Abstract

BackgroundEarly childhood environmental exposures, possibly infections, may be responsible for triggering islet autoimmunity and progression to type 1 diabetes (T1D). The Environmental Determinants of Diabetes in the Young (TEDDY) follows children with increased HLA-related genetic risk for future T1D. TEDDY asks parents to prospectively record the child’s infections using a diary book. The present paper shows how these large amounts of partially structured data were reduced into quantitative data-sets and further categorized into system-specific infectious disease episodes. The numbers and frequencies of acute infections and infectious episodes are shown.MethodsStudy subjects (n = 3463) included children who had attended study visits every three months from age 3 months to 4 years, without missing two or more consecutive visits during the follow-up. Parents recorded illnesses prospectively in a TEDDY Book at home. The data were entered into the study database during study visits using ICD-10 codes by a research nurse. TEDDY investigators grouped ICD-10 codes and fever reports into infectious disease entities and further arranged them into four main categories of infectious episodes: respiratory, gastrointestinal, other, and unknown febrile episodes. Incidence rate of infections was modeled as function of gender, HLA-DQ genetic risk group and study center using the Poisson regression.ResultsA total of 113,884 ICD-10 code reports for infectious diseases recorded in the database were reduced to 71,578 infectious episodes, including 74.0% respiratory, 13.1% gastrointestinal, 5.7% other infectious episodes and 7.2% febrile episodes. Respiratory and gastrointestinal infectious episodes were more frequent during winter. Infectious episode rates peaked at 6 months and began declining after 18 months of age. The overall infectious episode rate was 5.2 episodes per person-year and varied significantly by country of residence, sex and HLA genotype.ConclusionsThe data reduction and categorization process developed by TEDDY enables analysis of single infectious agents as well as larger arrays of infectious agents or clinical disease entities. The preliminary descriptive analyses of the incidence of infections among TEDDY participants younger than 4 years fits well with general knowledge of infectious disease epidemiology. This protocol can be used as a template in forthcoming time-dependent TEDDY analyses and in other epidemiological studies.Electronic supplementary materialThe online version of this article (doi:10.1186/s12887-015-0333-8) contains supplementary material, which is available to authorized users.

Highlights

  • Childhood environmental exposures, possibly infections, may be responsible for triggering islet autoimmunity and progression to type 1 diabetes (T1D)

  • Newborns invited into TEDDY study belong to either general population (GP) or are first-degree relatives (FDR) of a patient with T1D

  • If codes belonging to this category were reported within same week they were regarded as one Results Altogether 113,884 International classification of disease (ICD)-10 code reports for infectious diseases were extracted from the database of acute illnesses for the 3,463 children followed until 48 months of age

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Summary

Introduction

Possibly infections, may be responsible for triggering islet autoimmunity and progression to type 1 diabetes (T1D). The Environmental Determinants of Diabetes in the Young (TEDDY) follows children with increased HLA-related genetic risk for future T1D. The Environmental Determinants of Diabetes in the Young (TEDDY) study evaluates multiple environmental exposures in a prospective follow-up of children with increased genetic risk for T1D. The specific aim of TEDDY is to identify and characterize the environmental factors that may trigger T1D-related autoimmune process and/or promote progression to clinical T1D [1]. In TEDDY, prospective data on infectious exposures among study participants are being collected though a reporting system whereby parents monitor and record illnesses between clinical visits. The present study focuses on the parental reports of acute infectious illnesses

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