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Imaging Leukocyte Adhesion to the Vascular Endothelium at High Intraluminal Pressure
Published on: August 23, 2011
Cellular adhesion molecules and blood pressure: interaction with sex in a multi-ethnic population
Michelle A Miller1, Sally M Kerry, Derek G Cook
1Department of Community Health Sciences, St George's Hospital Medical School, London, UK. mmiller@sghms.ac.uk
Insights
Blood pressure associations with adhesion molecules differ by sex and age, particularly in premenopausal women. These findings may explain prior research inconsistencies and highlight potential menopause-related mechanisms.
Area of Science:
- Cardiovascular Science
- Biomarkers
- Epidemiology
Background:
- Adhesion molecules play a role in vascular health and inflammation.
- Previous studies on adhesion molecules and blood pressure have yielded inconsistent results.
- Understanding these relationships is crucial for cardiovascular disease risk assessment.
Purpose of the Study:
- To investigate the association between four specific soluble adhesion molecules and blood pressure.
- To examine these associations across different sexes and ethnic groups.
- To adjust for potential confounders including age, ethnicity, BMI, and smoking status.
Main Methods:
- Measurement of soluble P-selectin, E-selectin, ICAM-1, and VCAM-1 in plasma.
- Study population included 261 White, 188 African origin, and 215 South Asian individuals in England.
- Exclusion of participants with existing cardiovascular disease, diabetes, or on relevant medications.
Main Results:
- Soluble E-selectin showed a significant association with blood pressure after age adjustment.
- A significant interaction between sex and blood pressure (systolic, diastolic, pulse) was observed.
- In women, associations remained significant after full adjustment; in men, the association with diastolic pressure was abolished. Associations were most prominent in women under 50.
Conclusions:
- The relationship between adhesion molecules and blood pressure is specific to the molecule and influenced by sex and age.
- Menopause may modify the mechanisms linking blood pressure to adhesion molecule concentrations.
- These sex and age-specific differences may contribute to prior inconsistencies in the literature.
Objective:
To clarify the association between blood pressure and four different adhesion molecules, adjusting for potential confounders, in men and women from different ethnic origins.
Design And Methods:
The soluble (s) plasma adhesion molecules sP-selectin, sE-selectin, intracellular adhesion molecule-1 (sICAM-1) and vascular cell adhesion molecule-1 (sVCAM-1) were measured in 261 white (120 women), 188 African origin (99 women) and 215 South Asian (99 women) individuals living in England. All were free from coronary heart disease, stroke, other cardiovascular disease and diabetes, and were not receiving drug treatment for hypertension or high lipids, hormone replacement therapy or oral contraceptives.
Results:
After adjustment for age, only sE-selectin concentrations were significantly associated with blood pressure. There was a significant interaction of sex with systolic (P = 0.013), diastolic (P = 0.042) and pulse (P = 0.015) pressures. After adjustment for age, ethnicity, body mass index and smoking, the significant interaction of sex persisted and in women the associations with systolic (P < 0.001), diastolic (P < 0.001) or pulse (P = 0.004) pressure were unchanged, but in men the association with diastolic blood pressure was abolished. Finally, the association appeared to be present in women younger than 50 years, who were likely to be premenopausal.
Conclusions:
The relationship between adhesion molecules and blood pressure is adhesion molecule specific and varies with sex and age, which may partially explain previous inconsistencies in the literature. The mechanisms relating blood pressure to adhesion molecule concentrations are unknown, but they are likely to be modified by the menopause. These differences may relate to the production, clearance or cell-surface shedding of the adhesion molecules.
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