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

IF 1.1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Nucleosides, Nucleotides & Nucleic Acids Pub Date : 2024-11-01 DOI:10.1080/15257770.2024.2421302
Fulya Doğaner, Ahu Soyocak, Didem Turgut Coşan, Merih Özgen, Funda Berkan, Fezan Şahin Mutlu, İrfan Değirmenci, Hasan Veysi Güneş
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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 (p = 0.249, p = 0.754), while A1298C genotype and allele frequency distributions were found to be statistically significant (p = 0.002, p = 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.

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患有骨质疏松症的土耳其绝经后妇女的亚甲基四氢叶酸还原酶(MTHFR)C677T 和 A1298C 多态性。
骨质疏松症是一种常见的与年龄有关的骨骼疾病,其特点是骨组织的微观结构发生变化和骨量减少,尤其影响绝经后妇女。影响骨代谢的遗传和环境因素在骨质疏松症的发病中起着一定的作用。亚甲基四氢叶酸还原酶(MTHFR)是一种参与将同型半胱氨酸转化为蛋氨酸的重要酶。MTHFR 基因的遗传变异会导致这种酶的功能受损或失活。MTHFR 酶活性的降低和同型半胱氨酸水平的升高会影响骨代谢。本研究旨在调查土耳其绝经后妇女的 C677T 和 A1298C 多态性与骨质疏松症之间的关系。我们从 200 名志愿者身上提取了 DNA 样本。采用 PCR-RFLP 技术鉴定 MTHFR 基因多态性 C677T 和 A1298C。对分析结果的统计学意义进行了评估。绝经后骨质疏松症组和健康对照组的 C677T 基因型和等位基因频率分布无统计学差异(p = 0.249,p = 0.754),而 A1298C 基因型和等位基因频率分布有统计学意义(p = 0.002,p = 0.013)。我们的研究结果表明,在这一特定人群中,A1298C 多态性可能是与骨质疏松症相关的遗传因素。然而,C677T 多态性并没有显示出明显的联系。为了更全面地了解骨质疏松症的遗传基础,今后的研究必须扩大样本量,并考虑更多的遗传和环境因素。此外,考虑种族差异、基因与基因之间的相互作用以及基因与环境之间的相互作用也至关重要。这些见解可为针对不同人群中的骨质疏松症高危个体制定个性化预防和治疗策略提供参考。
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来源期刊
Nucleosides, Nucleotides & Nucleic Acids
Nucleosides, Nucleotides & Nucleic Acids 生物-生化与分子生物学
CiteScore
2.60
自引率
7.70%
发文量
91
审稿时长
6 months
期刊介绍: Nucleosides, Nucleotides & Nucleic Acids publishes research articles, short notices, and concise, critical reviews of related topics that focus on the chemistry and biology of nucleosides, nucleotides, and nucleic acids. Complete with experimental details, this all-inclusive journal emphasizes the synthesis, biological activities, new and improved synthetic methods, and significant observations related to new compounds.
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