Bio

Professional Education


  • Doctor of Philosophy, University of California San Francisco (2009)
  • Doctor of Philosophy, University of California Berkeley (2009)
  • Bachelor of Science, Stanford University, ME-BS (2004)

Stanford Advisors


Teaching

2013-14 Courses


Publications

Journal Articles


  • Hippocampal CA1 apical neuropil atrophy in mild Alzheimer disease visualized with 7-T MRI NEUROLOGY Kerchner, G. A., Hess, C. P., Hammond-Rosenbluth, K. E., Xu, D., Rabinovici, G. D., Kelley, D. A., Vigneron, D. B., Nelson, S. J., Miller, B. L. 2010; 75 (15): 1381-1387

    Abstract

    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.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 ?m.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.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.

    View details for Web of Science ID 000282884500015

    View details for PubMedID 20938031

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