Please use this identifier to cite or link to this item: http://hdl.handle.net/11054/2793
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dc.contributorThomson, R.en_US
dc.contributorOakey, H.en_US
dc.contributorHaynes, A.en_US
dc.contributorCraig, M.en_US
dc.contributorHarrison, L.en_US
dc.contributorWentworth, J.en_US
dc.contributorAnderson, A.en_US
dc.contributorAshwood, P.en_US
dc.contributorBarry, S.en_US
dc.contributorBrittain, B.en_US
dc.contributorBrown, J.en_US
dc.contributorColman, P.en_US
dc.contributorDavis, E.en_US
dc.contributorHamilton-Williams, E.en_US
dc.contributorHuynh, D.en_US
dc.contributorHuynh, T.en_US
dc.contributorKim, K.en_US
dc.contributorMcGorm, K.en_US
dc.contributorMorahan, G.en_US
dc.contributorRawlinson, W.en_US
dc.contributorSinnott, R.en_US
dc.contributorSoldatos, G.en_US
dc.contributorTye-Din, J.en_US
dc.contributorVuillermin, P.en_US
dc.contributorPenno, M.en_US
dc.contributorCouper, J.en_US
dc.date.accessioned2024-11-28T02:45:04Z-
dc.date.available2024-11-28T02:45:04Z-
dc.date.issued2024-
dc.identifier.govdoc02823en_US
dc.identifier.urihttp://hdl.handle.net/11054/2793-
dc.descriptionIncludes data from Ballarat Health Servicesen_US
dc.description.abstractIntroduction: The Environmental Determinants of Islet Autoimmunity (ENDIA) Study is an ongoing Australian prospective cohort study investigating how modifiable prenatal and early-life exposures drive the development of islet autoimmunity and type 1 diabetes (T1D) in children. In this profile, we describe the cohort’s parental demographics, maternal and neonatal outcomes and human leukocyte antigen (HLA) genotypes. Research design and methods: Inclusion criteria were an unborn child, or infant aged less than 6 months, with a first-degree relative (FDR) with T1D. The primary outcome was persistent islet autoimmunity, with children followed until a T1D diagnosis or 10 years of age. Demographic data were collected at enrollment. Lifestyle, clinical and anthropometric data were collected at each visit during pregnancy and clinical pregnancy and birth data were verified against medical case notes. Data were compared between mothers with and without T1D. HLA genotyping was performed on the ENDIA child and all available FDRs. Results: The final cohort comprised 1473 infants born to 1214 gestational mothers across 1453 pregnancies, with 80% enrolled during pregnancy. The distribution of familial T1D probands was 62% maternal, 28% paternal and 11% sibling. The frequency of high-risk HLA genotypes was highest in T1D probands, followed by ENDIA infants, and lowest among unaffected family members. Mothers with T1D had higher rates of pregnancy complications and perinatal intervention, and larger babies of shorter gestation. Parent demographics were comparable to the Australian population for age, parity and obesity. A greater percentage of ENDIA parents were Australian born, lived in a major city and had higher socioeconomic advantage and education. Conclusions: This comprehensive profile provides the context for understanding ENDIA’s scope, methodology, unique strengths and limitations. Now fully recruited, ENDIA will provide unique insights into the roles of early-life factors in the development of islet autoimmunity and T1D in the Australian environment.en_US
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dc.titleEnvironmental Determinants of Islet Autoimmunity (ENDIA) longitudinal prospective pregnancy to childhood cohort study of Australian children at risk of type 1 diabetes: Parental demographics and birth information.en_US
dc.typeJournal Articleen_US
dc.type.specifiedArticleen_US
dc.bibliographicCitation.titleBMJ Open Diabetes Research & Careen_US
dc.bibliographicCitation.volume12en_US
dc.bibliographicCitation.issue4en_US
dc.bibliographicCitation.stpagee004130en_US
dc.subject.healththesaurusCOHORT STUDIESen_US
dc.subject.healththesaurusDIABETES MELLITUSen_US
dc.subject.healththesaurusTYPE 1en_US
dc.subject.healththesaurusISLET AUTOIMMUNITYen_US
dc.subject.healththesaurusPREGNANCYen_US
dc.identifier.doihttps://doi.org/10.1136/bmjdrc-2024-004130en_US
Appears in Collections:Research Output

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