Department of Neurology, Jeju National University Hospital, Jeju National University College of Medicine, Jeju, Korea

Similar documents
DND. Phenotypic Features of Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Subjects with R544C Mutation

Cerebral autosomal-dominant arteriopathy with subcortical

CADASIL: structural MR imaging changes and apolipoprotein E genotype S E V E N

Three-Dimensional MRI Analysis of Individual Volume of Lacunes in CADASIL

Cerebral small vessel disease

Confluent Thalamic Hyperintensities in CADASIL

Brain Atrophy Is Related to Lacunar Lesions and Tissue Microstructural Changes in CADASIL

Lacunar Infarcts Are the Main Correlate With Cognitive Dysfunction in CADASIL

Patient with vertigo, dizziness and depression

Cerebral autosomal dominant arteriopathy with subcortical. Clinical Sciences

Grey matter volume alterations in CADASIL: a voxel-based morphometry study

Brain tissue and white matter lesion volume analysis in diabetes mellitus type 2

SUPPLEMENTAL MATERIAL

Vascular Dementia. Laura Pedelty, PhD MD The University of Illinois at Chicago and Jesse Brown VA Medical Center

Characterizing cerebral small vessel disease with a focus on CADASIL as a genetic model -an MRI based approach

NEUROPSYCHOMETRIC TESTS

Magnetic resonance imaging (MRI) has the potential to

Department of Neurology, Soonchunhyang University Bucheon Hospital, Bucheon, Korea

Cover Page. The handle holds various files of this Leiden University dissertation.

Turkish Title: Akut Eş Zamanlı Subkortikal Infarktların Neden Olduğu Progresif Bulber Paralizi ile Prezente olan CADASIL Olgusu

Supplementary Note. Patient #1 Additional Details

Silent Cerebral Microbleeds on T2*-Weighted MRI. Correlation with Stroke Subtype, Stroke Recurrence, and Leukoaraiosis

Cerebral Autosomal-Dominant Arteriopathy with Subcortical

PRESERVE: How intensively should we treat blood pressure in established cerebral small vessel disease? Guide to assessing MRI scans

Multimodal MRI in Cerebral Small Vessel Disease Its Relationship With Cognition and Sensitivity to Change Over Time

CADASIL: a short review of the literature and a description of the first family from Greece

Complete Recovery of Perfusion Abnormalities in a Cardiac Arrest Patient Treated with Hypothermia: Results of Cerebral Perfusion MR Imaging

Silent Cerebral Strokes: Clinical Outcomes and Management

Neuroradiological, clinical and genetic characterization of new forms of hereditary leukoencephalopathies

Diffusion Magnetic Resonance Histograms as a Surrogate Marker and Predictor of Disease Progression in CADASIL A Two-Year Follow-Up Study

2018 The Author(s). This open access article is distributed under a Creative Commons Attribution (CC-BY) 4.0 license.

Case 9511 Hypertensive microangiopathy

Magnetic resonance imaging, image analysis:visual scoring of white matter

FILE / PERIVENTRICULAR MICROVASCULAR ISCHEMIC CHANGES EBOOK

Injuries of neural tracts in a patient with CADASIL: a diffusion tensor imaging study

Supplementary Online Content

Estimating the Validity of the Korean Version of Expanded Clinical Dementia Rating (CDR) Scale

Subcortical lacunar lesions: an MR imaging fi nding in patients with CADASIL T H R E E

Role of MRI in acute disseminated encephalomyelitis

MRI and differential diagnosis in patients suspected of having MS

Genetic Testing of CADASIL Syndrome. Populations Interventions Comparators Outcomes Individuals: With suspected CADASIL syndrome.

MRI of Pathological Aging Brain

Chapter 11 summary definitief ineke brands.indd :57:59

P oirier et al classified lacunar infarcts into three types:

The comparisons of phenotype and genotype between CADASIL and CADASILlike patients and population-specific evaluation of CADASIL scale in China

The Reliability and Validity of the Korean Instrumental Activities of Daily Living (K-IADL)

Carotid Atherosclerotic Markers in CADASIL

On-line Table 1: Dementia diagnoses and related ICD codes for the diagnostic groups a

HYPERTENSIVE ENCEPHALOPATHY

Can a tissue sample help us understand a major genetic cause of stroke & vascular dementia?

The current state of healthcare for Normal Aging, Mild Cognitive Impairment, & Alzheimer s Disease

University of Bristol - Explore Bristol Research

September 26 28, 2013 Westin Tampa Harbour Island. Co-sponsored by

The Epidemiology of Stroke and Vascular Risk Factors in Cognitive Aging

White matter hyperintensities correlate with neuropsychiatric manifestations of Alzheimer s disease and frontotemporal lobar degeneration

Neuropsychiatric Manifestations in Vascular Cognitive Impairment Patients with and without Dementia

Patients with Alzheimer s disease with multiple microbleeds: relation with cerebrospinal fluid biomarkers and cognition 2.4

Clinical Research on Treating Senile Dementia by Combining Acupuncture with Acupoint-Injection

ORIGINAL COMMUNICATION. Abstract Reduced cerebrovascular reactivity has been reported in patients with cerebral autosomal

Association of White Matter Lesions and Lacunar Infarcts With Executive Functioning

ORIGINAL ARTICLE Neuroscience INTRODUCTION MATERIALS AND METHODS

Asymptomatic lacunar infarcts, white matter lesions, cerebral

Downloaded from Binswanger s Disease. Binswanger s Disease

Significant cognitive improvement with cholinesterase inhibition in AD with cerebral amyloid angiopathy

Interactive Cases: Demyelinating Diseases and Mimics. Disclosures. Case 1 25 yo F with nystagmus; look for tumor 4/14/2017

THE ROLE OF ACTIVITIES OF DAILY LIVING IN THE MCI SYNDROME

Introduction, use of imaging and current guidelines. John O Brien Professor of Old Age Psychiatry University of Cambridge

As life span rises, dementia has become a growing public. Stroke Compendium. Vascular Cognitive Impairment. Circulation Research Compendium on Stroke

Common and uncommon differential diagnosis of cerebral microhemorrhages

Zhenyu Jia, MD,* Wasif Mohammed, MD,* Yiru Qiu, MD, Xunning Hong, MD,* and Haibin Shi, MD, PhD*

Lambros Messinis PhD. Neuropsychology Section, Department of Neurology, University of Patras Medical School

Mild Cognitive Impairment (MCI)

Edinburgh Research Explorer

Genetic Testing for CADASIL Syndrome

Diffusion-Weighted and Conventional MR Imaging Findings of Neuroaxonal Dystrophy

Procedia - Social and Behavioral Sciences 159 ( 2014 ) WCPCG 2014

W hite matter high intensity lesions (WML) on T2

Cognitive Impairment and Magnetic Resonance Changes in Multiple Sclerosis. Background

Imaging in Pediatric `neurohiv Dr Jackie Hoare Head of Liaison Psychiatry Groote Schuur Hospital, UCT

Four Tissue Segmentation in ADNI II

Starting or Resuming Anticoagulation or Antiplatelet Therapy after ICH: A Neurology Perspective

Department of Psychology, Sungkyunkwan University, Seoul, Korea

Yong-Bum Kim, M.D., Kwang-Ho Lee, M.D., Soo-Joo Lee, M.D., Duk-L. Na, M.D., Soo-Jin Cho, M.D., Chin-Sang Chung, M.D., Won-Yong Lee M.D.

Department of Neurology, College of Medicine, Chungnam National University Hospital, Daejeon, Korea

CSF Aβ1-42 predicts cognitive impairment in de novo PD patients

Sicle-cell disease and silent cerebral infarcts evaluated with magnetic resonance imaging

Title:Cognitive profile in patients with a first-ever lacunar infarct with and without silent lacunes: a comparative study.

Motor Function Recovery in Stroke Patients with Corona Radiata Infarct: 4 Case Studies

Primary Central Nervous System Lymphoma with Lateral Ventricle Involvement

DEMENTIA? 45 Million. What is. WHAT IS DEMENTIA Dementia is a disturbance in a group of mental processes including: 70% Dementia is not a disease

King s Research Portal

Magnetic Resonance Imaging. Basics of MRI in practice. Generation of MR signal. Generation of MR signal. Spin echo imaging. Generation of MR signal

Neuroimaging for dementia diagnosis. Guidance from the London Dementia Clinical Network

A characteristic feature of acute haematomas in the brain on echo-planar diffusion-weighted imaging

Neuroimaging predictors of death and dementia in a cohort of older stroke survivors

Men and women are affected Male and Female larger amounts of intracranial CSF

Dementia. Stephen S. Flitman, MD Medical Director 21st Century Neurology

fmri and Voxel-based Morphometry in Detection of Early Stages of Alzheimer's Disease

Cover Page. The handle holds various files of this Leiden University dissertation.

Transcription:

ORIGINAL ARTICLE J Clin Neurol 2011;7:210-214 Print ISSN 1738-6586 / On-line ISSN 2005-5013 http://dx.doi.org/10.3988/jcn.2011.7.4.210 Open Access Effects of Lacunar Infarctions on Cognitive Impairment in Patients with Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Jung Seok Lee, a Jay Chol Choi, a Sa-Yoon Kang, a Ji-Hoon Kang, a Hae Ri Na, b Ji-Kang Park c a Department of Neurology, Jeju National University Hospital, Jeju National University College of Medicine, Jeju, Korea b Department of Neurology, Bobath Memorial Hospital, Seongnam, Korea c Department of Radiology, Jeju National University College of Medicine, Jeju, Korea Background and PurposezzCerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited microangiopathy caused by mutations in the Notch3 gene. Although previous studies have shown an association between lacunar infarction and cognitive impairment, the relationship between MRI parameters and cognition remains unclear. In this study we investigated the influence of MRI parameters on cognitive impairment in CADASIL. Received April 14, 2011 Revised May 11, 2011 Accepted May 11, 2011 Correspondence Jung Seok Lee, MD Department of Neurology, Jeju National University Hospital, Jeju National University College of Medicine, 15 Aran 13-gil, Jeju 690-767, Korea Tel +82-64-717-1268 Fax +82-64-717-1630 E-mail nrlee71@yahoo.co.kr MethodszzWe applied a prospective protocol to 40 patients. MRI analysis included the normalized volume of white-matter hyperintensities (nwmhs), number of lacunes, and number of cerebral microbleeds. Cognition was assessed with the aid of psychometric tests [Mini-Mental State Examination (MMSE), Alzheimer s Disease Assessment Scale-cognition (ADAS-cog), Trail-Making Test, and Stroop interference (Stroop IF)]. ResultszzA multivariate regression analysis revealed that the total number of lacunes influenced the performance in the MMSE, ADAS-cog, and Stroop IF, while nwmhs had a strong univariate association with ADAS-cog and Stroop IF scores. However, this association disappeared in the multivariate analysis. ConclusionszzThese findings demonstrate that the number of lacunes is the main predictive factor of cognitive impairment in CADASIL. J Clin Neurol 2011;7:210-214 Key Wordszz cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy, lacunes, cerebral microbleeds, white-matter hyperintensities. Introduction Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited angiopathy caused by mutations in the Notch3 gene. 1 The characteristic features include recurrent ischemic stroke, migraine, mood disturbances, apathy, and cognitive impairment. 2 Cognitive impairment is the second most frequent clinical manifestation, with executive dysfunction and slowness of cognitive processing speed cc This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. present in most patients. 3 The cognitive profile in CADASIL is characteristic of vascular dementia and is similar to that reported for sporadic subcortical ischemic vascular dementia. 4 MRI plays a major role in the diagnosis of CADASIL. Typical MRI findings include multiple focal lacunar infarcts and diffuse T2-weighted hyperintensities of the cerebral white matter. 5 Recent MRI studies have shown that cognitive impairment is associated with neuroimaging measures in CADASIL, but that there are conflicting results. 6-11 Some researchers have observed an association between the number of lacunar infarctions and the severity of cognitive impairment, 6-8 while other also found cognitive impairment to be associated with ventricular enlargement, 8 brain atrophy, 9 and cerebral microbleeds (CMBs). 8,10 In the present study we examined several different MRI pa- 210 Copyright 2011 Korean Neurological Association

Lee JS et al. rameters and determined their effect on cognitive impairment in patients with CADASIL. Methods Between April 2008 and May 2009, we enrolled 59 consecutive patients who had genetically confirmed CADASIL. Patients who did not undergo a prospective MRI protocol (n=8) or a comprehensive neuropsychological protocol (n=11) were excluded, resulting in the final inclusion of 40 patients in the study. The vascular risk factors were recorded, including hypertension, diabetes mellitus, and hypercholesterolemia. Hypertension was defined as blood pressures of >140/90 mm Hg on different occasions or use of an antihypertensive agent. Diabetes mellitus was defined as a fasting glucose level of 126 mg/dl, a PP2 test level of 200 mg/dl, or the use of antidiabetes medication. Hypercholesterolemia was defined as a total serum cholesterol level of >240 mg/dl. This study was approved by the institutional review board, and informed consent was obtained from patients. All patients received a standardized battery of neuropsychological tests. Global cognitive function was assessed with the Mini-Mental State Examination (MMSE) 12 and the Alzheimer s Disease Assessment Scale-cognition (ADAS-cog), 13,14 which includes tests for orientation, language, ideational and constructional praxis, and memory. Executive function was assessed using the Trail-Making Test part B (TMT-B) 15-17 and the color interference section of the Stroop Color and Word test (Stroop IF). 18 The neuropsychological examinations were performed by a trained neuropsychologist who was blinded to the patients imaging results. MRI scans were obtained with a 1.5-T system (Siemens, Sonata, Germany). The brain imaging protocol, which used a slice thickness of 5 mm and an interslice gap of 1.5 mm, employed the following parameters: T1-weighted images [time to echo (TE)=9.3 ms and time to repeat (TR)=550 ms], T2*-weighted gradient echo planar images (TE=20 ms and TR=600 ms), and fluid attenuated inversion recovery (FLAIR) images (TE=135 ms, TR=8,100 ms, and inversion time=2,100 ms). Lacunar infarcts were defined as parenchymal defects not extending to the cortical gray matter with a signal intensity of cerebrospinal fluid in all sequences and more than 2 mm in diameter. The total number of lacunar infarctions was counted manually by two observers. Lesions located in the lower third of the corpus striatum of the basal ganglia were excluded. 19 CMBs were defined as focal areas of round signal loss on T2*-weighted gradient echo planar images with a diameter of less than 10 mm. 20 The total number of CMBs was counted manually by two observers. Areas of symmetric hypointensity in the basal ganglia were excluded. White-matter hyperintensities (WMHs) were defined as whitematter areas with increased signal intensities on FLAIR images. All FLAIR axial sections from the base of the cerebellum to the vertex were analyzed. A masking and thresholding technique was used (Analyze 8.1, Biomedical Imaging, Mayo Clinic, Rochester, MN, USA) (Fig. 1). The total volume of WMHs was calculated automatically by multiplying the lesion area by the section thickness. WMH volume was normalized for total brain volume by dividing the individual WMH volume by the intracranial cavity volume [normalized WMH volume (nwmh)]. WMH volumes were measured by two investigators who were blinded to the clinical data. Data were analyzed using SPSS statistical software (version 12.0). The correlation between MMSE, ADAS-cog, and Stroop IF scores, and time to completion of the TMT-B versus MRI parameters (number of lacunes, number of CMBs, and nwmh) were analyzed by Spearman correlation, corrected for potential confounding by age. Linear regression models were used to assess the relative contribution of MRI parameters on clinical scales. Independent variables were the education level, number of lacunes, number of CMBs, and nwmh. We first used univariate regression models, followed by multivariate models. A p value of less than 0.05 was considered to be indicative of statistical significant. Results Descriptive data for all participants are reported in Table 1. Twenty-five (62.5%) of the 40 patients were men. The patients were aged 58.1±9.9 years (mean±sd; range, 38-74 years). The sites of the mutations were R544C (n=37), R578C (n=2), and R75P (n=1). Thirty-six subjects were symptomatic and 4 were asymptomatic. Ischemic stroke was the most frequent manifestation (n=20), followed by chronic headache (n=9), dementia (n=3), intracerebral hemorrhage (n=3), and seizure (n=1). Hypertension was present in 19 patients. Other risk factors included diabetes (n=2), hypercholesterolemia (n=7), and history of smoking (n=16). Twenty-four patients (60%) had lacunar infarctions, with 7.0±6.1 (range 1 to 20) per patient. CMBs were found in 21 (52.5%) patients, with 12.0±18.1 (range 1-81) per patient. The nwmh was 3.5±1.9. The MMSE and ADAS-cog scores were 27.9±2.9 and 11.8± 8.0, respectively. After adjustment for age, a significant association was found between the number of lacunes and the scores on all cognitive tests except TMT-B. A univariate analysis (Table 2) revealed an association between the MMSE score and the number of lacunes (p=0.005). Furthermore, the ADAS-cog score was associated with the number of lacunes (p<0.001) and nwmh (p=0.002). The total number of lacunes and nwmh showed trends toward poor performance in the TMT-B (p=0.084 and p= 0.083, respectively). The Stroop IF score was associated with the www.thejcn.com 211

Lacunar Infarctions and CADASIL A B C D number of lacunes (p<0.001) and nwmh (p=0.019). There was no significant association between the scores on any of the cognitive tests and the number of CMBs. A higher education level was associated with better performance in all cognitive tests except the Stroop IF. The results of the multivariate regression analysis are summarized in Table 3. The number of lacunes was an independent predictor of cognitive impairment for all cognitive tests in the multivariate analysis. There was also a significant independent effect of education level on all cognitive tests. nwmhs was associated with ADAS-cog and Stroop IF scores. However, the multivariate analysis found no significant association with nwmhs. Discussion We found that the number of lacunes was the most important predictor of cognitive impairment in patients with CADASIL. Of the candidate variables investigated in our study, education level, number of lacunes, and nwmh showed univariate associations with cognitive scales. However, only the number of lacunes 212 J Clin Neurol 2011;7:210-214 Fig. 1. An example of the volumetric analysis. Whole brain volume was calculated after removing nonbrain tissue (B) and the ventricles (C). The volume of the white-matter hyperintensity was calculated semiautomatically using threshold filtering (D). and education level remained significant in multivariate modeling. This is consistent with previous studies finding an association between the number of lacunar infarctions and the severity of cognitive impairment.6-9 The association between MRI parameters and clinical scales (cognitive function and disability) has been described previously for Caucasians.6-10 However, no studies have investigated clinical and MRI correlates in Asian patients with CADASIL. This is the first study to demonstrate that the number of lacunes is a major contributor to cognitive impairment in non-caucasian CADASIL patients. Our data show that the number of lacunes is negatively correlated with specific executive function as well as global cognitive function. The number of lacunes was independently associated with Stroop IF scores, which were sensitive discriminators between patients with CADASIL and healthy subjects in the early disease stages, as reported previously.3 In addition, lacunar infarcts were independent predictors of global cognitive decline as assessed by MMSE and ADAS-cog. ADAS-cog is one of the most widely used scales for measuring cognitive impairment. However, an association between the number of lacunes and ADAS-cog scores has not been described before in

Lee JS et al. Table 1. Demographic, cognitive, and MRI data of the study subjects Clinical data Age, years 58.1±9.9 Male sex 25 (62.5) Education, years 10.5±4.3 History of hypertension 19 (47.5) History of Diabetes Mellitus 2 (5) 0 History of hypercholesterolemia 07 (17.5) Current or previous smoking 16 (40) 0 Cognitive and functional data MMSE 27.9±2.9 ADAS-cog 11.8±8.0 Trail-Making Test, part B, time 061.3±48.6 Trail-Making Test, part B, errors 00.9±1.1 Stroop IF 00.41±0.67 MRI markers nwmh 03.5±1.9 Number of lacunes 04.2±5.8 Number of CMBs 006.6±14.6 Data are mean±sd or n (%) values. MMSE: Mini-Mental State Examination, ADAS-cog: Alzheimer s Disease Assessment Scale-cognition, Stroop IF: Stroop interference, nwmh: normalized volume of white-matter hyperintensities, CMBs: cerebral microbleeds. CADASIL. It is unusual that no significant correlation was found between the number of lacunes and time to completion of the TMT-B in the present study. However, there was a trend toward an association between the number of lacunes and poor performance in the TMT-B (p=0.084). Moreover, a significant association was found between these two parameters after correcting for age and education level (p=0.04, r=0.35). Recent studies of the relationship between CMBs and cognition have produced conflicting results, with some showing no association between the two, 6,7 whereas others indicating a possible association with cognition. 8-10 One prospective study found longitudinal associations between CMBs and cognitive decline. 8 However, the number of patients in that analysis (n=25) was too small to draw definitive conclusions. Our study found that CMBs were not associated with cognitive scales in the univariate analysis. We cannot exclude the possibility that CMBs contributed to cognitive impairment in CADASIL. However, our results suggest that the impact of CMBs on cognition is less significant than that of the number of lacunar infarctions. We also found that the association between nwmhs and cognitive scales was present in the univariate analysis, but this association disappeared in the final multivariate model. These findings are in line with previous studies showing the importance of lacunar lesions but not WMH volume in patients with CADA- SIL. 6-9 Our study was subject to several limitations. First, the number of lacunar infarcts and CMBs at each cerebral location were Table 2. Univariate analysis of the effect of MRI parameters on cognitive function Cognitive test Lacunes nwmh CMBs beta p beta p beta p MMSE -0.44 0.005-0.31 0.053 ns ns ADAS-cog 0.61 <0.001 0.47 0.002 ns ns TMT-B (time) 0.29 0.084 0.29 0.083 ns ns Stroop IF 0.58 <0.001 0.37 0.019 ns ns Lacunes: number of lacunar infarcts, beta: standardized beta, ns: not significant at p=0.05. nwmh: normalized white-matter hyperintensities volume, CMBs: cerebral microbleeds, MMSE: Mini-Mental State Examination, ADAScog: Alzheimer s Disease Assessment Scale-cognition, TMT-B: Trail-Making Test part B, Stroop IF: Stroop interference. Table 3. Multivariate analysis of the effect of MRI parameters on cognitive function after adjustment for age and years of education Cognitive test Lacunes nwmh CMBs beta p beta p beta p MMSE -0.41 0.004 ns ns ns ns ADAS-cog 0.58 <0.001 ns ns ns ns TMT-B (time) 0.28 0.04 ns ns ns ns Stroop IF 0.55 <0.001 ns ns ns ns nwmh: normalized white-matter hyperintensities volume, CMBs: cerebral microbleeds, MMSE: Mini-Mental State Examination, ADAScog: Alzheimer s Disease Assessment Scale-cognition, TMT-B: Trail-Making Test part B, Stroop IF: Stroop interference. not quantified, and hence we were unable to determine the correlation between regional MRI abnormalities and cognitive scales. Second, we were not able to measure the volume of individual lacunar infarcts and CMBs, which may have affected www.thejcn.com 213

Lacunar Infarctions and CADASIL cognitive deficits. Third, we could not evaluate the degree of brain atrophy, which has been reported to be an important predictor of cognitive impairment. Finally, R544C in exon 11 accounted for 92.5% of the mutations in our study. Thus, our findings may not be fully representative of the wider CADASIL population. 21,22 In conclusion, we found that the total number of lacunes was associated with poor performance in the MMSE, ADAS-cog, and Stroop IF. These findings suggest that the number of lacunes can be used as a predictive factor of cognitive impairment in non-caucasian patients with CADASIL. However, since this was a cross-sectional study, further prospective studies are needed to elucidate the association between MRI parameters and cognitive impairment. Conflicts of Interest The authors have no financial conflicts of interest. Acknowledgements This work was supported by the research grant of the Jeju National University in 2008. REFERENCES 1. Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, et al. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature 1996;383:707-710. 2. Chabriat H, Vahedi K, Iba-Zizen MT, Joutel A, Nibbio A, Nagy TG, et al. Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Lancet 1995;346:934-939. 3. Peters N, Opherk C, Danek A, Ballard C, Herzog J, Dichgans M. The pattern of cognitive performance in CADASIL: a monogenic condition leading to subcortical ischemic vascular dementia. Am J Psychiatry 2005; 162:2078-2085. 4. Benisty S, Hernandez K, Viswanathan A, Reyes S, Kurtz A, O Sullivan M, et al. Diagnostic criteria of vascular dementia in CADASIL. Stroke 2008;39:838-844. 5. O Sullivan M, Jarosz JM, Martin RJ, Deasy N, Powell JF, Markus HS. MRI hyperintensities of the temporal lobe and external capsule in patients with CADASIL. Neurology 2001;56:628-634. 6. Viswanathan A, Gschwendtner A, Guichard JP, Buffon F, Cumurciuc R, O Sullivan M, et al. Lacunar lesions are independently associated with disability and cognitive impairment in CADASIL. Neurology 2007;69: 172-179. 7. Liem MK, van der Grond J, Haan J, van den Boom R, Ferrari MD, Knaap YM, et al. Lacunar infarcts are the main correlate with cognitive dysfunction in CADASIL. Stroke 2007;38:923-928. 8. Liem MK, Lesnik Oberstein SA, Haan J, van der Neut IL, Ferrari MD, van Buchem MA, et al. MRI correlates of cognitive decline in CADA- SIL: a 7-year follow-up study. Neurology 2009;72:143-148. 9. Viswanathan A, Godin O, Jouvent E, O Sullivan M, Gschwendtner A, Peters N, et al. Impact of MRI markers in subcortical vascular dementia: a multi-modal analysis in CADASIL. Neurobiol Aging 2010;31: 1629-1636. 10. Viswanathan A, Guichard JP, Gschwendtner A, Buffon F, Cumurcuic R, Boutron C, et al. Blood pressure and haemoglobin A1c are associated with microhaemorrhage in CADASIL: a two-centre cohort study. Brain 2006;129:2375-2383. 11. Jouvent E, Viswanathan A, Mangin JF, O Sullivan M, Guichard JP, Gschwendtner A, et al. Brain atrophy is related to lacunar lesions and tissue microstructural changes in CADASIL. Stroke 2007;38:1786-1790. 12. Kang Y, Na DL, Hahn S. A validity study on the Korean mini-mental state examination (K-MMSE) in dementia patients. J Korean Neurol Assoc 1997;15:300-308. 13. Rosen WG, Mohs RC, Davis KL. A new rating scale for Alzheimer s disease. Am J Psychiatry 1984;141:1356-1364. 14. Suh GH, Mohs RC. Development of the Korean version of Alzheimers Disease Assessment Scale (ADAS-K) to assess cognition in dementia. J Korean Geriatr Soc 2003;7:269-277. 15. Reitan RM. Trail Making Test. Manual for Administration and Scoring. Bloomington, IN: Indiana University, 1959. 16. Yi H, Chin J, Lee BH, Kang Y, Na DL. Development and validation of Korean version of Trail Making Test for elderly persons. Dement Neurocognitive Disord 2007;6:54-66. 17. Madureira S, Verdelho A, Ferro J, Basile AM, Chabriat H, Erkinjuntti T, et al. Development of a neuropsychological battery for the Leukoaraiosis and Disability in the Elderly Study (LADIS): experience and baseline data. Neuroepidemiology 2006;27:101-116. 18. Golden C, Freshwater SM. Stroop Color and Word Test. Wood Dale, IL: Stoelting, 2002. 19. Bokura H, Kobayashi S, Yamaguchi S. Distinguishing silent lacunar infarction from enlarged Virchow-Robin spaces: a magnetic resonance imaging and pathological study. J Neurol 1998;245:116-122. 20. Koennecke HC. Cerebral microbleeds on MRI: prevalence, associations, and potential clinical implications. Neurology 2006;66:165-171. 21. Kang SY, Oh JH, Kang JH, Choi JC, Lee JS. Nerve conduction studies in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. J Neurol 2009;256:1724-1727. 22. Lee JS, Choi JC, Kang SY, Kang JH, Lee SH, Kim JH, et al. Olfactory identification deficits in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Eur Neurol 2010;64:280-285. 214 J Clin Neurol 2011;7:210-214