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Review
. 2021 Oct 1:2021:4461311.
doi: 10.1155/2021/4461311. eCollection 2021.

Epidemiological Research Advances in Vascular Calcification in Diabetes

Affiliations
Review

Epidemiological Research Advances in Vascular Calcification in Diabetes

Haipeng Yao et al. J Diabetes Res. .

Abstract

Vascular calcification is the transformation of arterial wall mesenchymal cells, particularly smooth muscle cells (SMCs), into osteoblast phenotypes by various pathological factors. Additionally, vascular transformation mediates the abnormal deposition of calcium salts in the vascular wall, such as intimal and media calcification. Various pathological types have been described, such as calcification and valve calcification. The incidence of vascular calcification in patients with diabetes is much higher than that in nondiabetic patients, representing a critical cause of cardiovascular events in patients with diabetes. Because basic research on the clinical transformation of vascular calcification has yet to be conducted, this study systematically expounds on the risk factors for vascular calcification, vascular bed differences, sex differences, ethnic differences, diagnosis, severity assessments, and treatments to facilitate the identification of a new entry point for basic research and subsequent clinical transformation regarding vascular calcification and corresponding clinical evaluation strategies.

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Conflict of interest statement

The authors have no conflicts of interest to declare that are relevant to the content of this article.

References

    1. Hjortnaes J., New S. E., Aikawa E. Visualizing novel concepts of cardiovascular calcification. Trends in Cardiovascular Medicine . 2013;23(3):71–79. doi: 10.1016/j.tcm.2012.09.003. - DOI - PMC - PubMed
    1. Xue X., Zhizhi C., Zhaoyu L. Research progress on the regulatory mechanism of vascular smooth muscle cells in vascular calcification. Journal of Clinical Cardiovascular Disease . 2020;36(327):93–96.
    1. Chen N. X., Duan D., O'Neill K. D., Moe S. M. High glucose increases the expression of Cbfa1 and BMP-2 and enhances the calcification of vascular smooth muscle cells. Nephrology, Dialysis, Transplantation . 2006;21(12):3435–3442. doi: 10.1093/ndt/gfl429. - DOI - PubMed
    1. Kapustin A. N., Davies J. D., Reynolds J. L., et al. Calcium regulates key components of vascular smooth muscle cell-derived matrix vesicles to enhance mineralization. Circulation Research . 2011;109(1):e1–e12. doi: 10.1161/CIRCRESAHA.110.238808. - DOI - PubMed
    1. Wang Y., Shan J., Yang W., Zheng H., Xue S. High mobility group box 1 (HMGB1) mediates high-glucose-induced calcification in vascular smooth muscle cells of saphenous veins. Inflammation . 2013;36(6):1592–1604. doi: 10.1007/s10753-013-9704-1. - DOI - PubMed

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