Evidence map›Paper›PMID 36817608›Full record

ArticleFrontiers in endocrinology2023

Increased levels of anti-BSA antibodies in children with Down syndrome.

Sian L Grace, Georgina L Mortimer, Aizhan Kozhakhmetova, Jamie Leveret, Richard Newton, Koit Reimand, Julian P H Shield, Raivo Uibo, Alistair J K Williams, Kathleen M Gillespie

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 25% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. 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

10 authors at 3 institutions in 2 countries.

Sian L GraceBristol Medical School, University of Bristol, Bristol, United Kingdom.
Georgina L MortimerBristol Medical School, University of Bristol, Bristol, United Kingdom.
Aizhan KozhakhmetovaBristol Medical School, University of Bristol, Bristol, United Kingdom.
Jamie LeveretBristol Medical School, University of Bristol, Bristol, United Kingdom.
Richard NewtonDepartment of Neurology, Royal Manchester Children's Hospital, Manchester, United Kingdom.
Koit ReimandDepartment of Immunology, Institute of Bio- and Translational Medicine, University of Tartu, Tartu, Estonia.
Julian P H ShieldNational Institute for Health and Care Research (NIHR) Bristol Biomedical Research Centre, Nutrition Theme, University of Bristol, Bristol, United Kingdom.
Raivo UiboDepartment of Immunology, Institute of Bio- and Translational Medicine, University of Tartu, Tartu, Estonia.
Alistair J K WilliamsBristol Medical School, University of Bristol, Bristol, United Kingdom.
Kathleen M GillespieBristol Medical School, University of Bristol, Bristol, United Kingdom.
University of Bristol · GBUniversity of Tartu · EERoyal Manchester Children's Hospital · GB

Funding

Department of Health
6 · The paper itself

Abstract

Introduction: Autoimmune diabetes occurs more often in the first 2 years of life in children with Down syndrome (DS) compared with the general population. We previously observed increased frequencies of islet autoantibodies, including insulin autoantibodies (IAA), in children with DS. Assays for IAA using Methods: Samples were available from two populations with DS: one from the UK, (UK DS cohort n=106, 58 male, median age 12.5 years) and one from Estonia (Estonian DS cohort: n=121, 65 male, median age 9.75 years). A UK control population was provided by sex and age-matched healthy siblings of probands participating in the Bart's Oxford (BOX) family study of type 1 diabetes. A competitive-displacement radiobinding assay (RBA) and a Dissociation Enhanced Lanthanide Fluoroimmunoassay (DELFIA) were developed to measure and confirm anti-BSA antibody levels. HLA class II genotype was analysed by PCR using sequence specific primers (PCR-SSP). Results: Overall, levels of anti-BSA antibodies were increased in those with DS compared with controls (p<0.0001) but this was not HLA associated. Conclusion: Increased levels of anti-BSA antibodies may reflect a defect in immune maturation or increased gut permeability in children with DS, increasing their risk of developing autoimmunity.

Indexed as

Diabetes Mellitus, Type 1Down SyndromeAnimalsAutoantibodiesCattleChildFemaleHumansInsulinIodine RadioisotopesMaleSerum Albumin, BovineAutoantibodiesInsulinIodine-125Iodine RadioisotopesSerum Albumin, Bovineautoimmunebovine serum albuminDown syndromeislet autoantibodiestype 1 diabetes

Identifiers

PMID36817608
PMCPMC9935828
OpenAlexW4319161576

What OpenQuestion 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 OpenQuestion graph.