Mannose binding lectin as a marker for coronary artery disease in hypertension

Authors

  • M Dilagamari
  • V.Amuthavalli

Keywords:

Mannose binding lectin (MBL) • Hypertension • Coronary artery disease • Atherosclerosis • Inflammation

Abstract

Background

According to The Framingham Heart Study and the Epidemiology of Cardiovascular Diseases hypertension is an

independent risk factor for cardiovascular disease (1). Inflammation plays a major role in atherosclerosis. Markers

of innate immunity have been shown to predict the development of coronary artery disease. MBL (Mannose binding

lectin) being a component of innate immunity can be used as a marker of cardiovascular risk in hypertension.

Aim & Objectives:

The study was conducted to evaluate the risk of coronary artery disease in recently diagnosed hypertensive patients

by estimating serum mannose binding lectin levels

Materials & Methods:

This cross sectional case control study was conducted among 180 subjects who were divided into three groups as

follows

Group A : 60 recently diagnosed hypertensive patients ( < 6 months duration )

Group B : 60 hypertensive patients who had myocardial infarction recently (< 7 days)

Group C : 60 age & sex matched healthy controls

Serum levels of MBL was evaluated in the three groups using ELISA technique. Collected data were analysed

statistically.

Results & Conclusion:

The serum MBL levels were significantly elevated in hypertensive patients (mean = 823.45 ng/mL; Range – 772 to

875 ng/mL) and in hypertensive with myocardial infarction (mean = 1163.39 ng/mL; Range – 945 to 1381 ng/mL) as

compared with control population (mean = 607.15 ng/mL; Range – 513 to 701 ng/mL) with p value of 0.001. From

the ROC curve, it has been determined that MBL has sensitivity of 93% & specificity of 96%) with a positive

predictive value of 96% & negative predictive value of 84.65%.

Our findings suggested the determination of MBL status may serve as a potential marker for early identification of

patients at risk of cardiovascular complications, pending further validation studies.

 

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Published

2025-04-13