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Polymorphisms in folate-metabolizing genes chromosome damage and risk of Down syndrome in Italian women: identification of key factors using artificial neural networks

机译:意大利女性的叶酸代谢基因多态性染色体损伤和唐氏综合症的风险:使用人工神经网络识别关键因素

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摘要

BackgroundStudies in mothers of Down syndrome individuals (MDS) point to a role for polymorphisms in folate metabolic genes in increasing chromosome damage and maternal risk for a Down syndrome (DS) pregnancy, suggesting complex gene-gene interactions. This study aimed to analyze a dataset of genetic and cytogenetic data in an Italian group of MDS and mothers of healthy children (control mothers) to assess the predictive capacity of artificial neural networks assembled in TWIST system in distinguish consistently these two different conditions and to identify the variables expressing the maximal amount of relevant information to the condition of being mother of a DS child.The dataset consisted of the following variables: the frequency of chromosome damage in peripheral lymphocytes (BNMN frequency) and the genotype for 7 common polymorphisms in folate metabolic genes (MTHFR 677C>T and 1298A>C, MTRR 66A>G, MTR 2756A>G, RFC1 80G>A and TYMS 28bp repeats and 1494 6bp deletion). Data were analysed using TWIST system in combination with supervised artificial neural networks, and a semantic connectivity map.
机译:背景对唐氏综合症患者(MDS)的母亲进行的研究指出,叶酸代谢基因的多态性在增加染色体损伤和唐氏综合症(DS)妊娠的母亲风险中起着重要作用,表明复杂的基因-基因相互作用。这项研究旨在分析意大利MDS组和健康儿童母亲(对照母亲)的遗传和细胞遗传学数据集,以评估在TWIST系统中组装的人工神经网络的预测能力,以始终如一地区分这两种不同情况并确定数据集由以下变量组成:外周淋巴细胞的染色体损伤频率(BNMN频率)和叶酸代谢中7种常见多态性的基因型基因(MTHFR 677C> T和1298A> C,MTRR 66A> G,MTR 2756A> G,RFC1 80G> A和TYMS 28bp重复和1494 6bp缺失)。使用TWIST系统结合监督的人工神经网络和语义连接图来分析数据。

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