Evidence map›Paper›PMID 32537543›Full record

ArticleJournal of the Endocrine Society2020

Risk of Islet and Celiac Autoimmunity in Cotwins of Probands With Type 1 Diabetes.

Taylor M Triolo, Laura Pyle, Sona Seligova, Liping Yu, Peter A Gottlieb, Andrea K Steck

Open access · goldAbstract read
In one paragraph

Article in Journal of the Endocrine Society, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 95% of its field
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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

6 authors at 2 institutions in 1 country.

Taylor M TrioloUniversity of Colorado Anschutz Medical Campus - The Barbara Davis Center for Diabetes, Aurora, Colorado.ORCID 0000-0003-4796-6542
Laura PyleUniversity of Colorado Anschutz Medical Campus, Pediatrics, Aurora, Colorado.ORCID 0000-0001-5577-8221
Sona SeligovaUniversity of Colorado Anschutz Medical Campus - The Barbara Davis Center for Diabetes, Aurora, Colorado.
Liping YuUniversity of Colorado Anschutz Medical Campus - The Barbara Davis Center for Diabetes, Aurora, Colorado.
Peter A GottliebUniversity of Colorado Anschutz Medical Campus - The Barbara Davis Center for Diabetes, Aurora, Colorado.
Andrea K SteckUniversity of Colorado Anschutz Medical Campus - The Barbara Davis Center for Diabetes, Aurora, Colorado.
University of Colorado Anschutz Medical Campus · USColorado School of Public Health · US

Funding

University of Colorado Anschutz Medical Campus DRCP30DK116073 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI LORI SUSSEL · 2020 to 2026
$10.8M
K12 Career DevelopmentK12DK094712 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI STECK, ANDREA · 2011 to 2021
$4.5M
NIDDK NIH HHS K12 DK094712NIDDK NIH HHS P30 DK116073
6 · The paper itself

Abstract

contextConcordance for persistent islet autoimmunity (IA) and type 1 diabetes in monozygotic twins after probands are diagnosed is variable (30%-70%). Risk for development of IA in dizygotic twins is thought to be similar to nontwin siblings. Little is known in regard to the development of celiac autoimmunity (CDA) in twins of subjects with type 1 diabetes.

objectiveOur aim was to investigate the development of IA and CDA in cotwins of probands with type 1 diabetes.

methodsSince 1995, the Twin Family Study has followed 336 twins (168 twin probands with type 1 diabetes and 168 cotwins) for a median of 14 years (interquartile range:10-18 years). Cotwins were followed for the development of IA, type 1 diabetes, and CDA.

resultsIn monozygotic cotwins, cumulative incidence by age 20 was 14% for IA and 10% for CDA. Development of IA and CDA by age 20 was 9% and 12% in dizygotic cotwins, respectively. While the numbers are small, IA by age 30 years was 26% in monozygotic and 39% in dizygotic twins. In proportional hazards models, the proband's younger age at diagnosis, but not sex or human leukocyte antigen were associated with time to IA and CDA in cotwins.

conclusionCDA risk by age 20 in cotwins was 10% to 12%. With long-term follow-up, cumulative incidence for IA is high in dizygotic twins, similar to monozygotic twins, suggesting a role of possible early environmental factors shared by type 1 diabetes discordant cotwins.

Indexed as

celiac autoimmunityepidemiologyislet autoimmunitytwinstype 1 diabetes

Identifiers

PMID32537543
PMCPMC7278281
OpenAlexW3025959643

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.