Evidence map›Paper›PMID 29404673›Full record

ArticleDiabetologia2018

Coxsackievirus B1 infections are associated with the initiation of insulin-driven autoimmunity that progresses to type 1 diabetes.

Amir-Babak Sioofy-Khojine, Jussi Lehtonen, Noora Nurminen, Olli H Laitinen, Sami Oikarinen, Heini Huhtala, Outi Pakkanen, Tanja Ruokoranta, Minna M Hankaniemi, Jorma Toppari and 5 more

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In one paragraph

Article in Diabetologia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
10.5field-weighted citation impact, top 1% 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

66 citing papers in PubMed, 1 synthesis or guideline pooled it, 97 citations in OpenAlex.

  1. Association BetweenFrontiers in endocrinology · 2021
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  10. COVID-19-Induced Diabetes Mellitus: Comprehensive Cellular and Molecular Mechanistic Insights.Pathophysiology : the official journal of the International Society for Pathophysiology · 2024
    Review
  11. Early Onset of Type 1 Diabetes in Kuwait: Distinct Clinical, Metabolic, and Immunological Characteristics.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2024
    Article
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  18. International journal of molecular sciences · 2023
    Article
  19. Review
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6 more citing papers are in PubMed but not listed here.

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 6 institutions in 1 country.

Amir-Babak Sioofy-KhojineDepartment of Virology, Faculty of Medicine and Life Sciences, University of Tampere, PL 100, 33014 Tampereen yliopisto, Tampere, Finland. Amirbabak.sioofy.khojine@staff.uta.fi.
Jussi LehtonenDepartment of Virology, Faculty of Medicine and Life Sciences, University of Tampere, PL 100, 33014 Tampereen yliopisto, Tampere, Finland.
Noora NurminenDepartment of Virology, Faculty of Medicine and Life Sciences, University of Tampere, PL 100, 33014 Tampereen yliopisto, Tampere, Finland.
Olli H LaitinenDepartment of Virology, Faculty of Medicine and Life Sciences, University of Tampere, PL 100, 33014 Tampereen yliopisto, Tampere, Finland.
Sami OikarinenDepartment of Virology, Faculty of Medicine and Life Sciences, University of Tampere, PL 100, 33014 Tampereen yliopisto, Tampere, Finland.
Heini HuhtalaFaculty of Social Sciences, University of Tampere, Tampere, Finland.
Outi PakkanenVactech Ltd, Tampere, Finland.
Tanja RuokorantaVactech Ltd, Tampere, Finland.
Minna M HankaniemiVactech Ltd, Tampere, Finland.
Jorma ToppariInstitute of Biomedicine, Research Centre of Integrative Physiology and Pharmacology, University of Turku, Turku, Finland.
Mari Vähä-MäkiläInstitute of Biomedicine, Research Centre of Integrative Physiology and Pharmacology, University of Turku, Turku, Finland.
Jorma IlonenImmunogenetics Laboratory, Institute of Biomedicine, University of Turku, Turku, Finland.
Riitta VeijolaDepartment of Paediatrics, PEDEGO Research Unit, Medical Research Centre, Oulu University, Hospital and University of Oulu, Oulu, Finland.
Mikael KnipChildren's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Heikki HyötyDepartment of Virology, Faculty of Medicine and Life Sciences, University of Tampere, PL 100, 33014 Tampereen yliopisto, Tampere, Finland.
Tampere University · FITampere University · FITurku University Hospital · FIPirkanmaa Hospital District · FIUniversity of Oulu · FIUniversity of Turku · FI

Funding

Juvenile Diabetes Research Foundation International 2-SRA-2014-311-Q-RSuomen Akatemia 288671The European Commission 261441
6 · The paper itself

Abstract

aims/hypothesisIslet autoimmunity usually starts with the appearance of autoantibodies against either insulin (IAA) or GAD65 (GADA). This categorises children with preclinical type 1 diabetes into two immune phenotypes, which differ in their genetic background and may have different aetiology. The aim was to study whether Coxsackievirus group B (CVB) infections, which have been linked to the initiation of islet autoimmunity, are associated with either of these two phenotypes in children with HLA-conferred susceptibility to type 1 diabetes.

methodsAll samples were from children in the Finnish Type 1 Diabetes Prediction and Prevention (DIPP) study. Individuals are recruited to the DIPP study from the general population of new-born infants who carry defined HLA genotypes associated with susceptibility to type 1 diabetes. Our study cohort included 91 children who developed IAA and 78 children who developed GADA as their first appearing single autoantibody and remained persistently seropositive for islet autoantibodies, along with 181 and 151 individually matched autoantibody negative control children, respectively. Seroconversion to positivity for neutralising antibodies was detected as the surrogate marker of CVB infections in serial follow-up serum samples collected before and at the appearance of islet autoantibodies in each individual.

resultsCVB1 infections were associated with the appearance of IAA as the first autoantibody (OR 2.4 [95% CI 1.4, 4.2], corrected p = 0.018). CVB5 infection also tended to be associated with the appearance of IAA, however, this did not reach statistical significance (OR 2.3, [0.7, 7.5], p = 0.163); no other CVB types were associated with increased risk of IAA. Children who had signs of a CVB1 infection either alone or prior to infections by other CVBs were at the highest risk for developing IAA (OR 5.3 [95% CI 2.4, 11.7], p < 0.001). None of the CVBs were associated with the appearance of GADA. CONCLUSIONS/

interpretationCVB1 infections may contribute to the initiation of islet autoimmunity being particularly important in the insulin-driven autoimmune process.

Indexed as

Antibodies, NeutralizingAutoantibodiesAutoimmune DiseasesAutoimmunityChildChild, PreschoolCohort StudiesCoxsackievirus InfectionsDiabetes Mellitus, Type 1Disease ProgressionEnterovirusFemaleFinlandGenotypeHumansInfantAntibodies, NeutralizingAutoantibodiesInsulinCoxsackievirus group BGlutamic acid decarboxylase autoantibody (GADA)Insulin autoantibody (IAA)Islet autoimmunityLogistic regressionPlaque reduction assayType 1 Diabetes Prediction and Prevention (DIPP)Virus neutralising antibodies

Identifiers

PMID29404673
OpenAlexW2793314137

What OpenQuestion holds

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Registered trials

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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.