Evidence map›Paper›PMID 42898234›Full record

ArticleJournal of the Endocrine Society2026

Development and validation of a model using routine clinical features to improve diabetes diagnosis.

Alan L Hutchison, Simar Narula, Brandon Faubert, Celeste C Thomas, Mary E Rinella, Raghavendra G Mirmira, William F Parker

Abstract read
In one paragraph

Article in Journal of the Endocrine Society, 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

7 authors.

Alan L HutchisonDepartment of Medicine, Section of Gastroenterology, Hepatology and Nutrition, University of Chicago Medicine, Chicago, IL 60637, USA.ORCID https://orcid.org/0000-0003-4161-0772
Simar NarulaDepartment of Medicine, Section of Gastroenterology, Hepatology and Nutrition, University of Chicago Medicine, Chicago, IL 60637, USA.ORCID https://orcid.org/0009-0001-0291-635X
Brandon FaubertDepartment of Medicine, Section of Hematology and Oncology, University of Chicago Medicine, Chicago, IL 60637, USA.ORCID https://orcid.org/0000-0002-2886-886X
Celeste C ThomasDepartment of Medicine, Section of Endocrinology, Diabetes and Metabolism, University of Chicago Medicine, Chicago, IL 60637, USA.ORCID https://orcid.org/0000-0002-0379-2459
Mary E RinellaDepartment of Medicine, Section of Gastroenterology, Hepatology and Nutrition, University of Chicago Medicine, Chicago, IL 60637, USA.ORCID https://orcid.org/0000-0003-0620-9705
Raghavendra G MirmiraDepartment of Medicine, Section of Endocrinology, Diabetes and Metabolism, University of Chicago Medicine, Chicago, IL 60637, USA.ORCID https://orcid.org/0000-0002-5013-6075
William F ParkerDepartment of Medicine, Section of Pulmonary and Critical Care, University of Chicago Medicine, Chicago, IL 60637, USA.ORCID https://orcid.org/0000-0002-6000-3153

Funding

Research Training in Digestive Health, Diseases, and NutritionT32DK007074 · NIDDK · UNIVERSITY OF CHICAGO · PI EUGENE B CHANG · 1986 to 2026
$11.3M
Transcriptional Mechanisms Governing Beta Cell DifferentiationR01DK060581 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Raghavendra G Mirmira · 2002 to 2026
$8.5M
The Integrated Stress Response in Human Islets During Early T1DU01DK127786 · NIDDK · UNIVERSITY OF CHICAGO · PI EVANS-MOLINA, CARMELLA, MIRMIRA, RAGHAVENDRA G · 2020 to 2025
$7.1M
Validation of small molecule 12-lipoxygenase inhibitors in metabolic diseaseR01DK105588 · NIDDK · UNIVERSITY OF CHICAGO · PI KULKARNI, ROHIT N., MIRMIRA, RAGHAVENDRA G · 2015 to 2024
$5.5M
Improving the efficiency and equity of critical care allocation during a crisis with place-based disadvantage indicesR01LM014263 · NLM · UNIVERSITY OF CHICAGO · PI William F Parker · 2023 to 2026
$2.0M
Integrating fairness, efficiency, and resilience into a continuous distribution system for heart transplant allocationR01HL176972 · NHLBI · UNIVERSITY OF CHICAGO · PI Kiran Kaur Khush, William F Parker · 2026 to 2026
$1.6M
Mending a Broken Heart Allocation System with Machine LearningK08HL150291 · NHLBI · UNIVERSITY OF CHICAGO · PI PARKER, WILLIAM F · 2020 to 2024
$713k
Mechanisms of Dysglycemia in People with Cirrhosis and Liver Transplant RecipientsK23DK146188 · NIDDK · UNIVERSITY OF CHICAGO · PI Alan Louis Hutchison · 2026 to 2026
$188k
NHLBI NIH HHS K08 HL150291NHLBI NIH HHS R01 HL176972NIDDK NIH HHS K23 DK146188NIDDK NIH HHS R01 DK060581NIDDK NIH HHS R01 DK105588NIDDK NIH HHS T32 DK007074NIDDK NIH HHS U01 DK127786NLM NIH HHS R01 LM014263
6 · The paper itself

Abstract

Context: Hemoglobin A1c (A1c) and fasting plasma glucose (FPG) miss diabetes diagnosis in many individuals, but the alternative, oral glucose tolerance testing (OGTT), is difficult to obtain. Objective: This work aimed to develop and validate a model to identify diabetes missed by A1c and FPG but detected by OGTT and associate its outcomes with mortality. Methods: We trained machine-learning models using National Health and Nutrition Examination Survey (NHANES) data, applied them to corresponding National Center for Health Statistics mortality data, and externally validated the models with Diabetes Prevention Program Outcomes Study (DPPOS) data. We tested models including the A1c, vital signs, complete blood count, and comprehensive metabolic panel with and without the FPG. This retrospective analysis included NHANES study participants from 1999 to 2016 and DPPOS study participants from 1996 to 2020. Main outcome measures included the area under the receiver operating curve, sensitivity, and specificity of models to detect diabetes. Results: The A1c/FPG+ model had better sensitivity for DPPOS individuals with A1c less than 6.5% (48 mmol/mol) and FPG less than 126 mg/dL compared to a logistic regression of A1c and FPG and recalibrated FPG for individuals both on (0.69 vs 0.53 vs 0.57, respectively) and off (0.75 vs 0.65 vs 0.68, respectively) medication. NHANES participants without diabetes but with A1c/FPG+-predicted diabetes had elevated risk of mortality compared to those without A1c/FPG+-predicted diabetes (HR = 1.4; Conclusion: Machine-learning models can improve the detection of individuals who would need OGTT assessment to diagnose diabetes using standard nonfasting laboratory values and vital signs with and without FPG.

Indexed as

diabetesdiagnosismachine learningoral glucose tolerance test

Identifiers

PMID42898234
PMCPMC13677441

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.