Evidence map›Paper›PMID 33855205›Full record

ArticleEndocrinology, diabetes & metabolism2021

Beta cell function in participants with single or multiple islet autoantibodies at baseline in the TEDDY Family Prevention Study: TEFA.

Maria Månsson Martinez, Falastin Salami, Helena Elding Larsson, Jorma Toppari, Åke Lernmark, Jukka Kero, Riitta Veijola, Jaakko J Koskenniemi, Päivi Tossavainen, Markus Lundgren and 5 more

Open access · goldAbstract read
In one paragraph

Article in Endocrinology, diabetes & metabolism, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.7field-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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Impact of screening programmes for type 1 diabetes in youth: A systematic review and meta-analysis.Diabetic medicine : a journal of the British Diabetic Association · 2026
    Pooled it
  2. Review
  3. Article
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  5. 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

15 authors at 3 institutions in 2 countries.

Maria Månsson MartinezDepartment of Clinical Sciences, Lund University/CRC, Skåne University Hospital, Malmö, Sweden.ORCID https://orcid.org/0000-0002-3320-1226
Falastin SalamiDepartment of Clinical Sciences, Lund University/CRC, Skåne University Hospital, Malmö, Sweden.
Helena Elding LarssonDepartment of Clinical Sciences, Lund University/CRC, Skåne University Hospital, Malmö, Sweden.
Jorma ToppariDepartment of Pediatrics, Turku University Hospital, Turku, Finland.
Åke LernmarkDepartment of Clinical Sciences, Lund University/CRC, Skåne University Hospital, Malmö, Sweden.
Jukka KeroDepartment of Pediatrics, Turku University Hospital, Turku, Finland.
Riitta VeijolaDepartment of Pediatrics, PEDEGO Research Unit, MRC Oulu, University of Oulu and Oulu University Hospital, Oulu, Finland.
Jaakko J KoskenniemiDepartment of Pediatrics, Turku University Hospital, Turku, Finland.
Päivi TossavainenDepartment of Pediatrics, PEDEGO Research Unit, MRC Oulu, University of Oulu and Oulu University Hospital, Oulu, Finland.ORCID https://orcid.org/0000-0003-0388-9039
Markus LundgrenDepartment of Clinical Sciences, Lund University/CRC, Skåne University Hospital, Malmö, Sweden.
Henrik BorgDepartment of Clinical Sciences, Lund University/CRC, Skåne University Hospital, Malmö, Sweden.
Anastasia KatsarouDepartment of Clinical Sciences, Lund University/CRC, Skåne University Hospital, Malmö, Sweden.
Marlena MaziarzDepartment of Clinical Sciences, Lund University/CRC, Skåne University Hospital, Malmö, Sweden.
Carina TörnDepartment of Clinical Sciences, Lund University/CRC, Skåne University Hospital, Malmö, Sweden.
TEDDY Family (TEFA) Study Group
Lund University · SEUniversity of Turku · FIOulu University Hospital · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: The aim of the present study was to assess beta cell function based on an oral glucose tolerance test (OGTT) in participants with single islet autoantibody or an intravenous glucose tolerance test (IvGTT) in participants with multiple islet autoantibodies. Materials and methods: Healthy participants in Sweden and Finland, between 2 and 49.99 years of age previously identified as positive for a single (n = 30) autoantibody to either insulin, glutamic acid decarboxylase, islet antigen-2, zinc transporter 8 or islet cell antibodies or multiple autoantibodies (n = 46), were included. Participants positive for a single autoantibody underwent a 6-point OGTT while participants positive for multiple autoantibodies underwent an IvGTT. Glucose, insulin and C-peptide were measured from OGTT and IvGTT samples. Results: All participants positive for a single autoantibody had a normal glucose tolerance test with 120 minutes glucose below 7.70 mmol/L and HbA1c values within the normal range (<42 mmol/mol). Insulin responses to the glucose challenge on OGTT ranged between 13.0 and 143 mIU/L after 120 minutes with C-peptide values between 0.74 and 4.60 nmol/L. In Swedish participants, the first-phase insulin response (FPIR) on IvGTT was lower in those positive for three or more autoantibodies (n = 13; median 83.0 mIU/L; range 20.0-343) compared to those with two autoantibodies (n = 15; median 146 mIU/L; range 19.0-545; Conclusion: Participants positive for a single autoantibody appeared to have a normal beta cell function. Participants positive for three or more autoantibodies had a lower FPIR as compared to participants with two autoantibodies, supporting the view that their beta cell function had deteriorated.

Indexed as

FamilyAdolescentAdultAutoantibodiesBiomarkersBlood GlucoseChildChild, PreschoolC-Reactive ProteinDiabetes Mellitus, Type 1FemaleFinlandGlucose Tolerance TestGlutamate DecarboxylaseGlycated HemoglobinHumansAutoantibodiesBiomarkersBlood GlucoseC-Reactive ProteinGlutamate DecarboxylaseGlycated Hemoglobinhemoglobin A1c protein, humanInsulinHbA1cintravenous glucose tolerance testoral glucose tolerance test

Identifiers

PMID33855205
PMCPMC8029501
OpenAlexW3094646230

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.