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Published on: January 28, 2020
Correlation between plasma asymmetric dimethylarginine and different types of coronary heart disease
Yu Cao1, Kan Yang, Zhihui Zhang
1Department of Cardiology, Third Xiangya Hospital, Central South University, Changsha 410013, China.
Insights
Plasma asymmetric dimethylarginine (ADMA) levels are elevated in patients with acute coronary syndrome (ACS), suggesting ADMA may serve as a key biomarker for ACS and related heart conditions.
Area of Science:
- Cardiovascular Medicine
- Biomarker Discovery
- Clinical Chemistry
Background:
- Coronary heart disease (CHD) encompasses stable angina pectoris (SAP) and acute coronary syndrome (ACS).
- Endothelial dysfunction plays a critical role in the pathogenesis of CHD.
- Asymmetric dimethylarginine (ADMA) is an endogenous inhibitor of nitric oxide synthase, impacting endothelial function.
Purpose of the Study:
- To investigate plasma levels of ADMA, nitric oxide (NO), and von Willebrand factor (vWF) in patients with SAP and ACS.
- To determine the correlation between ADMA levels and the presence of SAP or ACS.
Main Methods:
- A cohort of 143 subjects was categorized into non-CHD, SAP, and ACS groups.
- Plasma concentrations of ADMA, NO, and vWF were measured in all participants.
- Statistical analyses were performed to correlate biomarker levels with CHD status.
Main Results:
- ADMA levels were significantly higher in the ACS group compared to non-CHD and SAP groups (P<0.05).
- NO levels were decreased in both SAP and ACS groups, with a more pronounced reduction in ACS.
- vWF levels were elevated in both SAP and ACS groups compared to the non-CHD group.
Conclusions:
- Elevated plasma ADMA levels are strongly associated with acute coronary syndrome.
- ADMA shows potential as a valuable clinical marker for the diagnosis and management of ACS.
Objective:
To monitor the changes of plasma asymmetric dimethylarginine (ADMA), nitric oxide (NO), and von Willebrand factor (vWF) levels in patients with stable angina pectoris (SAP) or acute coronary syndrome (ACS) and to evaluate the correlation between ADMA and different types of coronary heart disease.
Methods:
A total of 143 subjects were divided into a non-CHD group, a SAP group and an ACS group. Plasma levels of ADMA, NO and vWF were examined and their correlation with SAP or ACS was analyzed.
Results:
Compared with the non-CHO or the SAP group, ADMA level was elevated in the ACS group (P<0.05). The ADMA level tended to increase in the SAP group compared with the non-CHD group, but had no significant difference (P>0.05). Compared with the non-CHD group, NO level was decreased in both the SAP and ACS group (P<0.05), and it decreased more in ACS group than that in the SAP group (P<0.05); vWF levels were increased in both the SAP and ACS group compared with the non-CHD group (P<0.05). There was no significant difference in the plasma levels of vWF in the SAP and the ACS group (P>0.05).
Conclusion:
The change of plasma ADMA level is closely correlated with acute coronary syndrome. ADMA might be a clinical marker for acute coronary syndrome.
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