Meeting Banner
Abstract #3729

3D Co-Registration of MRI and Histology in a Mouse Model of Obesity and Non-Alcoholic Fatty Liver Disease

Eli Gibson1, 2, Lanette J. Friesen-Waldner, 23, Amanda M. Hamilton2, Emeline J. Ribot2, Trevor P. Wade3, 4, Curtis N. Wiens5, Kundan Thind, 23, Jacqueline K. Harris3, Nica M. Borradaile6, Charles A. McKenzie1, 3, Aaron D. Ward1, 2

1Biomedical Engineering, University of Western Ontario, London, Ontario, Canada; 2Robarts Research Institute, London, Ontario, Canada; 3Medical Biophysics, University of Western Ontario, London, Ontario, Canada; 4Robarts Research Institute , London, Ontario, Canada; 5Physics and Astronomy, University of Western Ontario, London, Ontario, Canada; 6Physiology and Pharmacology, University of Western Ontario, London, Ontario, Canada

Validation of quantitative MRI for non-invasive quantification of liver fat ideally uses accurate registration to an accepted reference standard (e.g. histology). We demonstrate accurate co-registration of murine in vivo 3D whole-body water-only and fat-only images to stained histological liver images. Three 129/SVJ mice were fed a high fat diet to induce hepatic steatosis and obesity, imaged using 3D quantitative IDEAL MRI at 3T, then sectioned on a cryomicrotome, where 3D optical and histology images were collected. We successfully co-registered MR-optical images and optical-histology images interactively using thin-plate-spline transformations with mean target registration errors of 0.7 mm and 0.1 mm, respectively.

Keywords

accepted accurate acquisition alcoholic animal appear appearance approved astronomy audience automated bifurcations biomedical biophysics bird block body built cage calories cancer care chairs chosen clarity coil collected compound correspondence corresponds cross curved custom denote denoted diagnosis diet digitized discovery disease diseases distances distorted distribution embedding engineering epidemic errors euclidean fatty feasibility fewer frozen full fund globules hepatic histological histology homologous ideal ideally illustrate immediately in vivo incidence indicates induce institution intensity interactively investigators japan landmark landmarks liquid liver magnification manifestation manually medical metabolic mice model models monitoring months mouse nitrogen noninvasive obesity oblique optical overlaid pairs part pharmacology physics physiology pixel placed plate post primary program protocol quantification quantified quantitative rectangles registered registration resolution respectively rising samples scanner section sectioned sectioning sections serially slice slices space spline stained subcommittee successfully support surface syndrome system tape target technologies thick thin tissue transfer transformation validation vessel view visual volumetric wade ward water waterloo western whole