Evidence map›Paper›PMID 42523204›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Predictive Autoantibodies Before the Diagnosis of Type I Diabetes in Adults.

Peter D Burbelo, Robert Nee, Julio A Huapaya, Richard Plasse, Myungjin Kim, Sarah Gordon, Giovanni Di Pasquale, John A Chiorini, Stephen Olson

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
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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.

Peter D BurbeloAdeno-Associated Virus Biology Section, National Institute of Dental and Craniofacial Research, NIH, Bethesda, MD 20892.ORCID 0000-0003-1717-048X
Robert NeeWalter Reed National Military Medical Center, Bethesda, Maryland, 20889.
Julio A HuapayaCritical Care Medicine Department, National Heart, Lung, and Blood Institute, NIH, Bethesda, MD 20892.
Richard PlasseWalter Reed National Military Medical Center, Bethesda, Maryland, 20889.
Myungjin KimWalter Reed National Military Medical Center, Bethesda, Maryland, 20889.
Sarah GordonWalter Reed National Military Medical Center, Bethesda, Maryland, 20889.
Giovanni Di PasqualeAdeno-Associated Virus Biology Section, National Institute of Dental and Craniofacial Research, NIH, Bethesda, MD 20892.
John A ChioriniAdeno-Associated Virus Biology Section, National Institute of Dental and Craniofacial Research, NIH, Bethesda, MD 20892.
Stephen OlsonWalter Reed National Military Medical Center, Bethesda, Maryland, 20889.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent epidemiologic studies indicate that adult-onset type 1 diabetes (AOT1D) is more common than childhood-onset type 1 diabetes, yet it remains clinically underrecognized. Because little is known about the emergence of islet autoantibodies in AOT1D, we conducted a retrospective study using electronic medical records from the United States Military Health System and longitudinal serum samples from 169 individuals with AOT1D and 40 healthy controls obtained from the Department of Defense Serum Repository. Among 643 prediagnostic samples from individuals with AOT1D, IA-2 autoantibodies were the most prevalent (50%), followed by GADA (46%), IA-2β (34%), ZnT8-R (27%), and ZnT8-W (15%). Overall, 85% (144/169) of subjects were seropositive for at least one autoantibody prior to diagnosis. Analysis of the earliest available sample from all of the AOT1D cases, grouped into 5-year intervals preceding diagnosis, demonstrated a progressive increase in seropositivity over time: 38% of subjects were seropositive more than 20 years before diagnosis, increasing to 44% at 20-15 years, 59% at 15-10 years, 73% at 10-5 years, and 91% within 5 years of diagnosis. Among the 144 seropositive individuals, positivity for two or more autoantibodies was the most common pattern, occurring in 50% (72/144) of cases. Isolated GADA positivity (22%) and isolated IA-2/IA-2β positivity (24%) occurred at similar frequencies, whereas isolated ZnT8 positivity was uncommon (4%). Temporal analysis showed that isolated GADA positivity appeared earliest, with a median onset of 7.9 years before diagnosis, whereas multiple-autoantibody positivity, IA-2 positivity, and ZnT8 positivity emerged later, with median onsets of 4.6, 4.5, and 1.9 years before diagnosis, respectively. These findings extend observations from pediatric type 1 diabetes to adults and demonstrate that AOT1D-associated autoimmunity often begins decades before clinical diagnosis, highlighting a potentially important window for risk stratification and preventive intervention.

Identifiers

PMID42523204
PMCPMC13404221

What Socratic holds

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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 Socratic graph.