Abstract

BackgroundRheumatic Heart Disease (RHD), a chronic acquired heart disorder results from Acute Rheumatic Fever. It is a major public health concern in developing countries. In RHD, mostly the valves get affected. The present study investigated whether extracellular matrix remodelling in rheumatic valve leads to altered levels of collagen metabolism markers and if such markers can be clinically used to diagnose or monitor disease progression.MethodologyThis is a case control study comprising 118 subjects. It included 77 cases and 41 healthy controls. Cases were classified into two groups- Mitral Stenosis (MS) and Mitral Regurgitation (MR). Carboxy-terminal propeptide of type I procollagen (PICP), amino-terminal propeptide of type III procollagen (PIIINP), total Matrix Metalloproteinase-1(MMP-1) and Tissue Inhibitor of Metalloproteinase-1 (TIMP-1) were assessed. Histopathology studies were performed on excised mitral valve leaflets. A p value <0.05 was considered statistically significant.ResultsPlasma PICP and PIIINP concentrations increased significantly (p<0.01) in MS and MR subjects compared to controls but decreased gradually over a one year period post mitral valve replacement (p<0.05). In MS, PICP level and MMP-1/TIMP-1 ratio strongly correlated with mitral valve area (r = −0.40; r = 0.49 respectively) and pulmonary artery systolic pressure (r = 0.49; r = −0.49 respectively); while in MR they correlated with left ventricular internal diastolic (r = 0.68; r = −0.48 respectively) and systolic diameters (r = 0.65; r = −0.55 respectively). Receiver operating characteristic curve analysis established PICP as a better marker (AUC = 0.95; 95% CI = 0.91−0.99; p<0.0001). A cut-off >459 ng/mL for PICP provided 91% sensitivity, 90% specificity and a likelihood ratio of 9 in diagnosing RHD. Histopathology analysis revealed inflammation, scarring, neovascularisation and extensive leaflet fibrosis in diseased mitral valve.ConclusionsLevels of collagen metabolism markers correlated with echocardiographic parameters for RHD diagnosis.

Highlights

  • Rheumatic Heart Disease (RHD) is a chronic acquired disorder of heart

  • Plasma PICP and PIIINP concentrations increased significantly (p,0.01) in Mitral Stenosis (MS) and Mitral Regurgitation (MR) subjects compared to controls but decreased gradually over a one year period post mitral valve replacement (p,0.05)

  • In MS, PICP level and MMP1/Tissue Inhibitor of Metalloproteinase-1 (TIMP-1) ratio strongly correlated with mitral valve area (r = 20.40; r = 0.49 respectively) and pulmonary artery systolic pressure (r = 0.49; r = 20.49 respectively); while in MR they correlated with left ventricular internal diastolic (r = 0.68; r = 20.48 respectively) and systolic diameters (r = 0.65; r = 20.55 respectively)

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Summary

Introduction

Rheumatic Heart Disease (RHD) is a chronic acquired disorder of heart It is a major public health concern in Low and Middle Income Countries (LMICs) having a global prevalence of at least 15.6 million cases, with 282,000 new cases and demanding 233,000 deaths each year [1]. It results as a sequelae of Acute Rheumatic Fever (ARF), caused by autoimmune reactions following untreated Streptococcus pyogenes throat infection in genetically susceptible individuals [2]. Rheumatic Heart Disease (RHD), a chronic acquired heart disorder results from Acute Rheumatic Fever It is a major public health concern in developing countries. The present study investigated whether extracellular matrix remodelling in rheumatic valve leads to altered levels of collagen metabolism markers and if such markers can be clinically used to diagnose or monitor disease progression

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