The numbers of atherosclerosis
Atherosclerosis (ATS) is a chronic vascular disease which represents one of the major causes of morbidity and mortality worldwide. A number of modifiable risk factors for atherosclerosis have been described, such as smoking, dyslipidemia, high blood pressure, hypercholesterolemia, and diabetes mellitus, among others.
The first sign of ATS appears to be the presence of fatty streaks in arterial walls, which progressively develop into the so-called atheroma and vascular plaques. The clinical consequences of these plaques vary according to their location, the degree of resulting stenosis and their growth rate (1).
In particular, for what concerns carotid plaques, even though certain types of atheromata can remain stable for many years, others rupture (unstable or vulnerable plaques). Such event can lead to local thrombus formation and subsequent embolisation to the ipsilateral ophthalmic, middle cerebral, or anterior cerebral arteries. As a result, a number of clinical manifestations may ensue, such as ipsilateral amaurosis fugax or retinal infarction, controlateral body transient ischaemic attack (TIA) and stroke (2).
Since atherosclerosis is most frequently asymptomatic, it is difficult to determine its incidence with accuracy. However, coronary heart disease appears to be the leading cause of death in Western countries, with more than 370,000 deaths per year. A population study designed to investigate the prevalence of asymptomatic carotid atherosclerotis in the general population showed that its general prevalence could be as high as 25% in adults (3,4).
Pathogenesis of the atherosclerotic plaque
The etiopathogenesis of the atherosclerotic plaque is multifaceted. There is general agreement that atherosclerosis stems from low density lipoproteins (LDLs) accumulating in the arterial intima, where they are prone to undergo oxidative processes that stimulate the immune response (7).
As a result, endothelial cells and smooth muscle cells (SMCs) express adhesion molecules and other chemical mediators which, in turn, facilitate the transformation of monocytes into macrophages and, through the accumulation of intracellular lipid content, foam cells, which stack in several layers giving rise to the visible yellow-colored xanthomas or fatty streaks.
Smaller lipid pools deposit beneath the layers of foam cells determining intimal thickening, while larger and more confluent lipid clusters attract the invasion of macrophages and grow into necrotic cores (also named lipid-rich necrotic core). In the presence of a necrotic core, the lesion is named a fibroatheroma.
The loose fibrocellular tissue which forms the atherosclerotic lesion often proliferates and intervenes between the necrotic core and the luminal surface, forming the so-called fibrous cap. Likewise, the necrotic core can progressively calcify, sometimes occupying most of the plaque volume.
Subsequently, vasa vasorum grow into the atherosclerotic lesions; these plaque neovessels are typically fragile and permeable, predisposing to intraplaque bleedings. Alternatively, plaque hemorrhage may result from a ruptured fibrous cap (8).
During atherogenesis, mechanisms of remodeling take place; in particular, in expansive remodeling the lumen area is partially preserved until plaques are large, while in constrictive remodeling stenosis may result from progressive plaque growth or vascular bed shrinkage. While the two mechanisms often coexist, it is interesting to note that expansive remodeling typically occurs with fibroatheromas and positively correlates with plaque inflammation, medial atrophy, and necrotic core size; on the contrary, constrictive remodelling often contain lesions rich in fibrous tissue (9).
Plaque rupture/erosion is the most frequent cause of thrombosis. Through a structural defect in the fibrous cap, especially where the cap is thin and infiltrated by foam cells (thin-cap fibroatheromas; TCFAs), the highly thrombogenic core contacts the blood with the formation of a thrombus.
To characterize the severity and prognosis of plaques, several terms are used.
Plaque burden is a measure of the extent of atherosclerosis. It can be measured through a variety of descriptive methods, such as: plaque volume, extent of lesion along the arterial surface, coronary calcium score by Computed tomography (CT), intima-media thickness and plaque area by ultrasound (US) and ankle-brachial pressure index in peripheral vascular disease.
Plaque vulnerability describes the short-term risk of thrombosis. A number of histological features of rupture-prone plaques have been identified, such as: a TCFA with a large necrotic core and macrophage infiltration in the cap, big plaque size, expansive remodeling, neovascularization, intraplaque hemorrhage (IPH), adventitial inflammation and spotty calcifications (10).
The American Heart Association (AHA) proposed a plaque classification that identifies six types which are meant to reflect the temporal natural history of the disease. Type I: atherogenic lipoproteins and mononuclear infiltrates; medial thickening. Type II: fatty streaks. Type III: lipid particles disrupt the integrity of the SMCs. Type IV: typical atheromata (large extracellular lipid core). Type V: atheromata developing fibrous caps. Type Vb: largely calcified lesions. Type Vc: more fibrous connective tissue, little lipid and no calcium. Type VI: ruptured atherosclerotic plaque with IPH or thrombosis (11-13). The rationale for this classification is that the structural composition of the carotid plaque modifies with the progression of the disease and some phases appear to be more prone to acute vascular events than others; in fact, lesion types IV, V and VI are those typically involved in cerebrovascular events.
A change of perspective: from measuring stenosis to identifying vulnerability
For several years the degree of luminal stenosis had been considered the main factor affecting the severity of carotid atherosclerotic disease.
Indeed, a number of trials published along the course of the 1980s and 1990s, such as the European Carotid Surgery Trial (ECST), the North American Symptomatic Carotid Endarterectomy Trial (NASCET) and the Asymptomatic Carotid Atherosclerosis Study (ACAS), contributed to establishing the idea that the degree of luminal stenosis should be the reference point to indicate the appropriateness of carotid endarterectomy intervention (14-17) (Figure 1).
More recently, a growing body of scientific evidence suggests that plaque structure and composition may serve as a more reliable biomarker for the prediction of cerebrovascular ischemic events (18).
Morphological high risk features, such as intima-media thickness, lipid cores, thin fibrous caps and ulcerated plaques have shown high correlation with stroke, even in patients with mild to moderate stenosis. Conversely, high calcium content appears to correlate with more stable plaques (12,19).
Thus, while it is generally accepted that high-grade stenosis tends to associate with complicated plaques more frequently than nonstenotic asymptomatic lesions, a large number of scientific publications demonstrated that complicated plaques also occur with moderate stenosis. As a result, nowadays the recognition of high risk carotid artery lesions can no longer be based on the degree of stenosis alone (20).
In a cross-sectional observational study including 85 consecutive patients with anterior circulation embolic stroke of undetermined source, an association was observed with large but nonstenotic carotid artery plaques located ipsilateral to the brain lesion, rather than controlateral; the Authors suggest that nonstenotic plaque is an underestimated cause of stroke (21).
As part of a substudy of the AIM-HIGH (Atherothrombosis Intervention in Metabolic Syndrome with Low HDL/High Triglycerides: Impact on Global Health Outcomes) clinical trial, an investigation was carried out to evaluate whether carotid plaque features of vulnerability may serve as a marker of cardiovascular outcomes in patients with a known history of atherosclerotic disease. Results showed that lipid content and fibrous cap integrity strongly predicted systemic atherothrombotic risk (22).
A retrospective study, conducted in a matched cohort of Caucasian and East Asians patients with stable chest pain, aimed to investigate the reasons behind the lower prevalence of myocardial infarction in the East Asian population. Coronary atherosclerotic burden and plaque composition were compared via computed tomography angiography for the two subgroups; results showed that that east Asians appear to have a lower predominance of high risk noncalcified plaques (23).
Imaging of the carotid atherosclerotic plaque
What’s in the toolbox?
Up until carotid atherosclerosis risk was evaluated based on the degree of stenosis alone, diagnosis and classification of carotid plaques was possible only in advanced stages of the disease, when luminal stenosis became manifest through digital subtraction angiography (DSA) or organ perfusion techniques. Then, DSA represented the diagnostic gold standard thanks to its capability not only to measure stenosis, but also to predict plaque rupture by identifying ulceration and surface abnormalities (12).
However, thanks to recent advances in medical imaging, new opportunities emerged to explore and assess both lumen morphology and the lumen wall itself. Similarly, the shift of attention which took place in this field of literature away from stenosis and into aspects of vulnerability has spurred tremendous interest for the development of noninvasive techniques to identify the characterizing features of vulnerable plaques (24).
Before focusing with more detail into CT imaging features of vulnerable plaques, the present section will provide a panoramic view of the various diagnostic tools currently available.
US represents the first-line imaging modality in the evaluation of carotid artery plaques since it is relatively simple, inexpensive and widely available.
The measurement of intima media thickness (IMT) has been widely recognized as a marker of systemic atherosclerosis with a strong correlation to coronary artery disease (25,26). However, a number of recent studies indicate for IMT a poor prognostic value and, at present, the use of IMT to guide therapeutical decisions is not recommended (27). Besides, it has been observed that carotid atherosclerosis is focal and manifests with plaques while IMT is often measured deliberately in areas not affected by plaque formation; indeed, IMT and plaques are biologically and genetically distinct entities which represent different phenotypes of atherosclerosis and respond differentially to therapy (28).
As far as B-mode images are concerned, high lipid content and intraplaque haemorrhage appear echolucent, while calcium and fibrous tissue appear echogenic (29). However, most Authors agree that US cannot reliably discriminate lipid from IPH because of a substantial overlap in their echo-structure (30). Moreover, US is heavily limited by being a user-dependent methodology.
Contrast-enhanced ultrasound is an emerging technique that finds its rationale in the selective retention of contrast at specific sites of disease. There is evidence that plaque enhancement in contrast-enhanced ultrasound correlates with greater neovascularization at histology (31-34).
Moreover, current research is testing targeted micro-bubbles (attached to antibodies, small peptides, and glycoproteins such as VCAM-1 and P-selectin) designed to identify specific cell surface structures (35). However, molecular US imaging is limited by the fact that it can only assess intravascular events beyond a given threshold of molecular expression.
Recent research has tested the potentialities of 3D US in the evaluation of plaque burden. In particular, within the context of PESA (Progression of Early Subclinical Atherosclerosis) observational prospective cohort study, 4,184 volunteers (aged between 40 and 54 years and without a history of cardiovascular disease) underwent carotid and femoral 3-dimensional vascular ultrasound (3DVUS), with a follow up at 3 and 6 years. The Authors employed an automated 30-degree sweep capturing approximately 6 cm of arterial length, centered at the carotid bulb and at the femoral bifurcation. Results showed that measures of plaque burden correlate with common cardiovascular risk factors with a higher prognostic value than plaque detection alone (36). While this study gave significant contribution towards the definition of a reliable imaging method to appraise plaque burden, further research is needed in order to develop optimal semi-automated scanning systems, test the feasibility to include femoral plaque measurement (in addition to carotid measurement) in the clinical routine and establish whether the evaluation of a limited arterial segment can provide a comprehensive assessment of plaque burden (37).
Magnetic resonance imaging (MRI)
High-resolution MRI has been widely used to evaluate atherosclerotic plaques with a particular ability to characterize soft tissue components. It can identify with high accuracy, sensitivity and specificity the lipid rich necrotic core, thin and ruptured caps, IPH (38).
Serfaty et al. published an AHA classification of atherosclerotic plaque specifically adapted for MR imaging, highlighting the ability of MR to describe plaques on the basis of composition and morphology (39).
One of the earliest applications of nanotechnology in MRI exploited the phagocytic uptake of paramagnetic iron oxide particles by macrophages at the plaque level (40). More recently, target-specific contrast agents (bound to adhesion molecules, high-density lipoprotein, MMPs, macrophage scavenger receptors and fibrin) have been developed, which allow for a better representation of plaque components and reduce acquisition times.
However, MRI is signal-insensitive and has low spatial and temporal resolution, which translates in long scanning times. Moreover, it is complex, expensive and less readily available when compared to other imaging modalities.
Multi detector computed tomography angiography (MDCTA)
Recently, there has been growing interest in MDCTA as a non-invasive modality to characterize atherosclerotic plaques. When compared with MRI, CT is more signal-efficient and has higher spatial and temporal resolution.
MDCTA can also detect various important features associated with plaque vulnerability (41), which will be further analyzed in the next section.
Positron emission tomography (PET)
PET with F-18-fluorodeoxyglucose (FDG) is a molecular imaging technique that can illuminate metabolically active processes. It has been shown to detect ‘inflamed plaques’ by highlighting FDG uptake in macrophages at the plaque level.
In a cohort of 54 patients scheduled for carotid endarterectomy, Cocker et al. demonstrated a correlation between 18FDG uptake and the presence of markers of intraplaque inflammation at the immunohistologic analysis of the surgical specimen (such as macrophage-sensitive CD68 and leukocyte-sensitive CD45); moreover, results showed a greater degree of 18FDG uptake in symptomatic patients, especially those with a recent history of cerebrovascular events (<90 days), suggesting that 18FDG imaging with PET/CT may serve as a surrogate biomarker of plaque activity and allow for non-invasive interrogation of the inflammatory status of plaque (42). Similarly, a number of publications explored the capability of 18F-sodium fluoride PET to distinguish vulnerable from non-vulnerable plaques with promising results, with the potential to detect early stages of atherosclerotic development (43). Indeed, while macroscopic calcium seems to stabilize atherosclerotic plaques, microcalcific deposits appear to increase the risk of plaque rupture by amplifying mechanical stress at the level of fibrous cap. It is postulated that 18F-sodium fluoride replaces the hydroxyl groups of hydroxyapatite expressed in regions of active mineralization; hence, elevated 18F-sodium fluoride uptake in PET/CT imaging could suggest increased risk of mechanical failure, which translates in plaque instability (44). However, for the time being molecular imaging is less widely available and requires longer procedural times than other imaging options such as CT or MRI.
Immunoscintigraphy uses radioactive tracers (such as low-density lipoproteins, haematoporphyrin derivatives, fibronectin, immunoglobulins, platelets and antifibrin antibodies) that localize into vulnerable plaques.
A look into the future
Shear wave elastography (SWE) is a novel US method which could identify plaques prone to rupture measuring acoustic radiation propagation within the fibrous cap (45).
A number of serum biomarkers (mainly inflammatory and proteolytic markers such as: high-sensitivity C-reactive protein, IL-6, MMP-9, MMP-2, and tissue inhibitors of metalloproteinases) have shown to be highly predictive of plaque vulnerability (46).
Optical coherence tomography (OCT) is an invasive imaging technique which is capable of visualizing subsurface tissue in high detail (with a spatial resolution of 10 µm), demonstrating lipid content, fibrous cap thickness, and fibrous cap macrophage attenuation. So far, OCT has been employed in the study of the coronary artery bed, but preliminary research indicates it could also find application in the evaluation of carotid plaques (12).
Artificial intelligence could play a fundamental role in the future; in particular, deep learning might enable automated detection of quantitative biomarkers and provide risk stratification protocols that incorporate imaging features from different techniques (47,48).
CT imaging of the vulnerable plaque
Features of vulnerability
The use of CT in the evaluation of carotid plaques has received steadily growing attention in recent years, especially since the advent of multi detector CT scanners (MDCT), which enable fast and accurate acquisition of vascular structures with minimal discomfort to the patient. Additionally, CTA allows in the same session to evaluate extra- and intracranial vessels (from the aortic arch to the circle of Willis) and cerebral parenchymal abnormalities. CTA has been shown to have sensitivity and specificity comparable to those of DSA in the detection of carotid artery stenosis and plaque surface irregularities, but it can also show the vascular wall and provide significant information on plaque volume and composition (49). The present section will provide an overview of the main imaging biomarkers of vulnerable carotid plaques as they appear in MDCTA.
There is general agreement among Authors that IPH can be considered the most relevant imaging feature associated with plaque instability (50-54). It has also been demonstrated that IPH prevalently locates ipsilateral to embolic strokes of undetermined source (52).
In the past years, a significant number of publications have indicated MRI as the best imaging modality to detect IPH based on the oxidative state of haemoglobin, which can be highlighted using common imaging sequences (47). Besides, many Authors argue that CT is insensitive in the differentiation of fibrous, lipid, and intraplaque haemorrhage because of a substantial overlap in HU values for these tissues.
However, a number of recent publications have been challenging this concept, indicating that modern MDCTA, paired with dedicated segmentation software analysis, can provide equal or better results in the detection of soft tissue subcomponents of the plaque when compared to MRI.
In this regard, in a retrospective study by Saba et al. conducted on 91 patients who underwent CEA, CTA carotid plaque slices were matched and compared to the corresponding histologic section to determine the accuracy of CTA in the detection of IPH. Results showed that IPH is characterized by low average values of HU and that a threshold of 25 HU in the volume acquired after the administration of contrast medium provides excellent sensitivity and specificity for IPH (53).
Wintermark et al. conducted a study to compare CTA-derived plaque sections, analyzed via an automated classification computer algorithm, versus histologic corresponding slices as the gold standard. The authors observe that while much of the literature indicates MRI and US as the methodologies of choice to study the composition of carotid plaques, most publications on CT have been based on older-generation scanners and that the potential for modern MDCTA in this field is unexploited. Their study shows that the CT-derived algorithm provide excellent correlation with histologic examinations in the quantification of calcifications; lipid cores and IPH also show good correlation, although with some limitations when smaller areas of lesion are considered (51).
Another retrospective study by Saba et al., which included 123 subjects (246 carotid arteries), quantified the degree of stenosis and plaque composition using CTA. Subcomponent volumes of the plaque were analyzed via a dedicated semi-automatic segmentation software which uses an algorithm of iterative image restoration and subdivides tissue components into HU threshold classes. Expanding from the classic definition of three plaque types based on attenuation values described by de Weert et al. (lipid, mixed, calcified) (55), five classes were identified: calcium (>130 HU), fibrous tissue (60 to 130 HU), lipid tissues (<60 HU), lipid-IPH (26 to 59 HU), IPH (<25 HU). Relative percentages for each component were also calculated, including a ratio of IPH/lipid volume ranging from value 0 (no IPH) to value 1 (all the lipid plaque correspondent to IPH). Results showed a statistically significant difference for the lipid and, in particular, for the IPH volumes across the symptomatic and asymptomatic patient groups, confirming that IPH greater volumes correlate with symptoms and cerebrovascular events. Conversely, in asymptomatic subjects a higher relative percentage of calcium and lipid-IPH was found. The study demonstrated that it is not only the overall plaque volume to be predictive of ruptures, but also the relative percentage of plaque subcomponents, suggesting that the biomechanical characteristics of the plaque are involved in the triggering of acute cerebrovascular events. Additionally, this study provides proof of principle that MDCTA, coupled with the use of volumetric quantification analysis software, is a reliable modality to image even small changes in plaque composition (56). Moreover, CT offers a unique alternative in those patients who have a contraindication to undergoing MRI imaging (e.g., prosthesis or pacemaker). Similar results have been demonstrated in a number of other recent works (57,58).
Lipid-rich necrotic core (LRNC)
The presence of a LRNC has been associated with increased risk of stroke (59).
In a similar fashion to what has been earlier discussed with regards to IPH, many publications over the course of the years have contributed to the idea that CT is a low performer in the identification of LRNC, due to a substantial overlap in HU with IPH (both showing values <60 HU). However, a number of Authors bring forward the idea that recent technological advances in MDCTA and volumetric analysis software allow room for a redefinition of the role of CTA in this diagnostic field.
In particular, Saba et al. compared the accuracy of in vivo quantification of calcification, LRNC and matrix from CTA sections against the histological specimens of 31 endarterectomies (with a total of 239 cross sections) by using dedicated image processing algorithms. The Authors start from the assumption that MRI does not offer signal intensity values characteristic of the different soft tissue plaque components within a single sequence, making it necessary to perform a differential analysis across various sequences, resulting in complex and time-consuming protocols. Additionally, results published in most works adopt a dedicated neck coil to compensate for insufficient spatial resolution. Conversely, HU values in CTA have the potential to be more quantitative than MRI signal intensity. Results from this work showed high correlation with histologic specimens in the quantification of calcification, demonstrating that the overestimation of calcified plaques at CT angiography, often described and classically attributed the artifactual “blooming effect”, may be successfully overcome via the use of dedicated software algorithms. Similarly, the software demonstrated a low level of measurement bias for what concerns the quantification of LRNC. Therefore, the Authors conclude that algorithm approach not only enables an accurate quantification of calcification, but also provides satisfactory characterization of soft plaque subregions (60).
Thin fibrous cap (TFC)
There is evidence based on histological findings that an intact fibrous cap correlates with low risk of plaque rupture, whereas a TFC and fissured fibrous cap (FFC) are associated, respectively, with moderate and high risk. Thus, the typical unstable plaques appear as TFC covering a LRNC, which can be accurately documented via MRI (61,62) and CTA (63).
In particular, it was demonstrated with histological validation that in CTA the presence of FFC correlates with a higher degree of plaque enhancement when compared against non-fissured caps (64).
Inflammatory processes, often referred to by the term ‘plaque activity’, play a central role in plaque progression, with intraplaque neovascularisation being one of its typical signs and a prelude for neovessel rupture and haemorrhage (65).
There is evidence that CTA can detect and quantify intraplaque neovascularisation, which appears to be proportional to the amount of contrast enhancement (66).
A recent study demonstrated, in fifty-one patients admitted for ischemic stroke or transient ischemic attack (TIA), a strong correlation between maximum soft plaque thickness (assessed on CTA) and American Heart Association type VI plaques (previously defined by MRI) (69).
In a cross-sectional study, Gupta et al. retrospectively analyzed a series of carotid CTA performed in patients with high-grade carotid stenosis in order to assess the correlation between plaque thickness and stroke or transient ischemic attack (TIA) history. The Authors found that, compared with asymptomatic subjects, patients with symptomatic carotid disease showed much larger soft (non-calcified) plaque and total plaque thickness values; conversely, symptomatic patients had smaller hard (calcified) plaque thickness measurements. Moreover, the study showed for each 1-mm increase in soft plaque there was a 2.7 times greater odds of previous stroke or TIA (70).
Plaque surface can be classified as smooth, irregular (cavities from 0.3 to 0.9 mm) or ulcerated (cavities >1 mm) (71). In particular, ulcerations (Figure 2) are considered a marker of vulnerable plaques (72), although they may also represent relics of previously occurred ruptures (73).
de Weert et al. explored the correlation between plaque surface morphology (together with degree of stenosis and other cardiovascular risk factors) and cerebrovascular symptoms, demonstrating a higher incidence of complex plaques in symptomatic patients (74).
Plaque total volume and subcomponents
There is scientific evidence that the volume of the carotid artery plaque associates with plaque vulnerability and the incidence of stroke (77). In an US-based study designed to evaluate plaque progression in a cohort of 349 patients attending vascular prevention clinics, Wannarong et al. demonstrated that total plaque volume can predict cardiovascular outcomes more reliably than both IMT and total plaque area (78). The good spatial resolution of CT allows for a satisfactory analysis of both total plaque volume and of its subcomponents, especially when coupled with semi-automated software analysis based on HU thresholds and image restoration algorithms. Similar segmentation protocols have been tested using MRI, but the results were less convincing due to unsatisfactory spatial resolution (79).
As it was discussed earlier, while previous research indicated a higher sensitivity from MRI in discriminating between soft tissue components of the plaque, recent evidence suggests that modern MDCTA, coupled with dedicated software analysis, can discriminate accurately between lipid component and IPH (56).
With regards to the relative percentage of plaque subcomponents, as it was discussed earlier, there is evidence that fatty content associates with higher-risk lesions, while calcium appears to be a protective factor by supposedly stabilizing the plaque against biomechanical stress.
Saba et al. demonstrated an association between cerebral microbleeds, commonly seen in stroke patients and considered to be a harbinger of cerebral hemorrhage (80), and increased volume of carotid plaque fatty subcomponent. In this study, cerebral microbleeds were evaluated using a T2*-weighted gradient-recalled echo sequence, while carotid arteries were imaged in MDCTA (81).
A new type of CT scanner, dual energy CT, which works by postprocessing data relative to the attenuation values obtained from tissues scanned at multiple energy levels, has shown the ability to reduce artifacts related to the presence of calcium and quantify plaque calcifications with increased accuracy (82-84).
Present technique limitations
Despite MDCTA holding a significant potential to become the leading imaging modality for the study of carotid plaques, there are a number of technique limitations that must be highlighted.
First, as it was discussed in previous sections, there still is a certain degree of controversy in the literature with regards to the capability of CTA to reliably characterize soft tissue components, with some Authors indicating low sensitivity in the discrimination of lipid core and IPH, especially when small lesions are considered (54).
Other limitations described in the literature include beam-hardening artifacts associated with calcification (so-called ballooning artifacts, which can be partly reduced with post processing algorithms and DECT) and a high variability in patterns of plaque enhancement (which appears to be highly dependent on blood flow and time delay of image acquisition) (56,82,85).
The role of plaque imaging in the management of cardiovascular disease
Implementing research into the everyday clinical scenario
A growing number of recent scientific publications indicate that risk stratification in carotid atherosclerosis cannot rely on the quantification of luminal stenosis alone, but that newly introduced features of plaque vulnerability can be a more dependable predictor of acute vascular events. Even so, in the majority of institutions, US-based measurements of the degree of stenosis still represent the routine clinical examination to guide therapeutical approach.
In this scenario, MDCTA represents a potential candidate to become the imaging modality of choice in the characterization of carotid plaques, thanks to a number of advantages, such as: high spatial resolution, short acquisition times, large coverage in the Z-axis, access to a number of newly emerging post-processing techniques and a relatively easy to read interface for clinicians and surgeons (18).
Moreover, MDCTA is widely available in most clinical infrastructures and it is already integrated as standard care for most patients admitted for cerebrovascular incidents (12).
What do clinicians want to know?
Fundamentally, the imaging of carotid atherosclerosis is aimed at identifying patients with high risk of future cardiovascular events (especially among asymptomatic groups), guide therapeutical approaches and improve long-term outcomes (87).
When fully implemented in the clinical routine, the identification of higher risk biomarkers may warrant closer clinical follow-up and, possibly, expedite intensive medical treatment or revascularization in selected patient (47).
Furthermore, imaging provides support to the ongoing research in the field of new medical treatment. Indeed, imaging can provide objective assessment of a drug’s clinical efficacy before the ultimate step in drug evaluation (phase 3 trials, designed to assess impact on clinical end points) is initiated, involving the enrolment of large cohorts of patients, long follow-up periods and, typically, enormous costs. In other words, atherosclerosis imaging allows for the monitoring of early signals of therapeutical effects, which can inform researchers on which drugs hold a higher chance for success and merit to progress into phase 3 evaluation stages.
There is evidence that institutions that plan therapeutical approaches to cardiovascular disease by integrating clinical information with imaging biomarkers experience benefits in terms of cost-effectiveness (47,91).
Moreover, it has been demonstrated that CTA and MRI both prove more cost-effective than DSA (92); Sheahan et al. indicate that MRI appears to be more costly and time-consuming in the clinical routine when compared against MDCTA (60).
While scientific evidence suggests that imaging features of carotid plaque vulnerability outperform measurements of degree of stenosis in cerebrovascular risk stratification capabilities, a discrepancy still exists with the everyday clinical scenario since in most institutions such techniques are yet to find implementation in the clinical routine. In this context, CTA represents a strong candidate to become the imaging modality of choice in carotid plaque characterization, thanks to its excellent spatial resolution, short acquisition times, widespread availability and the capacity to accurately define plaque volume and subcomponents, especially when coupled with post-processing analysis techniques.
Provenance and Peer Review: This article was commissioned by the Guest Editor (Dr. Kosmas I. Paraskevas) for the series “Carotid Artery Stenosis and Stroke: Prevention and Treatment Part I” published in Annals of Translational Medicine. The article was sent for external peer review organized by the Guest Editor and the editorial office.
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/atm-2020-cass-13). The series “Carotid Artery Stenosis and Stroke: Prevention and Treatment Part I” was commissioned by the editorial office without any funding or sponsorship. The authors have no other conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
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