Evidence map›Paper›PMID 41757176›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Accounting for age-related increases in HbA1c more accurately quantifies risk of Type 1 Diabetes progression in islet autoantibody-positive adults.

Erin L Templeman, Nick Thomas, Susan Martin, Diane K Whereti, Maria J Redondo, Jennifer Sherr, Alessandra Petrelli, Laura M Jacobsen, Falastin Salami, Jacqueline Lonier and 6 more

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

5 · Who and what money

Authors and funding

16 authors.

Erin L TemplemanDepartment of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.ORCID 0009-0007-4306-7909
Nick ThomasDepartment of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
Susan MartinDepartment of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.ORCID 0000-0001-8746-0947
Diane K WheretiDepartment of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Maria J RedondoBaylor College of Medicine, Texas Children's Hospital, Houston, TX, USA.
Jennifer SherrYale University School of Medicine, New Haven, Conneticut, USA.
Alessandra PetrelliDepartment of Clinical Sciences and Community Health,University of Milan and Pio Albergo Trivulzio, Milan, Italy.
Laura M JacobsenDepartments of Pediatrics and Pathology, University of Florida, FL, USA.
Falastin SalamiDepartment of Clinical Sciences, Lund University, Sweden.
Jacqueline LonierDivision of Endocrinology, Columbia University Irving Medical Center, NY, USA.
Carmella Evans MolinaDepartment of Pediatrics, Indiana University School of Medicine, Indiana, Indianapolis, USA.
Jay SosenkoDivision of Endocrinology, University of Miami, Miami, Florida, USA.
Inês BarrosoDepartment of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.ORCID 0000-0001-5800-4520
Richard A OramDepartment of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
Emily K SimsDepartment of Pediatrics, Indiana University School of Medicine, Indiana, Indianapolis, USA.ORCID 0000-0002-4393-954X
Lauric A FerratDepartment of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.

Funding

Revision to the Coordinating Center for Type 1 Diabetes TrialNetU01DK106993 · NIDDK · UNIVERSITY OF SOUTH FLORIDA · PI JEFFREY P KRISCHER, SAMUEL S WU · 2019 to 2026
$181.3M
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
Mechanisms of Beta Cell Function in Health and DiseaseR01DK093954 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI EVANS-MOLINA, CARMELLA · 2011 to 2019
$3.5M
Implications of Changes in Islet Exosomal Cargo in Type 1 DiabetesR01DK133881 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI EVANS-MOLINA, CARMELLA, MIRMIRA, RAGHAVENDRA G · 2022 to 2025
$2.7M
Biomarkers Of Beta Cell Stress In Type 1 Diabetes (BetaMarker)UC4DK104166 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI EIZIRIK, DECIO LAKS, EVANS-MOLINA, CARMELLA · 2014 to 2014
$2.4M
Type 1 Diabetes Genetic Risk Score in TrialNetR01DK121843 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI REDONDO, MARIA JOSE · 2019 to 2023
$2.4M
Beta cell extracellular vesicles in health and diseaseR01DK121929 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI SIMS, EMILY K · 2020 to 2024
$2.0M
β cell miRNAs Function as Molecular Hubs of Type 1 Diabetes PathogenesisR01DK127308 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI EVANS-MOLINA, CARMELLA · 2021 to 2024
$1.7M
Precision administration of anti-thymocyte globulin with or without verapamil in adolescents and young adults with type 1 diabetesR01DK142858 · NIDDK · UNIVERSITY OF FLORIDA · PI Laura Jacobsen · 2025 to 2026
$1.5M
Development of a Predictive Response Signature to Anti-Thymocyte Globulin in Type 1 DiabetesK08DK128628 · NIDDK · UNIVERSITY OF FLORIDA · PI JACOBSEN, LAURA · 2021 to 2025
$618k
BLRD VA I01 BX001733NIDDK NIH HHS K08 DK128628NIDDK NIH HHS R01 DK093954NIDDK NIH HHS R01 DK121843NIDDK NIH HHS R01 DK121929NIDDK NIH HHS R01 DK127308NIDDK NIH HHS R01 DK133881NIDDK NIH HHS R01 DK142858NIDDK NIH HHS U01 DK106993NIDDK NIH HHS U01 DK127786NIDDK NIH HHS UC4 DK104166Wellcome Trust
6 · The paper itself

Abstract

Objective: HbA1c thresholds used to define dysglycemia in autoantibody-positive individuals at risk for type 1 diabetes do not account for age-related increases in HbA1c and may overestimate progression risk in adults. We evaluated whether age-adjusted HbA1c or a higher HbA1c threshold improves risk stratification across age groups. Research Design and Methods: We analyzed 5,024 autoantibody-positive relatives (3,720 children and 1,304 adults) participating in the TrialNet Pathway to Prevention study. Age-related HbA1c effects were modelled using 6,273 adults from the population-based Exeter 10,000 cohort. Progression risk was compared using the standard dysglycemia threshold (HbA1c ≥ 5.7% [39 mmol/mol]), age-adjusted HbA1c, and an alternative threshold of HbA1c ≥6.0% (42 mmol/mol). Results: Using HbA1c ≥5.7%, children had higher 1-year progression risk than adults among single autoantibody-positive participants (38% [95% CI 28, 47] vs. 13% [7.2, 19]) and multiple autoantibody-positive participants (55% [49, 60] vs. 38% [27, 47]; both p<0.001). Age adjustment reduced these differences; progression risk was similar among single autoantibody-positive participants (38% [28, 47] vs. 27% [13, 39]; p=0.32), with atienuated differences among multiple autoantibody-positive participants. An HbA1c threshold ≥6.0% yielded comparable progression risk between adults and children across autoantibody subgroups. In post hoc analyses, adults aged <30 years had progression risk similar to children (p=0.1). Conclusions: Age-related variation in HbA1c influences dysglycemia classification in adults at risk for type 1 diabetes. Age-adjusted HbA1c or a higher HbA1c threshold (≥6.0% [42 mmol/mol]) in adults ≥30 years identifies individuals with progression risk comparable to children and may improve age-specific risk stratification in prevention settings.

Identifiers

PMID41757176
PMCPMC12934852

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.