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Homocysteine and diabetes: Role in macrovascular and microvascular complications

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.jdiacomp.2020.107834

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Homocysteine; Diabetes mellitus; Macrovascular complications; Miaovascular complications; Cardiovascular disease

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Homocysteine’s role in the development of vascular complications in diabetes mellitus is still unclear, with conflicting results from studies. While lowering therapies can effectively reduce homocysteine levels, their impact on reducing cardiovascular disease risk remains uncertain, requiring further investigation, especially in diabetic patients.
Diabetes mellitus (DM) can lead to the development of macro- and miaovascular complications. Homocysteine (Hcy) may play a role in the development of cardiovascular (CV) diseases (CVDs). The role of Hcy in the development of the vascular complications associated with DM is not clearly defined. Despite a strong initial assumption regarding the importance of Hcy in DM and its complications, over time enthusiasm has waned because several studies showed unconvincing and occasionally contradictory results. A universal conclusion is not easy to draw given the diversity of studies (e.g. number of patients, design, folic acid and vitamin B status, ethnic differences, genetic background). For some complications, most results encourages further investigation. Impaired renal function is a major independent determinant of high total Hcy (tHcy) levels. However, the role of hyperhomocysteinaemia (HHcy) in the development of diabetic kidney disease (DKD) has yet to be determined. Hcylowering therapies can significantly decrease Hcy levels but their effects on CVD risk reduction are conflicting. Further studies are needed to determine the influence of Hcy-lowering therapy on CVD risk reduction, especially in patients with DM. (C) 2020 Elsevier Inc. All rights reserved.

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