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World J Gastroenterol. Jan 7, 2011; 17(1): 53-62
Published online Jan 7, 2011. doi: 10.3748/wjg.v17.i1.53
Optical molecular imaging for detection of Barrett’s-associated neoplasia
Nadhi Thekkek, Sharmila Anandasabapathy, Rebecca Richards-Kortum
Nadhi Thekkek, Rebecca Richards-Kortum, Department of Bioengineering, Rice University, Houston, TX 77005, United States
Sharmila Anandasabapathy, Division of Gastroenterology, Mount Sinai Medical Center, New York, NY 10029, United States
Author contributions: Thekkek N performed the research; Thekkek N, Anandasabapathy S and Richards-Kortum R reviewed the data; Thekkek N and Richards-Kortum R wrote the paper.
Supported by The National Institute of Health Grants BRP CA103830 and RO1 EB007594
Correspondence to: Rebecca Richards-Kortum, PhD, Professor, Department of Bioengineering, Rice University, 6100 Main St, MS 142, Houston, TX 77005, United States. rkortum@rice.edu
Telephone: +1-713-3483823 Fax: +1-713-3485877
Received: July 2, 2010
Revised: November 17, 2010
Accepted: November 24, 2010
Published online: January 7, 2011
Abstract

Recent advancements in the endoscopic imaging of Barrett’s esophagus can be used to probe a wide range of optical properties that are altered with neoplastic progression. This review summarizes relevant changes in optical properties as well as imaging approaches that measures those changes. Wide-field imaging approaches include narrow-band imaging that measures changes in light scattering and absorption, and autofluorescence imaging that measure changes in endogenous fluorophores. High-resolution imaging approaches include optical coherence tomography, endocytoscopy, confocal microendoscopy, and high-resolution microendoscopy. These technologies, some coupled with an appropriate contrast agent, can measure differences in glandular morphology, nuclear morphology, or vascular alterations associated with neoplasia. Advances in targeted contrast agents are further discussed. Studies that have explored these technologies are highlighted; as are the advantages and limitations of each.

Keywords: Barrett’s esophagus; Barrett’s metaplasia; Dysplasia; Esophageal adenocarcinoma; Endoscopy; Imaging