Evidence map›Paper›PMID 31123290›Full record

ArticleScientific reports2019

A Joint Modeling Approach for Childhood Meat, Fish and Egg Consumption and the Risk of Advanced Islet Autoimmunity.

Essi Syrjälä, Jaakko Nevalainen, Jaakko Peltonen, Hanna-Mari Takkinen, Leena Hakola, Mari Åkerlund, Riitta Veijola, Jorma Ilonen, Jorma Toppari, Mikael Knip and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 22 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

11 authors at 4 institutions in 1 country.

Essi SyrjäläHealth Sciences/Faculty of Social Sciences, Tampere University, Tampere, FI-33014, Finland. essi.syrjala@tuni.fi.ORCID http://orcid.org/0000-0002-5782-3089
Jaakko NevalainenHealth Sciences/Faculty of Social Sciences, Tampere University, Tampere, FI-33014, Finland.ORCID http://orcid.org/0000-0001-6295-0245
Jaakko PeltonenFaculty of Information Technology and Communication Sciences, Tampere University, Tampere, FI-33014, Finland.
Hanna-Mari TakkinenHealth Sciences/Faculty of Social Sciences, Tampere University, Tampere, FI-33014, Finland.
Leena HakolaHealth Sciences/Faculty of Social Sciences, Tampere University, Tampere, FI-33014, Finland.
Mari ÅkerlundHealth Sciences/Faculty of Social Sciences, Tampere University, Tampere, FI-33014, Finland.
Riitta VeijolaDepartment of Pediatrics, Medical Research Center, PEDEGO Research Unit, Oulu University Hospital and University of Oulu, Oulu, FI-90014, Finland.
Jorma IlonenImmunogenetics Laboratory, Institute of Biomedicine, University of Turku, Turku, FI-20520, Finland.
Jorma ToppariDepartment of Pediatrics, Turku University Hospital, Turku, FI-20521, Finland.
Mikael KnipChildren's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, FI-00281, Finland.ORCID http://orcid.org/0000-0003-0474-0033
Suvi M VirtanenHealth Sciences/Faculty of Social Sciences, Tampere University, Tampere, FI-33014, Finland.
Tampere University · FIUniversity of Turku · FIOulu University Hospital · FIUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several dietary factors have been suspected to play a role in the development of advanced islet autoimmunity (IA) and/or type 1 diabetes (T1D), but the evidence is fragmentary. A prospective population-based cohort of 6081 Finnish newborn infants with HLA-DQB1-conferred susceptibility to T1D was followed up to 15 years of age. Diabetes-associated autoantibodies and diet were assessed at 3- to 12-month intervals. We aimed to study the association between consumption of selected foods and the development of advanced IA longitudinally with Cox regression models (CRM), basic joint models (JM) and joint latent class mixed models (JLCMM). The associations of these foods to T1D risk were also studied to investigate consistency between alternative endpoints. The JM showed a marginal association between meat consumption and advanced IA: the hazard ratio adjusted for selected confounding factors was 1.06 (95% CI: 1.00, 1.12). The JLCMM identified two classes in the consumption trajectories of fish and a marginal protective association for high consumers compared to low consumers: the adjusted hazard ratio was 0.68 (0.44, 1.05). Similar findings were obtained for T1D risk with adjusted hazard ratios of 1.13 (1.02, 1.24) for meat and 0.45 (0.23, 0.86) for fish consumption. Estimates from the CRMs were closer to unity and CIs were narrower compared to the JMs. Findings indicate that intake of meat might be directly and fish inversely associated with the development of advanced IA and T1D, and that disease hazards in longitudinal nutritional epidemiology are more appropriately modeled by joint models than with naive approaches.

Indexed as

AdolescentAnimalsAutoantibodiesAutoimmunityChildChild, PreschoolCohort StudiesDiabetes Mellitus, Type 1DietDiet TherapyEggsFemaleFinlandFishesFood HypersensitivityGenetic Predisposition to DiseaseAutoantibodiesHLA-DQB1 antigenHLA-DQ beta-Chains

Identifiers

PMID31123290
PMCPMC6533366
OpenAlexW2945777765

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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.