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本文引用的文献

1
Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study.口腔面部裂隙与叶酸/一碳单位和维生素A代谢中的基因多态性:全通路关联研究
Genet Epidemiol. 2009 Apr;33(3):247-55. doi: 10.1002/gepi.20376.
2
Folate metabolism and the risk of Down syndrome.叶酸代谢与唐氏综合征风险
Downs Syndr Res Pract. 2008 Oct;12(2):93-7. doi: 10.3104/updates.2051.
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Smarter clustering methods for SNP genotype calling.用于单核苷酸多态性(SNP)基因分型的更智能聚类方法。
Bioinformatics. 2008 Dec 1;24(23):2665-71. doi: 10.1093/bioinformatics/btn509. Epub 2008 Sep 29.
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Estimation and testing for the effect of a genetic pathway on a disease outcome using logistic kernel machine regression via logistic mixed models.通过逻辑混合模型,使用逻辑核机器回归估计和检验遗传通路对疾病结局的影响。
BMC Bioinformatics. 2008 Jun 24;9:292. doi: 10.1186/1471-2105-9-292.
5
The prevalence of folate-remedial MTHFR enzyme variants in humans.人类中可通过补充叶酸纠正的亚甲基四氢叶酸还原酶(MTHFR)酶变体的患病率。
Proc Natl Acad Sci U S A. 2008 Jun 10;105(23):8055-60. doi: 10.1073/pnas.0802813105. Epub 2008 Jun 3.
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Two MTHFR polymorphisms, maternal B-vitamin intake, and CHDs.两种亚甲基四氢叶酸还原酶基因多态性、孕妇B族维生素摄入量与先天性心脏病
Birth Defects Res A Clin Mol Teratol. 2008 Jun;82(6):474-81. doi: 10.1002/bdra.20463.
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Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project.种族、性别与先天性心脏缺陷的发病率:来自国家唐氏综合征项目的报告
Genet Med. 2008 Mar;10(3):173-80. doi: 10.1097/GIM.0b013e3181634867.
8
A powerful and flexible multilocus association test for quantitative traits.一种用于数量性状的强大且灵活的多位点关联检验。
Am J Hum Genet. 2008 Feb;82(2):386-97. doi: 10.1016/j.ajhg.2007.10.010.
9
Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts.叶酸与一碳代谢基因多态性及其与口腔面部裂隙的关联。
Am J Med Genet A. 2008 Feb 15;146A(4):440-9. doi: 10.1002/ajmg.a.32162.
10
Importance of folate-homocysteine homeostasis during early embryonic development.早期胚胎发育过程中叶酸-同型半胱氨酸稳态的重要性。
Clin Chem Lab Med. 2007;45(12):1717-27. doi: 10.1515/CCLM.2007.345.

叶酸代谢途径基因的变异与唐氏综合征患者先天性心脏病风险相关。

Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.

机构信息

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA.

出版信息

Genet Epidemiol. 2010 Sep;34(6):613-23. doi: 10.1002/gepi.20518.

DOI:10.1002/gepi.20518
PMID:20718043
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3378053/
Abstract

Cardiac abnormalities are one of the most common congenital defects observed in individuals with Down syndrome. Considerable research has implicated both folate deficiency and genetic variation in folate pathway genes with birth defects, including both congenital heart defects (CHD) and Down syndrome (DS). Here, we test variation in folate pathway genes for a role in the major DS-associated CHD atrioventricular septal defect (AVSD). In a group of 121 case families (mother, father, and proband with DS and AVSD) and 122 control families (mother, father, and proband with DS and no CHD), tag SNPs were genotyped in and around five folate pathway genes: 5,10-methylenetetrahyrdofolate reductase (MTHFR), methionine synthase (MTR), methionine synthase reductase (MTRR), cystathionine beta-synthase (CBS), and the reduced folate carrier (SLC19A1, RFC1). SLC19A1 was found to be associated with AVSD using a multilocus allele-sharing test. Individual SNP tests also showed nominally significant associations with odds ratios of between 1.34 and 3.78, depending on the SNP and genetic model. Interestingly, all marginally significant SNPs in SLC19A1 are in strong linkage disequilibrium (r(2)> or = 0.8) with the nonsynonymous coding SNP rs1051266 (c.80A>G), which has previously been associated with nonsyndromic cases of CHD. In addition to SLC19A1, the known functional polymorphism MTHFR c.1298A was over-transmitted to cases with AVSD (P=0.05) and under-transmitted to controls (P=0.02). We conclude, therefore, that disruption of the folate pathway contributes to the incidence of AVSD among individuals with DS.

摘要

心脏异常是唐氏综合征患者最常见的先天性缺陷之一。大量研究表明,叶酸缺乏和叶酸途径基因的遗传变异与出生缺陷有关,包括先天性心脏缺陷(CHD)和唐氏综合征(DS)。在这里,我们研究了叶酸途径基因的变异是否与唐氏综合征相关的主要 CHD 房室间隔缺损(AVSD)有关。在 121 个病例家系(母亲、父亲和唐氏综合征伴 AVSD 的先证者)和 122 个对照组家系(母亲、父亲和唐氏综合征无 CHD 的先证者)中,对五个叶酸途径基因(5,10-亚甲基四氢叶酸还原酶(MTHFR)、蛋氨酸合成酶(MTR)、蛋氨酸合成酶还原酶(MTRR)、胱硫醚β-合酶(CBS)和还原型叶酸载体(SLC19A1、RFC1))周围的标签 SNP 进行了基因分型。使用多基因座等位基因共享检验发现 SLC19A1 与 AVSD 相关。个体 SNP 检验也显示出与 odds ratio 之间的名义显著性关联,其比值在 1.34 到 3.78 之间,具体取决于 SNP 和遗传模型。有趣的是,SLC19A1 中所有边缘显著的 SNP 都与非同义编码 SNP rs1051266(c.80A>G)处于强连锁不平衡状态(r²≥0.8),该 SNP 先前与非综合征型 CHD 病例有关。除了 SLC19A1 之外,已知的功能性多态性 MTHFR c.1298A 也向 AVSD 病例过度传递(P=0.05),向对照组传递不足(P=0.02)。因此,我们得出结论,叶酸途径的破坏导致唐氏综合征患者 AVSD 的发生率增加。