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      Toxoplasma gondii exposure may modulate the influence of TLR2 genetic variation on bipolar disorder: a gene–environment interaction study

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          Abstract

          Background

          Genetic vulnerability to environmental stressors is yet to be clarified in bipolar disorder (BD), a complex multisystem disorder in which immune dysfunction and infectious insults seem to play a major role in the pathophysiology. Association between pattern-recognition receptor coding genes and BD had been previously reported. However, potential interactions with history of pathogen exposure are yet to be explored.

          Methods

          138 BD patients and 167 healthy controls were tested for serostatus of Toxoplasma gondii, CMV, HSV-1 and HSV-2 and genotyped for TLR2 ( rs4696480 and rs3804099), TLR4 ( rs1927914 and rs11536891) and NOD2 ( rs2066842) polymorphisms (SNPs). Both the pathogen-specific seroprevalence and the TLR/NOD2 genetic profiles were compared between patients and controls followed by modelling of interactions between these genes and environmental infectious factors in a regression analysis.

          Results

          First, here again we observed an association between BD and Toxoplasma gondii ( p = 0.045; OR = 1.77; 95 % CI 1.01–3.10) extending the previously published data on a cohort of a relatively small number of patients (also included in the present sample). Second, we found a trend for an interaction between the TLR2 rs3804099 SNP and Toxoplasma gondii seropositivity in conferring BD risk ( p = 0.017, uncorrected).

          Conclusions

          Pathogen exposure may modulate the influence of the immunogenetic background on BD. A much larger sample size and information on period of pathogen exposure are needed in future gene–environment interaction studies.

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          Most cited references34

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          Diagnostic and statistical manual of mental disorders.

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            Global burden of disease in young people aged 10-24 years: a systematic analysis.

            Young people aged 10-24 years represent 27% of the world's population. Although important health problems and risk factors for disease in later life emerge in these years, the contribution to the global burden of disease is unknown. We describe the global burden of disease arising in young people and the contribution of risk factors to that burden. We used data from WHO's 2004 Global Burden of Disease study. Cause-specific disability-adjusted life-years (DALYs) for young people aged 10-24 years were estimated by WHO region on the basis of available data for incidence, prevalence, severity, and mortality. WHO member states were classified into low-income, middle-income, and high-income countries, and into WHO regions. We estimated DALYs attributable to specific global health risk factors using the comparative risk assessment method. DALYs were divided into years of life lost because of premature mortality (YLLs) and years lost because of disability (YLDs), and are presented for regions by sex and by 5-year age groups. The total number of incident DALYs in those aged 10-24 years was about 236 million, representing 15·5% of total DALYs for all age groups. Africa had the highest rate of DALYs for this age group, which was 2·5 times greater than in high-income countries (208 vs 82 DALYs per 1000 population). Across regions, DALY rates were 12% higher in girls than in boys between 15 and 19 years (137 vs 153). Worldwide, the three main causes of YLDs for 10-24-year-olds were neuropsychiatric disorders (45%), unintentional injuries (12%), and infectious and parasitic diseases (10%). The main risk factors for incident DALYs in 10-24-year-olds were alcohol (7% of DALYs), unsafe sex (4%), iron deficiency (3%), lack of contraception (2%), and illicit drug use (2%). The health of young people has been largely neglected in global public health because this age group is perceived as healthy. However, opportunities for prevention of disease and injury in this age group are not fully exploited. The findings from this study suggest that adolescent health would benefit from increased public health attention. None. Copyright © 2011 Elsevier Ltd. All rights reserved.
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              A rating scale for mania: reliability, validity and sensitivity.

              An eleven item clinician-administered Mania Rating Scale (MRS) is introduced, and its reliability, validity and sensitivity are examined. There was a high correlation between the scores of two independent clinicians on both the total score (0.93) and the individual item scores (0.66 to 0.92). The MRS score correlated highly with an independent global rating, and with scores of two other mania rating scales administered concurrently. The score also correlated with the number of days of subsequent stay in hospital. It was able to differentiate statistically patients before and after two weeks of treatment and to distinguish levels of severity based on the global rating.
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                Author and article information

                Contributors
                josemsoliveira@hotmail.com
                remi.kazma@gmail.com
                edith.lefloch@cng.fr
                meriem.bennabi@gmail.com
                nora_psy@yahoo.fr
                djaouida.bengoufa@aphp.fr
                mehdidahoun@gmail.com
                manierceline@gmail.com
                frank.bellivier@inserm.fr
                rajagopal.krishnamoorthy@gmail.com
                deleuze@cng.fr
                yolken@mail.jhmi.edu
                marion.leboyer@inserm.fr
                +33 1 42 49 48 90 , tamouza.ryad@gmail.com
                Journal
                Int J Bipolar Disord
                Int J Bipolar Disord
                International Journal of Bipolar Disorders
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                2194-7511
                20 May 2016
                20 May 2016
                2016
                : 4
                : 11
                Affiliations
                [ ]INSERM, U1160, Hôpital Saint Louis, Paris, France
                [ ]Fondation FondaMental, Créteil, France
                [ ]Centre National de Génotypage, CEA, Evry, France
                [ ]Faculté de Médecine, Université Paris-Est, Créteil, France
                [ ]AP-HP, DHU PePSY, Pôle de Psychiatrie, Hôpitaux Universitaires Henri Mondor, Créteil, France
                [ ]INSERM, U955, Psychiatrie Translationnelle, Créteil, France
                [ ]Laboratoire Jean Dausset and LabEx Transplantex, Hôpital Saint Louis, Paris, France
                [ ]Sorbonne Paris-Cité, Université Paris Diderot, Paris, France
                [ ]INSERM UMR-S1144-VariaPsy, Hôpital Fernand Widal, Paris, France
                [ ]Stanley Laboratory of Developmental Neurovirology, Johns Hopkins University Medical Center, Baltimore, USA
                [ ]Stanley Research Program, Sheppard Pratt, Baltimore, MD USA
                Article
                52
                10.1186/s40345-016-0052-6
                4875582
                27207565
                1076b125-832e-44a9-8f05-3864a7b1910a
                © Oliveira et al. 2016

                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
                : 20 January 2016
                : 5 May 2016
                Categories
                Research
                Custom metadata
                © The Author(s) 2016

                bipolar disorder,innate immunity,pathogen recognition receptor,genetic diversity,infection,gene–environment interaction

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