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Enhanced endothelial activation in diabetic patients with unstable angina and non-Q-wave myocardial infarction
N T Mulvihill1, J B Foley, R T Murphy
1Royal City of Dublin Hospital Research and Education Institute, Department of Cardiology, St James's Hospital, Dublin, Ireland. mulvihin@hotmail.com
Insights
Diabetic patients with acute coronary syndromes show elevated soluble E-selectin levels, indicating increased endothelial activation. This may explain the poorer prognosis observed in diabetic individuals with these conditions.
Area of Science:
- Cardiovascular Medicine
- Endocrinology
- Immunology
Background:
- Diabetes mellitus (DM) is linked to chronic endothelial dysfunction.
- Diabetic patients with acute coronary syndromes (ACS) face worse prognoses than non-diabetics.
- ACS involves inflammation and increased expression of cellular adhesion molecules (CAMs).
Purpose of the Study:
- To investigate soluble CAM levels in diabetic and non-diabetic patients with unstable angina (UA) and non Q-wave myocardial infarction (NQMI).
- To characterize the expression of soluble intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), E-selectin, and P-selectin.
Main Methods:
- Serum samples collected from UA/NQMI patients at presentation, 72 hours, and 3, 6, 12 months post-discharge.
- Soluble ICAM-1, VCAM-1, E-selectin, and P-selectin levels measured using ELISA.
- Study included 15 diabetic and 15 matched non-diabetic patients.
Main Results:
- Soluble E-selectin levels were significantly higher in diabetic patients at all time points (e.g., 74 ± 10 ng/ml vs. 47 ± 3 ng/ml at presentation, P < 0.03).
- Soluble P-selectin levels were lower in diabetic patients during follow-up (e.g., 134 ± 15 ng/ml vs. 225 ± 32 ng/ml at 3/12 months, P < 0.02).
- No significant differences in soluble ICAM-1 and VCAM-1 levels were found between groups.
Conclusions:
- Elevated soluble E-selectin in diabetic patients with UA/NQMI suggests enhanced endothelial activation.
- This endothelial activation may contribute to the adverse prognosis in diabetic patients with ACS.
- Further research is needed to explore the clinical implications of these findings.
Aims:
Diabetes mellitus (DM) is associated with chronic endothelial dysfunction. Diabetic patients presenting with acute coronary syndromes have a worse prognosis than non-diabetics. An acute inflammatory reaction at the site of coronary plaque rupture and increased expression of surface and soluble cellular adhesion molecules (CAMs) are pathological features of acute coronary syndromes. We set out to characterize the expression of soluble CAMs in patients with and without diabetes presenting with unstable angina (UA) and non Q-wave myocardial infarction (NQMI).
Methods:
Patients presenting with UA and NQMI had serum samples taken on presentation, after 72 h and then 3, 6 and 12 months after discharge. Levels of soluble intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), E-selectin and P-selectin were measured using an ELISA technique.
Results:
We studied 15 diabetic patients and 15 age- and sex-matched non-diabetic patients presenting with either UA or NQMI. Levels of soluble E-selectin were elevated in the diabetic patients in comparison with the non-diabetic patients at all measured time points: 74 +/- 10 ng/ml vs. 47 +/- 3 ng/ml, P < 0.03 at t = 0 h, 55 +/- 5 ng/ml vs. 38 +/- 2 ng/ml, P < 0.02 at t = 72 h. However, levels of soluble P-selectin were lower in the diabetic cohort during follow-up: 134 +/- 15 ng/ml vs. 225 +/- 32 ng/ml, P < 0.02 at t = 3/12 and 112 +/- 8 ng/ml vs. 197 +/- 23 ng/ml, P < 0.02 at t = 6/12. There was no significant difference in levels of soluble ICAM-1 and VCAM-1 between diabetic and non-diabetic patients.
Conclusions:
Levels of soluble E-selectin are significantly elevated in diabetic patients presenting with UA and NQMI in comparison with non-diabetics. This finding may reflect enhanced endothelial activation which may contribute to the adverse prognosis of diabetic patients with acute coronary syndromes.
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