3
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Parental asthma and risk of autism spectrum disorder in offspring: A population and family‐based case‐control study

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Summary

          Background

          Associations between parental asthma and prenatal exposure to asthma medications with offspring autism spectrum disorder ( ASD) have been reported. However, the associations might be confounded by unmeasured (genetic and shared environmental) familial factors.

          Objective

          We investigated the association between (a) maternal/paternal asthma and offspring ASD, and (b) prenatal exposures to β2‐agonists, other asthma medications and offspring ASD using cases and controls selected from the population as well as biological relatives with different degrees of relatedness.

          Methods

          We included all children (N = 1 579 263) born in Sweden 1992‐2007. A nested case‐control design was used to compare 22 894 ASD cases identified from the National Patient Register to (a) 228 940 age‐, county‐ and sex‐matched controls randomly selected from the population, (b) their eligible full‐siblings (n = 1267), (c) half‐siblings (n = 1323), (d) full‐cousins (n = 11 477) and (e) half‐cousins (n = 3337). Conditional logistic regression was used to estimate the odds ratios ( OR) and 95% confidence intervals ( CI) for ASD in children differentially exposed to parental asthma or prenatal asthma medications.

          Results

          Maternal asthma was associated with increased risk of offspring ASD ( OR 1.43, 95% CI 1.38‐1.49); there was a weaker association for paternal asthma ( OR 1.17, 95% CI 1.11‐1.23). The risk of offspring ASD in mothers with asthma showed similar estimates when adjusting for shared familial factors among paternal half‐siblings ( OR 1.20, 95% CI 0.80‐1.81), full‐cousins ( OR 1.28, 95% CI 1.16‐1.41) and half‐cousins ( OR 1.30, 95% CI 1.10‐1.54), albeit with wider confidence intervals. Prenatal exposure to asthma medications among subjects whose mothers had asthma was not associated with subsequent ASD.

          Conclusions and Clinical Relevance

          In this large observational study, parental asthma was associated with slightly elevated risk of ASD in offspring. More specifically, the increased risk by maternal asthma did not seem to be confounded by familial factors. There was no evidence of an association between asthma medications during pregnancy and offspring ASD.

          Related collections

          Most cited references40

          • Record: found
          • Abstract: found
          • Article: not found

          Preterm birth and mortality and morbidity: a population-based quasi-experimental study.

          Preterm birth is associated with increased mortality and morbidity. However, previous studies have been unable to rigorously examine whether confounding factors cause these associations rather than the harmful effects of being born preterm.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Critical need for family-based, quasi-experimental designs in integrating genetic and social science research.

            Researchers have identified environmental risks that predict subsequent psychological and medical problems. Based on these correlational findings, researchers have developed and tested complex developmental models and have examined biological moderating factors (e.g., gene-environment interactions). In this context, we stress the critical need for researchers to use family-based, quasi-experimental designs when trying to integrate genetic and social science research involving environmental variables because these designs rigorously examine causal inferences by testing competing hypotheses. We argue that sibling comparison, offspring of twins or siblings, in vitro fertilization designs, and other genetically informed approaches play a unique role in bridging gaps between basic biological and social science research. We use studies on maternal smoking during pregnancy to exemplify these principles.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Modeling an autism risk factor in mice leads to permanent immune dysregulation.

              Increasing evidence highlights a role for the immune system in the pathogenesis of autism spectrum disorder (ASD), as immune dysregulation is observed in the brain, periphery, and gastrointestinal tract of ASD individuals. Furthermore, maternal infection (maternal immune activation, MIA) is a risk factor for ASD. Modeling this risk factor in mice yields offspring with the cardinal behavioral and neuropathological symptoms of human ASD. In this study, we find that offspring of immune-activated mothers display altered immune profiles and function, characterized by a systemic deficit in CD4(+) TCRβ(+) Foxp3(+) CD25(+) T regulatory cells, increased IL-6 and IL-17 production by CD4(+) T cells, and elevated levels of peripheral Gr-1(+) cells. In addition, hematopoietic stem cells from MIA offspring exhibit altered myeloid lineage potential and differentiation. Interestingly, repopulating irradiated control mice with bone marrow derived from MIA offspring does not confer MIA-related immunological deficits, implicating the peripheral environmental context in long-term programming of immune dysfunction. Furthermore, behaviorally abnormal MIA offspring that have been irradiated and transplanted with immunologically normal bone marrow from either MIA or control offspring no longer exhibit deficits in stereotyped/repetitive and anxiety-like behaviors, suggesting that immune abnormalities in MIA offspring can contribute to ASD-related behaviors. These studies support a link between cellular immune dysregulation and ASD-related behavioral deficits in a mouse model of an autism risk factor.
                Bookmark

                Author and article information

                Contributors
                catarina.almqvist@ki.se
                Journal
                Clin Exp Allergy
                Clin. Exp. Allergy
                10.1111/(ISSN)1365-2222
                CEA
                Clinical and Experimental Allergy
                John Wiley and Sons Inc. (Hoboken )
                0954-7894
                1365-2222
                27 February 2019
                June 2019
                : 49
                : 6 ( doiID: 10.1111/cea.2019.49.issue-6 )
                : 883-891
                Affiliations
                [ 1 ] Department of Medical Epidemiology and Biostatistics Karolinska Institutet Stockholm Sweden
                [ 2 ] Woolcock Insitute of Medical Research University of Sydney Sydney New South Wales Australia
                [ 3 ] Obstetrics and Gynaecology Unit Södersjukhuset Stockholm Sweden
                [ 4 ] Center of Neurodevelopmental Disorders at Karolinska Institutet (KIND) Center for Psychiatric Research Department of Women's & Children's Health Karolinska Institutet & Child and Adolescent Psychiatry Stockholm Health Care Services Stockholm County Council Stockholm Sweden
                [ 5 ] Curtin Autism Research Group School of Occupational Therapy, Social Work and Speech Pathology Curtin University Perth Western Australia Australia
                [ 6 ] School of Medical Sciences Örebro University Örebro Sweden
                [ 7 ] Department of Psychological and Brain Sciences Indiana University Bloomington Indiana USA
                [ 8 ] Pediatric Allergy and Pulmonology Unit Astrid Lindgren Children's Hospital Karolinska University Hospital Stockholm Sweden
                Author notes
                [*] [* ] Correspondence

                Catarina Almqvist, Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.

                Email: catarina.almqvist@ 123456ki.se

                Author information
                https://orcid.org/0000-0002-1045-1898
                Article
                CEA13353
                10.1111/cea.13353
                6849600
                30742718
                fb6ce4b3-bd6d-4529-8b12-ff7feed7699e
                © 2019 The Authors. Clinical & Experimental Allergy Published by John Wiley & Sons Ltd

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 14 June 2018
                : 08 November 2018
                : 18 November 2018
                Page count
                Figures: 2, Tables: 1, Pages: 9, Words: 6643
                Funding
                Funded by: Forskningsrådet om Hälsa, Arbetsliv och Välfärd , open-funder-registry 10.13039/501100006636;
                Award ID: 2015‐00289
                Funded by: HKH Kronprinsessan Lovisas förening för barnasjukvård
                Funded by: Vetenskapsrådet , open-funder-registry 10.13039/501100004359;
                Award ID: 340‐2013‐5867
                Funded by: Stockholms Läns Landsting , open-funder-registry 10.13039/501100004348;
                Funded by: Hjärt‐Lungfonden , open-funder-registry 10.13039/501100003793;
                Categories
                Original Article
                ORIGINAL ARTICLES
                Epidemiology of Allergic Disease
                Custom metadata
                2.0
                June 2019
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.1 mode:remove_FC converted:12.11.2019

                Immunology
                asthma,autism spectrum disorder,confounding,medications during pregnancy,nested case‐control

                Comments

                Comment on this article