Blood-brain barrier permeability is increased in normal-appearing white matter in patients with lacunar stroke and leucoaraiosis

被引:239
作者
Topakian, R. [1 ]
Barrick, T. R. [1 ]
Howe, F. A. [1 ]
Markus, H. S. [1 ]
机构
[1] St Georges Univ London, Ctr Clin Neurosci, London SW17 0RE, England
关键词
CONTRAST-ENHANCED MRI; ISCHEMIC LEUKOARAIOSIS; ALZHEIMERS-DISEASE; VASCULAR DEMENTIA; LESIONS; HYPERINTENSITIES; DYSFUNCTION; INFARCTION; ACCURATE; SUBTYPES;
D O I
10.1136/jnnp.2009.172072
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and aim The pathogenesis of cerebral small-vessel disease (SVD) is incompletely understood. Endothelial dysfunction has been implicated and may result in increased bloodebrain barrier (BBB) permeability with leakage of blood constituents into the vessel wall and white matter. We used contrast-enhanced MRI to determine whether there was any evidence for BBB permeability in the white matter of patients with SVD, and whether this was present not only in areas of leucoaraiosis (white-matter lesions) but also in normal-appearing white matter (NAWM). Methods Subjects underwent T1 volumetric MRI before and after bolus injection of contrast. Scanning was continued for 30 min postinjection to determine the contrast-enhancement time course. The mean signal intensity change was plotted against time to calculate the area under the curve values, a parameter related to BBB permeability. Automated brain segmentation and regions of interest analysis were performed to determine 'permeability' in different brain compartments. Results Compared with controls (n=15), the SVD patient group (n=24) had signal changes consistent with increased BBB permeability in NAWM (p=0.033). Multivariate regression analyses identified leucoaraiosis grade as an independent predictor of these permeability related signal changes in NAWM after adjustment for age, gender, weight, brain volume, area under the curve in the internal carotid arteries and cardiovascular risk factors. Conclusion This study provides evidence for increased BBB permeability in SVD, and this is particularly seen in SVD with leucoaraiosis. Its presence in NAWM would be consistent with it playing a causal role in disease pathophysiology.
引用
收藏
页码:192 / 197
页数:6
相关论文
共 31 条
[1]   Voxel-based morphometry - The methods [J].
Ashburner, J ;
Friston, KJ .
NEUROIMAGE, 2000, 11 (06) :805-821
[2]   CLASSIFICATION AND NATURAL-HISTORY OF CLINICALLY IDENTIFIABLE SUBTYPES OF CEREBRAL INFARCTION [J].
BAMFORD, J ;
SANDERCOCK, P ;
DENNIS, M ;
BURN, J ;
WARLOW, C .
LANCET, 1991, 337 (8756) :1521-1526
[3]   2 CLINICALLY DISTINCT LACUNAR INFARCT ENTITIES - A HYPOTHESIS [J].
BOITEN, J ;
LODDER, J ;
KESSELS, F .
STROKE, 1993, 24 (05) :652-656
[4]  
Evelhoch JL, 1999, JMRI-J MAGN RESON IM, V10, P254, DOI 10.1002/(SICI)1522-2586(199909)10:3<254::AID-JMRI5>3.0.CO
[5]  
2-9
[6]   Blood-brain barrier: Ageing and microvascular disease-systematic review and meta-analysis [J].
Farrall, Andrew J. ;
Wardlaw, Joanna M. .
NEUROBIOLOGY OF AGING, 2009, 30 (03) :337-352
[7]   MR SIGNAL ABNORMALITIES AT 1.5-T IN ALZHEIMER DEMENTIA AND NORMAL AGING [J].
FAZEKAS, F ;
CHAWLUK, JB ;
ALAVI, A ;
HURTIG, HI ;
ZIMMERMAN, RA .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1987, 149 (02) :351-356
[8]   White matter lesions in an unselected cohort of the elderly - Molecular pathology suggests origin from chronic hypoperfusion injury [J].
Fernando, Malee S. ;
Simpson, Julie E. ;
Matthews, Fiona ;
Brayne, Carol ;
Lewis, Claire E. ;
Barber, Robert ;
Kalaria, Raj N. ;
Forster, Gill ;
Esteves, Filomena ;
Wharton, Stephen B. ;
Shaw, Pamela J. ;
O'Brien, John T. ;
Ince, Paul G. .
STROKE, 2006, 37 (06) :1391-1398
[9]   ARTERIAL LESIONS UNDERLYING LACUNES [J].
FISHER, CM .
ACTA NEUROPATHOLOGICA, 1969, 12 (01) :1-&
[10]   Relation between age-related decline in intelligence and cerebral white-matter hyperintensities in healthy octogenarians: a longitudinal study [J].
Garde, E ;
Mortensen, EL ;
Krabbe, K ;
Rostrup, E ;
Larsson, HBW .
LANCET, 2000, 356 (9230) :628-634