Hippocampal CA1 apical neuropil atrophy in mild Alzheimer disease visualized with 7-T MRI

被引:151
作者
Kerchner, G. A. [1 ,2 ]
Hess, C. P. [3 ,4 ]
Hammond-Rosenbluth, K. E. [5 ,7 ]
Xu, D. [3 ,4 ]
Rabinovici, G. D. [2 ]
Kelley, D. A. C. [6 ]
Vigneron, D. B. [3 ,4 ]
Nelson, S. J. [3 ,4 ]
Miller, B. L. [2 ]
机构
[1] Stanford Univ, Sch Med, Dept Neurol & Neurol Sci, Stanford Ctr Memory Disorders, Stanford, CA 94305 USA
[2] Univ Calif San Francisco, Dept Neurol, Memory & Aging Ctr, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Radiol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, UCB Joint Grad Grp Bioengn, San Francisco, CA 94143 USA
[6] GE Healthcare Technol, Global Appl Sci Lab, San Francisco, CA USA
[7] Univ Calif Berkeley, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
HIGH-RESOLUTION MRI; TAU-PATHOLOGY; HUMAN BRAIN; ONSET; MICROSCOPY; DEMENTIA;
D O I
10.1212/WNL.0b013e3181f736a1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: In Alzheimer disease (AD), mounting evidence points to a greater role for synaptic loss than neuronal loss. Supporting this notion, multiple postmortem studies have demonstrated that the hippocampal CA1 apical neuropil is one of the earliest sites of pathology, exhibiting tau aggregates and then atrophy before there is substantial loss of the CA1 pyramidal neurons themselves. In this cross-sectional study, we tested whether tissue loss in the CA1 apical neuropil layer can be observed in vivo in patients with mild AD. Methods: We performed ultra-high-field 7-T MRI on subjects with mild AD (n = 14) and age-matched normal controls (n = 16). With a 2-dimensional T2*-weighted gradient-recalled echo sequence that was easily tolerated by subjects, we obtained cross-sectional slices of the hippocampus at an in-plane resolution of 195 mu m. Results: On images revealing the anatomic landmarks of hippocampal subfields and strata, we observed thinning of the CA1 apical neuropil in subjects with mild AD compared to controls. By contrast, the 2 groups exhibited no difference in the thickness of the CA1 cell body layer or of the entire CA1 subfield. Hippocampal volume, measured on a conventional T1-weighted sequence obtained at 3T, also did not differentiate these patients with mild AD from controls. Conclusions: CA1 apical neuropil atrophy is apparent in patients with mild AD. With its superior spatial resolution, 7-T MRI permits in vivo analysis of a very focal, early site of AD pathology. Neurology (R) 2010;75:1381-1387
引用
收藏
页码:1381 / 1387
页数:7
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