Evidence map›Paper›PMID 32939969›Full record

ArticlePediatric diabetes2020

Extended family history of type 1 diabetes in HLA-predisposed children with and without islet autoantibodies.

Salla Kuusela, Päivi Keskinen, Tytti Pokka, Mikael Knip, Jorma Ilonen, Paula Vähäsalo, Riitta Veijola

Open access · hybridAbstract read
In one paragraph

Article in Pediatric diabetes, 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
1.1field-weighted citation impact, top 20% 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, 9 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

Salla KuuselaDepartment of Pediatrics, PEDEGO Research Unit, Medical Research Center, University of Oulu, Oulu, Finland.ORCID 0000-0003-4945-3089
Päivi KeskinenDepartment for Children and Adolescents, Tampere University Hospital, Tampere, Finland.
Tytti PokkaDepartment of Pediatrics, PEDEGO Research Unit, Medical Research Center, University of Oulu, Oulu, Finland.
Mikael KnipTampere Centre for Child Health Research, Tampere University Hospital, Tampere, Finland.ORCID 0000-0003-0474-0033
Jorma IlonenImmunogenetics Laboratory, University of Turku, Turku, Finland.
Paula VähäsaloDepartment of Pediatrics, PEDEGO Research Unit, Medical Research Center, University of Oulu, Oulu, Finland.
Riitta VeijolaDepartment of Pediatrics, PEDEGO Research Unit, Medical Research Center, University of Oulu, Oulu, Finland.ORCID 0000-0002-6557-270X
Oulu University Hospital · FITampere University Hospital · FIUniversity of Helsinki · FIUniversity of Turku · FI

Funding

Juvenile Diabetes Research Foundation 1-SRA-2016-342-M-RJuvenile Diabetes Research Foundation 1-SRA-2019-732-M-B
6 · The paper itself

Abstract

objectiveThe aim of this study was to explore the extended family history of type 1 diabetes in children at genetic risk and define the impact of a positive family history on the development of islet autoimmunity and type 1 diabetes.

methodsThe subjects were participants in The Finnish Type 1 Diabetes Prediction and Prevention (DIPP) study and carried increased HLA-conferred risk for type 1 diabetes. The case children (N = 343) were positive for at least one islet autoantibody, and the control children (N = 343) matched by age, gender and class II HLA genotype were negative for islet autoantibodies at the time of data collection. Extended family history of type 1 diabetes was obtained by using a structured questionnaire.

resultsAmong children who were autoantibody positive and progressed to type 1 diabetes 62.2% (28/45) had at least one relative with type 1 diabetes. Interestingly, 57.8% of these children (26/45) had such a relative outside the nuclear family compared to 30.7% of children with no autoantibodies (P = .001), 35.2% of those with only classical islet cell antibodies (P = .006), and 35.2% of non-progressors with biochemical autoantibodies (P = 0.011). A positive history of type 1 diabetes in the paternal extended family was more common in children with multiple biochemical autoantibodies compared to those with only one biochemical autoantibody (P = .010). No association between the specificity of the first appearing autoantibody and family history of the disease was found.

conclusionsType 1 diabetes in relatives outside the nuclear family is a significant risk factor for islet autoimmunity and progression to clinical disease in HLA susceptible children.

Indexed as

AutoimmunityFamilyGenetic Predisposition to DiseaseAutoantibodiesChildChild, PreschoolDiabetes Mellitus, Type 1Disease ProgressionFemaleFinlandFollow-Up StudiesHumansIncidenceIslets of LangerhansMaleProspective StudiesAutoantibodiesislet cell antibodychildrenfamily historygenetic riskHLAislet autoimmunitytype 1 diabetes

Identifiers

PMID32939969
PMCPMC7702069
OpenAlexW3087385820

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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.