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Jonathan J. Wisco

Jonathan J. Wisco

BYU, Department of Physiology and Developmental Biology, Neuroscience Center, USA

Title: Peering into the Iron Window of Alzheimer’s Disease MR Imaging and Pathophysiology

Biography

Dr. Jonathan J. Wisco is Associate Professor and Director of the Laboratory for Translational Anatomy  of  Degenerative  Disease  and  Developmental  Disorders,  College  of  Life Sciences,
Department of Physiology and Developmental Biology, and Neuroscience Center at Brigham Young University, Provo, UT. He is also Associate Director of the BYU MRI Research Facility. Dr. Wisco holds an Adjunct Associate Professor position in the Department of Neurobiology and Anatomy at the University of Utah School of Medicine, Salt Lake City, UT

 

Abstract

The severity of pathological protein deposition, and concomitant iron presence distinguishes neurological disorders. Tissues with high amounts of protein or iron deposits have a characteristically rapid T2* MRI signal decay. Therefore, these tissue components do not appear on traditional MRI, as the NMR signal has already gone through multiple time constants of decay before any signal can be acquired. Ultra-short Echo Time (UTE) imaging, however, significantly reduces the time between the appearance of an NMR signal and its sampling, allowing for the measurement of iron-related pathology. We used a novel UTE sequence with a 3D cones k-space trajectory in a 3T Siemens scanner to image short T2* tissues in the amygdala and hippocampus in ex vivo, 20 mm thick coronal human brain slabs, each with known Alzheimer’s disease (AD) Braak VI taopathy or with cerebrovascular disease (CVD). We quantified the MR signal from tissues with T2* values of less than 1 ms at TEs of 0.25, 0.5,   0.8,

1.0, 2.0, 3.0, and 5.0 ms and TR of 12.1 ms (1 mm iso, FA=15 deg, FOV=15 cm2). Difference

images were then formed by subtracting the TE=5 ms images from the images acquired at the other TEs, effectively suppressing longer T2* tissues. T2* value in the AD amygdala and hippocampus as 4.8+/-1.9 ms (mean+/-SD), and T2* values in anatomically matching regions of the CVD brain was 2.2+/-1.1 ms. We analyzed tissue sections in these regions for the presence Abeta-42, tau, and CD-68 immunohistochemical reactivity, and enhanced Perl’s staining. We noted that the T2* signal decreased with the additive presence of amyloid plaques, tau tangles, non-heme iron, and activated microglia. UTE imaging may be a feasible method to visualize iron-related protein pathology. Future work will further examine the individual contributions of pathological proteins, non-heme iron, and inflammation to the T2* decay.