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      Cortical gyrification is abnormal in children with prenatal alcohol exposure

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          Abstract

          Objectives

          Prenatal alcohol exposure (PAE) adversely affects early brain development. Previous studies have shown a wide range of structural and functional abnormalities in children and adolescents with PAE. The current study adds to the existing literature specifically on cortical development by examining cortical gyrification in a large sample of children with PAE compared to controls. Relationships between cortical development and intellectual functioning are also examined.

          Experimental design

          Included were 92 children with PAE and 83 controls ages 9–16 from four sites in the Collaborative Initiative on FASD (CIFASD). All PAE participants had documented heavy PAE. All underwent a formal evaluation of physical anomalies and dysmorphic facial features. MRI data were collected using modified matched protocols on three platforms (Siemens, GE, and Philips). Cortical gyrification was examined using a semi-automated procedure.

          Principal observations

          Whole brain group comparisons using Monte Carlo z-simulation for multiple comparisons showed significantly lower cortical gyrification across a large proportion of the cerebral cortex amongst PAE compared to controls. Whole brain comparisons and ROI based analyses showed strong positive correlations between cortical gyrification and IQ (i.e. less developed cortex was associated with lower IQ).

          Conclusions

          Abnormalities in cortical development were seen across the brain in children with PAE compared to controls. Cortical gyrification and IQ were strongly correlated, suggesting that examining mechanisms by which alcohol disrupts cortical formation may yield clinically relevant insights and potential directions for early intervention.

          Highlights

          • Children exposed to alcohol prenatally have widespread abnormalities in the development of cortical gyrification.

          • Abnormally smooth cortex occurs in developmental insults that interfere with cell proliferation and neuronal migration.

          • In FASD, we observed that abnormally smooth cortex was strongly associated with lower IQ.

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          Most cited references57

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          A self-report measure of pubertal status: Reliability, validity, and initial norms.

          Puberty is a central process in the complex set of changes that constitutes the transition from childhood to adolescence. Research on the role of pubertal change in this transition has been impeded by the difficulty of assessing puberty in ways acceptable to young adolescents and others involved. Addressing this problem, this paper describes and presents norms for a selfreport measure of pubertal status. The measure was used twice annually over a period of three years in a longitudinal study of 335 young adolescent boys and girls. Data on a longitudinal subsample of 253 subjects are reported. The scale shows good reliability, as indicated by coefficient alpha. In addition, several sources of data suggest that these reports are valid. The availability of such a measure is important for studies, such as those based in schools, in which more direct measures of puberty may not be possible.
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            Specification of cerebral cortical areas.

            P Rakic (1988)
            How the immense population of neurons that constitute the human cerebral neocortex is generated from progenitors lining the cerebral ventricle and then distributed to appropriate layers of distinctive cytoarchitectonic areas can be explained by the radial unit hypothesis. According to this hypothesis, the ependymal layer of the embryonic cerebral ventricle consists of proliferative units that provide a proto-map of prospective cytoarchitectonic areas. The output of the proliferative units is translated via glial guides to the expanding cortex in the form of ontogenetic columns, whose final number for each area can be modified through interaction with afferent input. Data obtained through various advanced neurobiological techniques, including electron microscopy, immunocytochemistry, [3H]thymidine and receptor autoradiography, retrovirus gene transfer, neural transplants, and surgical or genetic manipulation of cortical development, furnish new details about the kinetics of cell proliferation, their lineage relationships, and phenotypic expression that favor this hypothesis. The radial unit model provides a framework for understanding cerebral evolution, epigenetic regulation of the parcellation of cytoarchitectonic areas, and insight into the pathogenesis of certain cortical disorders in humans.
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              A tension-based theory of morphogenesis and compact wiring in the central nervous system.

              Many structural features of the mammalian central nervous system can be explained by a morphogenetic mechanism that involves mechanical tension along axons, dendrites and glial processes. In the cerebral cortex, for example, tension along axons in the white matter can explain how and why the cortex folds in a characteristic species-specific pattern. In the cerebellum, tension along parallel fibres can explain why the cortex is highly elongated but folded like an accordion. By keeping the aggregate length of axonal and dendritic wiring low, tension should contribute to the compactness of neural circuitry throughout the adult brain.
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                Author and article information

                Contributors
                Journal
                Neuroimage Clin
                Neuroimage Clin
                NeuroImage : Clinical
                Elsevier
                2213-1582
                22 May 2017
                2017
                22 May 2017
                : 15
                : 391-400
                Affiliations
                [a ]University of Minnesota, Twin Cities, United States
                [b ]Children's Hospital of Los Angeles, University of Southern California, United States
                [c ]San Diego State University, United States
                [d ]Emory University, United States
                [e ]University of California, San Diego, United States
                Author notes
                [* ]Corresponding author at: Department of Psychiatry, University of Minnesota, F282/2A West, 2450 Riverside Ave., Minneapolis, MN 55454, United States.Department of PsychiatryUniversity of MinnesotaF282/2A West, 2450 Riverside Ave.MinneapolisMN55454United States jwozniak@ 123456umn.edu
                Article
                S2213-1582(17)30120-1
                10.1016/j.nicl.2017.05.015
                5447653
                28580296
                48bbe017-917a-4a88-bc55-4f22303c6325
                © 2017 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 17 November 2016
                : 18 April 2017
                : 21 May 2017
                Categories
                Regular Article

                fetal alcohol (fas, fasd),brain,mri,cortex,neuropsychology
                fetal alcohol (fas, fasd), brain, mri, cortex, neuropsychology

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