Prenatal fever and autism risk

Some studies suggest that prenatal infection increases risk of autism spectrum disorders (ASDs). This study was undertaken in a prospective cohort in Norway to examine whether we could find evidence to support an association of the prenatal occurrence of fever, a common manifestation of infection, w...

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Veröffentlicht in:Molecular psychiatry 2018-03, Vol.23 (3), p.759-766
Hauptverfasser: Hornig, M, Bresnahan, M A, Che, X, Schultz, A F, Ukaigwe, J E, Eddy, M L, Hirtz, D, Gunnes, N, Lie, K K, Magnus, P, Mjaaland, S, Reichborn-Kjennerud, T, Schjølberg, S, Øyen, A-S, Levin, B, Susser, E S, Stoltenberg, C, Lipkin, W I
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Sprache:eng
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Zusammenfassung:Some studies suggest that prenatal infection increases risk of autism spectrum disorders (ASDs). This study was undertaken in a prospective cohort in Norway to examine whether we could find evidence to support an association of the prenatal occurrence of fever, a common manifestation of infection, with ASD risk. Prospective questionnaires provided maternal exposure data; case status was established from clinical assessments and registry linkages. In a large, prospectively ascertained cohort of pregnant mothers and their offspring, we examined infants born ⩾32 weeks for associations between fever exposure in each trimester and ASD risk using logistic regression. Maternal exposure to second-trimester fever was associated with increased ASD risk, adjusting for presence of fever in other trimesters and confounders (adjusted odds ratio (aOR), 1.40; 95% confidence interval, 1.09–1.79), with a similar, but nonsignificant, point estimate in the first trimester. Risk increased markedly with exposure to three or more fever episodes after 12 weeks' gestation (aOR, 3.12; 1.28–7.63). ASD risk appears to increase with maternal fever, particularly in the second trimester. Risk magnified dose dependently with exposure to multiple fevers after 12 weeks' gestation. Our findings support a role for gestational maternal infection and innate immune responses to infection in the pathogenesis of at least some cases of ASD.
ISSN:1359-4184
1476-5578
DOI:10.1038/mp.2017.119