• 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

稽留流产患者母体甲基四氢叶酸还原酶基因突变

Maternal methyltetrahydrofolate reductase gene mutation in patients with missed abortions.

作者信息

Rady Helmy A

机构信息

Obst. & Gyn. Department, Faculty of Medicine, University of Alexandria, Alexandria, Egypt.

出版信息

J Taibah Univ Med Sci. 2017 Jul 14;13(1):93-96. doi: 10.1016/j.jtumed.2017.04.004. eCollection 2018 Feb.

DOI:10.1016/j.jtumed.2017.04.004
PMID:31435309
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6695003/
Abstract

BACKGROUND

Missed abortions are a common problem, often caused by thrombophilia in both recurring and non-recurring cases.

AIM

To determine whether the presence of a mutation in the methyltetrahydrofolate reductase () gene correlates with missed abortions.

PATIENTS AND METHODS

We selected two hundred patients for this study in two groups: the study group, which consisted of one hundred patients with a history of missed abortion; and the control group, which consisted of one hundred patients with no history of missed abortion.

RESULTS

Of the 200 patients, mutations in were only found in forty-four patients-thirty-four from the study group and ten from the control group.

CONCLUSIONS

gene mutation is a common cause of both recurring and non-recurring missed abortions.

摘要

背景

稽留流产是一个常见问题,在复发性和非复发性病例中通常由血栓形成倾向引起。

目的

确定亚甲基四氢叶酸还原酶()基因突变的存在是否与稽留流产相关。

患者与方法

我们将200名患者分为两组进行本研究:研究组,由100名有稽留流产病史的患者组成;对照组,由100名无稽留流产病史的患者组成。

结果

在200名患者中,仅在44名患者中发现了突变——研究组34名,对照组10名。

结论

基因突变是复发性和非复发性稽留流产的常见原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/880d/6695003/f62ed658a6e7/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/880d/6695003/f62ed658a6e7/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/880d/6695003/f62ed658a6e7/gr1.jpg

相似文献

1
Maternal methyltetrahydrofolate reductase gene mutation in patients with missed abortions.稽留流产患者母体甲基四氢叶酸还原酶基因突变
J Taibah Univ Med Sci. 2017 Jul 14;13(1):93-96. doi: 10.1016/j.jtumed.2017.04.004. eCollection 2018 Feb.
2
[Molecular diagnostic tests for thrombophilia in patients referred to genetic counseling clinic because due to recurrent pregnancy failure. One center's experience].[因复发性流产转诊至遗传咨询门诊患者的血栓形成倾向分子诊断检测。一家中心的经验]
Ginekol Pol. 2012 Mar;83(3):178-82.
3
The structure of immunocompetent decidual cells in recurrent missed abortions.复发性流产中免疫活性蜕膜细胞的结构
Vojnosanit Pregl. 2016 Apr;73(4):306-11. doi: 10.2298/VSP141226018R.
4
Evaluation of chromosomal abnormalities and common trombophilic mutations in cases with recurrent miscarriage.复发性流产病例中染色体异常和常见易栓症突变的评估
Afr Health Sci. 2014 Mar;14(1):216-22. doi: 10.4314/ahs.v14i1.34.
5
Inherited thrombophilia with recurrent pregnancy loss in Turkish women--a real phenomenon?土耳其女性中遗传性易栓症与复发性流产——一种真实存在的现象?
Ginekol Pol. 2012 Aug;83(8):598-603.
6
Paternal thrombophilic gene mutations are not associated with recurrent miscarriage.父系血栓形成倾向基因突变与复发性流产无关。
Am J Reprod Immunol. 2008 Oct;60(4):325-32. doi: 10.1111/j.1600-0897.2008.00630.x.
7
Thrombophilic gene mutations and recurrent spontaneous abortion: prothrombin mutation increases the risk in the first trimester.
Am J Reprod Immunol. 2001 Aug;46(2):124-31. doi: 10.1111/j.8755-8920.2001.460202.x.
8
How many missed abortions are caused by embryonic chromosomal abnormalities and what are their risk factors?有多少稽留流产是由胚胎染色体异常引起的,其危险因素有哪些?
Front Genet. 2023 Jan 4;13:1058261. doi: 10.3389/fgene.2022.1058261. eCollection 2022.
9
Effects of inherited thrombophilia in women with recurrent pregnancy loss.遗传性血栓形成倾向对复发性流产女性的影响。
Clin Exp Obstet Gynecol. 2011;38(4):347-50.
10
Methyltetrahydrofolate vs Folic Acid Supplementation in Idiopathic Recurrent Miscarriage with Respect to Methylenetetrahydrofolate Reductase C677T and A1298C Polymorphisms: A Randomized Controlled Trial.亚甲基四氢叶酸还原酶C677T和A1298C基因多态性相关的特发性复发性流产中甲基四氢叶酸与叶酸补充剂的比较:一项随机对照试验
PLoS One. 2015 Dec 2;10(12):e0143569. doi: 10.1371/journal.pone.0143569. eCollection 2015.

引用本文的文献

1
Exome sequencing identified novel variants in three Chinese patients with 5,10-methenyltetrahydrofolate synthetase deficiency.外显子组测序在三名患有5,10-亚甲基四氢叶酸合成酶缺乏症的中国患者中鉴定出了新的变异。
Front Genet. 2023 Sep 18;14:1236849. doi: 10.3389/fgene.2023.1236849. eCollection 2023.

本文引用的文献

1
Polymorphisms in the methylene tetrahydrofolate reductase and methionine synthase reductase genes and their correlation with unexplained recurrent spontaneous abortion susceptibility.亚甲基四氢叶酸还原酶和甲硫氨酸合酶还原酶基因多态性及其与不明原因复发性自然流产易感性的相关性。
Genet Mol Res. 2015 Jul 28;14(3):8500-8. doi: 10.4238/2015.July.28.19.
2
Multiple Inherited Thrombophilic Gene Polymorphisms in Spontaneous Abortions in Turkish Population.土耳其人群自然流产中多种遗传性血栓形成倾向基因多态性
Int J Mol Cell Med. 2015 Spring;4(2):120-7.
3
Metabolism and gene polymorphisms of the folate pathway in Brazilian women with history of recurrent abortion.
Rev Bras Ginecol Obstet. 2015 Feb;37(2):71-6. doi: 10.1590/SO100-720320140005223. Epub 2015 Feb 1.
4
Association between thrombophilia and the post-thrombotic syndrome: a systematic review and meta-analysis.血栓形成倾向与血栓后综合征的关系:系统评价和荟萃分析。
J Thromb Haemost. 2014 Jan;12(1):14-23. doi: 10.1111/jth.12447.
5
Cognitive behavior therapy for psychological distress in patients with recurrent miscarriage.认知行为疗法治疗复发性流产患者的心理困扰。
Psychol Res Behav Manag. 2013 Jul 19;6:37-43. doi: 10.2147/PRBM.S44327. Print 2013.
6
MTHFR C677T polymorphism, folate, vitamin B12 and homocysteine in recurrent pregnancy losses: a case control study among North Indian women.亚甲基四氢叶酸还原酶 C677T 多态性、叶酸、维生素 B12 和同型半胱氨酸与复发性流产的关系:一项在印度北部妇女中进行的病例对照研究。
J Perinat Med. 2013 Sep 1;41(5):549-54. doi: 10.1515/jpm-2012-0252.
7
Association of maternal and fetal MTHFR A1298C polymorphism with the risk of pregnancy loss: a study of an Indian population and a meta-analysis.母体和胎儿 MTHFR A1298C 多态性与妊娠丢失风险的关联:一项印度人群研究和荟萃分析。
Fertil Steril. 2013 Apr;99(5):1311-1318.e4. doi: 10.1016/j.fertnstert.2012.12.027. Epub 2013 Jan 26.
8
Association study between methylenetetrahydrofolate reductase polymorphisms and unexplained recurrent pregnancy loss: a meta-analysis.亚甲基四氢叶酸还原酶多态性与不明原因复发性妊娠丢失的相关性:荟萃分析。
Gene. 2013 Feb 10;514(2):105-11. doi: 10.1016/j.gene.2012.10.091. Epub 2012 Nov 29.
9
Plasma homocysteine and vitamin B12 serum levels, red blood cell folate concentrations, C677T methylenetetrahydrofolate reductase gene mutation and risk of recurrent miscarriage: a case-control study in Spain.血浆同型半胱氨酸和维生素 B12 血清水平、红细胞叶酸浓度、亚甲基四氢叶酸还原酶 C677T 基因突变与复发性流产的关系:西班牙的一项病例对照研究。
Clin Chem Lab Med. 2013 Mar 1;51(3):693-9. doi: 10.1515/cclm-2012-0452.
10
Placental vasculature in health and disease.胎盘血管在健康和疾病中的作用。
Semin Thromb Hemost. 2010 Apr;36(3):309-20. doi: 10.1055/s-0030-1253453. Epub 2010 May 20.