Clinical significance of markers of collagen metabolism in rheumatic mitral valve disease

PLoS One. 2014 Mar 6;9(3):e90527. doi: 10.1371/journal.pone.0090527. eCollection 2014.

Abstract

Background: Rheumatic 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.

Methodology: This 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.

Results: Plasma 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.

Conclusions: Levels of collagen metabolism markers correlated with echocardiographic parameters for RHD diagnosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Collagen / blood
  • Collagen / metabolism*
  • Extracellular Matrix / pathology
  • Female
  • Humans
  • Male
  • Middle Aged
  • Mitral Valve / pathology*
  • Mitral Valve Insufficiency / blood
  • Mitral Valve Insufficiency / diagnosis
  • Mitral Valve Insufficiency / metabolism
  • Mitral Valve Insufficiency / pathology
  • Mitral Valve Stenosis / blood
  • Mitral Valve Stenosis / diagnosis
  • Mitral Valve Stenosis / metabolism
  • Mitral Valve Stenosis / pathology
  • Rheumatic Heart Disease / blood
  • Rheumatic Heart Disease / diagnosis
  • Rheumatic Heart Disease / metabolism*
  • Rheumatic Heart Disease / pathology*
  • Sensitivity and Specificity
  • Young Adult

Substances

  • Biomarkers
  • Collagen

Grants and funding

This work is supported by grants from Council of Scientific and Industrial Research (CSIR), New Delhi, India (NWP 0004, MLP 115) to AB. TB and SM are recipients of fellowships from CSIR, New Delhi. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.