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Infant microbes and metabolites point to childhood neurodevelopmental disorders
Department of Microbiology and Cell Science, College of Agricultural and Life Sciences, University of Florida, Gainesville, FL 32603, USA.
Örebro University, School of Science and Technology.ORCID iD: 0000-0002-4382-4355
Department of Microbiology and Cell Science, College of Agricultural and Life Sciences, University of Florida, Gainesville, FL 32603, USA.
Department of Biomedical and Clinical Sciences, Division of Neurobiology, Linköping University, Linköping 58185, Sweden.
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2024 (English)In: Cell, ISSN 0092-8674, E-ISSN 1097-4172, Vol. 187, no 8, p. 1853-1873.e15Article in journal (Refereed) Published
Abstract [en]

This study has followed a birth cohort for over 20 years to find factors associated with neurodevelopmental disorder (ND) diagnosis. Detailed, early-life longitudinal questionnaires captured infection and antibiotic events, stress, prenatal factors, family history, and more. Biomarkers including cord serum metabolome and lipidome, human leukocyte antigen (HLA) genotype, infant microbiota, and stool metabolome were assessed. Among the 16,440 Swedish children followed across time, 1,197 developed an ND. Significant associations emerged for future ND diagnosis in general and for specific ND subtypes, spanning intellectual disability, speech disorder, attention-deficit/hyperactivity disorder, and autism. This investigation revealed microbiome connections to future diagnosis as well as early emerging mood and gastrointestinal problems. The findings suggest links to immunodysregulation and metabolism, compounded by stress, early-life infection, and antibiotics. The convergence of infant biomarkers and risk factors in this prospective, longitudinal study on a large-scale population establishes a foundation for early-life prediction and intervention in neurodevelopment.

Place, publisher, year, edition, pages
Cell Press, 2024. Vol. 187, no 8, p. 1853-1873.e15
Keywords [en]
ASD, Akkermansia, Coprococcus, PFOA, antibiotics, equol, inflammation, otitis, pediatrics, tryptophan
National Category
Pediatrics
Identifiers
URN: urn:nbn:se:oru:diva-112922DOI: 10.1016/j.cell.2024.02.035ISI: 001233912800001PubMedID: 38574728Scopus ID: 2-s2.0-85189552628OAI: oai:DiVA.org:oru-112922DiVA, id: diva2:1849934
Funder
Swedish Child Diabetes FoundationForte, Swedish Research Council for Health, Working Life and Welfare, FAS2004-1775; FAS2004-1775Swedish Research Council, K2005-72X-11242-11A; K2008-69X-20826-01-4; K2008-69X-20826-01-4Region ÖstergötlandLinköpings universitet
Note

ABIS was supported by Barndiabetesfonden (Swedish Child Diabetes Foundation) ; Swedish Council for Working Life and Social Research grant/award numbers FAS2004-1775 and FAS2004-1775; Swedish Research Council grant/award numbers K2005-72X-11242-11A, K2008-69X-20826-01-4, and K2008-69X-20826-01-4; Östgöta Brandstodsbolag; Medical Research Council of Southeast Sweden (FORSS) ; JDRF Wallenberg Foundation grant/award number K98-99D-12813-01A; ALF and LFoU grants from Region Östergötland and Linköping University, Sweden; and the Joanna Cocozza Foundation. This research was funded by JDRF grant no. 1-INO-2018-637-A-N and supported by the "Inflammation in human early life: targeting impacts on life-course health" (INITIALISE) consortium funded by the Horizon Europe Program of the European Union under grant agreement 101094099. 

Available from: 2024-04-09 Created: 2024-04-09 Last updated: 2024-06-11Bibliographically approved

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Hyötyläinen, TuuliaOresic, Matej

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