BRIEF RESEARCH REPORT article
Symptomatic vs. Asymptomatic 20–40% Internal Carotid Artery Stenosis: Does the Plaque Size Matter?
- 1Department of Neurology, University Hospital Würzburg, Würzburg, Germany
- 2Department of Neurology, University Hospital of Essen, Essen, Germany
- 3Department of Neurology, University Hospital of Alexandria, Alexandria, Egypt
- 4Department of Neurology, Kantonssptial St. Gallen, St. Gallen, Switzerland
Background: Around 9–15% of ischemic strokes are related to internal carotid artery (ICA)-stenosis ≥50%. However, the extent to which ICA-stenosis <50% causes ischemic cerebrovascular events is uncertain. We examined the relation between plaque cross-sectional area and length and the risk of ischemic stroke or TIA among patients with ICA-stenosis of 20–40%.
Methods: We retrospectively identified patients admitted to the Department of Neurology, University Hospital of Würzburg, from January 2011 until September 2016 with ischemic stroke or TIA and concomitant ICA-stenosis of 20–40%, either symptomatic or asymptomatic. Plaque length and cross-sectional area were assessed on ultrasound scans.
Results: We identified 41 patients with ischemic stroke or TIA and ICA-stenosis of 20–40%; 14 symptomatic and 27 asymptomatic. The plaque cross-sectional area was significantly larger among symptomatic than asymptomatic ICA-stenosis; median values (IQR) were 0.45 (0.21–0.69) cm2 and 0.27 (0.21–0.38) cm2, p = 0.03, respectively. A plaque cross-sectional area ≥0.36 cm2 had a sensitivity of 71% and a specificity of 76% for symptomatic compared with asymptomatic ICA-stenosis. In a sex-adjusted multivariate logistic regression, a plaque cross-sectional area ≥0.36 cm2 and a plaque length ≥1.65 cm were associated with an OR (95% CI) of 5.54 (1.2–25.6), p = 0.028 and 1.78 (0.36–8.73), p = 0.48, respectively, for symptomatic ICA-stenosis.
Conclusion: Large plaques might increase the risk of ischemic stroke or TIA among patients with low-grade ICA-stenosis of 20–40%. Sufficiently powered prospective longitudinal cohort studies are needed to definitively test the stroke risk stratification value of carotid plaque length and cross-sectional area in the setting of current optimal medical treatment.
Internal carotid artery (ICA)-stenosis ≥50% causes around 9–15% of ischemic strokes (1). Evidence is accumulating that low-grade ICA-stenosis bears also a high-risk for ischemic stroke (2–5); if no optimal medical treatment is implemented, the annual ipsilateral stroke rate associated with mild-to-moderate asymptomatic ICA-stenosis is 0.1–1.6% compared to 2–3.3% among severe stenotic degrees (6, 7). Previous studies pointed to carotid plaque area as a useful parameter to stratify the risk of stroke and even to monitor preventive treatment of cerebrovascular and major vascular diseases (8, 9). In the current work, we investigated whether the carotid plaque cross-sectional area and/or length are more prominent among symptomatic than asymptomatic ICA-stenosis of 20–40%.
We conducted a subgroup analysis from a recently published cohort (10). In the current retrospective observational study, we included patients with an acute ischemic stroke or TIA admitted within 14 days of symptom onset, and a concomitant ipsilateral symptomatic ICA-stenosis of 20–40% (measured according to the NASCET criteria) without any other apparent stroke etiology according to the Trial of Org 10,172 in Acute Stroke Treatment (TOAST) (11), or a contralateral asymptomatic ICA-stenosis of 20–40% in the Department of Neurology (University Hospital of Würzburg) from January 2011 until September 2016. The exclusion criteria were: (1) ischemic stroke due to coronary angiography, carotid artery stenting, or carotid endarterectomy (CEA), (2) absence of ultrasound scans, or (3) bilateral stroke. In patients with bilateral ICA-stenosis of 20–40%, we included the symptomatic side in the present study and excluded the asymptomatic one to avoid including the same patient in the two study groups. All patients received the following minimal stroke work-up: routine blood tests within 24 h after index-TIA or index-stroke, ECG-monitoring with atrial fibrillation (AF) alarm for a minimum of 24-h, transthoracic echocardiography, extra- and transcranial color-coded duplex ultrasonography, and neuroimaging using computed tomography (CT) and/or magnetic resonance imaging (MRI).
Stroke was defined as acute-onset focal neurological deficits with a corresponding brain lesion in a vascular distribution showing hyperintensity in the diffusion-weighted images (DWI) with a corresponding hypointensity in the apparent diffusion coefficient (ADC) images and/or hypodensity in the cerebral CT. If the patient did not undergo cerebral MRI, stroke was diagnosed if the deficits persisted >24 h, with no other reasonable etiology. TIA was diagnosed if the deficits did not lead to brain lesions in the neuroimaging and the deficits persisted <24 h. Hypertension was defined as the presence of any of the followings: (1) persistent elevation of the systolic blood pressure ≥140 mmHg or diastolic blood pressure ≥90 mmHg requiring the initiation of antihypertensive drugs (12), or (2) if the patient was previously diagnosed with hypertension and has already received antihypertensive medications. Diabetes mellitus was defined according to the following criteria: (1) Hemoglobin A1c ≥ 6.5%, (2) Fasting blood glucose ≥126 mg/dl, (3) Blood glucose ≥200 mg/d, 2 h after oral glucose tolerance test (13), or (4) Previous diagnosis and treatment of diabetes mellitus. The patients were diagnosed as active smokers if they regularly consumed cigarettes within the previous 12 months. Atrial fibrillation (AF) was diagnosed according to the following criteria: (1) previously documented AF in the family physician's office prior to the index event or (2) 12-lead ECG or Holter ECG recorded after the index event showing loss of p-waves with irregular rapid heart rate and narrow QRS-complex for a duration of at least 30 s.
Ultrasound Assessment of the Plaque Length and Cross-Sectional Area
Ultrasound examination was conducted on a Toshiba AplioXG machine (Toshiba Medical Systems Corporation, Tochigi, Japan) using a 7.5 MHz linear array transducer. Ultrasound images were assessed in our picture archiving and communication system (PACS) by a single non-blinded examiner (AE). The hemodynamic criteria of the NASCET were used to measure the degree of stenosis (14). The stenotic length was measured from the most proximal to the most distal stenotic end, in the projection demonstrating the longest length, using a previously published method (10). The stenotic ends were defined according to the following criteria: (1) visible narrowing of the vascular lumen, (2) flow turbulence in the proximal stenotic end. For the distal end, this criterion was used to identify the distal end only in the presence of Doppler waves showing increased flow velocity. This is because there is no possible differentiation between a flow turbulence resulting from increased systolic flow velocity and that resulting from poststenotic flow disturbance, and/or (3) calcification shadowing. For the assessment of the plaque cross-sectional area, we used a previously published method (8, 15). First, we identified the projection demonstrating the largest cross-sectional area. Then we magnified the stored images in our PACS. Thereafter, we outlined the plaque edges using a cursor. Finally, the plaque cross-sectional area was displayed on the screen. Figure 1 demonstrates the measurement methods used for the plaque length and cross-sectional area.
Figure 1. Measurement method: Example for the method used to measure the plaque length (dashed red line) and cross-sectional area (dashed yellow) in a patient with symptomatic low-grade internal carotid artery stenosis of 20–40%.
Quantitative data were expressed using median and interquartile range, while qualitative data were expressed in absolute values and relative frequencies. To check for normality, we used a histogram and the Shapiro-Wilk test. Univariable statistical tests were conducted using χ2 test or Fischer exact test (if n < 5) for categorical data as well as Mann-Whitney U-test for continuous data. We calculated the sensitivity and specificity of plaque length and cross-sectional area using a receiver operating characteristic (ROC)-curve. An AUC > 0.5 indicates better prediction; values closer to 1 indicate more accurate prediction. Univariate binary logistic regression analyses were performed to measure the strength of association, measured as OR (95% CI), between the occurrence of ischemic stroke or TIA in relation to low-grade ICA-stenosis and other possibly related variables. Variables with a p < 0.1 and our two study variables (plaque cross-sectional area as well as plaque length) were further assessed in a multivariate logistic regression model. The fitness of this model was tested using a Hosmer-Lemeshow “goodness-of-fit” test. Data were analyzed in SPSS software package version 25 (SPSS, Chicago, IL, USA). P < 0.05 was considered statistically significant.
Four hundred eighty-nine patients, who received the ICD10-codes for stroke or TIA as well as ICA-stenosis, were screened for our inclusion and exclusion criteria. Forty-one patients (27 asymptomatic and 14 symptomatic ICA-stenosis) were included (See flow chart, Figure 2). The baseline characteristics are shown in Table 1. The risk factors were similar between the two groups. The plaque cross-sectional area was significantly larger and the length was insignificantly longer for symptomatic than asymptomatic ICA-stenosis; median (IQR) were 0.45 (0.21–0.69) cm2 and 0.27 (0.21–0.38) cm2, p = 0.03, as well as 1.7 (1.5–2.1), and 1.4 (1.1–1.8) cm, p = 0.15, respectively. Using a ROC-curve (Figure 3), a plaque cross-sectional area ≥0.36 cm2 and a plaque length ≥1.65 cm were found to have a sensitivity of 71 and 50% and a specificity of 76 and 64%, respectively, for symptomatic compared to asymptomatic ICA-stenosis (for cross-sectional area: AUC 0.72, 95% CI 0.53–0.91, p = 0.03, whereas for length: AUC 0.64, 95% CI 0.46–0.82, p = 0.16). In a sex-adjusted multivariate binary logistic regression model (Table 2), a plaque cross-sectional area ≥0.36 cm2 and a plaque length ≥1.65 cm were associated with an OR (95% CI) of 5.54 (1.2–25.6), p = 0.028, and 1.78 (0.36–8.73), p = 0.48, respectively, for symptomatic compared to asymptomatic ICA-stenosis. The Hosmer-Lemeshow “goodness-of-fit” test showed a non-significant difference between the observed and expected results with p = 0.076.
Figure 2. Flow chart showing the inclusion and exclusion criteria for patients enrolled in the present study. CA, carotid artery; CCA, common carotid artery; ICA, internal carotid artery; TIA, transient ischemic attack, iatrogenic stroke (5 cases after carotid endarterectomy, 1 case after coronary angiography). Of the 489 patients screened, only 41 patients met our inclusion and exclusion criteria.
Figure 3. Receiver operating characteristics curve (ROC) showing the relation between plaque surface area (blue) and length (green) with ipsilateral ischemic manifestations. A cut-off plaque cross-sectional area of ≥0.36 cm2 (indicated by the red circle) yielded a sensitivity of 71% and a specificity of 76% for the development of ipsilateral manifestations; AUC (95% CI) = 0.72 (0.53–0.91), p = 0.03. A cut-off plaque length of ≥1.65 cm (indicated by the red circle) yielded a sensitivity of 50% and a specificity of 64% for the development of ipsilateral manifestations; AUC (95% CI) = 0.64 (0.46–0.82), p = 0.16.
Table 2. Factors related to the occurrence of stroke or transient ischemic attack ipsilateral to a low-grade stenosis in the binary logistic regression models.
Plaque Size May Represent a High-Risk Plaque Feature
We found that the plaques of symptomatic low-grade ICA-stenosis of 20–40% had a significantly larger cross-sectional area and were insignificantly longer in comparison to asymptomatic ICA-stenosis of 20–40%. Among our patients with ICA-stenosis of 20–40%, a plaque cross-sectional area ≥0.36 cm2 had a sensitivity of 71% and a specificity of 76% with an OR (95% CI) of 5.54 (1.2–25.6) for symptomatic ICA-stenosis. We measured the plaque area using a method similar to previous studies. Taking the paucity of studies on plaque length into account, we considered several elements (narrowing of the vascular lumen, flow turbulence, increased flow velocity, and plaque calcification) to increase the accuracy of our measurement method for the plaque length. In line with our findings, the asymptomatic carotid stenosis and risk of stroke study (ACSRS) showed that increased plaque area, measured on ultrasound, is associated with increased future ipsilateral stroke rate from asymptomatic ICA-stenosis of 12–99% (NASCET) (15). The median (IQR) plaque area in the ACSRS study was 0.42 (0.27–0.6) cm2 and plaques >0.8 cm2 were noticeably associated with higher ipsilateral stroke risk. Of note, the ACSRC study included ICA-stenosis of 12–99%, whereas our study was restricted to ICA-stenosis of 20–40%. Moreover, previous studies reported that plaque thickness, length, and volume were more prominent on the ipsilateral side among patients with stroke (2, 4). Similarly, another study showed that carotid plaque volume of the endarterectomy specimens was larger in symptomatic than in asymptomatic ICA-stenosis (mean, 0.97 vs. 0.74 cm3, p < 0.001) (16). Furthermore, the total areas of all plaques in the right carotid artery, measured on ultrasound, were a strong predictor of ischemic stroke (9). Another study showed that the total carotid plaque areas on ultrasound in both carotid arteries were positively related to the combined 5-year risk of stroke, myocardial infarction, and vascular death (8). In a population-based study, larger plaque thickness (17), or carotid intima-media thickness (18, 19) were found to bear a higher risk for future major vascular events. Conversely, Nandalur et al. reported no difference between carotid plaque volume, measured by multidetector CT, among symptomatic compared to asymptomatic ICA-stenosis (20). Of note, a prominent inverse correlation between the degree and length of stenosis was reported among patients with symptomatic ICA-stenosis ≥ 70% but neither among symptomatic ICA-stenosis <70% nor among asymptomatic ICA-stenosis (10). Interestingly, statin was found to slow plaque progression, and even led to regression of the carotid plaques. This effect was mainly shown with maintaining the serum level of low-density lipoprotein <100 mg/dl independent of the statin dose (21). Plaque size can be used to stratify the cardio- or cerebrovascular risk and to monitor response to treatment (8, 15).
Other High-Risk Plaque Features
Several researchers investigated high-risk plaque features. Demarco et al. found that the following plaque features, assessed on magnetic resonance angiography (MRA), were more frequent among symptomatic mild-to-moderate ICA-stenosis compared to asymptomatic mild-to-moderate stenosis: thin or ruptured fibrous cap (100 vs. 36%, p = 0.006), lipid-rich necrotic core (100 vs. 39%, p = 0.022), and -to a lesser extent- plaque hemorrhage (86 vs. 33%, p = 0.055) (5). A meta-analysis showed that intraplaque hemorrhage (IPH), defined as the presence of a hyperintense signal within the carotid plaque on T1-weighted fat-suppressed MRI images, is associated with an annual stroke/TIA rate of 17.71% compared to 2.43% in relation to plaques without hemorrhage (22). The authors noted that IPH was associated with a hazard ratio [HR] of 5.69 (95% CI 2.98–10.87) for stroke/TIA. However, optimal medical treatment was not accurately implemented for patients included in the aforementioned meta-analysis; only 62% of the patients had a statin and 72% had an antiplatelet therapy, whereas data regarding further elements of optimal medical treatment are not available. Another meta-analysis identified the following high-risk ultrasound plaque features: plaque neovascularity (OR 19.68, 95% CI 3.14–123.16), complex plaque (OR 5.12, 95% CI 3.42–7.67), plaque ulceration (OR 3.58, 95% CI 1.66–7.71), plaque echolucency (OR 3.99, 95% CI 3.06–5.19), and intraplaque motion (OR = 1.57, 95% CI = 1.02–2.41) (23). Of note, hypoechoic plaque morphology is more often associated with intraplaque hemorrhage (24), and is notably related to fatal or disabling stroke (15). Plaque inflammation on PET/CT was also identified as a high-risk feature (25). Interestingly, the ACSRS study showed that the combination of high-risk clinical features, high-risk plaque features, and the degree of stenosis could better stratify the risk of ipsilateral stroke/TIA (15). The authors of the aforementioned study identified the following high-risk plaque features: hypoechoic plaque morphology or low gray scale median (GSM), increased plaque area, and the presence of discrete white areas without acoustic shadowing. For example, the authors showed a 5-year ipsilateral stroke rate of 70.4% among patients with the following combinations: asymptomatic ICA-stenosis of 50–82% (NASCET), history of contralateral stroke/TIA, discrete white areas, plaque area >0.8 cm2, and low GSM <15. Conversely, the 5-year ipsilateral stroke rate was as low as 1.9% for patients with the following combinations: asymptomatic ICA-stenosis 83–99% (NASCET), no history of contralateral stroke/TIA, absence of discrete white areas, plaque area <0.4 cm2, and GSM >30. Of note, the ACSRS study was conducted before the era of optimal medical treatment, so that the aforementioned 5-year ipsilateral stroke rates of 70.4% and 1.9% should be viewed with caution. This elucidates the importance of risk stratification using multiple high-risk clinical and plaque features rather than a single one. The follow-up of these features might be used to optimize medical treatment or to investigate new medical therapies for cerebrovascular and other major vascular events.
High-Risk Plaque Features Represent a Fruitful Subject for Future Research
More than 20 years ago, CEA was shown to provide an overall stroke prevention benefit in symptomatic patients with ICA-stenosis ≥50% (26–29). However, these data should be interpreted with caution, because they were conducted before the introduction of optimized medical treatment. The latter includes antiplatelets, statins, control of blood pressure and blood glucose level, smoking cessation, implementation of exercise programs, Mediterranean diet, and lifestyle modification, and was shown to significantly reduce the stroke risk among patients with asymptomatic ICA-stenosis (30, 31). Current optimized medical treatment is an established therapy for prevention of arterial disease complications, including patients with carotid stenosis, whether mild or severe, and it is a continually improving gold standard of care (32, 33), and should also be offered perioperatively before CEA (34). Best medical treatment seems to be as effective as CEA or carotid artery stenting for asymptomatic moderate-to-severe ICA-stenosis (30, 31, 33). Additionally, medical treatment is around 3–8 times more cost-effective than carotid procedures (33). Of note, under suboptimal medical treatment, the annual ipsilateral stroke rate associated with mild-to-moderate asymptomatic ICA-stenosis is 0.1–1.6% and 2–3.3% in severe asymptomatic ICA-stenosis (6, 7). Under best medical treatment, an average annual stroke rate among moderate-to-severe asymptomatic ICA-stenosis ranges from 0.3–3.1% (31). In the current work, large-sized plaques were shown to represent a high-risk plaque feature. The incidence of ipsilateral stroke associated with high-risk plaque features, and the protective effect of best medical treatment, as well as carotid procedures for those high-risk plaques, remain under-investigated. We recommend the assessment of this risk in future observational studies. If any subgroup can be identified with high-risk for ipsilateral stroke, despite best medical treatment, it is important to further test the cost-benefit ratio of carotid procedures for those patients in randomized trials before the results can be translated into the clinical practice.
We are aware of the following limitations: First, the sample size is small. However, this study was planned as a pilot study and serves as a proof-of-concept. Second, the design of the present study is retrospective and has to be confirmed in large prospective observational studies to stratify the risk related to different degrees of ICA-stenosis and high-risk plaque features. This allows assessing whether there is a subgroup with an ipsilateral stroke rate high enough to justify the conduction of trials of more intensive/different medical intervention and/or carotid procedures. Third, the assessment of the plaque length and surface area was performed by a non-blinded investigator, which represents another study limitation. Fourth, there is a bias of a sub-group analysis from a non-predefined primary outcome. Fifth, other individual risk factors, other plaque characteristics, and previous medications may have influenced our comparative analysis.
Large plaques might represent a high-risk marker for further complication of arterial disease including ipsilateral stroke among patients with low-grade ICA-stenosis. Sufficiently powered prospective longitudinal cohort studies are needed to definitively test the stroke risk stratification value of carotid plaque length and cross-sectional area in the setting of current optimal medical treatment. Plaque size, along with other high-risk plaque features and high-risk clinical features should be ideally used to optimize the medical treatment of patients with carotid stenosis as well as other atherosclerotic vascular diseases. Future observational studies are needed to stratify the risk of ipsilateral stroke associated with high-risk clinical features, along with high-risk plaque features among different stenotic degrees. This probably allows to identify subgroups of patients with a risk high enough to justify the conduction of future randomized trials.
The datasets generated for this study are available on request to the corresponding author.
Data collected within routine clinical care were used. Therefore, no specific approval was needed according to local regulations confirmed by the Ethics Board of the Medical Faculty of the University of Würzburg. Our Ethical Committee was consulted before the conduction of the study and the need for informed consent was waived because of the retrospective nature of the study.
AE collected the data, performed the measurements and the statistical analysis, and wrote the first draft. MS contributed to the ultrasound examinations. JV, MS, and FF supervised the work, provided consultations, and revised the manuscript. All authors were involved in the final approval of the version to be published, made a substantial contribution to the conception, design, and revision of the draft.
This publication was funded by the German Research Foundation (DFG) and the University of Wuerzburg in the funding programme Open Access Publishing.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: ischemic stroke, carotid atherosclerosis, carotid stenosis, plaque cross-sectional area, length of stenosis, carotid ultrasound
Citation: Elhfnawy AM, Volkmann J, Schliesser M and Fluri F (2019) Symptomatic vs. Asymptomatic 20–40% Internal Carotid Artery Stenosis: Does the Plaque Size Matter? Front. Neurol. 10:960. doi: 10.3389/fneur.2019.00960
Received: 29 April 2019; Accepted: 21 August 2019;
Published: 01 October 2019.
Edited by:Jean-Claude Baron, University of Cambridge, United Kingdom
Reviewed by:Miguel A. Barboza, University of Costa Rica, Costa Rica
Antonio Arauz, National Institute of Neurology and Neurosurgery (INNN), Mexico
Copyright © 2019 Elhfnawy, Volkmann, Schliesser and Fluri. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Ahmed Mohamed Elhfnawy, email@example.com