Role of Lipoprotein-associated phospholipase A2 (Lp-PLA2) in prediction and assessment of the severity of coronary artery disease in patients with type 2 Diabetes Mellitus Short title: Lp-PLA2 and coronary artery disease
Lp-PLA2 and coronary artery disease
Abstract
Background: Lipoprotein-associated phospholipase A2 (Lp-PLA2) is a specific biomarker associated with an increased risk of coronary artery disease (CAD) development. This study aims to determine the relationship between Lp-PLA2 activity and the risk of development and severity of CAD in patients with type 2 Diabetes mellitus (T2DM).
Methods: The cross-sectional study included 148 patients with T2DM, divided into two groups: patients with T2DM without confirmed CAD (n=56) and patients with T2DM and confirmed CAD (n=92), further divided into three subgroups based on the stage of CAD, and a control group of healthy individuals (n=44). Venous blood samples were collected from all participants to measure glucose, cholesterol, triglycerides, HDL, LDL, C-reactive protein, urea, and creatinine levels using standard photometric methods. Lp-PLA2 activity was measured using a chemiluminescent immunoassay method.
Results: Patients with T2DM and confirmed CAD had significantly higher Lp-PLA2 levels than those without confirmed CAD and healthy individuals. A significant difference in Lp-PLA2 levels was found between the group without CAD, the patients with CAD divided into subgroups according to disease stage, and the healthy control group. A positive correlation was observed between Lp-PLA2 and BMI, glycated hemoglobin, total cholesterol, and HDL cholesterol. The optimal cutoff value for Lp-PLA2 < 250 ng/ml yielded a diagnostic sensitivity of 95.65% and specificity of 88.64% for patients with T2DM and diagnosed CAD.
Conclusion: Lp-PLA2 can be used as a predictor for developing and assessing the severity of CAD in patients with T2DM.
References
Li D, Zhao L, Yu J, Zhang W, Du R, Liu X, et al. Lipoprotein-associated phospholipase A2 in coronary heart disease: Review and meta-analysis. Clin Chim Acta 2017; 465: 22-29.
New WHO statistics highlight increases in blood pressure and diabetes, other noncommunicable risk factors. Cent Eur J Public Health 2012; 20: 134-149.
Chen Y, Wang S, Li J, Fu Y, Chen P, Liu X, et al. The relationships between biological novel biomarkers Lp-PLA2 and CTRP-3 and CVD in patients with type 2 diabetes mellitus. J Diabetes 2024; 16(7): e13574.
Lee DY. Emerging Circulating Biomarkers for Enhanced Cardiovascular Risk Prediction. J Lipid Atheroscler 2024; 13(3): 262-279.
Zhu HA. Lp-PLA2, a Novel Potential Biomarker Predicting Cardiovascular Disease in Type 2 Diabetes Mellitus. Med Clin Rev 2016; 2: 11.
Zhang H, Gao Y, Wu D, Zhang D. The relationship of lipoprotein-associated phospholipase A2 activity with the seriousness of coronary artery disease. BMC Cardiovasc Disord 2020; 20, 295.
De Stefano A, Mannucci L, Tamburi F, Cardillo C, Schinzari F, Rovella V, et al. Lp-PLA2, a new biomarker of vascular disorders in metabolic diseases. Int J Immunopathol Pharmacol 2019; 33: 2058738419827154.
Zhang S, Wang J, Chen S, Zhang Y, He R, Wang X, et al. Serum levels of lipoprotein-associated phospholipase A2 are associated with coronary atherosclerotic plaque progression in diabetic and non-diabetic patients. BMC Cardiovasc Disord 2024; 24(1) :251.
Bargieł W, Cierpiszewska K, Maruszczak K, Pakuła A, Szwankowska D, Wrzesińska A, et al. Recognized and Potentially New Biomarkers-Their Role in Diagnosis and Prognosis of Cardiovascular Disease. Medicina 2021; 57(7): 701.
Baziar N, Nasli-Esfahani E, Djafarian K, Qorbani M, Hedayati M, Mishani MA, et al. The Beneficial Effects of Alpha Lipoic Acid Supplementation on Lp-PLA2 Mass and Its Distribution between HDL and apoB-Containing Lipoproteins in Type 2 Diabetic Patients: A Randomized, Double-Blind, Placebo-Controlled Trial. Oxid Med Cell Longev. 2020; 2020: 5850865.
Kurniawan LB, Rampo H, Soraya GV, Adnan E , Esa T, Widaningsih Y, et al. Effect of obesity, glucose control, lipid profiles, and blood pressure on Lp-PLA2 levels in type 2 Diabetes Mellitus patients. Obes Med 2021; 22: 100318
Naito R, Kasai T. Coronary artery disease in type 2 diabetes mellitus: Recent treatment strategies and future perspectives. World J Cardiol 2015; 7(3):119-24.
Nelson TL, Biggs ML, Kizer JR, Cushman M, Hokanson JE, Furberg CD, et al. Lipoprotein-associated phospholipase A2 (Lp-PLA2) and future risk of type 2 diabetes: results from the Cardiovascular Health Study. J Clin Endocrinol Metab 2012; 97(5): 1695-701.
Global Burden of Disease Collaborative Network. Global Burden of Disease Study 2021. Results. Institute for Health Metrics and Evaluation. 2024 (https://vizhub.healthdata.org/gbd-results/).
Garg S, Madhu SV, Suneja S. Lipoprotein associated phospholipase A2 activity & its correlation with oxidized LDL & glycaemic status in early stages of type-2 diabetes mellitus. Indian J Med Res 2015; 141(1): 107-14.
Chen YH, Li WC, Chen YC, Yeh WC, Yu W, Hung HY, et al. The correlation between lipoprotein associated phospholipase A2 and central overweight status. Int J Immunopathol Pharmacol. 2021; 35: 20587384211048562.
Sairam SG, Sola S, Barooah A, Javvaji SK, Jaipuria J, Venkateshan V, et al. The role of Lp-PLA2 and biochemistry parameters as potential biomarkers of coronary artery disease in Asian South-Indians: a case-control study. Cardiovasc Diagn Ther 2017; 7(6): 589-597.
Copyright (c) 2025 Irena Kostovska, Svetlana Cekovska, Katerina Tosheska Trajkovska, Danica Labudovic, Julijana Brezovska Kavrakova, Sonja Topuzovska, Hristina Ampova, Melda Emin, Elena Petrushevska Stanojevska, Natasa Nedeska Minova, Ognen Kostovski, Marjan Boshev

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