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Updated: May 13, 2026

A Human Ex Vivo Atherosclerotic Plaque Model to Study Lesion Biology
Published on: May 6, 2014
Fe(III) distribution varies substantially within and between atherosclerotic plaques
H Gustafsson1, M Hallbeck, M Norell
1Department of Medical and Health Sciences (IMH), Division of Radiological Sciences, Linköping University, Linköping, Sweden; Center for Medical Image Science and Visualization (CMIV), Linköping University, Linköping, Sweden.
Iron(III) (Fe(III)) is more concentrated in vulnerable atherosclerotic plaques, indicating its role in plaque instability and rupture. Symptomatic patients showed higher Fe(III) levels, cap rupture, and macrophage activity.
Area of Science:
- Cardiovascular Research
- Oxidative Stress Biology
- Medical Imaging and Diagnostics
Background:
- Vulnerable atherosclerotic plaques pose a rupture risk due to structural weakness, potentially linked to oxidative stress.
- Redox-active iron, specifically Fe(III), is implicated in oxidative stress mechanisms within plaques.
Purpose of the Study:
- To investigate the distribution of Fe(III) in carotid atherosclerotic plaques.
- To correlate Fe(III) levels with plaque vulnerability and rupture.
Main Methods:
- Atherosclerotic plaques from 10 patients (symptomatic and asymptomatic) were analyzed.
- Plaque vulnerability assessed via ultrasound and immunohistochemistry.
- Fe(III) quantified using electron paramagnetic resonance spectroscopy.
Main Results:
- Significant intra-plaque Fe(III) concentration variations were observed.
- Symptomatic plaques exhibited higher Fe(III) levels compared to asymptomatic ones (0.36 ± 0.21 vs. 0.06 ± 0.04 nmol Fe(III)/mg tissue).
- Symptomatic plaques showed increased cap rupture and macrophage infiltration (31% ± 11% vs. 2.3% ± 2.3%).
Conclusions:
- Fe(III) distribution is heterogeneous within atherosclerotic plaques.
- Higher Fe(III) concentrations correlate with symptomatic plaques, cap rupture, and increased macrophage activity.
- Fe(III) may serve as a biomarker for atherosclerotic plaque vulnerability.
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