Regional white matter pathology in mild cognitive impairment - Differential influence of lesion type on neuropsychological functioning

被引:83
作者
Delano-Wood, Lisa [1 ]
Abeles, Norm [2 ]
Sacco, Joshua M. [2 ]
Wierenga, Christina E. [1 ]
Horne, Nikki R. [1 ]
Bozoki, Andrea [3 ]
机构
[1] Univ Calif San Diego, Sch Med, Dept Psychiat, La Jolla, CA 92093 USA
[2] Michigan State Univ, Sch Med, Dept Psychol, E Lansing, MI 48824 USA
[3] Michigan State Univ, Sch Med, Dept Neurol & Radiol, E Lansing, MI 48824 USA
关键词
cognition; deep white matter lesions; mild cognitive impairment; white matter hyperintensities; white matter lesions;
D O I
10.1161/STROKEAHA.107.502534
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose - Associations between regional white matter lesion pathology and neuropsychological performance across the aging spectrum are not well understood and, to date, research has been largely contradictory and inconclusive. The current study set out to clarify some of the inconsistencies in the literature by relating volumetric analyses of white matter lesions ( deep white matter lesions and periventricular lesions) to neuropsychological performance in a large clinical sample of older adults diagnosed with mild cognitive impairment. Methods - Seventy older adults with mild cognitive impairment were administered a comprehensive neuropsychological battery. White matter lesions identified on T2-weighted FLAIR images were quantified using a semi-automated volumetric approach ( pixel thresholding). Results - Results showed that, in contrast to performance on memory and naming tasks, total white matter lesions strongly predicted executive impairments, slowed processing speed, and visuospatial/construction difficulties. In addition, separate regression analyses demonstrated that results were primarily accounted for by deep white matter lesions ( but not periventricular lesions), most likely due to frontal-subcortical circuitry disruption. Moreover, deep white matter lesions, but not periventricular lesions, significantly predicted overall poorer neuropsychological functioning after controlling for age, education, and level of depression. Conclusions - Taken together, findings demonstrate a differential influence of lesion type on cognitive impairment in mild cognitive impairment and implicate deep white matter lesions as being most detrimental in terms of neuropsychological functioning. Clinical, theoretical, and methodological implications of these results are discussed.
引用
收藏
页码:794 / 799
页数:6
相关论文
共 44 条
[1]   VASCULAR DEMENTIA AND DEMENTIA OF THE ALZHEIMER TYPE - COGNITION, VENTRICULAR SIZE, AND LEUKO-ARAIOSIS [J].
AHARONPERETZ, J ;
CUMMINGS, JL ;
HILL, MA .
ARCHIVES OF NEUROLOGY, 1988, 45 (07) :719-721
[2]  
[Anonymous], [No title captured]
[3]  
[Anonymous], 1985, HALSTEAD REITAN NEUR
[4]   White matter structural integrity in healthy aging adults and patients with Alzheimer disease - A magnetic resonance imaging study [J].
Bartzokis, G ;
Cummings, JL ;
Sultzer, D ;
Henderson, VW ;
Nuechterlein, KH ;
Mintz, J .
ARCHIVES OF NEUROLOGY, 2003, 60 (03) :393-398
[5]   Mild cognitive impairment -: Long-term course of four clinical subtypes [J].
Busse, A. ;
Hensel, A. ;
Guehne, U. ;
Angermeyer, M. C. ;
Riedel-Heller, S. G. .
NEUROLOGY, 2006, 67 (12) :2176-2185
[6]   A total score for the CERAD neuropsychological battery [J].
Chandler, MJ ;
Lacritz, LH ;
Hynan, LS ;
Barnard, HD ;
Allen, G ;
Deschner, M ;
Weiner, MF ;
Cullum, CM .
NEUROLOGY, 2005, 65 (01) :102-106
[7]   FRONTAL-SUBCORTICAL CIRCUITS AND HUMAN-BEHAVIOR [J].
CUMMINGS, JL .
ARCHIVES OF NEUROLOGY, 1993, 50 (08) :873-880
[8]  
de Groot JC, 2000, ANN NEUROL, V47, P145
[9]  
de Mendonça A, 2005, EUR J NEUROL, V12, P125
[10]   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