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      Gene–environment interaction of monoamine oxidase A in relation to antisocial behaviour: current and future directions

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          Abstract

          Since the pioneering finding of Caspi and co-workers in 2002 that exposure to childhood maltreatment predicted later antisocial behaviour (ASB) in male carriers of the low-activity MAOA-uVNTR allele, frequent replication studies have been published. Two meta-analyses, one in 2006 and the other in 2014, confirmed the original findings by Caspi and co-workers. In the present paper, we review the literature, note some methodological aspects of candidate gene–environment interaction (cG×E) studies and suggest some future directions. Our conclusions are as follows. (1) The direction of the effect in a cG×E model may differ according to the positive and negative environmental background of the population. (2) There is a predictor-intersection problem such that when measuring one type of maltreatment in a person, other kinds of maltreatment often co-occur. Other forms of abuse are implicitly considered in statistical models; therefore, it is difficult to draw conclusions about the effects of timing and the severity of different forms of stressful life events in relation to ASB. (3) There is also an outcome-intersection problem because of the major intersection of ASB and other forms of mental health problems. It is likely that the G×E with MAOA is related to a common unmeasured factor. (4) For the G×E model, in which the effect of the gene on the outcome variable is dependent on other predictor variables, theoretically, hypothesis-driven statistical modelling is needed.

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          Cultural Violence

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            Genetic sensitivity to the environment: the case of the serotonin transporter gene and its implications for studying complex diseases and traits.

            Evidence of marked variability in response among people exposed to the same environmental risk implies that individual differences in genetic susceptibility might be at work. The study of such Gene-by-Environment (GxE) interactions has gained momentum. In this article, the authors review research about one of the most extensive areas of inquiry: variation in the promoter region of the serotonin transporter gene (SLC6A4; also known as 5-HTT) and its contribution to stress sensitivity. Research in this area has both advanced basic science and generated broader lessons for studying complex diseases and traits. The authors evaluate four lines of evidence about the 5-HTT stress-sensitivity hypothesis: 1) observational studies about the serotonin transporter linked polymorphic region (5-HTTLPR), stress sensitivity, and depression in humans; 2) experimental neuroscience studies about the 5-HTTLPR and biological phenotypes relevant to the human stress response; 3) studies of 5-HTT variation and stress sensitivity in nonhuman primates; and 4) studies of stress sensitivity and genetically engineered 5-HTT mutations in rodents. The authors then dispel some misconceptions and offer recommendations for GxE research. The authors discuss how GxE interaction hypotheses can be tested with large and small samples, how GxE research can be carried out before as well as after replicated gene discovery, the uses of GxE research as a tool for gene discovery, the importance of construct validation in evaluating GxE research, and the contribution of GxE research to the public understanding of genetic science.
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              A functional polymorphism in the monoamine oxidase A gene promoter.

              We describe a new polymorphism upstream of the gene for monoamine oxidase A (MAOA), an important enzyme in human physiology and behavior. The polymorphism, which is located 1.2 kb upstream of the MAOA coding sequences, consists of a 30-bp repeated sequence present in 3, 3.5, 4, or 5 copies. The polymorphism is in linkage disequilibrium with other MAOA and MAOB gene markers and displays significant variations in allele frequencies across ethnic groups. The polymorphism has been shown to affect the transcriptional activity of the MAOA gene promoter by gene fusion and transfection experiments involving three different cell types. Alleles with 3.5 or 4 copies of the repeat sequence are transcribed 2-10 times more efficiently than those with 3 or 5 copies of the repeat, suggesting an optimal length for the regulatory region. This promoter region polymorphism may be useful as both a functional and an anonymous genetic marker for MAOA.
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                Author and article information

                Contributors
                kent.nilsson@ltv.se
                Journal
                J Neural Transm (Vienna)
                J Neural Transm (Vienna)
                Journal of Neural Transmission
                Springer Vienna (Vienna )
                0300-9564
                1435-1463
                7 June 2018
                7 June 2018
                2018
                : 125
                : 11
                : 1601-1626
                Affiliations
                [1 ]ISNI 0000 0004 1936 9457, GRID grid.8993.b, Centre for Clinical Research, , Uppsala University, County Hospital, ; Västerås, Sweden
                [2 ]ISNI 0000 0004 1936 9457, GRID grid.8993.b, Department of Neuroscience, Science for Life Laboratory, , Uppsala University, ; Uppsala, Sweden
                [3 ]ISNI 0000 0004 1936 9457, GRID grid.8993.b, Department of Neuroscience, , Uppsala University, ; Uppsala, Sweden
                Author information
                http://orcid.org/0000-0002-8853-2508
                Article
                1892
                10.1007/s00702-018-1892-2
                6224008
                29881923
                be22c44c-9f00-42f3-b0e0-622ad493d061
                © The Author(s) 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 14 February 2018
                : 29 May 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100003792, Hjärnfonden;
                Funded by: Swedish Alcohol Monopoly Research Council
                Funded by: the Swedish Council for Working Life and Social Research (FAS)
                Funded by: the Uppsala and Örebro Regional Research Council
                Funded by: the Fredrik and Ingrid Thurings Foundation
                Funded by: the County Council of Västmanland
                Funded by: the Söderström König Foundation
                Award ID: SLS-559921, SLS-655791, SLS-745221
                Award Recipient :
                Funded by: the Svenska Spel Research Foundation
                Funded by: FundRef http://dx.doi.org/10.13039/100007435, Åke Wiberg Stiftelse;
                Award ID: M15-0239
                Award Recipient :
                Funded by: the Swedish Research Council for Health, Working Life and Welfare (FORTE)
                Award ID: 2015-00897
                Award Recipient :
                Funded by: Marie Skłodowska Curie fellow
                Funded by: the Swedish Research Council
                Award ID: VR: 2015-00495
                Award Recipient :
                Funded by: EU FP7-People-Cofund
                Award ID: INCA 600398
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100009252, Science for Life Laboratory;
                Funded by: Bertil Hållsten’s Research Fund
                Categories
                Translational Neurosciences - Review Article
                Custom metadata
                © Springer-Verlag GmbH Austria, part of Springer Nature 2018

                antisocial personality disorder,brunner syndrome,conduct disorder,genetic association studies,gene–environment interaction,genetic susceptibility,juvenile delinquency,monoamine oxidase a,review

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