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Updated: Sep 21, 2025

Glycoproteomics of the Extracellular Matrix: A Method for Intact Glycopeptide Analysis Using Mass Spectrometry
Published on: April 21, 2017
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.
Abstract:
Cardiovascular disease (CVD) in Mucopolysaccharidosis Type IVA (Morquio A), signified by valvular disease and cardiac hypertrophy, is the second leading cause of death and remains untouched by current therapies. Enzyme replacement therapy (ERT) is the gold-standard treatment for MPS disorders including Morquio A. Early administration of ERT improves outcomes of patients from childhood to adulthood while posing new challenges including prognosis of CVD and ERT's negligible effect on cardiovascular health. Thus, having accurate biomarkers for CVD could be critical. Here we show that cathepsin S (CTSS) and elastin (ELN) can be used as biomarkers of extracellular matrix remodeling in Morquio A disease. We found in a cohort of 54 treatment naïve Morquio A patients and 74 normal controls that CTSS shows promising attributes as a biomarker in young Morquio A children. On the other hand, ELN shows promising attributes as a biomarker in adolescent and adult Morquio A. Plasma/urine keratan sulfate (KS), and urinary glycosaminoglycan (GAG) levels were significantly higher in Morquio A patients (p < 0.001) which decreased with age of patients. CTSS levels did not correlate with patients' phenotypic severity but differed significantly between patients (median range 5.45-8.52 ng/mL) and normal controls (median range 9.61-15.9 ng/mL; p < 0.001). We also studied α -2-macroglobulin (A2M), C-reactive protein (CRP), and circulating vascular cell adhesion molecule-1 (sVCAM-1) in a subset of samples to understand the relation between ECM biomarkers and the severity of CVD in Morquio A patients. Our experiments revealed that CRP and sVCAM-1 levels were lower in Morquio A patients compared to normal controls. We also observed a strong inverse correlation between urine/plasma KS and CRP (p = 0.013 and p = 0.022, respectively) in Morquio A patients as well as a moderate correlation between sVCAM-1 and CTSS in Morquio A patients at all ages (p = 0.03). As the first study to date investigating CTSS and ELN levels in Morquio A patients and in the normal population, our results establish a starting point for more elaborate studies in larger populations to understand how CTSS and ELN levels correlate with Morquio A severity.
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