Evidence map›Paper›PMID 41654821›Full record

ArticleBMC medicine2026

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 Javier Hernandez

Abstract read
In one paragraph

Article in BMC medicine, 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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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Boomer B OlsenDepartment of Internal Medicine, University of Utah, Salt Lake City, UT, USA. Boomer.Olsen@hsc.utah.edu.
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, USA.
Edgar Javier 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
NHLBI NIH HHS 1R38HL167282-01NHLBI NIH HHS U01HL128711
6 · The paper itself

Abstract

backgroundWhile diabetes-related complications have been widely investigated, the burden of infectious diseases across the diabetes spectrum remains relatively understudied.

methodsWe 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.

resultsPatients 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 most infections among patients with either T1D, T2D, or 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).

conclusionsOur 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.

Indexed as

Communicable DiseasesDiabetes ComplicationsDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2Prediabetic StateAdolescentAdultAgedBayes TheoremFemaleHumansMaleMiddle AgedRisk FactorsYoung AdultBayesian methodsInfection riskPrediabetesType 1 diabetesType 2 diabetes

Identifiers

PMID41654821
PMCPMC12977889

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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.