• 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

相似文献

1
Correlation of MTHFR C677T Polymorphism with Male Infertility among Indian Population: Case-Control Study.印度人群中MTHFR基因C677T多态性与男性不育的相关性:病例对照研究
J Pharm Bioallied Sci. 2024 Jul;16(Suppl 3):S2809-S2814. doi: 10.4103/jpbs.jpbs_207_24. Epub 2024 Jul 18.
2
MTHFR A1298C polymorphism and idiopathic male infertility.亚甲基四氢叶酸还原酶A1298C基因多态性与特发性男性不育症
J Postgrad Med. 2010 Oct-Dec;56(4):267-9. doi: 10.4103/0022-3859.70935.
3
Methylenetetrahydrofolate reductase C677T polymorphism is not associated with male infertility in a South Indian population.亚甲基四氢叶酸还原酶 C677T 多态性与南印度人群男性不育症无关。
Andrologia. 2012 May;44 Suppl 1:252-9. doi: 10.1111/j.1439-0272.2011.01172.x. Epub 2011 Jul 6.
4
Role of 677C→T polymorphism a single substitution in methylenetetrahydrofolate reductase (MTHFR) gene in North Indian infertile men.677C→T多态性(亚甲基四氢叶酸还原酶(MTHFR)基因中的一个单碱基替换)在北印度不育男性中的作用。
Mol Biol Rep. 2014 Feb;41(2):573-9. doi: 10.1007/s11033-013-2894-7. Epub 2013 Dec 24.
5
MTHFR-c 677C>T polymorphism and male infertility: An analysis in a cohort of Pakistani men.亚甲基四氢叶酸还原酶(MTHFR)基因c.677C>T多态性与男性不育:巴基斯坦男性队列研究分析
Rev Int Androl. 2022 Oct-Dec;20(4):274-280. doi: 10.1016/j.androl.2021.05.001. Epub 2022 Aug 2.
6
Association of the C677T (rs1801133) polymorphism with idiopathic male infertility in a local Pakistani population.巴基斯坦当地人群中C677T(rs1801133)基因多态性与特发性男性不育的关联
Balkan J Med Genet. 2016 Aug 2;19(1):51-62. doi: 10.1515/bjmg-2016-0007. eCollection 2016 Jul 1.
7
Methylenetetrahydrofolate reductase C677T polymorphism is associated with increased risk of coronary artery disease in young South African Indians.亚甲基四氢叶酸还原酶C677T基因多态性与南非年轻印度裔人群患冠状动脉疾病的风险增加有关。
Gene. 2015 Oct 15;571(1):28-32. doi: 10.1016/j.gene.2015.06.044. Epub 2015 Jun 18.
8
MTHFR C677T predisposes to POAG but not to PACG in a North Indian population: a case control study.在北印度人群中,亚甲基四氢叶酸还原酶(MTHFR)C677T基因多态性易导致原发性开角型青光眼(POAG),而非原发性闭角型青光眼(PACG):一项病例对照研究。
PLoS One. 2014 Jul 23;9(7):e103063. doi: 10.1371/journal.pone.0103063. eCollection 2014.
9
Association of C677T transition of the human methylenetetrahydrofolate reductase (MTHFR) gene with male infertility.人类亚甲基四氢叶酸还原酶(MTHFR)基因C677T突变与男性不育的相关性
Reprod Fertil Dev. 2016 Apr;28(6):785-94. doi: 10.1071/RD14186.
10
Prospective study of MTHFR genetic polymorphisms as a possible etiology of male infertility.MTHFR基因多态性作为男性不育可能病因的前瞻性研究。
Genet Mol Res. 2014 Mar 24;13(3):6367-74. doi: 10.4238/2014.March.24.26.

引用本文的文献

1
MTHFR Gene Polymorphisms: A Single Gene with Wide-Ranging Clinical Implications-A Review.亚甲基四氢叶酸还原酶基因多态性:一个具有广泛临床意义的单基因——综述
Genes (Basel). 2025 Apr 8;16(4):441. doi: 10.3390/genes16040441.

本文引用的文献

1
Associations of C677T polymorphism in methylenetetrahydrofolate reductase (MTHFR) gene with male infertility risk: A meta-analysis.亚甲基四氢叶酸还原酶(MTHFR)基因C677T多态性与男性不育风险的关联:一项荟萃分析。
Eur J Obstet Gynecol Reprod Biol. 2017 May;212:101-109. doi: 10.1016/j.ejogrb.2017.03.004. Epub 2017 Mar 4.
2
Short-term FSH treatment and sperm maturation: a prospective study in idiopathic infertile men.短期促卵泡激素治疗与精子成熟:一项针对特发性不育男性的前瞻性研究。
Andrology. 2017 May;5(3):414-422. doi: 10.1111/andr.12333. Epub 2017 Mar 15.
3
Association of the C677T (rs1801133) polymorphism with idiopathic male infertility in a local Pakistani population.巴基斯坦当地人群中C677T(rs1801133)基因多态性与特发性男性不育的关联
Balkan J Med Genet. 2016 Aug 2;19(1):51-62. doi: 10.1515/bjmg-2016-0007. eCollection 2016 Jul 1.
4
Microarray Technology for the Diagnosis of Fetal Chromosomal Aberrations: Which Platform Should We Use?用于诊断胎儿染色体畸变的微阵列技术:我们应使用哪个平台?
J Clin Med. 2014 Jun 20;3(2):663-78. doi: 10.3390/jcm3020663.
5
Association between genetic polymorphisms in folate-related enzyme genes and infertile men with non-obstructive azoospermia.叶酸相关酶基因多态性与非梗阻性无精子症不育男性之间的关联。
Syst Biol Reprod Med. 2015;61(5):286-92. doi: 10.3109/19396368.2015.1049752. Epub 2015 Jul 21.
6
DNA fragmentation in brighter sperm predicts male fertility independently from age and semen parameters.精子发光度中的DNA碎片化独立于年龄和精液参数可预测男性生育能力。
Fertil Steril. 2015 Sep;104(3):582-90.e4. doi: 10.1016/j.fertnstert.2015.06.005. Epub 2015 Jul 4.
7
FSH treatment of male idiopathic infertility improves pregnancy rate: a meta-analysis.FSH 治疗男性特发性不育症可提高妊娠率:一项荟萃分析。
Endocr Connect. 2015 Sep;4(3):R46-58. doi: 10.1530/EC-15-0050. Epub 2015 Jun 25.
8
Association study of folate-related enzymes (MTHFR, MTR, MTRR) genetic variants with non-obstructive male infertility in a Polish population.波兰人群中叶酸相关酶(MTHFR、MTR、MTRR)基因变异与非梗阻性男性不育的关联研究。
Genet Mol Biol. 2015 Mar;38(1):42-7. doi: 10.1590/S1415-475738120140179. Epub 2014 Mar 17.
9
Lack of association between genetic polymorphisms in three folate-related enzyme genes and male infertility in the Chinese population.中国人群中三个叶酸相关酶基因的遗传多态性与男性不育之间无关联。
J Assist Reprod Genet. 2015 Mar;32(3):369-74. doi: 10.1007/s10815-014-0423-9. Epub 2015 Jan 13.
10
The relationship between methylenetetrahydrofolate reductase c.677TT genotype and oligozoospermia in infertile male patients living in the Trakya region of Turkey.土耳其特拉凯地区不育男性患者亚甲基四氢叶酸还原酶c.677TT基因型与少精子症的关系。
Andrologia. 2015 Nov;47(9):1068-74. doi: 10.1111/and.12380. Epub 2014 Nov 26.

印度人群中MTHFR基因C677T多态性与男性不育的相关性:病例对照研究

Correlation of MTHFR C677T Polymorphism with Male Infertility among Indian Population: Case-Control Study.

作者信息

More Akash, Anjankar Namrata, Shrivastava Jarul, Nair Nancy, Jadhav Ritesh

机构信息

Clinical Embryology, Acharya Vinoba Bhave Rural Hospital, Datta Meghe Institute of Higher Education and Research, Maharashtra, India.

Clinical Embryology, School of Allied Health Sciences, Datta Meghe Institute of Higher Education and Research, Maharashtra, India.

出版信息

J Pharm Bioallied Sci. 2024 Jul;16(Suppl 3):S2809-S2814. doi: 10.4103/jpbs.jpbs_207_24. Epub 2024 Jul 18.

DOI:10.4103/jpbs.jpbs_207_24
PMID:39346466
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11426628/
Abstract

This case-control study investigated the correlation between male infertility in India and the methylenetetrahydrofolate reductase (MTHFR) C677T variant. Infertile males were utilized as the case group in the study, whereas fertile individuals served as the control group. The C677T polymorphism was genotyped using PCR-RFLP analysis (polymerase chain reaction-restriction fragment length polymorphism). The Chi-square test and odds ratio calculation were implemented in the statistical analysis method for assessing the correlation between the C677T mutation and infertility. The results of this study revealed that the case group (9.4%) had a substantially greater prevalence of the C677T variation than the control group (1.6%). The C677T variation is significantly associated with male infertility by the Chi-square test ( value: 0.006). According to these results, the MTHFR gene›s C677T variation may increase the incidence of male infertility in the Indian population. Additional evaluations were also conducted to investigate the association between the C677T variation and particular infertility indicators. The C677T variation has been demonstrated to have been significantly correlated with a low or missing sperm count (p 0.05). These findings highlight the potential function of the MTHFR gene in reproductive health and advance our understanding of the genetic underpinnings of male infertility. It is encouraged to investigate the underlying mechanisms and additional investigation of the underlying mechanisms and to support the creation of individualized approaches to diagnosing and managing male infertility.

摘要

这项病例对照研究调查了印度男性不育与亚甲基四氢叶酸还原酶(MTHFR)C677T变异之间的相关性。不育男性被用作研究中的病例组,而有生育能力的个体作为对照组。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析对C677T多态性进行基因分型。在统计分析方法中采用卡方检验和比值比计算来评估C677T突变与不育之间的相关性。本研究结果显示,病例组(9.4%)中C677T变异的患病率显著高于对照组(1.6%)。通过卡方检验(值:0.006),C677T变异与男性不育显著相关。根据这些结果,MTHFR基因的C677T变异可能会增加印度人群中男性不育的发生率。还进行了其他评估以研究C677T变异与特定不育指标之间的关联。已证明C677T变异与精子数量少或无精子显著相关(p<0.05)。这些发现突出了MTHFR基因在生殖健康中的潜在作用,并增进了我们对男性不育遗传基础的理解。鼓励对潜在机制进行研究以及进一步调查,并支持制定诊断和管理男性不育的个性化方法。