Measuring cerebral atrophy and white matter hyperintensity burden to predict the rate of cognitive decline in Alzheimer disease.
Measuring cerebral atrophy and white matter hyperintensity burden to predict the rate of cognitive decline in Alzheimer disease.
复制标题
DOI:
10.1001/archneur.65.9.1202
复制
发表时间:
2008-09
影响因子:
--
通讯作者:
Stern, Yaakov
中科院分区:
文献类型:
--
作者:
Brickman, Adam M.;Honig, Lawrence S.;Scarmeas, Nikolaos;Tatarina, Oksana;Sanders, Linda;Albert, Marilyn S.;Brandt, Jason;Blacker, Deborah;Stern, Yaakov
Although non-specific, cerebral atrophy and white matter hyperintensities (WMH) are features of the neurodegeneration associated with Alzheimer’s disease (AD). The purpose of the current study was to determine if baseline measurements of cerebral atrophy and WMH predict the rate of future cognitive decline in AD. Data were drawn from the Predictors Study, a longitudinal study that enrolls mild AD patients and re-asseses them every six months with the Columbia modified Mini Mental State Examination (mMMS; 0–57). MR images were analyzed to determine the severity of WMH (Scheltens Scale) and the degree of atrophy (bicaudate ratio). Generalized estimating equations (GEE) were used to determine whether severity of baseline MRI measurements and their interaction predicted the rate of mMMS decline at subsequent visits. Three university-based AD centers in the United States (Predictors Study). Eighty-four AD patients from the Predictors Study received structural MRI at baseline and were selected for analysis. They had an average of 6 follow-up evaluations. Cognitive (Columbia modified Mini-Mental State Examination). Generalized estimating equation models demonstrated that degree of baseline atrophy (β = −0.316, p = 0.036), severity of WMH (β = −0.173, p = 0.028), and their interaction (β = − 6.061, p = 0.018) predicted rate of decline in mMMS scores. Both degree of cerebral atrophy and severity of WMH are associated with the rapidity of cognitive decline in AD. Atrophy and WMH may interact to have a synergistic effect on future decline, such that AD patients with a high degree of both have a particularly precipitous cognitive course. These findings lend further support to the hypothesis that cerebrovascular pathology contributes to the clinical syndrome of Alzheimer’s disease.
登录
查看更多内容
影响因子:
9.9
作者:
Jack, CR;Shiung, MM;Petersen, RC
通讯作者:
Petersen, RC
影响因子:
2.4
作者:
Englund, E
通讯作者:
Englund, E
影响因子:
2.5
作者:
Duarte, Audrey;Hayasaka, Satoru;Weiner, Michael
通讯作者:
Weiner, Michael
影响因子:
9.9
作者:
Gurol, ME;Irizarry, MC;Greenberg, SM
通讯作者:
Greenberg, SM
影响因子:
--
作者:
Burns, JM;Church, JA;Buckner, RL
通讯作者:
Buckner, RL