Objectives We investigated the prevalence and long-term risk associated with intracranial atherosclerosis identified during routine evaluation.
Design This study presents data from a prospective cohort of patients admitted to our stroke unit for thrombolysis evaluation.
Setting and participants We included 652 with a final diagnosis of ischaemic stroke or transient ischaemic attack (TIA) from April 2009 to December 2011. All patients were acutely evaluated with cerebral CT and CT angiography (CTA). Acute radiological examinations were screened for intracranial arterial stenosis (IAS) or intracranial arterial calcifications (IAC). Intracranial stenosis was grouped into 30–50%, 50–70% and >70% lumen reduction. The extent of IAC was graded as number of vessels affected.
Primary and secondary outcome measure Patients were followed until July 2013. Recurrence of an ischaemic event (stroke, ischaemic heart disease (IHD) and TIA) was documented through the national chart system. Poor outcome was defined as death or recurrence of ischaemic event.
Results 101 (15.5%) patients showed IAS (70: 30–50%, 29: 50–70% and 16: >70%). Two-hundred and fifteen (33%) patients had no IAC, 339 (52%) in 1–2 vessels and 102 (16%) in >2 vessels. During follow-up, 53 strokes, 20 TIA and 14 IHD occurred, and 95 patients died. The risk of poor outcome was significantly different among different extents of IAS as well as IAC (log-rank test p<0.01 for both). In unadjusted analysis IAS and IAC predicted poor outcome and recurrent ischaemic event. When adjusted, IAS and IAC independently increased the risk of a recurrent ischaemic event (IAS: HR 1.67; CI 1.04 to 2.64 and IAC: HR 1.22; CI 1.02 to 1.47).
Conclusions Intracranial atherosclerosis detected during acute evaluation predicts an increased risk of recurrent stroke.
- STROKE MEDICINE
This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/
Statistics from Altmetric.com
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Strengths and limitations of this study
The high degree of generalisability due to the unselected patient population.
The consistent use of CT-angiography (CTA).
The acute CTA performance that might lead to an underestimation of the true prevalence of intracranial arterial stenosis due to thrombus formation.
Ischaemic stroke remains a leading cause of disability and death worldwide, and one of six persons suffers a stroke during their lifetime. Intracranial atherosclerosis represents a risk factor of stroke, however, varying incidence and significance worldwide have been reported.1–6 Even though intracranial arterial atherosclerosis is traditionally assumed most prevalent in patients of Asian descent, limited evidence is available as to the prevalence and prognostic significance of intracranial atherosclerosis in a European stroke population.
Overall, two markers of intracranial atherosclerotic changes are recognised on CT-based imaging of patients with stroke: intracranial arterial stenosis (IAS) and diffused intracranial arterial calcifications (IAC).
IAS has in recent years received much attention in relation to possible treatment interventions, especially with regard to endovascular procedures7 and pharmacological treatment.8 Though most attention has been focused on stenosis with severe lumen reduction, postmortem studies have shown that even lumen reductions of 30% can potentially give rise to embolism or thrombus.9 This finding indicates that patients with 30% stenosis could potentially be at increased risk of recurrent stroke.
IAC is assumed to reflect the atherosclerotic burden and can be assessed by means of simple non-contrast CT.10 ,11 Even though these lesions do not necessarily cause lumen reduction and may represent a more diffused atherosclerotic process—limited evidence suggests their link to recurrent ischaemic events in patients with stroke.12
Because intracranial atherosclerosis may represent an important and potentially modifiable risk factor for recurrent ischaemic events in an European stroke population, we aimed at (1) establishing the incidence of IAS and calcifications in an acute northern European thrombolysis population identified during acute radiological examination; (2) identifying potential modifiable risk-factors; and (3) assessing whether intracranial atherosclerosis identified during acute stroke evaluation predicts poor long-term outcome.
This study is based on a prospective cohort of stroke or patients with transient ischaemic attack (TIA) admitted to Copenhagen University Hospital—Bispebjerg with symptoms of acute stroke within 4.5 h and worked up for recanalisation therapy. The hospital has a catchment area for acute stroke of 1.7 million inhabitants on even dates, sharing the function with another hospital.
Patients admitted from April 2009 to December 2011 with a CT angiography (CTA) of diagnostic quality on admission and a discharge diagnosis of stroke or TIA were prospectively included in the cohort.
On arrival, all patients underwent physical and neurological examination, and the National Institute of Health Stroke Scale (NIHSS) score was obtained along with standard biochemistry, ECG and vital values. All patients underwent non-contrast CT—and in patients without contra indications, CTA was performed. Intravenous thrombolysis was administered according to general guidelines. In all non-thrombolysed patients with stroke or TIA, 300 mg of aspirin was administered.
Acute CT scans were performed using 64-section MDCT (Philips Brilliance 64 TM; Philips Medical Systems, Best, the Netherlands) with non-contrast CT cerebrum (120 kVp, 500 mAs; 5 mm slice thickness reconstruction). CTA was performed from aortic arch to vertex (120 kVp, 295 mAs; collimation 64×0.625 mm (isotropic voxel resolution)) with contrast injection, Omnipaque 350 mg/mL, 5 mL/s, monitored by bolus tracking in the descending aorta and scanned with fixed 3 s post-tracking delay (0.9 mm slice reconstruction).
All images during the study period were reviewed by a consultant neuroradiologist (AFC) blinded to all clinical data using a standardised method. Thoracocervicale and intracranial arteries from the aortic arch and cranially were evaluated. An extracranial carotid artery stenosis was considered significant, if a lumen reduction >70% was demonstrated.
All major intracranial vessels, (internal carotid artery, anterior cerebral artery, middle cerebral artery (MCA), posterior cerebral artery, basilar artery (B) and vertebral artery (V)) were screened for stenosis stratified into three categories of lumen reduction (30–50%, 50–70% and >70%) in accordance with standard WASID criteria for grading of IAS.13 We defined percentage of stenosis of an intracranial artery as follows Percentage of
where D (stenosis) is the diameter of the artery at the site of the most severe stenosis and D (normal) is the diameter of the proximal normal artery.13 If the proximal segment was diseased, contingency sites were chosen to measure D (normal): distal artery (second choice) or feeding artery (third choice). IAS was graded as symptomatic, if supplying a vascular area with radiological signs of acute ischaemia and no other obvious cause (eg, acute occlusion) was present.
We employed a semiquantitative score for the number of vessels calcified according to a presence or absence of calcified foci.12
Data extraction and definitions
Data were prospectively collected from all patients on a daily basis from charts and by direct interview. All previous concurrent medical conditions (stroke/TIA, ischaemic heart disease (IHD), congestive heart failure and periphery artery disease) were confirmed by registrations in previous medical charts.
Hypertension was defined as either use of antihypertensive medication or at least three blood pressure measurements above 140/90 mm Hg taken at least 1 h apart and at least 24 h after stroke onset—or a diagnosis of hypertension in the outpatient clinic. Diabetes was defined as use of antidiabetic medication, or a fasting glucose >9 mmol/L—or glycosylated haemoglobin >6.5%. Hypercholesterolaemia was defined as use of lipid-lowering medication—or plasma cholesterol > 5 mmol/L. IHD was defined as prior myocardial infarction or prior coronary by-pass surgery—or prior percutaneous coronary intervention. Atrial fibrillation was defined as a history of atrial fibrillation or at least 30 s of atrial fibrillation documented by telemetry or ECG in 12 leads. A history of smoking was defined as present use of tobacco in any form or a smoking history of at least 3 pack-years. Excessive use of alcohol was defined as consumption of more than 250 g alcohol/week for men and 170 g for women. Glomerular filtration rate was estimated on the basis of the creatine-level14
Prior to discharge, all patients with ischaemic stroke or TIA were prescribed an antiplatelet treatment regimen (clopidogrel—or aspirin and dipyridamole in combination). Patients with diagnosed atrial fibrillation were prescribed oral anticoagulation treatment, mainly warfarin, but dabigatran was used in some cases. All patients with thrombotic stroke were prescribed a statin and antihypertensives aiming at a maximum systolic value of 130 mm Hg.
All patients were followed up after discharge through the national online chart system until 1 July 2013. Recurrent event was defined as ischaemic stroke, TIA or IHD as documented by discharge cards. Recurrent stroke or TIA were considered present, if diagnosed by radiographic imaging studies, or if a consultant neurologist in the patient's discharge card confirmed the diagnosis. Recurrent IHD was defined as either ST-segment elevation myocardial infarction (STEMI) or non-STEMI (NSTEMI) diagnosed by ECG change or enzyme level increase, unstable angina pectoris, coronary by-pass surgery or percutaneous coronary intervention. Poor outcome was defined as either recurrent event or death within the follow-up period.
No formal sample size calculations were performed. The patient flow in the study period determined the sample size.
Categorical data were compared among groups using χ2 test. Ordinal or discrete risk factors were represented using median values and compared using Mann-Whitney U test. If variables were normally distributed, they were compared using Student’s’ t test, otherwise a non-parametric alternative (Mann-Whitney U test) was used. Missing values were excluded from the calculations.
To assess the association between risk factors and the presence of intracranial atherosclerosis, a multinomial logistic regression model was used. All risk factors from table 2 that proved a group difference of p<0.1 were entered in a backward stepwise multinomial logistic regression.
Survival was assessed using Kaplan-Meyer curves. In order to ensure sufficient group size in the Kaplan-Meier curves, we grouped 50–70% and >70% stenosis as >50%. Calcifications were grouped into three groups: one without and two groups with calcifications divided by the total median number of calcified arteries in the cohort. We conducted univariate Cox proportional hazard model analysis of characteristics in table 2 (not including medical history—stroke, TIA or myocardial infarction—due to potential interaction with other characteristics). We transferred characteristics that in the univariate model proved p<0.1 to the multivariate model. Patients lost to follow-up were censured the day they were lost. A general significance level of p<0.05 was employed. Statistical analysis was performed using SPSS V.20 statistical software (IBM Corp, Armonk, New York, USA).
During the study period, 924 patients were admitted with acute stroke symptoms. The final population thus comprised 652 patients with ischaemic stroke or TIA (figure 1). Only 34 patients (5.2%) had other ethnicity than Scandinavian, of whom 3 (0.5%) were of Asian descent.
Prevalence of intracranial atherosclerosis
A total of 115 IAS were observed in 101 (15.5%) patients (table 1). Of these 45 (39%) had a severe lumen reduction of >50%. Only one patient underwent endovascular procedures with stenting of a >70% basilar artery stenosis. This patient remained in the cohort due to failure of revascularisation. Three patients had a symptomatic stenosis (all above 50% lumen reduction and all in the MCA). IAC in one or more vessels was observed in 441 (68%: figure 2), and median number of vessels involved was two. This number was used to group patients with moderate calcifications (1–2 vessels calcified) from patients with extensive lesions (>2 vessels calcified).
Based on the baseline characteristics (table 2), a multinomial logistical regression was performed to determine the risk factor profile of IAC and IAS (table 3). Age was an independent predictor of IAC as well as IAS. In addition, atherosclerotic lesions in the aorta and former IHD were independent predictors in IAC as well as IAS. Hypertension, former stroke, hypercholesterolaemia and extracranial carotid stenosis were independent predictors of IAS (table 3).
Outcome after stroke
Of the 652 patients included in this analysis, 13 were lost to follow-up after hospital discharge—all foreign citizens, who had a stroke while visiting Copenhagen. The median (IQR) follow-up time was 815.5 days (607–1124 days). During the follow-up time, 87 ischaemic events were registered (53 strokes, 20 TIA and 14 IHD), and 95 patients died. Kaplan-Meier curves for poor outcome (death or ischaemic events) are presented in figure 3A,B. A significant difference in risk of poor outcome was present when stratified for the extent of both IAS as well as IAC (log-rank test p<0.01 in figure 3A and B). The probability of poor outcome past the first year after index event for patients with no IAS (0.16 CI 0.10 to 0.22) and no IAC (0.10 CI 0.03 to 0.22) was substantially lower than in patients with >50% IAS (0.27 CI 0.09 to 0.49) and >2 vessels IAC (0.30 CI 0.18 to 0.43). In crude estimates, both the burden of IAC (per vessels increase) and lumen reduction of any significant degree (IAS>30%) were associated with recurrent ischaemic events and poor outcome (table 4). When adjusted for other risk factors, the burden of IAC emerged as an independent predictor for recurrent event or death (HR 1.18; CI 1.03 to 1.36/vessel increase). If only recurrent ischaemic events (stroke, TIA and MI) were considered, both IAC and IAS emerged as independent risk factors for recurrent event (HR 1.67; CI 1.04 to 2.64 and HR 1.22; CI 1.02 to 1.47, respectively).
In this study, intracranial atherosclerosis was not an unusual finding in North European patients with ischaemic stroke and TIA. The process of developing atherosclerotic lesions seemed to be part of a global and time-dependent process of atherosclerotic development in the body, marked by progressing age along with accompanying lesions in the aortic arch and former myocardial infarction. In addition, more severe atherosclerotic lesions (lesions with lumen reduction—IAS) were linked to a more severe risk profile accompanied by extracranial carotid stenosis as well as traditional stroke risk factors as hypertension and hypercholesterolaemia. We furthermore observed that the risk of a poor outcome increased with the burden of intracranial atherosclerotic disease being highest in patients with >50% IAS and >2 vessels IAC. Both IAS (>30%) and IAC burden were independently associated with risk of recurrent ischaemic event.
The primary strength of this study is the high degree of generalisability due to the unselected patient population. This cohort of unselected patients further allows us to compare consecutive patients with stroke or TIA with intracranial atherosclerosis against a control group comprised of similar patients with stroke or TIA without intracranial atherosclerosis. Further, our national online chart system made sure that all patients with permanent stay in Denmark could be followed up, and recurrent events could be assessed from discharge cards. Only patients not seeking medical help for recurrent events have been missed. Another important strength of this study is the consistent use of CTA in the population and the blinded standardised imaging evaluation.
The primary limitations of this study are that the true prevalence of IAS probably is underestimated due to the acute setting, in which the CTA was performed. IAS may have been mistaken as acute vascular occlusions due to superimposed thrombus. However, in the present study, the aim is to assess the impact of stenosis identified during acute evaluation and their implication and signal value on the prognosis of the patients.
CTA has been shown to process a sensitivity and specificity of 97– 99.5%, respectively in detecting IAS>50% compared to DSA and to be superior to MR angiography.15 ,16 A number of studies have used transcranial Doppler to detect stenosis. Although, transcranial doppler (TCD) is non-invasive and performs well in the middle-cerebral artery, it is highly observer dependent and has poor sensitivity and specificity in the posterior vasculature.17
It is known that the prevalence of intracranial atherosclerosis varies with ethnicity. In direct comparison between ethnic groups in the population of Manhattan, persons with Caucasian ancestry have a lower burden of large vessel disease compared to people of Hispanic and African-American descent.4 ,18 This is supported by studies reporting the prevalence of IAS to be as high as 30–50% in Asian stroke populations1 ,3 ,5 ,6 and 7–12% in asymptomatic populations.19 ,20 The incidence of documented symptomatic intracranial stenosis in populations of Europe is reported to be 2.2–6.5%.21–23 This number may represent the tip of the iceberg. A newer cross-sectional CTA-based study elaborated by Homburg et al2 revealed a prevalence of stenotic lesions of 23% (30–99% stenosis). Our finding of a prevalence of 15.5% is in accordance with Homburg et al revealing that intracranial atherosclerotic disease is a relevant and prevalent problem in European stroke population. The reason for this ethnic difference in prevalence is likely due to genetic and lifestyle differences between ethnic groups.
The direct comparison of the prevalence of IAC among studies is hampered by differences in the methods of quantifying its extent.11 ,24–26 However, IAC is likely to reflect atherosclerotic burden.10 ,11
Our finding that age is a risk factor for atherosclerotic disease is in accordance with almost all previous studies.2 ,11 ,19 ,24 ,26 ,27 It is likely that the process of atherosclerosis in the intracranial vasculatures is of a progressive nature and linked to ongoing atherosclerotic processes in other body parts.24 ,28 ,29 In this study, we identified hypertension and hypercholesterolaemia as risk factors for only IAS, and not IAC. This finding is not in accordance with other studies identifying especially hypertension as an important risk factor for IAC.26 However, we believe that the pooling of patients with various degrees of IAC—from patients with one vessel calcified and thus a weak risk-factor profile together with patients with more extensive IAC burden and thus a heavier risk factor profile—may have led to this conclusion.
In the present study, we were not able to identify diabetes as a risk factor for intracranial atherosclerosis. Diabetes is in general believed to be a risk factor for IAC and IAS.2 ,9 ,20 ,26 ,27 This finding may be due to ethnic differences in the incidence of diabetes.30
Prognostic studies of patients with IAS have predominantly been focusing on symptomatic lesions22 ,31 and thus contain an ill-fitting prognostic value on the general population with stroke with varying degrees of intracranial atherosclerosis and with a low prevalence of symptomatic stenosis. Studies on prognosis in more general populations with stroke have been performed in Asian patients with stroke with a much higher rate of IAS32 showing a clear link to recurrent ischaemic events.
In order to prevent further ischaemic events in patients with IAS, efforts as balloon angioplasty and stenting have been attempted. The recent SAMMPRIS trial found no benefit of stenting the intracranial stenotic lesions compared to aggressive medical therapy, especially due to an unacceptable rate of periprocedural complications.7 This finding is further supported by results from the WASID trial proposing that the recurrence rate in patients with symptomatic artery stenosis can be reduced by strict risk-factor modification.33 This suggests a possible beneficial effect of stricter risk factor control and aggressive medical prophylaxis in patients with lumen-reducing lesions IAS.
The prognostic value of IAC has only been investigated in a smaller single-centre study elaborated by Bugnicourt et al.12 This study found that IAC provided an independent risk factor for recurrent vascular event and death. This finding is supported by our data and indicates that the burden of IAC should be assessed as a factor in poststroke risk assessment similar to artery stenosis and atrial fibrillation.
To our knowledge, this is the first study to investigate the impact of radiological findings of intracranial atherosclerosis (IAS and IAC) detected during acute evaluation on recurrent vascular events and death in a large well-defined cohort of patients admitted within 4.5 h of stroke onset. With the results of the present study in hand, it seems that the problem of preventing recurrent ischaemia in patients with intracranial atherosclerosis is still very much alive.
In summary, this study shows that radiological markers of intracranial atherosclerosis are prevalent in North European patients with symptoms of acute stroke and appear linked to a global process of atherosclerotic disease. Our results suggest that intracranial atherosclerosis in consecutive patients with stroke or TIA entail a dramatic increase in risk of poor outcome compared to patients with stroke or TIA without intracranial atherosclerosis. Furthermore, IAS or IAC independently increases the risk of recurrent ischaemic events. So far, risk-factor modification and aggressive medical therapy remain first line treatments in this patient group.
The authors would like to thank nurses and doctors of the Department of Neurology, Bispebjerg University Hospital.
Contributors CO designed the study, gathered data, performed statistical analysis, interpreted the results and drafted the manuscript. AA, CK, JKN and IH gathered data. AFC gathered data and interpreted the results. SR interpreted results. HC designed the study and interpreted the results.
Funding This research received no specific grant from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests CO holds research grants from the Lundbeck Foundation and from Eva and Henry Fraenkels Memorial Foundation. HC holds a research grant from the Capital Region of Denmark.
Ethics approval The registry was approved by the Danish Data Protection Agency file no. 2010-41-5205 in accordance with Danish law.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement No additional data are available.