Evidence map›Paper›PMID 39188918›Full record

ArticleFrontiers in endocrinology2024

Risk for progression to type 1 diabetes in first-degree relatives under 50 years of age.

Ines Urrutia, Rosa Martinez, Begona Calvo, Irene Marcelo, Laura Saso-Jimenez, Idoia Martinez de Lapiscina, Jose Ramon Bilbao, Luis Castano, Itxaso Rica, Collaborative Working Group

Abstract readMulticenter Study
In one paragraph

Article in Frontiers in endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Type 1 Diabetes Mellitus Pathogenesis: Mechanisms, Early Diagnostic Strategies, and Emerging Therapeutic Approaches.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
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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

10 authors.

Ines UrrutiaBiobizkaia Health Research Institute, Barakaldo, Spain.
Rosa MartinezBiobizkaia Health Research Institute, Barakaldo, Spain.
Begona CalvoBiobizkaia Health Research Institute, Barakaldo, Spain.
Irene MarceloHospital de Mataró - Consorci Sanitari del Maresme, Barcelona, Spain.
Laura Saso-JimenezBiobizkaia Health Research Institute, Barakaldo, Spain.
Idoia Martinez de LapiscinaBiobizkaia Health Research Institute, Barakaldo, Spain.
Jose Ramon BilbaoBiobizkaia Health Research Institute, Barakaldo, Spain.
Luis Castano *Biobizkaia Health Research Institute, Barakaldo, Spain.
Itxaso Rica *Biobizkaia Health Research Institute, Barakaldo, Spain.
Collaborative Working Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The detection of pancreatic autoantibodies in first-degree relatives of patients with type 1 diabetes (T1D) is considered a risk factor for disease. Novel available immunotherapies to delay T1D progression highlight the importance of identifying individuals at risk who might benefit from emerging treatments. The objective was to assess the autoimmunity in first-degree relatives of patients with T1D, estimate the time from autoimmunity detection to the onset of clinical diabetes, and identify the associated risk factors. Methods: Retrospective multicenter study of 3,015 first-degree relatives of patients with T1D recruited between 1992 and 2018. Pancreatic autoantibodies (IAA, GADA, IA2A, and ZnT8A) were determined by radioimmunoassay, starting the analyses at diagnosis of the proband. All those with positive autoimmunity and normal fasting blood glucose without clinical symptoms of diabetes were followed up in the study. The progression rate to T1D was assessed according to sex, relationship with the proband, age at autoimmunity detection, type/number of autoantibodies, and HLA-DRB1 genotype. Cox proportional-hazard models and Kaplan-Meier survival plots were used for statistical analyses. Results: Among the relatives, 21 progenitors [43.7 years (IQR: 38.1-47.7)] and 27 siblings [7.6 years (IQR: 5.8-16.1)] had positive autoantibodies. Of these, 54.2% (95% CI: 39.2%-68.6%) developed T1D (age at autoimmunity detection 11 months to 39 years) in a median of 5 years (IQR: 3.6-8.7; ranged from 0.9 to 22.6 years). Risk factors associated with faster progression to T1D were multiple autoimmunity and <20 years at autoimmunity detection. Younger relatives (<20 years) with multiple autoantibodies had a 5-year cumulative risk of developing diabetes of 52.9% (95% CI: 22.1%-71.6%) and a 20-year risk of 91.2% (95% CI: 50.5%-98.4%). The 20-year risk decreased to 59.9% (95% CI: 21.9%-79.5%) if only one risk factor was met and to 35.7% (95% CI: 0.0%-66.2%) if the relative was older than 20 years with one autoantibody. Conclusions: In first-degree relatives with autoimmunity, the time to progression to T1D is faster in children and adolescents with multiple autoantibodies. Young adults are also at risk, which supports their consideration in screening strategies for people at risk of developing T1D.

Indexed as

AutoantibodiesDiabetes Mellitus, Type 1Disease ProgressionAdolescentAdultAutoimmunityChildChild, PreschoolFamilyFemaleFollow-Up StudiesGenetic Predisposition to DiseaseHumansMaleMiddle AgedRetrospective StudiesAutoantibodiesautoimmunityfirst-degree relativespancreatic autoantibodiespredictionrisktype 1 diabetes

Identifiers

PMID39188918
PMCPMC11345149

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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.