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Published on: January 28, 2020
Circulating cathepsin K as a potential novel biomarker of coronary artery disease
Xian Wu Cheng1, Ryosuke Kikuchi, Hideki Ishii
1Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan. xianwu@med.nagoya-u.ac.jp
Insights
Elevated levels of Cathepsin K (CatK) are closely associated with coronary artery disease (CAD). CatK is a potent collagenase and a novel biomarker for detecting CAD presence.
Area of Science:
- Biochemistry
- Cardiovascular Medicine
- Biomarker Discovery
Background:
- Cathepsin K (CatK) is a potent mammalian collagenase implicated in atherosclerosis.
- Its role in coronary artery disease (CAD) prevalence requires investigation.
Purpose of the Study:
- To investigate the association between circulating Cathepsin K (CatK) levels and the prevalence of coronary artery disease (CAD).
Main Methods:
- Plasma CatK, I-PINP, and ICTP levels were measured in 252 CAD patients and 132 controls.
- Coronary angiography and intravascular ultrasound were performed.
- Statistical analyses included linear and logistic regression.
Main Results:
- CAD patients exhibited significantly higher CatK levels and ICTP/I-PINP ratios compared to controls.
- CatK levels positively correlated with ICTP/I-PINP ratios and plaque volume.
- CatK was an independent predictor of CAD and correlated inversely with fibrous volume.
Conclusions:
- High circulating CatK levels are closely linked to the presence of CAD.
- Cathepsin K emerges as a novel and significant biomarker for coronary artery disease.
Background:
Cathepsin K (CatK) is one of the most potent mammalian collagenases involved in atherosclerosis-based vascular disease. We investigated whether circulating CatK is associated with the prevalence of coronary artery disease (CAD).
Methods:
Two-hundred fifty-two consecutive subjects were enrolled from among patients who underwent coronary angiography and intravascular ultrasound analyses. One-hundred thirty-two age-matched subjects served as controls. Plasma CatK, intact procollagen type I N-terminal propeptide (I-PINP), and linked carboxy-terminal telopeptide of collagen type I (ICTP) were measured.
Results:
Patients with CAD had higher CatK levels (44.0 ± 31.2 versus 15.5 ± 8.3 ng/mL, P < 0.001) and ICTP/I-PINP ratios (0.2 ± 0.1 versus 0.04 ± 0.03, P < 0.001) than the controls. Patients with acute coronary syndrome had higher CatK levels than those with stable angina pectoris. Overall, linear regression analysis showed that the CatK levels correlated positively with ICTP/I-PINP ratios (r = 0.41, P < 0.001). Multiple logistic regression analysis showed that CatK levels were independent predictors of CAD (odds ratio, 1.15; 95% CI, 1.07 to 1.23; P < 0.01). Furthermore, CatK levels were also correlated positively with percent plaque volumes and inversely with percent fibrous volumes by intravascular ultrasound.
Conclusions:
These data indicated that high levels of CatK are closely linked with the presence of CAD and that CatK serves as a novel biomarker for CAD.
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