Abstract
COVID-19 infection (COronaVIrus Disease 2019) is associated with dyslipidemia and cardiovascular complications. It has been proven that a high content of low-density lipoproteins (LDL) and, especially, oxidized LDL (oxLDL) causes cholesterol accumulation in blood vessel walls and significantly increases the risk of atherosclerosis and other cardiovascular diseases (CVD). Aim. The aim of the work was to determine oxLDL content in the blood of 82 patients with diabetes mellitus (DM), who had a coronavirus infection between 2020 and 2022. Material and methods. Blood was obtained by standard venipuncture and stored in EDTA tubes. Plasma was separated by centrifugation for 10 min after blood collection. Samples were stored at -80
°C until use. OxLDL was determined using enzyme-linked immunosorbent assay kits (Elabscience, USA). Results. It was shown that oxLDL level in the blood of patients with type 2 DM (T2DM) and, especially, patients who had recovered from COVID-19, was significantly higher than in the blood of healthy people. There is also a significant difference between patients with mild and severe forms of COVID-19. In the absence of treatment with hypoglycemic drugs in patients who had recovered from COVID-19, the level of oxLDL increases significantly, especially in the absence of insulin treatment. The effect of treatment was more pronounced in patients with COVID-19, and when treated with inhibitors of sodium-dependent glucose cotransporter type 2 (SGLT2i), the level of oxLDL decreased almost to control values. Therefore, oxLDL levels remain elevated in diabetic patients who have recovered from COVID-19, although lower than in the acute disease. Conclusions. OxLDL levels in the blood of diabetic patients who have recovered from COVID-19 remain elevated, although lower than in the acute form of the disease. Treatment with hypoglycemic drugs may be a promising strategy to reduce oxLDL levels, and therefore the risk of atherosclerosis, in individuals who have recovered from COVID-19. OxLDL levels may be an important marker of post-COVID syndrome.
References
Lima-Martínez MM, Carrera Boada C, Madera-Silva MD, Marín W, Contreras M. COVID-19 and diabetes: A bidirectional relationship. Clin Investig Arterioscler. 2021 May-Jun;33(3):151-7. English, Spanish. doi: 10.1016/j.arteri.2020.10.001.
Liu Y, Lou X. The bidirectional association between metabolic syndrome and long-COVID-19. Diabetes Metab Syndr Obes. 2024 Oct 9;17:3697-710. doi: 10.2147/DMSO.S484733.
Mukkawar RV, Reddy H, Rathod N, Kumar S, Acharya S. The long-term cardiovascular impact of COVID-19: pathophysiology, clinical manifestations, and management. Cureus. 2024 Aug 10;16(8):e66554. doi: 10.7759/cureus.66554.
Sharma SK, Mohan A, Upadhyay V. Long COVID syndrome: An unfolding enigma. Indian J Med Res. 2024 Jun;159(6):585-600. doi: 10.25259/IJMR_1449_23.
Greenhalgh T, Sivan M, Perlowski A, Nikolich JŽ. Long COVID: a clinical update. Lancet. 2024 Aug 17;404(10453):707-24. doi: 10.1016/S0140-6736(24)01136-X.
Khatana C, Saini NK, Chakrabarti S, Saini V, Sharma A, Saini RV, et al. Mechanistic Insights into the Oxidized Low-Density Lipoprotein-Induced Atherosclerosis. Oxid Med Cell Longev. 2020 Sep 15;2020:5245308. doi: 10.1155/2020/5245308.
Tronko ND, Pushkarev VM, Sokolova LK, Pushkarev VV, Kovzun OI. Molecular mechanisms of pathogenesis of diabetes and its complications. Kyiv: Publishing house Medkniga; 2018. 264 p.
Kočar E, Režen T, Rozman D. Cholesterol, lipoproteins, and COVID-19: basic concepts and clinical applications. Biochim Biophys Acta Mol Cell Biol Lipids. 2021 Feb;1866(2):158849. doi:10.1016/j.bbalip.2020.158849.
Sokolova L, Pushkarev V, Pushkarev V, Kovzun O, Tronko M. Diabetes mellitus and atherosclerosis. The role of inflammatory processes in pathogenesis. International Journal of Endocrinology (Ukraine). 2017;13(7):486-98. doi:10.22141/2224-0721.13.7.2017. 115747.
Yan Y, Song D, Wu J, Wang J. Long non-coding RNAs link oxidized low-density lipoprotein with the inflammatory response of macrophages in atherogenesis. Front Immunol. 2020 Jan 30;11:24. doi: 10.3389/fimmu.2020.00024.
