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卵巢早衰女性中 和 基因变化的评估:一项病例对照研究。 (你提供的原文中“ 和 ”部分内容缺失,请补充完整以便更准确翻译)

Evaluation of the and Gene changes in women with premature ovarian failure: A case-control study.

作者信息

Akhavansales Zhima, Mosadeghmehrjardi Alimohammad, Reza Ashrafzadeh Hamid, Fakhteh Yavari Shadnaz, Taher Tahoori Mohammad, Bitaraf Sani Morteza, Mohammadi Mahnaz, Montazeri Fateme, Ghasemi Nasrin

机构信息

Department of Immunology, Faculty of Medicine, International Campus, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.

Department of Traditional Pharmacy, Faculty of Traditional Medicine, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Int J Reprod Biomed. 2023 Jan 9;20(12):1007-1012. doi: 10.18502/ijrm.v20i12.12561. eCollection 2022 Dec.

DOI:10.18502/ijrm.v20i12.12561
PMID:36819201
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9928975/
Abstract

BACKGROUND

Premature ovarian failure (POF), is menopause occurring before the age of 40, affecting 1-3% of women worldwide. The risk of POF increases with altered immunological parameters such as and genes, which play a fundamental role in embryogenesis and cellular homeostasis.

OBJECTIVE

The study aimed to investigate the potential role of and genes in POF pathogenesis.

MATERIALS AND METHODS

In this case-control study, the polymorphisms of -670A/G and IVS2nt_124A/G apoptotic genes were analyzed in 51 Iranian women suffering from POF, and 61 healthy controls. Isolation of DNA was done using the salting-out method, and genotypic analysis was performed for all the subjects using the polymerase chain reaction-restriction fragment length polymorphism method.

RESULTS

Our results revealed that homozygous -670A/A and G/G, and heterozygous -670A/G are not significantly different between cases and controls (p = 0.99). Also, in different genotyping models of IVS2nt_124, polymorphisms were not related to POF risk (p = 0.23).

CONCLUSION

There is no statistical association between these polymorphisms and POF risk in women referred to genetic counseling clinics.

摘要

背景

卵巢早衰(POF)是指在40岁之前出现的绝经,影响全球1%-3%的女性。POF的风险会随着免疫参数的改变而增加,如 和 基因,这些基因在胚胎发育和细胞稳态中起着重要作用。

目的

本研究旨在探讨 和 基因在POF发病机制中的潜在作用。

材料与方法

在这项病例对照研究中,对51名患有POF的伊朗女性和61名健康对照者分析了凋亡基因-670A/G和IVS2nt_124A/G的多态性。采用盐析法提取DNA,并使用聚合酶链反应-限制性片段长度多态性方法对所有受试者进行基因分型分析。

结果

我们的结果显示,病例组和对照组之间纯合子-670A/A和G/G以及杂合子-670A/G没有显著差异(p = 0.99)。此外,在IVS2nt_124的不同基因分型模型中,多态性与POF风险无关(p = 0.23)。

结论

在前往遗传咨询诊所的女性中,这些多态性与POF风险之间没有统计学关联。

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本文引用的文献

1
Position statement on the diagnosis and management of premature/primary ovarian insufficiency (except Turner Syndrome).关于诊断和管理原发性/早发性卵巢功能不全(特纳综合征除外)的立场声明。
Ann Endocrinol (Paris). 2021 Dec;82(6):555-571. doi: 10.1016/j.ando.2021.09.001. Epub 2021 Sep 8.
2
FAS-670A>G gene polymorphism and the risk of allograft rejection after organ transplantation: a systematic review and meta-analysis.FAS-670A>G基因多态性与器官移植后同种异体移植排斥反应的风险:一项系统评价和荟萃分析。
Blood Res. 2021 Mar 31;56(1):17-25. doi: 10.5045/br.2021.2020201.
3
Investigating the rate of different ovarian response in in vitro fertilization cycles based on estrogen receptor beta +1730 polymorphism: A cross-sectional study.基于雌激素受体β +1730多态性研究体外受精周期中不同卵巢反应率:一项横断面研究。
Int J Reprod Biomed. 2020 Jul 22;18(7):509-516. doi: 10.18502/ijrm.v13i7.7368. eCollection 2020 Jul.
4
Esculentoside A rescues granulosa cell apoptosis and folliculogenesis in mice with premature ovarian failure.海参苷A可挽救卵巢早衰小鼠的颗粒细胞凋亡和卵泡发生。
Aging (Albany NY). 2020 Aug 5;12(17):16951-16962. doi: 10.18632/aging.103609.
5
Intraovarian injection of autologous human mesenchymal stem cells increases estrogen production and reduces menopausal symptoms in women with premature ovarian failure: two case reports and a review of the literature.卵巢内注射自体人间充质干细胞可增加雌激素生成并减轻卵巢早衰女性的更年期症状:两例病例报告及文献综述
J Med Case Rep. 2020 Jul 18;14(1):108. doi: 10.1186/s13256-020-02426-5.
6
Pathways Involved in Premature Ovarian Failure: A Systematic Review of Experimental Studies.涉及卵巢早衰的途径:实验研究的系统评价。
Curr Pharm Des. 2020;26(18):2087-2095. doi: 10.2174/1381612826666200316160145.
7
Identification of a FAS/FASL haplotype associated with endometriosis in Iranian patients.鉴定与伊朗患者子宫内膜异位症相关的 FAS/FASL 单倍型。
Gynecol Endocrinol. 2020 Mar;36(3):261-264. doi: 10.1080/09513590.2019.1655729. Epub 2019 Sep 30.
8
Cell death: a review of the major forms of apoptosis, necrosis and autophagy.细胞死亡:细胞凋亡、坏死和自噬的主要形式综述。
Cell Biol Int. 2019 Jun;43(6):582-592. doi: 10.1002/cbin.11137. Epub 2019 Apr 25.
9
The Roles of Different Stem Cells in Premature Ovarian Failure.不同干细胞在卵巢早衰中的作用
Curr Stem Cell Res Ther. 2020;15(6):473-481. doi: 10.2174/1574888X14666190314123006.
10
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Infect Genet Evol. 2016 Apr;39:92-98. doi: 10.1016/j.meegid.2016.01.013. Epub 2016 Jan 13.