Mucopolysaccharidosis Type IVA: Extracellular Matrix Biomarkers in Cardiovascular Disease

Brittany Montavon1, Linda E Winter1, Qi Gan1

  • 1Department of Pediatrics, School of Medicine, Saint Louis University, St. Louis, MO, United States.

Insights

Cardiovascular disease (CVD) in Morquio A is a major concern. New biomarkers, cathepsin S (CTSS) for children and elastin (ELN) for adults, show promise for monitoring extracellular matrix remodeling in this rare genetic disorder.

Area of Science:

  • Biochemistry
  • Genetics
  • Medical Research

Background:

  • Cardiovascular disease (CVD) is a leading cause of mortality in Mucopolysaccharidosis Type IVA (Morquio A), characterized by valvular disease and cardiac hypertrophy.
  • Current therapies, including enzyme replacement therapy (ERT), have limited impact on cardiovascular health, highlighting the need for effective biomarkers.
  • Accurate biomarkers are critical for monitoring CVD progression and treatment efficacy in Morquio A patients.

Purpose of the Study:

  • To identify and validate novel biomarkers for extracellular matrix (ECM) remodeling associated with CVD in Morquio A.
  • To investigate the potential of cathepsin S (CTSS) and elastin (ELN) as biomarkers in different age groups of Morquio A patients.
  • To explore the correlation between ECM biomarkers and other inflammatory markers in Morquio A.

Main Methods:

  • Analysis of plasma and urine samples from 54 treatment-naïve Morquio A patients and 74 healthy controls.
  • Quantification of CTSS and ELN levels using biochemical assays.
  • Measurement of keratan sulfate (KS), glycosaminoglycan (GAG), C-reactive protein (CRP), and soluble vascular cell adhesion molecule-1 (sVCAM-1) levels.

Main Results:

  • CTSS demonstrated potential as a biomarker in young Morquio A children, while ELN showed promise in adolescents and adults.
  • Plasma/urine KS and urinary GAG levels were significantly elevated in Morquio A patients and decreased with age.
  • CRP and sVCAM-1 levels were lower in Morquio A patients compared to controls, with significant correlations observed between KS and CRP, and sVCAM-1 and CTSS.

Conclusions:

  • CTSS and ELN represent promising novel biomarkers for ECM remodeling in Morquio A, with age-specific utility.
  • These findings provide a foundation for larger studies to correlate CTSS and ELN levels with Morquio A severity and CVD.
  • The study establishes a starting point for developing targeted monitoring strategies for cardiovascular complications in Morquio A.

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