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      Environmental Risk Factors in Han and Uyghur Children with Dyslexia: A Comparative Study

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          Abstract

          Background

          Several studies have been conducted to explore risk factors for dyslexia. However, most studies examining dyslexia have been skewed toward Western countries, and few have considered two nationalities simultaneously. This study focused on differences in dyslexia prevalence and potential environmental risk factors between Han and Uyghur children.

          Methods

          A cross-sectional study was conducted in Kashgar and Aksu, cities in Xinjiang province, China. A two-stage sampling strategy was used to recruit 2,854 students in grades 3–6 from 5 primary schools in 5 districts; 2,348 valid student questionnaires were included in the analysis. Dyslexia checklists for Chinese and Uyghur children and pupil rating scales were used to identify children with dyslexia. Questions related to the home literacy environment and reading ability were used to evaluate potential environmental risk factors. Single factor analysis and multivariate logistic regression were used to examine prevalence and risk factors for dyslexia.

          Results

          Dyslexia prevalence differed significantly between Han (3.9%) and Uyghur (7.0%) children ( P < 0.05), and the boy-to-girl diagnosis ratio was almost 2:1. Multiple logistic regression analysis showed that ethnic differences in dyslexia prevalence between Han and Uyghur children could have occurred because of factors such as mother’s occupation ( P = 0.02, OR = 0.04, 95% CI = 0.01–0.68) and the frequency with which parents told stories ( P = 0.00, OR = 4.50, 95% CI = 1.67–12.11).

          Conclusions

          The prevalence of dyslexia was high in all children, particularly those in the Uyghur group. Environmental factors could have been responsible for some of the differences observed. The results contribute to the early identification and management of dyslexia in children from these two groups and research examining developmental dyslexia and differences in racial genetics.

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          Most cited references18

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          Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.

          Linkage between developmental dyslexia (DD) and chromosome 6p has been replicated in a number of independent samples. Recent attempts to identify the gene responsible for the linkage have produced inconsistent evidence for association of DD with a number of genes in a 575-kb region of chromosome 6p22.2, including VMP, DCDC2, KIAA0319, TTRAP, and THEM2. We aimed to identify the specific gene or genes involved by performing a systematic, high-density (approximately 2-3-kb intervals) linkage disequilibrium screen of these genes in an independent sample, incorporating family-based and case-control designs in which dyslexia was defined as an extreme representation of reading disability. Using DNA pooling, we first observed evidence for association with 17 single-nucleotide polymorphisms (SNPs), 13 of which were located in the KIAA0319 gene (P<.01-.003). After redundant SNPs were excluded, 10 SNPs were individually genotyped in 223 subjects with DD and 273 controls. Those SNPs that were significant at P
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            Analysis of genomic admixture in Uyghur and its implication in mapping strategy.

            The Uyghur (UIG) population, settled in Xinjiang, China, is a population presenting a typical admixture of Eastern and Western anthropometric traits. We dissected its genomic structure at population level, individual level, and chromosome level by using 20,177 SNPs spanning nearly the entire chromosome 21. Our results showed that UIG was formed by two-way admixture, with 60% European ancestry and 40% East Asian ancestry. Overall linkage disequilibrium (LD) in UIG was similar to that in its parental populations represented in East Asia and Europe with regard to common alleles, and UIG manifested elevation of LD only within 500 kb and at a level of 0.1
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              A theoretical molecular network for dyslexia: integrating available genetic findings.

              Developmental dyslexia is a common specific childhood learning disorder with a strong heritable component. Previous studies using different genetic approaches have identified several genetic loci and candidate genes for dyslexia. In this article, we have integrated the current knowledge on 14 dyslexia candidate genes suggested by cytogenetic findings, linkage and association studies. We found that 10 of the 14 dyslexia candidate genes (ROBO1, KIAA0319, KIAA0319L, S100B, DOCK4, FMR1, DIP2A, GTF2I, DYX1C1 and DCDC2) fit into a theoretical molecular network involved in neuronal migration and neurite outgrowth. Based on this, we also propose three novel dyslexia candidate genes (SLIT2, HMGB1 and VAPA) from known linkage regions, and we discuss the possible involvement of genes emerging from the two reported genome-wide association studies for reading impairment-related phenotypes in the identified network.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                14 July 2016
                2016
                : 11
                : 7
                : e0159042
                Affiliations
                [1 ]Medical School, University of Shihezi, Xinjiang, China
                [2 ]Medical School, Quzhou College of Technology, Zhejiang, China
                University of Perugia, ITALY
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: HZ XPZ. Performed the experiments: HZ XPZ YC BPZ. Analyzed the data: HZ XPZ. Contributed reagents/materials/analysis tools: XZ. Wrote the paper: HZ.

                Author information
                http://orcid.org/0000-0001-7881-8644
                Article
                PONE-D-15-46183
                10.1371/journal.pone.0159042
                4944905
                27416106
                4c99e230-1e40-49d9-8d4e-7e7dbb0a3f26
                © 2016 Zhao et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 21 October 2015
                : 19 May 2016
                Page count
                Figures: 1, Tables: 3, Pages: 15
                Funding
                Funded by: The National Natural Science Foundation of China
                Award ID: 81360434
                Award Recipient : Xiang Peng Zuo
                The National Natural Science Foundation of China Project No. 81360434.
                Categories
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