Cerebral white matter rarefaction has both neurodegenerative and vascular causes and may primarily be a distal axonopathy

被引:7
作者
Beach, Thomas G. [1 ,7 ]
Sue, Lucia, I [1 ]
Scott, Sarah [1 ]
Intorcia, Anthony J. [1 ]
Walker, Jessica E. [1 ]
Arce, Richard A. [1 ]
Glass, Michael J. [1 ]
Borja, Claryssa, I [1 ]
Cline, Madison P. [1 ]
Hemmingsen, Spencer J. [1 ]
Qiji, Sanaria [1 ]
Stewart, Analisa [1 ]
Martinez, Kayleigh N. [1 ]
Krupp, Addison [1 ]
McHattie, Rylee [1 ]
Mariner, Monica [1 ]
Lorenzini, Ileana [1 ]
Kuramoto, Angela [1 ]
Long, Kathy E. [1 ]
Tremblay, Cecilia [1 ]
Caselli, Richard J. [2 ]
Woodruff, Bryan K. [2 ]
Rapscak, Steven Z. [3 ]
Belden, Christine M. [1 ]
Goldfarb, Danielle [1 ]
Choudhury, Parichita [1 ]
Driver-Dunckley, Erika D. [2 ]
Mehta, Shyamal H. [2 ]
Sabbagh, Marwan N. [4 ]
Shill, Holly A. [4 ]
Atri, Alireza [1 ,5 ,6 ]
Adler, Charles H. [2 ]
Serrano, Geidy E. [1 ]
机构
[1] Banner Sun Hlth Res Inst, Sun City, AZ USA
[2] Mayo Clin, Dept Neurol, Scottsdale, AZ USA
[3] Banner Alzheimers Inst, Tucson, AZ USA
[4] Barrow Neurol Inst, Phoenix, AZ USA
[5] Harvard Med Sch, Boston, MA USA
[6] Brigham & Womens Hosp, Boston, MA USA
[7] Banner Sun Hlth Res Inst, Civin Lab Neuropathol, 10515 W St Fe Dr, Sun City, AZ 85351 USA
关键词
Alzheimer disease; Hyperintensity; Lacunar infarct; Leukoaraiosis; Microscopic infarct; Small vessel disease; Vascular cognitive impairment; ALZHEIMERS-DISEASE; SEX-DIFFERENCES; RISK-FACTORS; NEUROFIBRILLARY CHANGES; CORTICAL MICROINFARCTS; BINSWANGERS-DISEASE; WEIGHT-LOSS; DEMENTIA; LESIONS; BRAIN;
D O I
10.1093/jnen/nlad026
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cerebral white matter rarefaction (CWMR) was considered by Binswanger and Alzheimer to be due to cerebral arteriolosclerosis. Renewed attention came with CT and MR brain imaging, and neuropathological studies finding a high rate of CWMR in Alzheimer disease (AD). The relative contributions of cerebrovascular disease and AD to CWMR are still uncertain. In 1181 autopsies by the Arizona Study of Aging and Neurodegenerative Disorders (AZSAND), large-format brain sections were used to grade CWMR and determine its vascular and neurodegenerative correlates. Almost all neurodegenerative diseases had more severe CWMR than the normal control group. Multivariable logistic regression models indicated that Braak neurofibrillary stage was the strongest predictor of CWMR, with additional independently significant predictors including age, cortical and diencephalic lacunar and microinfarcts, body mass index, and female sex. It appears that while AD and cerebrovascular pathology may be additive in causing CWMR, both may be solely capable of this. The typical periventricular pattern suggests that CWMR is primarily a distal axonopathy caused by dysfunction of the cell bodies of long-association corticocortical projection neurons. A consequence of these findings is that CWMR should not be viewed simply as "small vessel disease" or as a pathognomonic indicator of vascular cognitive impairment or vascular dementia.
引用
收藏
页码:457 / 466
页数:10
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