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dc.date.accessioned2017-08-25T14:35:38Z
dc.date.available2017-08-25T14:35:38Z
dc.date.created2017-08-11T15:38:44Z
dc.date.issued2017
dc.identifier.citationMahic, Milada Che, Xiaoyu Mjaaland, Siri . Epidemiological and Serological Investigation into the Role of Gestational Maternal Influenza Virus Infection and Autism Spectrum Disorders. mSphere. 2017, 2(3)
dc.identifier.urihttp://hdl.handle.net/10852/57463
dc.description.abstractThe literature concerning gestational maternal influenza virus infection and risk of autism spectrum disorders (ASD) is inconclusive. To address this uncertainty, we obtained information from questionnaires and samples from the Autism Birth Cohort, a prospective birth cohort comprising mothers, fathers, and offspring recruited in Norway in 1999 to 2008. Through questionnaires, referrals, and linkages to the Norwegian National Patient Registry, we identified 338 mothers of children with ASD and 348 frequency-matched controls for whom plasma samples that had been collected midpregnancy and after delivery were available for influenza virus serology via luciferase immunoprecipitation and hemagglutinin inhibition assays for influenza virus strains circulating during the study period. Assay data were combined to define serological status and integrated with self-reports of influenza-like illness to estimate ASD risk. Neither influenza A nor influenza B virus infection was associated with increased ASD risk. Integration of reports of symptoms of influenza-like illness with serology revealed an increase in risk for seropositive women with symptoms, but this increase did not achieve statistical significance (a level of P < 0.05) in the comparison with seronegative women without symptoms (adjusted odds ratio, 1.93; 95% confidence interval, 0.95 to 3.89; P = 0.068). Although chance may explain our findings, the magnitude of the potential association may be of biological importance, and dismissing our findings could result in failure to detect a bona fide association (type II error). If the association is true, we posit that the risk is due to activation of the maternal immune system following infection rather than direct fetal infection. Data on levels of cytokines or other mediators of inflammation would allow us to test the validity of this hypothesis.en_US
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleEpidemiological and Serological Investigation into the Role of Gestational Maternal Influenza Virus Infection and Autism Spectrum Disordersen_US
dc.typeJournal articleen_US
dc.creator.authorMahic, Milada
dc.creator.authorChe, Xiaoyu
dc.creator.authorMjaaland, Siri
cristin.unitcode185,53,18,72
cristin.unitnameK.G. Jebsen Senter for influensavaksine-part UiO
cristin.ispublishedtrue
cristin.fulltextoriginal
dc.identifier.cristin1485836
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=mSphere&rft.volume=2&rft.spage=&rft.date=2017
dc.identifier.jtitlemSphere
dc.identifier.volume2
dc.identifier.issue3
dc.identifier.pagecount8
dc.identifier.doi10.1128/mSphere.00159-17
dc.identifier.urnURN:NBN:no-60195
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn2379-5042
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/57463/2/Mahic_2017_Epi.pdf
dc.type.versionPublishedVersion
cristin.articleide00159-17


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