Related Experiment Video
Updated: Apr 16, 2026

Visualizing Leukocyte Rolling and Adhesion in Angiotensin II-Infused Mice: Techniques and Pitfalls
Published on: January 4, 2018
The relationship between vascular inflammation and target organ damage in hypertensive crises
Mustafa Karabacak1, Mehmet Yigit2, Kenan Ahmet Turkdogan2
1Department of Cardiology, Isparta State Hospital, Isparta, Turkey.
Insights
Hypertensive crises with target organ damage show higher vascular inflammation markers, including monocyte chemoattractant protein-1 (MCP-1). These findings suggest MCP-1 may play a role in developing organ damage during hypertensive emergencies.
Area of Science:
- Cardiovascular Medicine
- Inflammation Biology
- Nephrology
Background:
- Hypertensive crises increase cardiovascular risks, with target organ damage (TOD) worsening outcomes.
- Monocyte chemoattractant protein-1 (MCP-1) is a key mediator in recruiting monocytes to inflamed vasculature.
Purpose of the Study:
- To investigate the association between vascular inflammation and the development of TOD in patients experiencing hypertensive crises.
- To evaluate plasma levels of MCP-1 as a potential biomarker for TOD in this patient group.
Main Methods:
- A comparative study included 33 patients with TOD and 30 patients without TOD.
- Evaluated parameters included routine labs, neutrophil-lymphocyte ratio, uric acid, C-reactive protein (CRP), high-sensitivity CRP, and plasma MCP-1.
Main Results:
- Patients with hypertensive crises exhibited elevated neutrophil counts, white blood cells, high-sensitivity CRP, and uric acid.
- Significantly higher levels of CRP and MCP-1 were observed in the TOD group compared to those without TOD.
Conclusions:
- Plasma MCP-1 levels are significantly elevated in hypertensive crisis patients with TOD.
- Increased vascular inflammation, indicated by higher MCP-1, is suggested to be associated with TOD development in hypertensive crises.
Objective:
Hypertensive crises, divided depending on the presence of target organ damage (TOD), are associated with increased cardiovascular mortality and morbidity. Monocyte chemoattractant protein-1 (MCP-1) is responsible for the recruitment of monocytes to sites of vascular inflammation. The aim of this study was to evaluate the role of vascular inflammation in development of TOD.
Method:
The patients were categorized according to the presence of TOD. Thirty-three patients (15 female; mean age, 68 ± 12 y) with TOD and 30 patients (14 female; mean age, 64 ± 12 y) without TOD were included to the study. In addition to routine laboratory parameters, neutrophil-lymphocyte ratio, uric acid, C-reactive protein (CRP), high sensitive CRP, and plasma MCP-1 levels were evaluated.
Results:
Neutrophil counts, white blood cells, high sensitive CRP, and uric acid levels were higher in patients with hypertensive crises. More importantly, CRP (7.2 mg/dL [2-37.8 mg/dL] vs 4.6 mg/dL [1.5-14 mg/dL] vs 2.7 mg/dL [1-8.1 mg/dL], P < .01) and MCP-1 levels (546 pg/mL [236-1350 pg/mL] vs 407 pg/mL [78-942 pg/mL] vs 264 pg/mL [34-579 pg/mL], P < .01) were higher in the group with TOD compared with other groups.
Conclusion:
In conclusion, plasma MCP-1 levels were significantly higher in patients with TOD. According to our results, we suggest that increased vascular inflammation and MCP-1 levels might be associated with the development of TOD in hypertensive crisis.
More Related Videos
Related Concept Videos
Hypertension III: Clinical Manifestations and Diagnostic Studies
Hypertension II: Pathophysiology
Inflammatory Response I: Vascular and Cellular
Disorders of the Autonomic Nervous System
Raynaud's disease, also known as Raynaud's...
Hypertension and Regulation of Blood Pressure
Vascular Spasm

