Evidence map›Paper›PMID 35314671›Full record

ArticleNature communications2022

Progression of type 1 diabetes from latency to symptomatic disease is predicted by distinct autoimmune trajectories.

Bum Chul Kwon, Vibha Anand, Peter Achenbach, Jessica L Dunne, William Hagopian, Jianying Hu, Eileen Koski, Åke Lernmark, Markus Lundgren, Kenney Ng and 4 more

Abstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Trial
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  6. Review
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  11. Article
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  13. Article
  14. The immunology of type 1 diabetes.Nature reviews. Immunology · 2024
    Review
  15. Review
  16. Article
  17. Screening and Prevention of Type 1 Diabetes: Where Are We?The Journal of clinical endocrinology and metabolism · 2023
    Review
  18. Article
  19. Article
  20. 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

14 authors.

Bum Chul Kwon *Center for Computational Health, IBM Research, Cambridge, MA, USA. bumchul.kwon@us.ibm.com.ORCID 0000-0002-9391-6274
Vibha Anand *Center for Computational Health, IBM Research, Cambridge, MA, USA.ORCID 0000-0001-8605-5712
Peter AchenbachInstitute of Diabetes Research, Helmholtz Zentrum München, German Research Center for Environmental Health, Munich-Neuherberg, Germany.ORCID 0000-0001-6720-2684
Jessica L DunneJDRF, New York, NY, USA.ORCID 0000-0002-0134-4177
William HagopianPacific Northwest Research Institute, Seattle, WA, USA.ORCID 0000-0003-2979-0475
Jianying HuCenter for Computational Health, IBM Research, Yorktown Heights, NY, USA.ORCID 0000-0001-7753-886X
Eileen KoskiCenter for Computational Health, IBM Research, Yorktown Heights, NY, USA.ORCID 0000-0003-3621-9613
Åke LernmarkDepartment of Clinical Sciences Malmö, Lund University CRC, Skåne University Hospital, Malmö, Sweden.ORCID 0000-0003-1735-0499
Markus LundgrenDepartment of Clinical Sciences Malmö, Lund University CRC, Skåne University Hospital, Malmö, Sweden.ORCID 0000-0001-6394-7689
Kenney NgCenter for Computational Health, IBM Research, Cambridge, MA, USA.ORCID 0000-0003-0792-070X
Jorma ToppariInstitute of Biomedicine and Centre for Population Health Research, University of Turku, and Department of Pediatrics, Turku University Hospital, Turku, Finland.ORCID 0000-0003-2228-334X
Riitta VeijolaUniversity of Oulu and Oulu University Hospital, Department of Pediatrics, PEDEGO Research Unit, Oulu, Finland.ORCID 0000-0002-6557-270X
Brigitte I FrohnertUniversity of Colorado, Denver, CO, USA.
T1DI Study Group

Funding

University of Colorado Anschutz Medical Campus DRCP30DK116073 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI LORI SUSSEL · 2020 to 2026
$10.8M
Natural History of Pre-Diabetic Autoimmunity (DAISY)R01DK032493 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI REWERS, MARIAN J · 1986 to 2024
$9.3M
Natural History of Pre-diabetic Autoimmunity (DAISY)R37DK032493 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI REWERS, MARIAN J · 2001 to 2010
$8.0M
Multiple Autoantigens/Multiple Epitopes of Type 1DMR01DK032083 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI MICHELS, AARON W · 1986 to 2025
$6.9M
ISLET CELL MEMBRANE ANTIBODIES IN DIABTESR01DK026190 · NIDDK · UNIVERSITY OF WASHINGTON · PI HAMPE, CHRISTIANE S · 1986 to 2016
$4.9M
Nutrigenetics & -genomics of Vitamin D and Omega-3 Fatty Acids in Type 1 DiabetesR01DK104351 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI NORRIS, JILL M · 2014 to 2018
$2.9M
MULTIPLE AUTOANTIGENS OF PRETYPE I DMR37DK032083 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI EISENBARTH, GEORGE S · 1992 to 1999
–
NIDDK NIH HHS P30 DK116073NIDDK NIH HHS R01 DK026190NIDDK NIH HHS R01 DK032083NIDDK NIH HHS R01 DK032493NIDDK NIH HHS R01 DK104351NIDDK NIH HHS R37 DK032083NIDDK NIH HHS R37 DK032493
6 · The paper itself

Abstract

Development of islet autoimmunity precedes the onset of type 1 diabetes in children, however, the presence of autoantibodies does not necessarily lead to manifest disease and the onset of clinical symptoms is hard to predict. Here we show, by longitudinal sampling of islet autoantibodies (IAb) to insulin, glutamic acid decarboxylase and islet antigen-2 that disease progression follows distinct trajectories. Of the combined Type 1 Data Intelligence cohort of 24662 participants, 2172 individuals fulfill the criteria of two or more follow-up visits and IAb positivity at least once, with 652 progressing to type 1 diabetes during the 15 years course of the study. Our Continuous-Time Hidden Markov Models, that are developed to discover and visualize latent states based on the collected data and clinical characteristics of the patients, show that the health state of participants progresses from 11 distinct latent states as per three trajectories (TR1, TR2 and TR3), with associated 5-year cumulative diabetes-free survival of 40% (95% confidence interval [CI], 35% to 47%), 62% (95% CI, 57% to 67%), and 88% (95% CI, 85% to 91%), respectively (p < 0.0001). Age, sex, and HLA-DR status further refine the progression rates within trajectories, enabling clinically useful prediction of disease onset.

Indexed as

Diabetes Mellitus, Type 1Islets of LangerhansAutoantibodiesAutoimmunityChildDisease ProgressionGenotypeHLA-DR AntigensHumansAutoantibodiesHLA-DR Antigens

Identifiers

PMID35314671
PMCPMC8938551

What Socratic 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 Socratic graph.