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      The impact of maternal smoking during pregnancy on depressive and anxiety behaviors in children: the Norwegian Mother and Child Cohort Study

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          Abstract

          Background

          Maternal smoking during pregnancy (MSDP) is associated with multiple adverse childhood outcomes including externalizing behaviors. However, the association between MSDP and internalizing (anxiety and depressive) behaviors in offspring has received less investigation. We aimed to assess the association between MSDP and childhood internalizing (anxiety and depressive) behaviors in a very large, well-characterized cohort study.

          Methods

          We assessed the association between MSDP and internalizing behaviors in offspring utilizing information drawn from 90,040 mother-child pairs enrolled in the Norwegian Mother and Child Cohort Study. Mothers reported smoking information, including status and frequency of smoking, twice during pregnancy. Mothers also reported their child’s internalizing behaviors at 18 months, 36 months, and 5 years. Associations between MSDP and childhood internalizing behaviors, including dose-response and timing of smoking in pregnancy, were assessed at each time point.

          Results

          MSDP was associated with increased internalizing behaviors when offspring were aged 18 months (B = 0.11, P <0.001) and 36 months (B = 0.06, P <0.01), adjusting for numerous potential confounders. Higher rates of smoking (e.g., >20 cigarettes per day) were associated with higher levels of internalizing behaviors. Maternal smoking during early pregnancy appeared to be the critical period for exposure.

          Conclusions

          We found evidence supporting a potential role for MSDP in increasing internalizing (anxiety and depressive) behaviors in offspring. We also found evidence supportive of a possible causal relationship, including dose-dependency and support for a predominant role of early pregnancy exposure. Further investigation utilizing genetically informed designs are warranted to assess this association.

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          Most cited references48

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          How well can a few questionnaire items indicate anxiety and depression?

          There is a need for a short form questionnaire with known psychometric characteristics that may be used as an indicator of level of global mental distress. A weighted sum of 5 questions from the Symptom Check List (SCL) anxiety and depression subscales (SCL-25) correlates at r = 0.92 with the global SCL-25 score. The alpha reliability for the (5-item) short form questionnaire was 0.85%. Age differences seemed to be trivial, and sex differences were moderate. Descriptive statistics for short form scores in a large, representative sample are given.
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            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.
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              Cholinergic systems in brain development and disruption by neurotoxicants: nicotine, environmental tobacco smoke, organophosphates.

              Acetylcholine and other neurotransmitters play unique trophic roles in brain development. Accordingly, drugs and environmental toxicants that promote or interfere with neurotransmitter function evoke neurodevelopmental abnormalities by disrupting the timing or intensity of neurotrophic actions. The current review discusses three exposure scenarios involving acetylcholine systems: nicotine from maternal smoking during pregnancy, exposure to environmental tobacco smoke (ETS), and exposure to the organophosphate insecticide, chlorpyrifos (CPF). All three have long-term, adverse effects on specific processes involved in brain cell replication and differentiation, synaptic development and function, and ultimately behavioral performance. Many of these effects can be traced to the sequence of cellular events surrounding the trophic role of acetylcholine acting on its specific cellular receptors and associated signaling cascades. However, for chlorpyrifos, additional noncholinergic mechanisms appear to be critical in establishing the period of developmental vulnerability, the sites and type of neural damage, and the eventual outcome. New findings indicate that developmental neurotoxicity extends to late phases of brain maturation including adolescence. Novel in vitro and in vivo exposure models are being developed to uncover heretofore unsuspected mechanisms and targets for developmental neurotoxicants.
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                Author and article information

                Contributors
                steven.moylan@deakin.edu.au
                KristinBrun.Gustavson@fhi.no
                Simon.Overland@iuh.uib.no
                e.b.karevold@psykologi.uio.no
                felice@barwonhealth.org.au
                juliep@barwonhealth.org.au
                mikebe@barwonhealth.org.au
                Journal
                BMC Med
                BMC Med
                BMC Medicine
                BioMed Central (London )
                1741-7015
                3 February 2015
                3 February 2015
                2015
                : 13
                : 1
                : 24
                Affiliations
                [ ]School of Medicine, Deakin University, Geelong, Victoria 3220 Australia
                [ ]Division of Mental Health, Norwegian Institute of Public Health, Oslo, NO-0403 Norway
                [ ]Faculty of Psychology, University of Bergen, Bergen, N-5020 Norway
                [ ]Department of Psychology, University of Oslo, Oslo, NO-0316 Norway
                [ ]NorthWest Academic Centre, Department of Medicine, The University of Melbourne, St Albans, Victoria 3021 Australia
                [ ]Department of Psychiatry, Orygen Research Centre, and the Florey Institute for Neuroscience Mental Health, The University of Melbourne, Melbourne, Parkville Victoria 3052 Australia
                [ ]Barwon Health, Geelong, Victoria 3220 Australia
                Article
                257
                10.1186/s12916-014-0257-4
                4314755
                25644294
                dab95c19-a369-4733-9a63-b3ee7d17efe1
                © Moylan et al.; licensee BioMed Central. 2015

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 9 May 2014
                : 12 December 2014
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2015

                Medicine
                anxiety,depression,cigarette smoking,pregnancy,obstetrics,psychiatry
                Medicine
                anxiety, depression, cigarette smoking, pregnancy, obstetrics, psychiatry

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