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Klotho gene polymorphism as a susceptibility factor for oxidative DNA damage in coronary artery disease

Year 2023, Volume: 27 Issue: 5, 2079 - 2086, 28.06.2025

Abstract

The Klotho protein has been linked to the promotion of cardiovascular health maintenance through its capacity to enhance resistance against oxidative stress, thereby exerting protective effects. The potential involvement of Klotho gene polymorphisms in the regulation of human aging and age-related disorders, including coronary artery disease, chronic renal disease, osteoporosis, and stroke, is under investigation. The objective of our research was to investigate the association between the rs9527025 (Cys370Ser) polymorphism of the Klotho gene and coronary artery calcification, as well as the potential link between the rs9527025 polymorphism and oxidative DNA damage. The study involved a sample of 90 patients who had undergone coronary angiography. The genotyping of Cys370Ser in exon 2 of the Klotho gene was performed using the polymerase chain reaction. The evaluation of oxidative DNA damage was conducted using the alkaline comet test. The findings of the study revealed that there was no statistically significant association between the distribution of alleles in the Klotho SNPs and the occurrence of coronary artery disorders. In the meantime, the total comet score frequency was significantly associated with the rs9527025 polymorphism. The results of our study indicate that Klotho gene variants, particularly the C370S polymorphism (rs9527025), might play a role in influencing oxidative DNA damage in age-related diseases, such as coronary artery disease. In consequence, larger studies are required to confirm the association between Klotho deficiency and the progression of cardiovascular disease in order to elucidate risk factors for coronary artery disease and develop potential therapeutic strategies.

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There are 25 citations in total.

Details

Primary Language English
Subjects Pharmaceutical Toxicology
Journal Section Articles
Authors

Seher Karslı 0000-0002-4036-0399

Selma Yazar 0000-0003-2626-4066

Mehmet Karaca 0000-0001-8771-0539

Türkan Yurdun 0000-0002-2554-1204

Publication Date June 28, 2025
Published in Issue Year 2023 Volume: 27 Issue: 5

Cite

APA Karslı, S., Yazar, S., Karaca, M., Yurdun, T. (2025). Klotho gene polymorphism as a susceptibility factor for oxidative DNA damage in coronary artery disease. Journal of Research in Pharmacy, 27(5), 2079-2086.
AMA Karslı S, Yazar S, Karaca M, Yurdun T. Klotho gene polymorphism as a susceptibility factor for oxidative DNA damage in coronary artery disease. J. Res. Pharm. July 2025;27(5):2079-2086.
Chicago Karslı, Seher, Selma Yazar, Mehmet Karaca, and Türkan Yurdun. “Klotho Gene Polymorphism As a Susceptibility Factor for Oxidative DNA Damage in Coronary Artery Disease”. Journal of Research in Pharmacy 27, no. 5 (July 2025): 2079-86.
EndNote Karslı S, Yazar S, Karaca M, Yurdun T (July 1, 2025) Klotho gene polymorphism as a susceptibility factor for oxidative DNA damage in coronary artery disease. Journal of Research in Pharmacy 27 5 2079–2086.
IEEE S. Karslı, S. Yazar, M. Karaca, and T. Yurdun, “Klotho gene polymorphism as a susceptibility factor for oxidative DNA damage in coronary artery disease”, J. Res. Pharm., vol. 27, no. 5, pp. 2079–2086, 2025.
ISNAD Karslı, Seher et al. “Klotho Gene Polymorphism As a Susceptibility Factor for Oxidative DNA Damage in Coronary Artery Disease”. Journal of Research in Pharmacy 27/5 (July 2025), 2079-2086.
JAMA Karslı S, Yazar S, Karaca M, Yurdun T. Klotho gene polymorphism as a susceptibility factor for oxidative DNA damage in coronary artery disease. J. Res. Pharm. 2025;27:2079–2086.
MLA Karslı, Seher et al. “Klotho Gene Polymorphism As a Susceptibility Factor for Oxidative DNA Damage in Coronary Artery Disease”. Journal of Research in Pharmacy, vol. 27, no. 5, 2025, pp. 2079-86.
Vancouver Karslı S, Yazar S, Karaca M, Yurdun T. Klotho gene polymorphism as a susceptibility factor for oxidative DNA damage in coronary artery disease. J. Res. Pharm. 2025;27(5):2079-86.