医学
萎缩
心脏病学
内科学
磁共振成像
白质
大脑大小
高强度
前瞻性队列研究
病理
放射科
作者
Raoul P. Kloppenborg,Paul J. Nederkoorn,Anne M. Grool,Koen L. Vincken,Willem P.Th.M. Mali,Michel Vermeulen,Y. van der Graaf,Mirjam I. Geerlings
出处
期刊:Neurology
[Ovid Technologies (Wolters Kluwer)]
日期:2012-11-01
卷期号:79 (20): 2029-2036
被引量:85
标识
DOI:10.1212/wnl.0b013e3182749f02
摘要
ABSTRACT
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.
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