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土耳其绝经后骨质疏松症女性的亚甲基四氢叶酸还原酶(MTHFR)C677T和A1298C基因多态性

Methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms in Turkish postmenopausal women with osteoporosis.

作者信息

Doğaner Fulya, Soyocak Ahu, Turgut Coşan Didem, Özgen Merih, Berkan Funda, Şahin Mutlu Fezan, Değirmenci İrfan, Güneş Hasan Veysi

机构信息

Department of Molecular Biology and Genetics, Faculty of Science and Letters, Aksaray University, Aksaray, Turkiye.

Department of Medical Biology, Faculty of Medicine, Istanbul Aydin University, Istanbul, Turkiye.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2025;44(10):783-792. doi: 10.1080/15257770.2024.2421302. Epub 2024 Nov 1.

Abstract

Osteoporosis is a common age-related skeletal disease, characterized by changes in the microarchitectural structure of bone tissue and decreased bone mass, especially affecting postmenopausal women. Genetic and environmental factors affecting bone metabolism play a role in the development of osteoporosis. Methylenetetrahydrofolate reductase (MTHFR) is an important enzyme involved in the conversion of homocysteine to methionine. Genetic variations in the MTHFR gene lead to impaired function or inactivation of this enzyme. A decrease in MTHFR enzyme activity and an increase in homocysteine levels affect bone metabolism. In this study, we aimed to investigate the relationship between C677T and A1298C polymorphisms and osteoporosis in Turkish postmenopausal women. DNA samples were extracted from 200 volunteers. The PCR-RFLP technique was used to identify the MTHFR gene polymorphisms C677T and A1298C. The statistical significance of the analysis's results was assessed. C677T genotype and allele frequency distributions were not statistically different between postmenopausal osteoporosis and healthy control groups ( = 0.249,  = 0.754), while A1298C genotype and allele frequency distributions were found to be statistically significant ( = 0.002,  = 0.013). The results of our study showed that the A1298C polymorphism may be a genetic factor associated with osteoporosis in this specific population. However, the C677T polymorphism did not show a significant connection. To gain a more comprehensive understanding of the genetic basis of osteoporosis, future research with larger sample sizes and the consideration of additional genetic and environmental factors is essential. Additionally, it is crucial to account for ethnic disparities, gene-gene interactions, and gene-environment interplays. These insights can inform the development of personalized preventive and therapeutic strategies for individuals at risk of osteoporosis in diverse populations.

摘要

骨质疏松症是一种常见的与年龄相关的骨骼疾病,其特征是骨组织微结构变化和骨量减少,尤其影响绝经后女性。影响骨代谢的遗传和环境因素在骨质疏松症的发生发展中起作用。亚甲基四氢叶酸还原酶(MTHFR)是参与同型半胱氨酸转化为甲硫氨酸的一种重要酶。MTHFR基因的遗传变异导致该酶功能受损或失活。MTHFR酶活性降低和同型半胱氨酸水平升高会影响骨代谢。在本研究中,我们旨在调查土耳其绝经后女性中C677T和A1298C多态性与骨质疏松症之间的关系。从200名志愿者中提取DNA样本。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术鉴定MTHFR基因多态性C677T和A1298C。评估分析结果的统计学意义。绝经后骨质疏松症组与健康对照组之间的C677T基因型和等位基因频率分布无统计学差异(=0.249,=0.754),而A1298C基因型和等位基因频率分布具有统计学意义(=0.002,=0.013)。我们的研究结果表明,A1298C多态性可能是该特定人群中与骨质疏松症相关的遗传因素。然而,C677T多态性未显示出显著关联。为了更全面地了解骨质疏松症的遗传基础,未来需要进行更大样本量的研究,并考虑其他遗传和环境因素。此外,考虑种族差异、基因-基因相互作用和基因-环境相互作用至关重要。这些见解可为不同人群中骨质疏松症高危个体制定个性化的预防和治疗策略提供依据。

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