48 research outputs found

    Obesity and brain structure in schizophrenia - ENIGMA study in 3021 individuals

    Get PDF
    Schizophrenia is frequently associated with obesity, which is linked with neurostructural alterations. Yet, we do not understand how the brain correlates of obesity map onto the brain changes in schizophrenia. We obtained MRI-derived brain cortical and subcortical measures and body mass index (BMI) from 1260 individuals with schizophrenia and 1761 controls from 12 independent research sites within the ENIGMA-Schizophrenia Working Group. We jointly modeled the statistical effects of schizophrenia and BMI using mixed effects. BMI was additively associated with structure of many of the same brain regions as schizophrenia, but the cortical and subcortical alterations in schizophrenia were more widespread and pronounced. Both BMI and schizophrenia were primarily associated with changes in cortical thickness, with fewer correlates in surface area. While, BMI was negatively associated with cortical thickness, the significant associations between BMI and surface area or subcortical volumes were positive. Lastly, the brain correlates of obesity were replicated among large studies and closely resembled neurostructural changes in major depressive disorders. We confirmed widespread associations between BMI and brain structure in individuals with schizophrenia. People with both obesity and schizophrenia showed more pronounced brain alterations than people with only one of these conditions. Obesity appears to be a relevant factor which could account for heterogeneity of brain imaging findings and for differences in brain imaging outcomes among people with schizophrenia

    Large-scale analysis of structural brain asymmetries in schizophrenia via the ENIGMA consortium

    Get PDF
    BACKGROUND Left-right asymmetry is an important organizing feature of the healthy brain that may be altered in schizophrenia, but most studies have used relatively small samples and heterogeneous approaches, resulting in equivocal findings. We carried out the largest case-control study of structural brain asymmetries in schizophrenia (N = 11,095), using a single image analysis protocol. METHODS We included T1-weighted data from 46 datasets (5,080 affected individuals and 6,015 controls) from the ENIGMA Consortium. Asymmetry indexes were calculated for global and regional cortical thickness, surface area, and subcortical volume measures. Differences of asymmetry were calculated between affected individuals and controls per dataset, and effect sizes were meta-analyzed across datasets. Analyses were also performed with respect to the use of antipsychotic medication and other clinical variables, as well as age and sex. Case-control differences in a multivariate context were assessed in a subset of the data (N = 2,029). RESULTS Small average differences between cases and controls were observed for asymmetries in cortical thickness, specifically of the rostral anterior cingulate (d = −0.08, pFDR = 0.047) and the middle temporal gyrus (d = −0.07, pFDR = 0.048), both driven primarily by thinner cortices in the left hemisphere in schizophrenia. These asymmetries were not significantly associated with the use of antipsychotic medication or other clinical variables. Older individuals with schizophrenia showed a stronger average leftward asymmetry of pallidum volume than older controls (d = 0.08, pFDR = 9.0 × 10−3). The multivariate analysis revealed that 7% of the variance across all structural asymmetries was explained by case-control status (F = 1.87, p = 1.25 × 10−5). CONCLUSIONS Altered trajectories of asymmetrical brain development and/or lifespan asymmetry may contribute to schizophrenia pathophysiology. Small case-control differences of brain macro-structural asymmetry may manifest due to more substantial differences at the molecular, cytoarchitectonic or circuit levels, with functional relevance for lateralized cognitive processes

    Virtual Ontogeny of Cortical Growth Preceding Mental Illness

    Get PDF
    Background: Morphology of the human cerebral cortex differs across psychiatric disorders, with neurobiology and developmental origins mostly undetermined. Deviations in the tangential growth of the cerebral cortex during pre/perinatal periods may be reflected in individual variations in cortical surface area later in life. Methods: Interregional profiles of group differences in surface area between cases and controls were generated using T1-weighted magnetic resonance imaging from 27,359 individuals including those with attention-deficit/hyperactivity disorder, autism spectrum disorder, bipolar disorder, major depressive disorder, schizophrenia, and high general psychopathology (through the Child Behavior Checklist). Similarity of interregional profiles of group differences in surface area and prenatal cell-specific gene expression was assessed. Results: Across the 11 cortical regions, group differences in cortical area for attention-deficit/hyperactivity disorder, schizophrenia, and Child Behavior Checklist were dominant in multimodal association cortices. The same interregional profiles were also associated with interregional profiles of (prenatal) gene expression specific to proliferative cells, namely radial glia and intermediate progenitor cells (greater expression, larger difference), as well as differentiated cells, namely excitatory neurons and endothelial and mural cells (greater expression, smaller difference). Finally, these cell types were implicated in known pre/perinatal risk factors for psychosis. Genes coexpressed with radial glia were enriched with genes implicated in congenital abnormalities, birth weight, hypoxia, and starvation. Genes coexpressed with endothelial and mural genes were enriched with genes associated with maternal hypertension and preterm birth. Conclusions: Our findings support a neurodevelopmental model of vulnerability to mental illness whereby prenatal risk factors acting through cell-specific processes lead to deviations from typical brain development during pregnancy

    Widespread white matter microstructural differences in schizophrenia across 4322 individuals:Results from the ENIGMA Schizophrenia DTI Working Group

    Get PDF
    The regional distribution of white matter (WM) abnormalities in schizophrenia remains poorly understood, and reported disease effects on the brain vary widely between studies. In an effort to identify commonalities across studies, we perform what we believe is the first ever large-scale coordinated study of WM microstructural differences in schizophrenia. Our analysis consisted of 2359 healthy controls and 1963 schizophrenia patients from 29 independent international studies; we harmonized the processing and statistical analyses of diffusion tensor imaging (DTI) data across sites and meta-analyzed effects across studies. Significant reductions in fractional anisotropy (FA) in schizophrenia patients were widespread, and detected in 20 of 25 regions of interest within a WM skeleton representing all major WM fasciculi. Effect sizes varied by region, peaking at (d=0.42) for the entire WM skeleton, driven more by peripheral areas as opposed to the core WM where regions of interest were defined. The anterior corona radiata (d=0.40) and corpus callosum (d=0.39), specifically its body (d=0.39) and genu (d=0.37), showed greatest effects. Significant decreases, to lesser degrees, were observed in almost all regions analyzed. Larger effect sizes were observed for FA than diffusivity measures; significantly higher mean and radial diffusivity was observed for schizophrenia patients compared with controls. No significant effects of age at onset of schizophrenia or medication dosage were detected. As the largest coordinated analysis of WM differences in a psychiatric disorder to date, the present study provides a robust profile of widespread WM abnormalities in schizophrenia patients worldwide. Interactive three-dimensional visualization of the results is available at www.enigma-viewer.org.Molecular Psychiatry advance online publication, 17 October 2017; doi:10.1038/mp.2017.170

    Cortical brain abnormalities in 4474 individuals with schizophrenia and 5098 control subjects via the enhancing neuro Imaging genetics through meta analysis (ENIGMA) Consortium

    Get PDF
    BACKGROUND: The profile of cortical neuroanatomical abnormalities in schizophrenia is not fully understood, despite hundreds of published structural brain imaging studies. This study presents the first meta-analysis of cortical thickness and surface area abnormalities in schizophrenia conducted by the ENIGMA (Enhancing Neuro Imaging Genetics through Meta Analysis) Schizophrenia Working Group. METHODS: The study included data from 4474 individuals with schizophrenia (mean age, 32.3 years; range, 11-78 years; 66% male) and 5098 healthy volunteers (mean age, 32.8 years; range, 10-87 years; 53% male) assessed with standardized methods at 39 centers worldwide. RESULTS: Compared with healthy volunteers, individuals with schizophrenia have widespread thinner cortex (left/right hemisphere: Cohen's d = -0.530/-0.516) and smaller surface area (left/right hemisphere: Cohen's d = -0.251/-0.254), with the largest effect sizes for both in frontal and temporal lobe regions. Regional group differences in cortical thickness remained significant when statistically controlling for global cortical thickness, suggesting regional specificity. In contrast, effects for cortical surface area appear global. Case-control, negative, cortical thickness effect sizes were two to three times larger in individuals receiving antipsychotic medication relative to unmedicated individuals. Negative correlations between age and bilateral temporal pole thickness were stronger in individuals with schizophrenia than in healthy volunteers. Regional cortical thickness showed significant negative correlations with normalized medication dose, symptom severity, and duration of illness and positive correlations with age at onset. CONCLUSIONS: The findings indicate that the ENIGMA meta-analysis approach can achieve robust findings in clinical neuroscience studies; also, medication effects should be taken into account in future genetic association studies of cortical thickness in schizophrenia

    Allogamy-Autogamy Switch Enhance Assortative Mating in the Allotetraploid Centaurea seridis L. Coexisting with the Diploid Centaurea aspera L. and Triggers the Asymmetrical Formation of Triploid Hybrids

    Full text link
    [EN] Hybridization between tetraploids and its related diploids is generally unsuccessful in Centaurea, hence natural formation of triploid hybrids is rare. In contrast, the diploid Centaurea aspera and the allotetraploid C. seridis coexist in several contact zones where a high frequency of triploid hybrids is found. We analyzed the floral biology of the three taxa to identify reproductive isolation mechanisms that allow their coexistence. Flowering phenology was recorded, and controlled pollinations within and between the three taxa were performed in the field. Ploidy level and germination of progeny were also assessed. There was a 50% flowering overlap which indicated a phenological shift. Diploids were strictly allogamous and did not display mentor effects, while tetraploids were found to be highly autogamous. This breakdown of self-incompatibility by polyploids is first described in Centaurea. The asymmetrical formation of the hybrid was also found: all the triploid intact cypselae came from the diploid mothers pollinated by the pollen of tetraploids. Pollen and eggs from triploids were totally sterile, acting as a strong triploid block. These prezygotic isolation mechanisms ensured higher assortative mating in tetraploids than in diploids, improving its persistence in the contact zones. However these mechanisms can also be the cause of the low genetic diversity and high genetic structure observed in C. seridis.Ferriol Molina, M.; Garmendia, A.; Ana Gonzalez; Merle Farinós, HB. (2015). Allogamy-Autogamy Switch Enhance Assortative Mating in the Allotetraploid Centaurea seridis L. Coexisting with the Diploid Centaurea aspera L. and Triggers the Asymmetrical Formation of Triploid Hybrids. PLoS ONE. 10(10):1-13. doi:10.1371/journal.pone.0140465S1131010Jiao, Y., Wickett, N. J., Ayyampalayam, S., Chanderbali, A. S., Landherr, L., Ralph, P. E., … dePamphilis, C. W. (2011). Ancestral polyploidy in seed plants and angiosperms. Nature, 473(7345), 97-100. doi:10.1038/nature09916Wood, T. E., Takebayashi, N., Barker, M. S., Mayrose, I., Greenspoon, P. B., & Rieseberg, L. H. (2009). The frequency of polyploid speciation in vascular plants. Proceedings of the National Academy of Sciences, 106(33), 13875-13879. doi:10.1073/pnas.0811575106ROMASCHENKO, K., ERTUǦRUL, K., SUSANNA, A., GARCIA-JACAS, N., UYSAL, T., & ARSLAN, E. (2004). New chromosome counts in the Centaurea Jacea group (Asteraceae, Cardueae) and some related taxa. Botanical Journal of the Linnean Society, 145(3), 345-352. doi:10.1111/j.1095-8339.2004.00292.xHardy, O. J., de Loose, M., Vekemans, X., & Meerts, P. (2001). Allozyme segregation and inter-cytotype reproductive barriers in the polyploid complex Centaurea jacea. Heredity, 87(2), 136-145. doi:10.1046/j.1365-2540.2001.00862.xKOUTECKÝ, P., BAĎUROVÁ, T., ŠTECH, M., KOŠNAR, J., & KARÁSEK, J. (2011). Hybridization between diploidCentaurea pseudophrygiaand tetraploidC. jacea(Asteraceae): the role of mixed pollination, unreduced gametes, and mentor effects. Biological Journal of the Linnean Society, 104(1), 93-106. doi:10.1111/j.1095-8312.2011.01707.xKoutecký, P. (2012). A diploid drop in the tetraploid ocean: hybridization and long-term survival of a singular population of Centaurea weldeniana Rchb. (Asteraceae), a taxon new to Austria. Plant Systematics and Evolution, 298(7), 1349-1360. doi:10.1007/s00606-012-0641-5Mráz, P., Španiel, S., Keller, A., Bowmann, G., Farkas, A., Šingliarová, B., … Müller-Schärer, H. (2012). Anthropogenic disturbance as a driver of microspatial and microhabitat segregation of cytotypes of Centaurea stoebe and cytotype interactions in secondary contact zones. Annals of Botany, 110(3), 615-627. doi:10.1093/aob/mcs120Olšavská, K., & Löser, C. J. (2013). Mating System and Hybridization of the Cyanus triumfetti and C. montanus Groups (Asteraceae). Folia Geobotanica, 48(4), 537-554. doi:10.1007/s12224-013-9155-3Španiel, S., Marhold, K., Hodálová, I., & Lihová, J. (2008). Diploid and Tetraploid Cytotypes of Centaurea stoebe (Asteraceae) in Central Europe: Morphological Differentiation and Cytotype Distribution Patterns. Folia Geobotanica, 43(2), 131-158. doi:10.1007/s12224-008-9008-7HARDY, O. J., VANDERHOEVEN, S., DE LOOSE, M., & MEERTS, P. (2000). Ecological, morphological and allozymic differentiation between diploid and tetraploid knapweeds (Centaurea jacea) from a contact zone in the Belgian Ardennes. New Phytologist, 146(2), 281-290. doi:10.1046/j.1469-8137.2000.00631.xFerriol, M., Garmendia, A., Ruiz, J. J., Merle, H., & Boira, H. (2012). Morphological and molecular analysis of natural hybrids between the diploidCentaurea asperaL. and the tetraploidC. seridisL. (Compositae). Plant Biosystems - An International Journal Dealing with all Aspects of Plant Biology, 146(sup1), 86-100. doi:10.1080/11263504.2012.727878Ferriol, M., Merle, H., & Garmendia, A. (2014). Microsatellite evidence for low genetic diversity and reproductive isolation in tetraploidCentaurea seridis(Asteraceae) coexisting with diploidCentaurea asperaand triploid hybrids in contact zones. Botanical Journal of the Linnean Society, 176(1), 82-98. doi:10.1111/boj.12194Garmendia, A., Ferriol, M., Juarez, J., Zając, A., Kałużny, K., & Merle, H. (2015). A rare case of a natural contact zone in Morocco between an autopolyploid and an allopolyploid ofCentaurea asperawith sterile tetraploid hybrids. Plant Biology, 17(3), 746-757. doi:10.1111/plb.12284Petit, C., Bretagnolle, F., & Felber, F. (1999). Evolutionary consequences of diploid–polyploid hybrid zones in wild species. Trends in Ecology & Evolution, 14(8), 306-311. doi:10.1016/s0169-5347(99)01608-0Thorsson, A. T., Palsson, S., Sigurgeirsson, A., & Anamthawat-Jonsson, K. (2007). Morphological Variation among Betula nana (diploid), B. pubescens (tetraploid) and their Triploid Hybrids in Iceland. Annals of Botany, 99(6), 1183-1193. doi:10.1093/aob/mcm060Husband And, B. C., & Schemske, D. W. (2000). Ecological mechanisms of reproductive isolation between diploid and tetraploidChamerion angustifolium. Journal of Ecology, 88(4), 689-701. doi:10.1046/j.1365-2745.2000.00481.xKruskal, W. H., & Wallis, W. A. (1952). Use of Ranks in One-Criterion Variance Analysis. Journal of the American Statistical Association, 47(260), 583-621. doi:10.1080/01621459.1952.10483441Dunn, O. J. (1961). Multiple Comparisons among Means. Journal of the American Statistical Association, 56(293), 52-64. doi:10.1080/01621459.1961.10482090HARVILLE, D. A. (1974). Bayesian inference for variance components using only error contrasts. Biometrika, 61(2), 383-385. doi:10.1093/biomet/61.2.383McCullagh, P., & Nelder, J. A. (1989). Generalized Linear Models. doi:10.1007/978-1-4899-3242-6Lambert, D. (1992). Zero-Inflated Poisson Regression, with an Application to Defects in Manufacturing. Technometrics, 34(1), 1. doi:10.2307/1269547Vuong, Q. H. (1989). Likelihood Ratio Tests for Model Selection and Non-Nested Hypotheses. Econometrica, 57(2), 307. doi:10.2307/1912557Ferriol, M., Llorens, L., Gil, L., & Boira, H. (2008). Influence of phenological barriers and habitat differentiation on the population genetic structure of the balearic endemic Rhamnus ludovici-salvatoris Chodat and R. alaternus L. Plant Systematics and Evolution, 277(1-2), 105-116. doi:10.1007/s00606-008-0110-3Colas, B., Olivieri, I., & Riba, M. (2001). Spatio-temporal variation of reproductive success and conservation of the narrow-endemic Centaurea corymbosa (Asteraceae). Biological Conservation, 99(3), 375-386. doi:10.1016/s0006-3207(00)00229-9Felber, F., & Bever, J. D. (1997). Effect of triploid fitness on the coexistence of diploids and tetraploids. Biological Journal of the Linnean Society, 60(1), 95-106. doi:10.1111/j.1095-8312.1997.tb01485.xPeckert, T., & Chrtek, J. (2006). Mating interactions between coexisting dipoloid, triploid and tetraploid cytotypes ofHieracium Echioides (Asteraceae). Folia Geobotanica, 41(3), 323-334. doi:10.1007/bf02904945HUSBAND, B. C. (2004). The role of triploid hybrids in the evolutionary dynamics of mixed-ploidy populations. Biological Journal of the Linnean Society, 82(4), 537-546. doi:10.1111/j.1095-8312.2004.00339.xStebbins, G. L. (1950). Variation and Evolution in Plants. doi:10.7312/steb94536Barringer, B. C. (2007). Polyploidy and self-fertilization in flowering plants. American Journal of Botany, 94(9), 1527-1533. doi:10.3732/ajb.94.9.1527Borges, L. A., Souza, L. G. R., Guerra, M., Machado, I. C., Lewis, G. P., & Lopes, A. V. (2012). Reproductive isolation between diploid and tetraploid cytotypes of Libidibia ferrea (= Caesalpinia ferrea) (Leguminosae): ecological and taxonomic implications. Plant Systematics and Evolution, 298(7), 1371-1381. doi:10.1007/s00606-012-0643-3Greiner, R., & Oberprieler, C. (2012). The role of inter-ploidy block for reproductive isolation of the diploid Leucanthemum pluriflorum Pau (Compositae, Anthemideae) and its tetra- and hexaploid relatives. Flora - Morphology, Distribution, Functional Ecology of Plants, 207(9), 629-635. doi:10.1016/j.flora.2012.07.001Ferrer, M. M., & Good-Avila, S. V. (2006). Macrophylogenetic analyses of the gain and loss of self-incompatibility in the Asteraceae. New Phytologist, 173(2), 401-414. doi:10.1111/j.1469-8137.2006.01905.xSun, M., & Ritland, K. (1998). Mating system of yellow starthistle (Centaurea solstitialis), a successful colonizer in North America. Heredity, 80(2), 225-232. doi:10.1046/j.1365-2540.1998.00290.xHusband, B. C., & Sabara, H. A. (2003). Reproductive isolation between autotetraploids and their diploid progenitors in fireweed, Chamerion angustifolium (Onagraceae). New Phytologist, 161(3), 703-713. doi:10.1046/j.1469-8137.2004.00998.xAwadalla, P., & Ritland, K. (1997). Microsatellite variation and evolution in the Mimulus guttatus species complex with contrasting mating systems. Molecular Biology and Evolution, 14(10), 1023-1034. doi:10.1093/oxfordjournals.molbev.a025708Reinartz, J. A., & Les, D. H. (1994). Bottleneck-Induced Dissolution of Self-Incompatibility and Breeding System Consequences in Aster furcatus (Asteraceae). American Journal of Botany, 81(4), 446. doi:10.2307/2445494Hiscock, S. J. (2000). Genetic control of self-incompatibility in Senecio squalidus L. (Asteraceae): a successful colonizing species. Heredity, 85(1), 10-19. doi:10.1046/j.1365-2540.2000.00692.xNIELSEN, L. R., SIEGISMUND, H. R., & PHILIPP, M. (2003). Partial self-incompatibility in the polyploid endemic species Scalesia affinis (Asteraceae) from the Galápagos: remnants of a self-incompatibility system? Botanical Journal of the Linnean Society, 142(1), 93-101. doi:10.1046/j.1095-8339.2003.00168.xSonnleitner, M., Weis, B., Flatscher, R., García, P. E., Suda, J., Krejčíková, J., … Hülber, K. (2013). Parental Ploidy Strongly Affects Offspring Fitness in Heteroploid Crosses among Three Cytotypes of Autopolyploid Jacobaea carniolica (Asteraceae). PLoS ONE, 8(11), e78959. doi:10.1371/journal.pone.0078959Cui, C., Ge, X., Gautam, M., Kang, L., & Li, Z. (2012). Cytoplasmic and Genomic Effects on Meiotic Pairing inBrassicaHybrids and Allotetraploids from Pair Crosses of Three Cultivated Diploids. Genetics, 191(3), 725-738. doi:10.1534/genetics.112.140780Comai, L. (2005). The advantages and disadvantages of being polyploid. Nature Reviews Genetics, 6(11), 836-846. doi:10.1038/nrg1711Mráz, P. (2003). Mentor effects in the genusHieracium S.STR. (Compositae, Lactuceae). Folia Geobotanica, 38(3), 345-350. doi:10.1007/bf02803204Husband, B. C., Schemske, D. W., Burton, T. L., & Goodwillie, C. (2002). Pollen competition as a unilateral reproductive barrier between sympatric diploid and tetraploid Chamerion angustifolium. Proceedings of the Royal Society of London. Series B: Biological Sciences, 269(1509), 2565-2571. doi:10.1098/rspb.2002.2196Baldwin, S. J., & Husband, B. C. (2010). Genome duplication and the evolution of conspecific pollen precedence. Proceedings of the Royal Society B: Biological Sciences, 278(1714), 2011-2017. doi:10.1098/rspb.2010.220
    corecore