Cerebral small-vessel disease and progression of brain atrophy The SMART-MR study

被引:82
作者
Kloppenborg, R. P. [1 ,4 ]
Nederkoorn, P. J. [4 ]
Grool, A. M. [1 ]
Vincken, K. L. [2 ]
Mali, W. P. T. M. [3 ]
Vermeulen, M. [4 ]
van der Graaf, Y. [1 ]
Geerlings, M. I. [1 ]
机构
[1] Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Image Sci Inst, Utrecht, Netherlands
[3] Univ Med Ctr Utrecht, Dept Radiol, Utrecht, Netherlands
[4] Univ Amsterdam, Acad Med Ctr, Dept Neurol, NL-1105 AZ Amsterdam, Netherlands
关键词
WHITE-MATTER LESIONS; COGNITIVE DECLINE; HIPPOCAMPAL ATROPHY; RISK-FACTORS; FOLLOW-UP; RATES; LACUNES; VOLUMES; LADIS; AD;
D O I
10.1212/WNL.0b013e3182749f02
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: To investigate whether severity and progression of periventricular and deep white matter lesions (WML) and lacunar infarcts were associated with progression of brain atrophy. Methods: Within the SMART-MR study, a prospective cohort on MRI changes in patients with symptomatic atherosclerotic disease, 565 patients (57 +/- 9 years) without large infarcts had vascular screening and 1.5 T MRI at baseline and after a mean follow-up of 3.9 years. With automated brain segmentation, total brain, cortical gray matter, ventricular, and WML volumes were estimated and expressed relative to intracranial volume (%). Lacunar infarcts were rated manually. Results: Using linear regression analyses adjusted for demographics and vascular risk factors, periventricular WML volume at baseline was associated with greater decrease in cortical gray matter volume (B = -1.73%, 95% confidence interval [CI] -3.15% to -0.30%, per 1% WML volume increase) and greater increase in ventricular volume (B = 0.12%, 95% CI 0.04% to 0.20%). Progression of periventricular WML volume corresponded with a greater decrease in cortical gray matter volume (B = -0.45%, 95% CI -0.9% to 0%) and greater increase in ventricular volume (B = 0.15%, 95% CI 0.1% to 0.2%). Presence of lacunar infarcts was associated with greater decline in total brain volume (B = -0.25%, 95% CI -0.49% to -0.01%) and progression of lacunar infarcts with a greater decrease of total brain (B = -0.30%, 95% CI -0.59% to 0.01%) and cortical gray matter volume (B = -0.81%, 95% CI -1.43% to -0.20%). Conclusions: In patients with symptomatic atherosclerotic disease, presence and progression of periventricular WML and lacunar infarcts is associated with greater progression of brain atrophy independent of vascular risk factors. Neurology (R) 2012; 79: 2029-2036
引用
收藏
页码:2029 / 2036
页数:8
相关论文
共 28 条
[1]   Probabilistic segmentation of white lesions in MR imaging [J].
Anbeek, P ;
Vincken, KL ;
van Osch, MJP ;
Bisschops, RHC ;
van der Grond, J .
NEUROIMAGE, 2004, 21 (03) :1037-1044
[2]   CEREBRAL WHITE-MATTER LESIONS, VASCULAR RISK-FACTORS, AND COGNITIVE FUNCTION IN A POPULATION-BASED STUDY - THE ROTTERDAM STUDY [J].
BRETELER, MMB ;
VANSWIETEN, JC ;
BOTS, ML ;
GROBBEE, DE ;
CLAUS, JJ ;
VANDENHOUT, JHW ;
VANHARSKAMP, F ;
TANGHE, HLJ ;
DEJONG, PTVM ;
VANGIJN, J ;
HOFMAN, A .
NEUROLOGY, 1994, 44 (07) :1246-1252
[3]   PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE [J].
COCKCROFT, DW ;
GAULT, MH .
NEPHRON, 1976, 16 (01) :31-41
[4]   White matter lesions are associated with progression of medial temporal lobe atrophy in Alzheimer disease [J].
de Leeuw, Frank-Erik ;
Korf, Esther ;
Barkhof, Frederik ;
Scheltens, Philip .
STROKE, 2006, 37 (09) :2248-2252
[5]   Use of hippocamal and amygdalar volumes on magnetic resonance imaging to predict dementia in cognitively intact elderly people [J].
den Heijer, T ;
Geerlings, MI ;
Hoebeek, FE ;
Hofman, A ;
Koudstaal, PJ ;
Breteler, MMB .
ARCHIVES OF GENERAL PSYCHIATRY, 2006, 63 (01) :57-62
[6]   Age effects on atrophy rates of entorhinal cortex and hippocampus [J].
Du, AT ;
Schuff, N ;
Chao, LL ;
Kornak, J ;
Jagust, WJ ;
Kramer, JH ;
Reed, BR ;
Miller, BL ;
Norman, D ;
Chui, HC ;
Weiner, MW .
NEUROBIOLOGY OF AGING, 2006, 27 (05) :733-740
[7]   White matter lesions are associated with cortical atrophy more than entorhinal and hippocampal atrophy [J].
Du, AT ;
Schuff, N ;
Chao, LL ;
Kornak, J ;
Ezekiel, F ;
Jagust, WJ ;
Kramer, JH ;
Reed, BR ;
Miller, BL ;
Norman, D ;
Chui, HC ;
Weiner, MW .
NEUROBIOLOGY OF AGING, 2005, 26 (04) :553-559
[8]   Risk factors for progression of brain atrophy in aging - Six-year follow-up of normal subjects [J].
Enzinger, C ;
Fazekas, F ;
Matthews, PM ;
Ropele, S ;
Schmidt, H ;
Smith, S ;
Schmidt, R .
NEUROLOGY, 2005, 64 (10) :1704-1711
[9]   Medial temporal atrophy rather than white matter hyperintensities predict cognitive decline in stroke survivors [J].
Firbank, Michael J. ;
Burton, Emma J. ;
Barber, Robert ;
Stephens, Sally ;
Kenny, Rose Anne ;
Ballard, Clive ;
Kalaria, Raj. N. ;
O'Brien, John T. .
NEUROBIOLOGY OF AGING, 2007, 28 (11) :1664-1669
[10]   Brain atrophy and white matter hyperintensity change in older adults and relationship to blood pressure [J].
Firbank, Michael J. ;
Wiseman, Rebecca M. ;
Burton, Emma J. ;
Saxby, Brian K. ;
O'Brien, John T. ;
Ford, Gary A. .
JOURNAL OF NEUROLOGY, 2007, 254 (06) :713-721