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Serum ADMA concentration-- an independent factor determining FMD impairment in cardiac syndrome X
Maciej Haberka1, Katarzyna Mizia-Stec, Zbigniew Gasior
1Department of Cardiology, Medical University of Silesia, Katowice, Poland. mhaberka@op.pl
Insights
Endothelial dysfunction in Cardiac Syndrome X (CSX) is linked to impaired vascular reactivity. Asymmetric dimethylarginine (ADMA) is the sole independent factor identified as causing flow-mediated vasodilatation (FMD) impairment in CSX patients.
Area of Science:
- Cardiology
- Vascular Biology
- Biochemistry
Background:
- Cardiac Syndrome X (CSX) is characterized by chest pain despite normal coronary angiograms.
- The precise mechanisms underlying reduced endogenous vascular reactivity in CSX remain unclear.
- Endothelial dysfunction is a suspected contributor to CSX pathophysiology.
Purpose of the Study:
- To investigate serum markers including total nitric oxide (NO), asymmetric dimethylarginine (ADMA), and platelet-derived growth factor (PDGF) in CSX patients.
- To determine the relationship between these serum markers and ultrasound-assessed endothelial function and vascular remodeling.
- To identify key factors contributing to impaired vascular reactivity in CSX.
Main Methods:
- A case-control study involving 43 CSX patients and 21 healthy controls.
- High-resolution ultrasound was used to measure flow-mediated vasodilatation (FMD), nitroglycerine-mediated vasodilatation (NMD), and intima-media thickness (IMT) of carotid arteries.
- Serum levels of total NO, ADMA, and PDGF were quantified and analyzed.
Main Results:
- CSX patients exhibited significantly lower FMD and higher IMT compared to controls (P < 0.05).
- Mean serum total NO levels were significantly higher in CSX patients than in controls (P < 0.0001).
- Serum ADMA concentration was identified as the independent factor significantly associated with FMD impairment in CSX patients.
Conclusions:
- Asymmetric dimethylarginine (ADMA) is the primary independent determinant of impaired flow-mediated vasodilatation (FMD) in patients with Cardiac Syndrome X (CSX).
- While total nitric oxide (NO) levels were elevated in CSX, ADMA emerged as the critical factor for endothelial dysfunction.
- These findings highlight the role of ADMA in the vascular abnormalities observed in CSX.
Unlabelled:
Mechanisms of decreased endogenous vascular reactivity in individuals with cardiac syndrome X (CSX) are not fully understood.
Aim:
To evaluate the following serum markers: total nitric oxide (NO), asymmetric dimethylarginine (ADMA), platelet-derived growth factor (PDGF), and to establish their relation to ultrasound indexes of endothelial function and structural remodeling in CSX patients.
Method:
The study group consisted of 43 CSX patients (mean age: 56.3 +/- 9 years), while the control group included 21 healthy subjects (mean age: 54.86 +/- 6.9 years). The high-resolution ultrasound was performed to measure: flow-mediated vasodilatation (FMD), nitroglycerine-mediated vasodilatation (NMD) and intima-media thickness (IMT) of carotid arteries.
Results:
In CSX patients, significantly lower FMD (9.06 +/- 3.2%) and significantly higher IMT (0.667 +/- 0.14 mm) values were observed compared to healthy individuals (17.42 +/- 8.4%, 0.571 +/- 0.2 mm; P < 0.05). Mean total NO serum concentration was significantly higher in the CSX group (48.2 +/- 18.2 micromol/L) as compared to controls (32.1 +/- 1.4 micromol/L; P < 0.0001). There were no differences in serum ADMA and PDGF levels. In CSX patients, FMD values correlated with NO (r = 0.323; P = 0.039) and ADMA (r = -0.387; P = 0.012) serum levels; however, there were no significant correlations between NO and ADMA concentrations.
Conclusion:
Serum ADMA concentration is the only independent factor determining FMD impairment.
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