MR mismatch profiles in patients with intracranial ... - SAGE Journals

Journal of Cerebral Blood Flow & Metabolism (2009) 29, 1138–1145 & 2009 ISCBFM All rights reserved 0271-678X/09 $32.00 www.jcbfm.com

MR mismatch profiles in patients with intracranial atherosclerotic stroke: a comprehensive approach comparing stroke subtypes Suk Jae Kim1, Jin Myoung Seok1, Oh Young Bang1, Gyeong-Moon Kim1, Keon Ha Kim2, Pyoung Jeon2, Chin-Sang Chung1, Kwang Ho Lee1, Jeffry R Alger3 and David S Liebeskind3 1

Department of Neurology, Stroke and Cerebrovascular Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea; 2Department of Radiology, Stroke and Cerebrovascular Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea; 3 Department of Neurology, Stroke Center, University of California, Los Angeles, California, USA

Most clinical trials have focused on the presence of perfusion- and diffusion-weighted imaging (PWI–DWI) mismatch by more than 20%, and different stroke subtypes were lumped together. We hypothesized that intracranial large artery atherosclerotic stroke (IC-LAA) would show different PWI–DWI and magnetic resonance angiography (MRA)–DWI mismatch profiles, compared with other stroke subtypes. Consecutive patients underwent pretreatment multiparametric magnetic resonance imaging for the acute middle cerebral artery infarcts within 6 h of symptom onset. We assessed the difference in the DWI–PWI mismatch ratio, severity of hypoperfusion, and MRA–DWI mismatch among the stroke subtypes. Of 86 patients, 19 (22.1%) had IC-LAA; 42 (48.8%) cardioembolic stroke, 15 (17.4%) extracranial-LAA, and 10 (11.6%) had cryptogenic embolic stroke. Although the volume of the penumbra was not different among the groups, the mismatch ratio was higher (P = 0.003) and the severity of hypoperfusion was lower in the IC-LAA group (P = 0.001). The MRA–DWI mismatch was more prevalent in the IC-LAA group than in other groups (P < 0.001). Collateral grading, assessed in 41 patients, was more likely to be intermediate/excellent in the ICLAA group (P < 0.001). Multivariate testing revealed that a larger mismatch ratio and less severe hypoperfusion, and MRA–DWI mismatch were independently associated with IC-LAA. Our data show that patients with IC-LAA had different mismatch profiles, which were related to better collaterals, compared with other subtypes. Journal of Cerebral Blood Flow & Metabolism (2009) 29, 1138–1145; doi:10.1038/jcbfm.2009.38; published online 15 April 2009 Keywords: atherosclerosis; collaterals; ischemic; magnetic resonance imaging; perfusion; stroke

Introduction Multiparametric magnetic resonance imaging (MRI), including diffusion-weighted imaging (DWI) and perfusion-weighted imaging (PWI), has increasingly been used in clinical practice for selecting patients for recanalization therapy after stroke (Albers et al, 2006; Furlan et al, 2006; Hacke et al, 2005; Hjort et al, Correspondence: Dr OY Bang, Department of Neurology and the Stroke and Cerebrovascular Center, Samsung Medical Center, Sungkyunkwan University, 50 Irwon-dong, Gangnam-gu, Seoul 135-710, South Korea. E-mail: [email protected] This study was supported by a grant of the Korean Healthcare Technology R&D Project, Ministry of Health and Welfare, Republic of Korea (A080044) to B.O.Y. Received 9 February 2009; revised 13 March 2009; accepted 18 March 2009; published online 15 April 2009

2005; Kohrmann et al, 2006). Hyperintense DWI lesions can appear within 30 to 60 mins from the onset of infarction, whereas PWI defines an area of hypoperfusion. Thus, the mismatch between areas of hypoperfusion and areas of decreased diffusion on MRI have been suggested to be a penumbra zone, although many uncertainties remain (Kidwell et al, 2003). Most clinical trials have focused on the presence of PWI–DWI mismatch by more than 20%. However, the severity of hypoperfusion and vascular status and the extent of hypoperfusion determine tissue fate. Recently, Lansberg and colleagues of the Diffusion and Perfusion Imaging Evaluation for Understanding Stroke Evolution (DEFUSE) trial group reported that the magnetic resonance angiography (MRA)–DWI mismatch model could identify patients with stroke who are likely to benefit from reperfusion therapy (Lansberg et al, 2008). In addition,

Mismatch profile in intracranial atherosclerosis$ SJ Kim et al 1139

few studies have looked at differences in the hypoperfusion pattern among stroke subtypes; patients with different stroke subtypes were lumped together as one group. Most recent studies on hypoperfusion have been performed in Western countries, where the prevalence of intracranial large artery atherosclerotic stroke (IC-LAA) is much lower than in Asian countries; thus, relatively little attention has been devoted to this type of stroke mechanism. Intracranial large artery atherosclerotic stroke accounts for one-quarter to one-third of all strokes in Asian patients (Kieffer et al, 1967; Liu et al, 1996; Wong et al, 1998). Although the stroke classifications used widely in clinical trials (Adams et al, 1993; Ay et al, 2005) classify IC-LAA and extracranial large artery atherosclerotic stroke (EC-LAA) together, there are accumulating evidences that these two types of stroke differ in terms of ethnicity, risk factors, natural history, mechanism, and long-term recurrence (Inzitari et al, 1990; Shin et al, 2005; Uehara et al, 2005; Kang et al, 2003; Wong et al, 2002). Our hypothesis was that IC-LAA would show different PWI–DWI and MRA–DWI mismatch profiles, compared with the other stroke subtypes.

Materials and methods Patient Selection Our analysis was performed on data collected in a prospective registry of patients who were eligible for recanalization therapy for acute infarct of the middle cerebral artery (MCA), and who were evaluated with diffusion–perfusion MRI. This study analyzed consecutive patients encountered at a University Medical Center from June 2005 to July 2008. Inclusion criteria for this study were: (1) presentation within 6 h of symptom onset; (2) performance of pretreatment MRI, including DWI, PWI, and MRA; (3) acute ischemic lesions within the MCA distribution on DWI or perfusion defects within the MCA territory on PWI; and (d) a NIHSS (National Institute of Health Stroke Scale) score of Z4 points at the time of pretreatment MRI. In this study, we included atherosclerotic, cardioembolic (CE), and cryptogenic embolic stroke. Patients with small arterial occlusive stroke (n = 17), unclassified stroke (n = 7), other causes (n = 6), other cryptogenic strokes (n = 9), or incomplete work-ups (n = 8) were excluded (Ay et al, 2005). The local institutional review board approved the study.

Patients Grouping Stroke subtypes were determined according to the SSSTOAST (Stop Stroke Study Trial of Org 10172 in Acute Stroke Treatment) classification (Ay et al, 2005), with the following modifications: patients with atherosclerotic stroke were divided into IC-LAA and EC-LAA. Intracranial large artery atherosclerotic stroke was diagnosed when the initial angiography showed symptomatic atherosclerotic intracranial arterial stenosis of Z50% or occlusion, and

when neither a cardiac nor an extracranial arterial embolic source could be identified. The large intracranial arterial system included the intracranial portion of the internal carotid artery (ICA) and the M1 portion of the MCA. If the M2 portion of the MCA showed stenosis or occlusion in isolation , the patient was included as IC-LAA with one of the three additional findings, namely concomitant stenotic lesions on the contralateral M1 portion of the MCA or the intracranial portion of the ICA, or the intracranial portion of the vertebral artery or the basilar artery. Extracranial large artery atherosclerotic stroke was diagnosed if there was symptomatic extracranial arterial stenosis of Z50% or occlusion without evidence of CE. Cryptogenic embolic stroke was diagnosed when there was an angiographic evidence of an abrupt cutoff, consistent with a blood clot, within otherwise angiographically normal-looking intracranial arteries, or imaging evidence of the complete recanalization of an earlier occluded artery, or the presence of multiple acute infarctions that had occurred closely in time, without a detectable abnormality in the relevant vessels. Stroke subtype and phenotype were diagnosed by consensus of two stroke neurologists (O.Y.B. and G.M.K.).

Magnetic Resonance Imaging Methods and Image Analysis Magnetic resonance imaging was performed using a 3.0T unit (Achieva, Philips Medical Systems, Best, The Netherlands). The typical stroke MRI protocol consisted of DWI, PWI, T2 gradient-echo imaging, gadoliniumenhanced T1-weighted imaging, and vascular images (three-dimensional time-of-flight MRA and contrastenhanced MRA, including extracranial ICA and vertebral artery). The DWI parameters were as follows: TR (repetition time), 3,000 msecs; TE (echo time), 46 msecs; matrix, 128 128; 3 directions; FOV (field of view), 24 cm; section thickness, 5 mm; and intersection gap, 2 mm. Diffusionweighted imaging was obtained with b-values of 0 and 1,000 secs/mm2. PWI was performed using gradient-echo and echo-planar sequences with the following parameters: TR, 1,500 msecs; TE, 35 msecs; flip angle, 401; matrix, 128 128, FOV 24 cm; section thickness, 5 mm; and intersection gap, 2 mm. We selected a definition on the basis of the perfusion parameter Tmax, which is the time to peak MR signal intensity change after deconvolution; Tmax perfusion lesion maps were generated by deconvolution of an arterial input function and tissue concentration curves, on the basis of earlier methods (Ostergaard et al, 1996). Data analysis was performed with software developed in-house, using the IDL (Interactive Data Language) produced by ITT Visual Systems (Boulder, CO, USA). Magnetic resonance imaging volume measurements were performed by one of authors (K.H.K.), blinded to the clinical information. For each patient, DWI and PWI lesion volumes were outlined automatically with subsequent manual corrections, and the volumes were calculated using a computer-assisted volumetric analysis program (Medical Image Processing, Analysis and Visualization, version 2.1, CIT, NIH). The mismatch ratio was defined as the ratio of PWI lesion volume of Tmax Z2 secs to DWI Journal of Cerebral Blood Flow & Metabolism (2009) 29, 1138–1145


lesion volume. The perfusion defect severity (%) was defined as the ratio of Tmax Z8 secs to Tmax Z2 secs lesion volume (PWI volume of Tmax Z8 secs/PWI volume of Tmax Z2 secs) 100. The MRA rating and MRA–DWI mismatch was defined according to the prespecified MRA–DWI mismatch criteria (Lansberg et al, 2008). For the intracranial ICA and M1 segment of the MCA, 1 = normal; 2 = reduced flow; and 3 = occlusion. For the M2 segment of the MCA, 1 = normal and 2 = abnormal. The MRA–DWI mismatch was defined as an MRA score of 3 and a DWI lesion volume < 25 mL or an MRA score of 2 and a DWI lesion volume < 15 mL. The MRA was rated independently by two stroke neurologists (S.J.K. and J.M.S.) who were only informed of the symptomatic hemisphere of the patient. The third opinion (by P.J.) was obtained in cases of disagreement.

Conventional Angiographic Study Some of the patients underwent comprehensive cerebral angiography, including injection of both ICAs and the dominant vertebral artery, with assessment through the late venous phase. The angiographic collateral grade was evaluated using the ASITN/SIR Collateral Flow Grading System on pretreatment angiography (Higashida et al, 2003). This angiographic scale assigns patients to grade 0 (no visible collateral to the ischemic site), grade 1 (slow collaterals to the periphery of the ischemic site with persistence of some of the defect), grade 2 (rapid collaterals to the periphery of ischemic site with persistence of some of the defect and to only a portion of the ischemic territory), grade 3 (collaterals with slow but complete angiographic blood flow of the ischemic bed by the late venous phase), and grade 4 (complete and rapid collateral blood flow to the vascular bed in the entire ischemic territory by retrograde perfusion). In this study, scores of 0 and 1 were designated as poor collateral flow; grades 2 and 3, as intermediate; and grade 4, as excellent. The collateral grade was rated independently by two stroke neurologists (S.J.K. and J.M.S.) who were only informed of the symptomatic hemisphere of the patient. The third opinion (P.J.) was obtained in cases of disagreement.

Statistical Analysis The differences in the clinical, laboratory, and radiologic characteristics among stroke subtypes were evaluated using one-way ANOVA (analysis of variance) or Kruskall– Wallis test for continuous variables, Pearson’s w2 or Fisher’s exact test for categorical variables. The independent t-test or Mann–Whitney U-test was used for evaluating differences in the aforementioned factors between IC-LAA and other stroke subtypes. In addition, a multivariate logistic regression analysis was performed to predict the independent contribution of factors in IC-LAA compared with other stroke mechanisms. Variables from univariate analyses at P < 0.1 were considered to represent explanatory variables and were entered together into the multivariate analysis. P-values < 0.05 were deemed to be statistically significant. All statistical analyses were performed using Journal of Cerebral Blood Flow & Metabolism (2009) 29, 1138–1145

commercially available software (SPSS for Windows, version 13.0; SPSS Inc., Chicago, IL, USA).

Results Of the 98 patients who met the inclusion criteria during the study period, a total of 86 patients (50 men and 36 women; age, 66.4±13.0 years) were included in this study. Twelve patients were excluded owing to the failure of post-MRI processing or selection of the wrong arterial input function. Pretreatment MRI and conventional cerebral angiography were performed at 3.2±1.5 h (range, 0.9 to 7.4) and 5.6±1.9 h (range, 2.6 to 8.7), respectively. Clinical and laboratory characteristics of patients, classified by stroke subtype, are presented in Table 1. Male gender and hypertension were more frequently observed in patients with EC-LAA, whereas atrial fibrillation was more prevalent in patients with CE. Hyperlipidemia was more frequent in patients with EC-LAA, but was not significantly so. The NIHSS score on admission was lower in patients with IC-LAA than in those with CE. Age, diabetes, smoking habits, coronary heart disease, stroke/transient ischemic attack (TIA) history, onset to pretreatment MRI time, and other laboratory findings did not differ among the groups. Radiologic characteristics of different stroke mechanisms are illustrated in Table 2. The volumes of initial penumbra were not different among the groups. However, the mismatch ratio and the severity of perfusion defect differed by stroke subtype (Figure 1). Compared with other stroke mechanisms, IC-LAA had a much higher mismatch ratio (P = 0.003) and lower severity of perfusion defect (P = 0.001) (Figure 2). The majority of IC-LAA had MRA–DWI mismatch, whereas < 50% of patients in other stroke subtypes had MRA–DWI mismatch (P < 0.001). Of patients who showed total occlusion of symptomatic vessels on conventional angiography, we compared conventional angiographic collateral grading among different stroke mechanisms (n = 41). According to this, patients in the IC-LAA group were more likely to have intermediate or excellent collateral flow, whereas those of other groups were more likely to have poor collateral flow (Table 2). Clinical and radiologic features independently associated with IC-LAA were analyzed by multiple logistic regression (Table 3). After adjusting for covariates; model 1 (not including MRA–DWI mismatch as an explanatory variable) revealed an independent association with IC-LAA in the higher half of the mismatch ratio (OR (odds ratio), 4.84; 95% CI (95% confidence interval), 1.35 to 17.34) and lower half of the severity of perfusion defect (OR, 6.21; 95% CI, 1.14 to 33.74). On the contrary, in model 2 (including MRA–DWI mismatch as an explanatory variable) the MRA–DWI mismatch (OR, 15.81; 95% CI, 1.45 to 171.93) alone was independently associated with IC-LAA.


Table 1 Clinical and laboratory characteristics of patients according to the stroke subtypes Stroke subtypes

P

IC-LAA

CE

EC-LAA

Cryptogenic embolism

n = 19 (22.1%)

n = 42 (48.8%)

n = 15 (17.4%)

n = 10 (11.6%)

Male sex Mean age (s.d.) years Mean NIHSS on admission (s.d.)

9 (47.4%) 62 (12) 9.2 (3.5)

21 (50.0%) 68 (14) 14.3 (6.3)

14 (93.3%) 71 (9) 10.1 (6.5)

6 (60.0%) 64 (12) 11.0 (6.4)

Risk factors Hypertension Diabetes Hyperlipidemia Coronary heart disease Stroke/TIA history Mean onset to MRI time (s.d.) h

11 4 2 2 5 3.5

Laboratory findings Median glucose (IQR) mg/dL Mean Triglyceride (s.d.) mg/dL

129 (27) 132 (65)

No. of patients

(57.9%) (21.1%) (10.5%) (10.5%) (26.3%) (1.2)

23 10 8 7 13 3.1

(54.8%) (23.8%) (19.0%) (16.7%) (31.0%) (1.8)

129 (45.5) 97 (42)

14 6 7 6 8 3.0

(93.3%) (40.0%) (46.7%) (40.0%) (53.3%) (1.2)

142.5 (61.5) 141 (87)

6 5 1 1 4 3.2

(60.0%) (50.0%) (10.0%) (10.0%) (40.0%) (1.7)

132.5 (89.5) 110 (63)

Among subtypes

IC-LAA versus other subtypes

0.014 0.177 0.013

0.281 0.066 0.002

0.044 0.243 0.066 0.158 0.371 0.725

0.617 0.383 0.338 0.505 0.375 0.280

0.623 0.065

0.416 0.075

CE, cardioembolic; EC-LAA, extracranial large artery atherosclerotic stroke; HDL, high-density lipoprotein; IC-LAA, intracranial large artery atherosclerotic stroke; LDL, low-density lipoprotein; MRI, magnetic resonance imaging; NIHSS, The National Institute of Health Stroke Scale; TIA, transient ischemic attack; IQR, interquartile range. Smoking habits, serum total cholesterol, HDL cholesterol, and LDL cholesterol did not differ among the groups (P > 0.2). Atrial fibrillation was exclusively observed in the CE group (83.3%).

Table 2 Radiologic characteristics of patients according to the stroke subtypes Stroke subtypes

No. of patients

IC-LAA

CE

EC-LAA

Cryptogenic embolism

n = 19 (22.1%)

n = 42 (48.8%)

n = 15 (17.4%)

n = 10 (11.6%)

Mean DWI lesion volume (s.d.) mL 5.4 (7.4) 132.6 (105.3) Mean initial penumbra volume (s.d.) mLa Median mismatch ratio (IQR)b 26.4 (63.2) 19.8 (17.3) Mean severity of perfusion defect c (s.d.) % No. of patients with MRA–DWI 18 (94.7%) mismatchd Conventional angiographic collateral grading score 0–1 2–3 4

P

n=9 0 (0%) 6 (66.7%) 3 (33.3%)

45.4 (61.2) 102.8 (83.0)

9.9 (14.8) 99.5 (97.2)

19.0 (34.9) 89.1 (116.9)

4.0 (11.0) 45.8 (24.1)

8.3 (52.9) 24.0 (21.3)

15 (35.7%) n = 21 16 (76.2%) 5 (23.8%) 0 (0%)

7 (46.7%) n=6 3 (50.0%) 2 (33.3%) 1 (16.7%)

Among subtypes

IC-LAA versus other subtypes

0.017 0.530

0.045 0.213

7.3 (84.0) 23.5 (27.5)

0.012 < 0.001

0.003 0.001

6 (60%)

< 0.001

< 0.001

0.001

< 0.001

n=5 3 (60.0%) 2 (40.0%) 0 (0%)

CE, cardioembolic; DWI, diffusion-weighted imaging; EC-LAA, extracranial large artery atherosclerotic stroke; IC-LAA, intracranial large artery atherosclerotic stroke; MRA, magnetic resonance angiography; MRI, magnetic resonance imaging; PWI, perfusion-weighted imaging; IQR, interquartile range. a PWI volume of Tmax Z2 secs—DWI volume. b Ratio of PWI lesion volume of Tmax Z2 secs to DWI lesion volume. c Ratio of Tmax Z8 secs lesion volume to Tmax Z2 secs lesion volume: (PWI volume of Tmax Z8 secs/PWI volume of Tmax Z2 secs 100). d An MRA score of 2 and a DWI lesion volume < 15 mL, or an MRA score of 3, and a DWI lesion volume < 25 mL.

Discussion Intracranial large artery atherosclerotic stroke is one of the major causes of stroke in Asians and in blacks. In our study, the prevalence of patients with IC-LAA

was 22.1% among Korean patients with acute ischemic stroke who were eligible for recanalization therapy. Many studies have evaluated predictors for favorable outcome after recanalization therapy for acute ischemic stroke. However, earlier studies have Journal of Cerebral Blood Flow & Metabolism (2009) 29, 1138–1145


Figure 1 (A) Quartile of mismatch ratio. The majority of IC-LAA (78.9%) is included in the 3rd and 4th quartile (mismatch ratio Z9), but only 21.1% in the 1st and 2nd quartile (mismatch ratio < 9). (B) Severity of perfusion defect. Most of IC-LAA (89.5%) are included in the 1st and 2nd quartile (hypoperfusion severity < 41%), but only 10.5% in the 3rd and 4th quartile (hypoperfusion severity Z41%).

Figure 2 Typical examples of DWI and PWI in patients with different stroke mechanisms.

largely not addressed stroke mechanisms, especially IC-LAA (Albers et al, 2006; Clark et al, 1999; Davis et al, 2008; Furlan et al, 2006; Hacke et al, 1995, 1998, 2005; The National Institute of Neurological Disorders and Stroke rt-PA Stroke Study Group, 1995). To our knowledge, this is the first study regarding the PWI–DWI and MRA–DWI mismatch profiles in patients with IC-LAA, compared with other stroke subtypes. Journal of Cerebral Blood Flow & Metabolism (2009) 29, 1138–1145

The major findings of our study were that patients with IC-LAA had PWI–DWI (larger mismatch ratio but less severe hypoperfusion) and MRA–DWI mismatch profiles, which have been reported to be associated with favorable outcomes after recanalization therapy (Albers et al, 2006; Furlan et al, 2006; Hacke et al, 2005; Hjort et al, 2005; Kohrmann et al, 2006; Lansberg et al, 2008; Bang et al, 2008). In this study, we have considered several different


Table 3 Logistic regression analysis: clinical and radiologic features associated with IC-LAA Univariate analysis

Multivariate testing Model 1

OR Clinical and laboratory findings Age, per 1 year increase NIHSS on admission, per 1 point increase Triglyceride, per 1 mg/dL increase

0.96 0.89 1.01

Radiologic findings DWI lesion volume, per 1 mL increase Higher half of mismatch ratioa Lower half of severity of perfusion defectb MRA–DWI mismatchc

1.00 6.72 7.32 25.07

Model 2

OR (95% CI)

P-value

4.84 (1.35–17.34) 6.21 (1.14–33.74)

0.016 0.034

OR (95% CI)

P-value

15.81 (1.45–171.93)

0.023

CI, confidence interval; DWI, diffusion-weighted imaging; IC-LAA, intracranial large artery atherosclerotic stroke; MRA, magnetic resonance angiography; NIHSS, National Institute of Health Stroke Scale; OR, odds ratio; PWI, perfusion-weighted imaging. Model 1: not including MRA–DWI mismatch as an explanatory variable. Model 2: including MRA–DWI mismatch as an explanatory variable. a Ratio of PWI lesion volume of Tmax Z2 secs to DWI lesion volume. b Ratio of Tmax Z8 secs lesion volume to Tmax Z2 secs lesion volume: (PWI volume of Tmax Z8 secs/PWI volume of Tmax Z2 secs 100). c An MRA score of 2 and a DWI lesion volume < 15 mL or an MRA score of 3 and a DWI lesion volume < 25 mL.

mismatch profiles simultaneously (using DWI, PWI, and MRA data) to characterize the penumbra zone, for the following reasons. First, the ideal PWI–DWI mismatch definition was not settled yet, and there have been growing evidences that a simple diffusion–perfusion mismatch model may not accurately identify the ischemic penumbra (Kidwell et al, 2003). Most clinical trials defined the diffusion– perfusion mismatch as PWI–DWI ratio 1.2 using Tmax delay of Z2 secs and PWI–DWI volume Z10 mL. However, the optimal PWI–DWI mismatch ratio and the threshold of hypoperfusion were not evaluated comprehensively. Second, most earlier studies have focused on the extent of hypoperfusion, but the severity of hypoperfusion may also be an important determinant of tissue fate of hypoperfused region after recanalization. Patients with good collaterals had relatively larger areas of only mildly hypoperfused tissue than those with poor collaterals, and infarct growth within the penumbral zone was smaller when collaterals were better (Bang et al, 2008). Finally, the DEFUSE trial group has recently reported that the MRA–DWI mismatch model is a novel approach to select who is likely to benefit from reperfusion in a 3- to 6-h time window after symptom onset (Lansberg et al, 2008). They suggest that this model is restively easy to assess, but more powerful than the PWI–DWI mismatch model. The results of our study suggest that patients with IC-LAA may show more favorable clinical outcomes after recanalization than those with other subtypes, especially CE. Further studies with data on infarct growth determined by serial MRI are needed to confirm our findings. In addition, in clinical trials of recanalization therapy for acute ischemic stroke, race and ethnicity should be considered in the analysis,

because the prevalence of IC-LAA differs among Asians, blacks, and Caucasians. The differences in PWI–DWI mismatch profiles and in MRA–DWI mismatch profile between IC-LAA and other subtypes may be related to differences in pretreatment collateral flow status; in this study, patients with IC-LAA had a good collateral grade than those with other subtypes. Collateral flow is an important indication for good treatment outcome after thrombolysis in acute stroke patients (Liebeskind, 2003). Using serial MRI data, we recently found that the pretreatment collateral grade was associated with infarct growth in patients undergoing endovascular recanalization therapy (Bang et al, 2008). The good collateral flows of IC-LAA may be explained by the speed of occlusion. In patients with CE and cryptogenic embolism, arterial occlusion occurs suddenly; hence, the time available for developing collaterals may be insufficient. Similar mechanisms may apply in EC-LAA, which are related to thromboembolism owing to plaque instability. Conversely, IC-LAA is associated with microembolism or hemodynamic instability (Wong et al, 2002). These mechanisms require a longer time for complete arterial occlusion, allowing the development of adequate collateral flow before the onset of stroke. There are several limitations to our study. First, this was a single-center trial with a modest sample size. Multicenter trials with larger cohorts and different study populations are warranted. Second, in this study, Tmax perfusion lesion maps (a timedomain parameter) were used to delineate perfusion defects. Although time-domain parameters have been increasingly used to determine diffusion– perfusion mismatch (Davis et al, 2005), further studies are needed to find differences between Journal of Cerebral Blood Flow & Metabolism (2009) 29, 1138–1145


IC-LAA and the other stroke subtypes using nontimedomain parameters, such as cerebral blood volume. Using Tmax perfusion lesion maps to select patients for recanalization therapy failed to show positive results in the recent DIAS-II (presented at the 16th European Stroke Conference, Glasgow, UK) and EPITHET (Effects of alteplase beyond 3 h after stroke in the Echoplanar Imaging Thrombolytic Evaluation Trial) trials (Davis et al, 2008). In conclusion, IC-LAA as stroke mechanism had a relatively larger salvageable area of less severe hypoperfusion and more frequent MRA–DWI mismatch profile. Good collateral flows of IC-LAA may explain these results. Larger, multicenter, confirmatory studies with long-term follow-up are needed to determine whether IC-LAA has different responses after recanalization therapy.

Conflict of interest The authors declare no conflict of interest.

References Adams HP, Jr, Bendixen BH, Kappelle LJ, Biller J, Love BB, Gordon DL, Marsh EE, III (1993) Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment. Stroke 24:35–41 Albers GW, Thijs VN, Wechsler L, Kemp S, Schlaug G, Skalabrin E, Bammer R, Kakuda W, Lansberg MG, Shuaib A, Coplin W, Hamilton S, Moseley M, Marks MP (2006) Magnetic resonance imaging profiles predict clinical response to early reperfusion: the diffusion and perfusion imaging evaluation for understanding stroke evolution (DEFUSE) study. Ann Neurol 60:508–17 Ay H, Furie KL, Singhal A, Smith WS, Sorensen AG, Koroshetz WJ (2005) An evidence-based causative classification system for acute ischemic stroke. Ann Neurol 58:688–97 Bang OY, Saver JL, Buck BH, Alger JR, Starkman S, Ovbiagele B, Kim D, Jahan R, Duckwiler GR, Yoon SR, Vinuela F, Liebeskind DS (2008) Impact of collateral flow on tissue fate in acute ischaemic stroke. J Neurol Neurosurg Psychiatry 79:625–9 Clark WM, Wissman S, Albers GW, Jhamandas JH, Madden KP, Hamilton S (1999) Recombinant tissue-type plasminogen activator (Alteplase) for ischemic stroke 3 to 5 hours after symptom onset. The ATLANTIS Study: a randomized controlled trial. Alteplase Thrombolysis for Acute Noninterventional Therapy in Ischemic Stroke. JAMA 282:2019–26 Davis SM, Donnan GA, Butcher KS, Parsons M (2005) Selection of thrombolytic therapy beyond 3 h using magnetic resonance imaging. Curr Opin Neurol 18:47–52 Davis SM, Donnan GA, Parsons MW, Levi C, Butcher KS, Peeters A, Barber PA, Bladin C, De Silva DA, Byrnes G, Chalk JB, Fink JN, Kimber TE, Schultz D, Hand PJ, Frayne J, Hankey G, Muir K, Gerraty R, Tress BM, Desmond PM (2008) Effects of alteplase beyond 3 h after stroke in the Echoplanar Imaging Thrombolytic Evaluation Trial (EPITHET): a placebo-controlled randomised trial. Lancet Neurol 7:299–309 Journal of Cerebral Blood Flow & Metabolism (2009) 29, 1138–1145

Furlan AJ, Eyding D, Albers GW, Al-Rawi Y, Lees KR, Rowley HA, Sachara C, Soehngen M, Warach S, Hacke W (2006) Dose Escalation of Desmoteplase for Acute Ischemic Stroke (DEDAS): evidence of safety and efficacy 3 to 9 hours after stroke onset. Stroke 37:1227–31 Hacke W, Albers G, Al-Rawi Y, Bogousslavsky J, Davalos A, Eliasziw M, Fischer M, Furlan A, Kaste M, Lees KR, Soehngen M, Warach S (2005) The Desmoteplase in Acute Ischemic Stroke Trial (DIAS): a phase II MRI-based 9-h window acute stroke thrombolysis trial with intravenous desmoteplase. Stroke 36:66–73 Hacke W, Kaste M, Fieschi C, Toni D, Lesaffre E, von Kummer R, Boysen G, Bluhmki E, Hoxter G, Mahagne MH, Hennerici M (1995) Intravenous thrombolysis with recombinant tissue plasminogen activator for acute hemispheric stroke. The European Cooperative Acute Stroke Study (ECASS). JAMA 274:1017–25 Hacke W, Kaste M, Fieschi C, von Kummer R, Davalos A, Meier D, Larrue V, Bluhmki E, Davis S, Donnan G, Schneider D, Diez-Tejedor E, Trouillas P (1998) Randomised double-blind placebo-controlled trial of thrombolytic therapy with intravenous alteplase in acute ischaemic stroke (ECASS II). Second European-Australasian Acute Stroke Study Investigators. Lancet 352:1245–51 Higashida RT, Furlan AJ, Roberts H, Tomsick T, Connors B, Barr J, Dillon W, Warach S, Broderick J, Tilley B, Sacks D (2003) Trial design and reporting standards for intraarterial cerebral thrombolysis for acute ischemic stroke. Stroke 34:e109–37 Hjort N, Butcher K, Davis SM, Kidwell CS, Koroshetz WJ, Rother J, Schellinger PD, Warach S, Ostergaard L (2005) Magnetic resonance imaging criteria for thrombolysis in acute cerebral infarct. Stroke 36:388–97 Inzitari D, Hachinski VC, Taylor DW, Barnett HJ (1990) Racial differences in the anterior circulation in cerebrovascular disease. How much can be explained by risk factors? Arch Neurol 47:1080–4 Kang DW, Chalela JA, Ezzeddine MA, Warach S (2003) Association of ischemic lesion patterns on early diffusion-weighted imaging with TOAST stroke subtypes. Arch Neurol 60:1730–4 Kidwell CS, Alger JR, Saver JL (2003) Beyond mismatch: evolving paradigms in imaging the ischemic penumbra with multimodal magnetic resonance imaging. Stroke 34:2729–35 Kieffer SA, Takeya Y, Resch JA, Amplatz K (1967) Racial differences in cerebrovascular disease. Angiographic evaluation of Japanese and American populations. Am J Roentgenol Radium Ther Nucl Med 101:94–9 Kohrmann M, Juttler E, Fiebach JB, Huttner HB, Siebert S, Schwark C, Ringleb PA, Schellinger PD, Hacke W (2006) MRI versus CT-based thrombolysis treatment within and beyond the 3 h time window after stroke onset: a cohort study. Lancet Neurol 5:661–7 Lansberg MG, Thijs VN, Bammer R, Olivot JM, Marks MP, Wechsler LR, Kemp S, Albers GW (2008) The MRA-DWI mismatch identifies patients with stroke who are likely to benefit from reperfusion. Stroke 39:2491–6 Liebeskind DS (2003) Collateral circulation. Stroke 34:2279–84 Liu HM, Tu YK, Yip PK, Su CT (1996) Evaluation of intracranial and extracranial carotid steno-occlusive diseases in Taiwan Chinese patients with MR angiography: preliminary experience. Stroke 27:650–3

Mismatch profile in intracranial atherosclerosis$ SJ Kim et al

Ostergaard L, Weisskoff RM, Chesler DA, Gyldensted C, Rosen BR (1996) High resolution measurement of cerebral blood flow using intravascular tracer bolus passages. Part I: Mathematical approach and statistical analysis. Magn Reson Med 36:715–25 Shin DH, Lee PH, Bang OY (2005) Mechanisms of recurrence in subtypes of ischemic stroke: a hospitalbased follow-up study. Arch Neurol 62:1232–7 The National Institute of Neurological Disorders and Stroke rt-PA Stroke Study Group (1995) Tissue plasminogen activator for acute ischemic stroke. N Engl J Med 333:1581–7

Uehara T, Tabuchi M, Mori E (2005) Risk factors for occlusive lesions of intracranial arteries in stroke-free Japanese. Eur J Neurol 12:218–22 Wong KS, Gao S, Chan YL, Hansberg T, Lam WW, Droste DW, Kay R, Ringelstein EB (2002) Mechanisms of acute cerebral infarctions in patients with middle cerebral artery stenosis: a diffusion-weighted imaging and microemboli monitoring study. Ann Neurol 52: 74–81 Wong KS, Huang YN, Gao S, Lam WW, Chan YL, Kay R (1998) Intracranial stenosis in Chinese patients with acute stroke. Neurology 50:812–3

1145

Journal of Cerebral Blood Flow & Metabolism (2009) 29, 1138–1145