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Endothelin-1 and nitric oxide levels in patients with mitral annulus calcification
Ahmet Camsari1, Hasan Pekdemir, Dilek Ciçek
1Department of Cardiology, Faculty of Medicine, Mersin University, Mersin, Turkey.
Insights
Patients with mitral annulus calcification (MAC) show elevated endothelin-1 (ET-1) and reduced nitric oxide (NOx) levels. These changes are more pronounced in severe MAC cases, suggesting a role in disease progression.
Area of Science:
- Cardiovascular Medicine
- Biochemistry
Background:
- Mitral annulus calcification (MAC) is a chronic degenerative condition.
- The roles of endothelin-1 (ET-1) and nitric oxide (NOx) in MAC pathogenesis are not fully understood.
Purpose of the Study:
- To investigate plasma levels of ET-1 and NOx in patients with MAC.
- To compare these levels with those in healthy subjects.
- To assess the correlation between ET-1/NOx levels and MAC severity.
Main Methods:
- Cross-sectional study comparing 39 MAC patients with 20 healthy controls.
- MAC patients were stratified into severe (Group A) and mild (Group B) subgroups.
- Plasma ET-1 and NOx levels were measured and compared across groups.
Main Results:
- MAC patients exhibited significantly higher ET-1 and lower NOx levels than controls.
- Severe MAC (Group A) showed higher ET-1 and lower NOx compared to mild MAC (Group B) and controls.
- ET-1 levels correlated with diabetes, coronary artery disease, and dyslipidemia.
Conclusions:
- Patients with MAC have an imbalance of ET-1 and NOx, with increased ET-1 and decreased NOx.
- This imbalance is particularly evident in severe MAC, indicating its potential contribution to disease severity.
Abstract:
Mitral annulus calcification (MAC) is a chronic degenerative noninflammatory process. The goal of this study was to determine endothelin-1 (ET-1) and nitric oxide (NOx) levels in patients with MAC and compare them with those in normal subjects. The study group included 39 patients [26 females (66%), age, 63 +/- 8 years] with MAC and 20 [11 females (55%), age, 61 +/- 7 years] healthy subjects. The patients were divided into two subgroups, group A with severe MAC and group B with mild MAC, according to the severity of the MAC. Plasma ET-1 levels were higher and NOx levels were lower in patients than controls [(6.5 +/- 5.6 pg/mL vs 3.7 +/- 2.9 pg/mL for ET-1 and 35.0 +/- 10.6 micromol/L vs 42.3 +/- 9.9 micromol/L for NOx; P < 0.05 for both)]. In the subgroups, ET-1 levels were higher in group A than group B (8.65 +/- 6.84 pg/mL vs 4.74 +/- 3.45 pg/mL, P < 0.05) and the control group (8.65 +/- 6.84 pg/mL vs 3.70 +/- 2.88 pg/mL, P < 0.05). There was no difference between group B and the control group. Plasma NOx levels were significantly decreased in group A compared to controls (32.22 +/- 11.88 micromol/L vs 42.25 +/- 9.99 micromol/L, P < 0.05). However, no significant difference was observed between group B (37.38 +/- 9.06 micromol/L) and the other groups. Diabetes mellitus, coronary artery disease, and dyslipidemia were significantly associated with ET-1 levels. However, this association was not observed for NOx. In conclusion, patients with MAC have increased ET-1 and decreased NOx levels. This seems to be more prominent in patients with severe MAC.
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