Evidence map›Paper›PMID 32011014›Full record

ArticleDiabetic medicine : a journal of the British Diabetic Association2020

Older age of childhood type 1 diabetes onset is associated with islet autoantibody positivity >30 years later: the Pittsburgh Epidemiology of Diabetes Complications Study.

R G Miller, L Yu, D J Becker, T J Orchard, T Costacou

Open access · greenAbstract read
In one paragraph

Article in Diabetic medicine : a journal of the British Diabetic Association, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. The relationship between GAD65 autoantibody and the risk of T1DM onset.Journal of diabetes and metabolic disorders · 2022
    Review
  3. Current Perspective on Auto-antibodies in Type 1 Diabetes.Indian journal of endocrinology and metabolism
    Article
  4. 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

5 authors at 2 institutions in 1 country.

R G MillerDepartment of Epidemiology, University of Pittsburgh, Pittsburgh, PA.ORCID 0000-0003-1845-8477
L YuSchool of Medicine, Barbara Davis Center, University of Colorado Denver, Aurora, CO, USA.
D J BeckerDepartment of Paediatrics, Division of Pediatric Endocrinology and Diabetes, University of Pittsburgh, Pittsburgh, PA.
T J OrchardDepartment of Epidemiology, University of Pittsburgh, Pittsburgh, PA.
T CostacouDepartment of Epidemiology, University of Pittsburgh, Pittsburgh, PA.ORCID 0000-0001-9303-3810
University of Pittsburgh · USUniversity of Colorado Denver · US

Funding

EPIDEMIOLOGY OF DIABETIC COMPLICATIONS--PHASE IIR01DK034818 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI COSTACOU, TINA · 1986 to 2019
$5.6M
American Diabetes Association 1-19-JDF-109NIDDK NIH HHS R01 DK034818NIDDK NIH HHS R01-DK034818Rossi Memorial FundUniversity of Pittsburgh Central Research Development Fund
6 · The paper itself

Abstract

aimsTo examine the association between islet autoantibody positivity and clinical characteristics, residual β-cell function (C-peptide) and prevalence of complications in a childhood-onset (age <17 years), long-duration (≥32 years) type 1 diabetes cohort.

methodsIslet autoantibodies (glutamic acid decarboxylase, insulinoma-associated protein 2 and zinc transporter-8 antibodies) were measured in the serum of participants who attended the 2011-2013 Pittsburgh Epidemiology of Diabetes Complications study follow-up examination (n=177, mean age 51 years, diabetes duration 43 years).

resultsPrevalences of islet autoantibodies were: glutamic acid decarboxylase, 32%; insulinoma-associated protein 2, 22%; and zinc transporter-8, 4%. Positivity for each islet autoantibody was associated with older age at diabetes onset (glutamic acid decarboxylase antibodies, P=0.03; insulinoma-associated protein 2 antibodies, P=0.001; zinc transporter-8 antibodies, P<0.0001). Older age at onset was also associated with an increasing number of autoantibodies (P = 0.001). Glutamic acid decarboxylase antibody positivity was also associated with lower HbA

conclusionsThe strong association between islet autoantibody positivity and older age at type 1 diabetes onset supports the hypothesis of a less aggressive, and thus more persistent, immune process in those with older age at onset. This observation suggests that there may be long-term persistence of heterogeneity in the underlying autoimmune process.

Indexed as

AdultAgedAge of OnsetAutoantibodiesCholesterolCholesterol, LDLC-PeptideDiabetes ComplicationsDiabetes Mellitus, Type 1FemaleGlycated HemoglobinHumansMaleMiddle AgedZinc Transporter 8anti-GAD65 autoantibodyAutoantibodiesCholesterolCholesterol, LDLC-PeptideGlycated Hemoglobinhemoglobin A1c protein, humanICA512 autoantibodySLC30A8 protein, humanZinc Transporter 8

Identifiers

PMID32011014
PMCPMC7369217
OpenAlexW3004726497

What OpenQuestion holds

Textmetadata
LicenceTDM
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.