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Elevated circulating P-selectin in insulin dependent diabetes mellitus
B Jilma1, P Fasching, C Ruthner
1Department of Clinical Pharmacology, Clinical Institute of Medical and Chemical Laboratory Diagnostics, Vienna, Austria.
Thrombosis and Haemostasis
|September 1, 1996
Summary
Patients with insulin dependent diabetes mellitus (IDDM) have higher plasma levels of circulating P-selectin (cP-selectin) and von Willebrand antigen (vWF-Ag). These findings support targeting P-selectin to prevent diabetes complications.
Area of Science:
- Endocrinology and Metabolism
- Vascular Biology
- Immunology
Background:
- Increased P-selectin expression is observed on platelets and choroidal microvessels in patients with insulin dependent diabetes mellitus (IDDM).
- This suggests a potential role for P-selectin in the pathophysiology of IDDM-related vascular issues.
Purpose of the Study:
- To investigate whether plasma concentrations of circulating P-selectin (cP-selectin) are elevated in patients with IDDM.
- To compare cP-selectin levels between non-smoking IDDM patients on intensified insulin therapy and healthy controls.
Main Methods:
- Prospective, cross-sectional, analyst-blinded study design.
- Plasma levels of cP-selectin and von Willebrand antigen (vWF-Ag) were measured using enzyme-linked immunoassays.
- Subjects were individually matched for sex, age, and body mass index, with 42 pairs analyzed.
Main Results:
- Median plasma cP-selectin levels were 21% higher in IDDM patients (285 ng/ml) compared to controls (236 ng/ml; p = 0.004).
- Median plasma vWF-Ag levels were 10% higher in IDDM patients (96 U/dl) than in controls (87 U/dl; p = 0.025).
- No significant correlation was found between plasma cP-selectin and vWF-Ag levels in either group.
Conclusions:
- Elevated plasma cP-selectin levels in IDDM patients align with increased P-selectin expression on platelets and microvessels.
- These findings provide a rationale for targeting P-selectin with small molecule inhibitors.
- Targeting P-selectin may help treat or prevent micro- and macrovascular complications associated with IDDM.