William C. Warger
Harvard University
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Radiology | 2012
Pál Maurovich-Horvat; Christopher L. Schlett; Hatem Alkadhi; Masataka Nakano; Paul Stolzmann; Marc Vorpahl; Hans Scheffel; Atsushi Tanaka; William C. Warger; Akiko Maehara; Shixin Ma; Matthias F. Kriegel; Ryan K. Kaple; Harald Seifarth; Fabian Bamberg; Gary S. Mintz; Guillermo J. Tearney; Renu Virmani; Udo Hoffmann
PURPOSE To establish an ex vivo experimental setup for imaging coronary atherosclerosis with coronary computed tomographic (CT) angiography, intravascular ultrasonography (US), and optical frequency domain imaging (OFDI) and to investigate their ability to help differentiate early from advanced coronary plaques. MATERIALS AND METHODS All procedures were performed in accordance with local and federal regulations and the Declaration of Helsinki. Approval of the local Ethics Committee was obtained. Overall, 379 histologic cuts from nine coronary arteries from three donor hearts were acquired, coregistered among modalities, and assessed for the presence and composition of atherosclerotic plaque. To assess the discriminatory capacity of the different modalities in the detection of advanced lesions, c statistic analysis was used. Interobserver agreement was assessed with the Cohen κ statistic. RESULTS Cross sections without plaque at coronary CT angiography and with fibrous plaque at OFDI almost never showed advanced lesions at histopathologic examination (odds ratio [OR]: 0.02 and 0.06, respectively; both P<.0001), while mixed plaque at coronary CT angiography, calcified plaque at intravascular US, and lipid-rich plaque at OFDI were associated with advanced lesions (OR: 2.49, P=.0003; OR: 2.60, P=.002; and OR: 31.2, P<.0001, respectively). OFDI had higher accuracy for discriminating early from advanced lesions than intravascular US and coronary CT angiography (area under the receiver operating characteristic curve: 0.858 [95% confidence interval {CI}: 0.802, 0.913], 0.631 [95% CI: 0.554, 0.709], and 0.679 [95% CI: 0.618, 0.740]; respectively, P<.0001). Interobserver agreement was excellent for OFDI and coronary CT angiography (κ=0.87 and 0.85, respectively) and was good for intravascular US (κ=0.66). CONCLUSION Systematic and standardized comparison between invasive and noninvasive modalities for coronary plaque characterization in ex vivo specimens demonstrated that coronary CT angiography and intravascular US are reasonably associated with plaque composition and lesion grading according to histopathologic findings, while OFDI was strongly associated. These data may help to develop initial concepts of sequential imaging strategies to identify patients with advanced coronary plaques.
Jacc-cardiovascular Imaging | 2010
Patrick Donnelly; Pál Maurovich-Horvat; Marc Vorpahl; Masataka Nakano; Ryan K. Kaple; William C. Warger; Atsushi Tanaka; Guillermo J. Tearney; Renu Virmani; Udo Hoffmann
NEW HIGH-RESOLUTION IMAGING TECHNOLOGIES HAVE ENHANCED OUR UNDERSTANDING OF THE CORONARY atherosclerotic disease process, and this atlas provides a multimodality pictorial review of the development of histologically verified coronary atherosclerosis. A modified American Heart Association
Biomedical Optics Express | 2013
Eman Namati; William C. Warger; Carolin Unglert; Jocelyn E. Eckert; Jeroen Hostens; Brett E. Bouma; Guillermo J. Tearney
Pulmonary alveoli have been studied for many years, yet no unifying hypothesis exists for their dynamic mechanics during respiration due to their miniature size (100-300 μm dimater in humans) and constant motion, which prevent standard imaging techniques from visualizing four-dimensional dynamics of individual alveoli in vivo. Here we report a new platform to image the first layer of air-filled subpleural alveoli through the use of a lightweight optical frequency domain imaging (OFDI) probe that can be placed upon the pleura to move with the lung over the complete range of respiratory motion. This device enables in-vivo acquisition of four-dimensional microscopic images of alveolar airspaces (alveoli and ducts), within the same field of view, during continuous ventilation without restricting the motion or modifying the structure of the alveoli. Results from an exploratory study including three live swine suggest that subpleural alveolar air spaces are best fit with a uniform expansion (r (2) = 0.98) over a recruitment model (r (2) = 0.72). Simultaneously, however, the percentage change in volume shows heterogeneous alveolar expansion within just a 1 mm x 1 mm field of view. These results signify the importance of four-dimensional imaging tools, such as the device presented here. Quantification of the dynamic response of the lung during ventilation may help create more accurate modeling techniques and move toward a more complete understanding of alveolar mechanics.
Journal of Biomedical Optics | 2012
Carolin Unglert; Eman Namati; William C. Warger; Linbo Liu; Hongki Yoo; DongKyun Kang; Brett E. Bouma; Guillermo J. Tearney
Abstract. Three-dimensional (3-D) visualization of the fine structures within the lung parenchyma could advance our understanding of alveolar physiology and pathophysiology. Current knowledge has been primarily based on histology, but it is a destructive two-dimensional (2-D) technique that is limited by tissue processing artifacts. Micro-CT provides high-resolution three-dimensional (3-D) imaging within a limited sample size, but is not applicable to intact lungs from larger animals or humans. Optical reflectance techniques offer the promise to visualize alveolar regions of the large animal or human lung with sub-cellular resolution in three dimensions. Here, we present the capabilities of three optical reflectance techniques, namely optical frequency domain imaging, spectrally encoded confocal microscopy, and full field optical coherence microscopy, to visualize both gross architecture as well as cellular detail in fixed, phosphate buffered saline-immersed rat lung tissue. Images from all techniques were correlated to each other and then to corresponding histology. Spatial and temporal resolution, imaging depth, and suitability for in vivo probe development were compared to highlight the merits and limitations of each technology for studying respiratory physiology at the alveolar level.
Journal of Biomedical Optics | 2012
Carolin Unglert; William C. Warger; Jeroen Hostens; Eman Namati; Reginald Birngruber; Brett E. Bouma; Guillermo J. Tearney
Abstract. Optical coherence tomography (OCT) has been increasingly used for imaging pulmonary alveoli. Only a few studies, however, have quantified individual alveolar areas, and the validity of alveolar volumes represented within OCT images has not been shown. To validate quantitative measurements of alveoli from OCT images, we compared the cross-sectional area, perimeter, volume, and surface area of matched subpleural alveoli from microcomputed tomography (micro-CT) and OCT images of fixed air-filled swine samples. The relative change in size between different alveoli was extremely well correlated (r>0.9, P<0.0001), but OCT images underestimated absolute sizes compared to micro-CT by 27% (area), 7% (perimeter), 46% (volume), and 25% (surface area) on average. We hypothesized that the differences resulted from refraction at the tissue–air interfaces and developed a ray-tracing model that approximates the reconstructed alveolar size within OCT images. Using this model and OCT measurements of the refractive index for lung tissue (1.41 for fresh, 1.53 for fixed), we derived equations to obtain absolute size measurements of superellipse and circular alveoli with the use of predictive correction factors. These methods and results should enable the quantification of alveolar sizes from OCT images in vivo.
Reference Module in Biomedical Sciences#R##N#Pathobiology of Human Disease#R##N#A Dynamic Encyclopedia of Disease Mechanisms | 2014
William C. Warger; Michalina Gora; Carolin Unglert; Brett E. Bouma; Guillermo J. Tearney
american thoracic society international conference | 2012
William C. Warger; Eman Namati; Carolin Unglert; Jocelyn E. Eckert; Jeroen Hostens; Brett E. Bouma; Guillermo J. Tearney
Archive | 2012
William C. Warger; Eman Namati; Guillermo J. Tearney; Brett Eugene Bouma; Carolin Unglert
Journal of the American College of Cardiology | 2012
Christopher L. Schlett; Pál Maurovich-Horvat; Fabian Bamberg; William C. Warger; Masataka Nakano; Atsushi Tanaka; Marc Vorpahl; Harald Seifarth; Maros Ferencik; Renu Virmani; Guillermo J. Tearney; Udo Hoffmann
Archive | 2011
Brett Eugene Bouma; Joseph A. Gardecki; James L. Hancock; Melissa Suter; Guillermo J. Tearney; George Velmahos; William C. Warger