgar J Hernandez

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. 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

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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

The trial behind it

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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

5 · Who and what money

Authors and funding

5 authors.

Boomer B OlsenDepartment of Internal Medicine, University of Utah, Salt Lake City, UT, USA.
Martin Tristani-FirouziDivision of Pediatric Cardiology, University of Utah School of Medicine, Salt Lake City, UT, USA.
Karen EilbeckDepartment of Biomedical Informatics, University of Utah, Salt Lake City, UT, USA.
Mark YandellDepartment of Human Genetics, Utah Center for Genetic Discovery, University of Utah, Salt Lake City, UT.
Edgar J HernandezDepartment of Biomedical Informatics, University of Utah, Salt Lake City, UT, USA.

Funding

Bridging the Gap between Genomics and Clinical Outcomes in CHDU01HL128711 · NHLBI · UNIVERSITY OF UTAH · PI TRISTANI-FIROUZI, MARTIN, YANDELL, MARK DOUGLAS · 2020 to 2024
$2.1M
Utah Stimulating Access to Research in ResidencyR38HL167282 · NHLBI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Margaret B Conroy, JOSEPH BARNEY STANFORD · 2023 to 2026
$924k
NHLBI NIH HHS R38 HL167282NHLBI NIH HHS U01 HL128711
6 · The paper itself

Abstract

Although many diabetes complications have been extensively studied, less is known about the burden of infectious diseases. We developed a Bayesian approach to compare infection risk across 9,476 patients with type 1 diabetes (T1D), 74,270 with type 2 diabetes (T2D), and 32,095 with prediabetes. Patients with T1D, T2D, and prediabetes had multifold increased risk for all organ system- and pathogen-based composite infection outcomes. We also quantified risk for 1,401 individual infection outcomes, finding increased risk for 880 in T1D, 1,047 in T2D, and 991 in prediabetes. Patients had increased risk for well-established diabetes-associated infections (e.g., mucormycosis) and less commonly associated infections (e.g., West Nile Virus encephalitis). Finally, we found disparities in risk across sociodemographic subgroups (i.e., age, sex, ethnicity, ancestry, and insurance status). Our comprehensive findings advance previous research by quantifying risk for wide-ranging infection outcomes across diverse patients with T1D, T2D, and prediabetes through an innovative Bayesian approach.

Identifiers

PMID40894172
PMCPMC12393658

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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.