• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

自然流产胚胎中亚甲基四氢叶酸还原酶(MTHFR C677T和A1298C)的流行基因型。

Prevalent genotypes of methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) in spontaneously aborted embryos.

作者信息

Bae Jeehyeon, Shin Seung Joo, Cha Sun Hee, Choi Dong Hee, Lee Suman, Kim Nam Keun

机构信息

Institute for Clinical Research, Bundang CHA General Hospital, College of Medicine, Seongnam, South Korea.

出版信息

Fertil Steril. 2007 Feb;87(2):351-5. doi: 10.1016/j.fertnstert.2006.06.027. Epub 2006 Nov 13.

DOI:10.1016/j.fertnstert.2006.06.027
PMID:17094971
Abstract

OBJECTIVE

To assess prevalent 5,10-methylenetetrahydrofolate reductase (MTHFR) polymorphisms in spontaneously aborted embryos.

DESIGN

A retrospectively analyzed, prospectively obtained database.

SETTING

Bundang CHA General Hospital and Kangnam CHA Hospital.

PATIENT(S): Ninety-four spontaneously aborted embryos at <20 weeks of gestational age.

INTERVENTION(S): None.

MAIN OUTCOME MEASURE

Genotype frequency of MTHFR C677T and A1298C polymorphisms in spontaneously aborted embryos.

RESULT(S): The aborted embryos exhibited both a significantly high frequency of the MTHFR 677CC genotype and a low frequency of the MTHFR 677CT genotype, compared to both the child and the adult control groups, respectively, whereas no significant change in the fetal MTHFR A1298C genotype frequency was observed. The combinative genotype of MTHFR 677CC/1298AC from the abortus had a high prevalence compared to the child controls. Further, the chromosomal integrity of the abortus did not affect the frequency of the MTHFR 677CC and 1298AC genotypes.

CONCLUSION

Spontaneously aborted embryos have a unique distribution of MTHFR C677T and A1289C polymorphisms, regardless of their chromosomal integrity.

摘要

目的

评估自然流产胚胎中5,10-亚甲基四氢叶酸还原酶(MTHFR)基因多态性的流行情况。

设计

一项回顾性分析的前瞻性获取数据库。

地点

盆唐CHA综合医院和江南CHA医院。

患者

94例孕龄小于20周的自然流产胚胎。

干预措施

无。

主要观察指标

自然流产胚胎中MTHFR C677T和A1298C基因多态性的基因型频率。

结果

与儿童和成人对照组相比,流产胚胎中MTHFR 677CC基因型频率显著较高,而MTHFR 677CT基因型频率较低,而胎儿MTHFR A1298C基因型频率未观察到显著变化。与儿童对照组相比,流产胚胎中MTHFR 677CC/1298AC的联合基因型患病率较高。此外,流产胚胎的染色体完整性不影响MTHFR 677CC和1298AC基因型的频率。

结论

自然流产胚胎具有独特的MTHFR C677T和A1289C基因多态性分布,与染色体完整性无关。

相似文献

1
Prevalent genotypes of methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) in spontaneously aborted embryos.自然流产胚胎中亚甲基四氢叶酸还原酶(MTHFR C677T和A1298C)的流行基因型。
Fertil Steril. 2007 Feb;87(2):351-5. doi: 10.1016/j.fertnstert.2006.06.027. Epub 2006 Nov 13.
2
Increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos.自然流产胚胎中亚甲基四氢叶酸还原酶C677T和A1298C突变等位基因联合出现的频率增加。
Eur J Hum Genet. 2002 Feb;10(2):113-8. doi: 10.1038/sj.ejhg.5200767.
3
Influence of combined methylenetetrahydrofolate reductase (MTHFR) and thymidylate synthase enhancer region (TSER) polymorphisms to plasma homocysteine levels in Korean patients with recurrent spontaneous abortion.亚甲基四氢叶酸还原酶(MTHFR)与胸苷酸合成酶增强子区域(TSER)基因多态性联合对韩国复发性自然流产患者血浆同型半胱氨酸水平的影响
Thromb Res. 2006;117(6):653-8. doi: 10.1016/j.thromres.2005.05.025. Epub 2005 Jun 27.
4
Polymorphisms of 5,10-methylenetetrahydrofolate reductase and risk of stomach cancer in a Korean population.韩国人群中5,10-亚甲基四氢叶酸还原酶多态性与胃癌风险
Anticancer Res. 2005 May-Jun;25(3B):2249-52.
5
Methylenetetrahydrofolate reductase gene, homocysteine and coronary artery disease: the A1298C polymorphism does matter. Inferences from a case study (Madeira, Portugal).亚甲基四氢叶酸还原酶基因、同型半胱氨酸与冠状动脉疾病:A1298C多态性至关重要。一项病例研究(葡萄牙马德拉岛)的推论
Thromb Res. 2008;122(5):648-56. doi: 10.1016/j.thromres.2008.02.005. Epub 2008 Apr 1.
6
Genotypes of the C677T and A1298C polymorphisms of the MTHFR gene as a cause of human spontaneous embryo loss.MTHFR基因C677T和A1298C多态性的基因型作为人类自然胚胎丢失的一个原因。
Hum Reprod. 2007 Dec;22(12):3249-54. doi: 10.1093/humrep/dem337. Epub 2007 Oct 25.
7
Association of the 5,10-methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) polymorphisms in Korean patients with adult acute lymphoblastic leukemia.韩国成人急性淋巴细胞白血病患者中5,10-亚甲基四氢叶酸还原酶(MTHFR C677T和A1298C)基因多态性的关联研究
Anticancer Res. 2007 Sep-Oct;27(5A):3419-24.
8
Methylenetetrahydrofolate reductase C677T polymorphism and the risk of unexplained recurrent pregnancy loss: a meta-analysis.亚甲基四氢叶酸还原酶C677T多态性与不明原因复发性流产的风险:一项荟萃分析。
Fertil Steril. 2006 Dec;86(6):1716-22. doi: 10.1016/j.fertnstert.2006.05.052. Epub 2006 Oct 30.
9
[C677T and A1298C mutation of the methylenetetrahydrofolate reductase gene in unexplained recurrent spontaneous abortion].不明原因复发性自然流产中甲基四氢叶酸还原酶基因的C677T和A1298C突变
Zhonghua Fu Chan Ke Za Zhi. 2004 Apr;39(4):238-41.
10
Association of the C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene with schizophrenia: association is significant in men but not in women.亚甲基四氢叶酸还原酶基因C677T和A1298C多态性与精神分裂症的关联:该关联在男性中显著,但在女性中不显著。
Prog Neuropsychopharmacol Biol Psychiatry. 2005 Sep;29(7):1113-23. doi: 10.1016/j.pnpbp.2005.06.022.

引用本文的文献

1
3'-UTR Polymorphisms in the Vascular Endothelial Growth Factor Gene (VEGF) Contribute to Susceptibility to Recurrent Pregnancy Loss (RPL).3'UTR 多态性在血管内皮生长因子基因(VEGF)中与复发性妊娠丢失(RPL)的易感性有关。
Int J Mol Sci. 2019 Jul 5;20(13):3319. doi: 10.3390/ijms20133319.
2
Genetic Variation of Methylenetetrahydrofolate Reductase (MTHFR) and Thymidylate Synthase (TS) Genes Is Associated with Idiopathic Recurrent Implantation Failure.亚甲基四氢叶酸还原酶(MTHFR)和胸苷酸合成酶(TS)基因的遗传变异与特发性反复种植失败相关。
PLoS One. 2016 Aug 25;11(8):e0160884. doi: 10.1371/journal.pone.0160884. eCollection 2016.
3
Polymorphisms in the MTHFR gene influence embryo viability and the incidence of aneuploidy.
MTHFR 基因多态性影响胚胎活力和非整倍体发生率。
Hum Genet. 2016 May;135(5):555-568. doi: 10.1007/s00439-016-1652-z. Epub 2016 Apr 11.
4
MTHFR C677T and A1298C Genotypes and Haplotypes in Slovenian Couples with Unexplained Infertility Problems and in Embryonic Tissues from Spontaneous Abortions.斯洛文尼亚患有不明原因不孕问题的夫妇以及自然流产胚胎组织中的亚甲基四氢叶酸还原酶(MTHFR)C677T和A1298C基因型与单倍型
Balkan J Med Genet. 2013 Jun;16(1):31-40. doi: 10.2478/bjmg-2013-0015.
5
Association of methylenetetrahydrofolate reductase (MTHFR 677C>T and 1298A>C) polymorphisms and haplotypes with silent brain infarction and homocysteine levels in a Korean population.亚甲基四氢叶酸还原酶(MTHFR 677C>T 和 1298A>C)多态性及单体型与韩国人群无症状性脑梗死及同型半胱氨酸水平的相关性。
Yonsei Med J. 2010 Mar;51(2):253-60. doi: 10.3349/ymj.2010.51.2.253. Epub 2010 Feb 12.
6
Methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms resulting in suboptimal oocyte maturation: a discussion of folate status, neural tube defects, schizophrenia, and vasculopathy.亚甲基四氢叶酸还原酶(MTHFR)基因多态性导致卵母细胞成熟欠佳:关于叶酸状态、神经管缺陷、精神分裂症和血管病变的讨论
J Exp Clin Assist Reprod. 2008 Jul 10;5:5. doi: 10.1186/1743-1050-5-5.