Radiolabelled probes for imaging of atherosclerotic plaques
1Department of Patho-Functional Bioanalysis, Graduate School of Pharmaceutical Sciences, Kyoto University 46-29 Yoshida Shimoadachi-cho, Sakyo-ku, Kyoto 606-8501, Japan.
Insights
Nuclear imaging techniques like PET and SPECT offer sensitive, quantitative detection of unstable atherosclerotic plaques. This review explores radiolabeled probes for molecular imaging, aiding early diagnosis and preventive treatments for cardiovascular disease.
Area of Science:
- Cardiovascular medicine
- Molecular imaging
- Nuclear medicine
Background:
- Cardiovascular disease is a leading global cause of death, often caused by unstable atherosclerotic plaque rupture.
- Current imaging methods (CT, MRI, US, IVUS) struggle with quantitative assessment of plaque instability.
- Early diagnosis of unstable plaques is crucial for preventive treatment of myocardial and brain infarction.
Purpose of the Study:
- To review the current state and future of radiolabeled probes for detecting atherosclerotic unstable plaques.
- To highlight the potential of nuclear imaging techniques for functional diagnosis of plaque instability.
- To discuss molecular targets associated with unstable plaques for imaging.
Main Methods:
- Review of existing literature on radiolabeled probes for nuclear imaging (PET, SPECT).
- Focus on molecular targets indicative of plaque instability: inflammation (macrophages), oxidative stress, apoptosis, and protease activity.
- Discussion of quantitative data acquisition and interpretation in nuclear imaging.
Main Results:
- Nuclear imaging (PET, SPECT) provides sensitive, in vivo, quantitative functional information about unstable plaques.
- Specific molecular characteristics of unstable plaques (inflammation, oxidative stress, apoptosis) are viable targets for radiolabeled probes.
- Advancements in radiolabeled probes are expanding the capabilities for detecting and characterizing atherosclerotic disease.
Conclusions:
- Nuclear imaging offers a promising approach for the sensitive and quantitative diagnosis of unstable atherosclerotic plaques.
- Radiolabeled probes targeting specific molecular markers can enable early detection and risk stratification.
- Further development of these probes is essential for improving preventive strategies against cardiovascular events.
Abstract:
Cardiovascular disease is the leading cause of death worldwide. Unstable atherosclerotic plaques are prone to rupture followed by thrombus formation, vessel stenosis, and occlusion and frequently lead to acute myocardial infarction and brain infarction. As such, unstable plaques represent an important diagnostic target in clinical settings and the specific diagnosis of unstable plaques would enable preventive treatments for cardiovascular disease. To date, various imaging methods such as computed tomography (CT), magnetic resonance imaging (MRI), ultrasound (US), and intravascular ultrasound (IVUS) have been widely used clinically. Although these methods have advantages in terms of spatial resolution and the ability to make detailed identification of morphological alterations such as calcifications and vessel stenosis, these techniques require skill or expertise to discriminate plaque instability, which is essential for early diagnosis and treatment and can present difficulties for quantitative estimation. On the other hand, nuclear imaging techniques such as positron emission tomography (PET) and single photon emission computed tomography (SPECT) can noninvasively collect quantitative information on the expression levels of functional molecules and metabolic activities in vivo and thus provide functional diagnoses of unstable plaques with high sensitivity. Specifically, unstable plaques are characterized by an abundance of invasive inflammatory cells (macrophages), increased oxidative stress that increases oxidized LDL and its receptor expressed on cells in the lesions, increased occurrence of apoptosis of macrophages and other cells involved in disease progression, increased protease expression and activity, and finally thrombus formation triggered by plaque rupture, which is the most important mechanism leading to the onset of infarctions and ischemic sudden death. Therefore, these characteristics can all be targets for molecular imaging by PET and SPECT. In this paper, we review the present state and future of radiolabelled probes that have been developed for detecting atherosclerotic unstable plaques with nuclear imaging techniques.
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