Detection of Dysplasia in Barrett's Esophagus With In Vivo Depth-Resolved Nuclear Morphology Measurements
Background & Aims Patients with Barrett's esophagus (BE) show increased risk of developing esophageal adenocarcinoma and are routinely examined using upper endoscopy with biopsy to detect neoplastic changes. Angle-resolved low coherence interferometry (a/LCI) uses in vivo depth-resolved nuc...
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Published in | Gastroenterology (New York, N.Y. 1943) Vol. 140; no. 1; pp. 42 - 50 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.01.2011
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Subjects | |
Online Access | Get full text |
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Summary: | Background & Aims Patients with Barrett's esophagus (BE) show increased risk of developing esophageal adenocarcinoma and are routinely examined using upper endoscopy with biopsy to detect neoplastic changes. Angle-resolved low coherence interferometry (a/LCI) uses in vivo depth-resolved nuclear morphology measurements to detect dysplasia. We assessed the clinical utility of a/LCI in the endoscopic surveillance of patients with BE. Methods Consecutive patients undergoing routine surveillance upper endoscopy for BE were recruited at 2 endoscopy centers. A novel, endoscope-compatible a/LCI system measured the mean diameter and refractive index of cell nuclei in esophageal epithelium at 172 biopsy sites in 46 patients. At each site, an a/LCI measurement was correlated with a concurrent endoscopic biopsy specimen. Each biopsy specimen was assessed histologically and classified as normal, nondysplastic BE, indeterminate for dysplasia, low-grade dysplasia (LGD), or high-grade dysplasia (HGD). The a/LCI data from multiple depths were analyzed to evaluate its ability to differentiate dysplastic from nondysplastic tissue. Results Pathology characterized 5 of the scanned sites as HGD, 8 as LGD, 75 as nondysplastic BE, 70 as normal tissue types, and 14 as indeterminate for dysplasia. The a/LCI nuclear size measurements separated dysplastic from nondysplastic tissue at a statistically significant ( P < .001) level for the tissue segment 200 to 300 μm beneath the surface with an accuracy of 86% (147/172). A receiver operator characteristic analysis indicated an area under the curve of 0.91, and an optimized decision point gave 100% (13/13) sensitivity and 84% (134/159) specificity. Conclusions These preliminary data suggest a/LCI is accurate in detecting dysplasia in vivo in patients with BE. |
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Bibliography: | NJS and AW were equally contributing co-senior authors. List of Contributions: NT, YZ, MTR, WJB & SCG operated the a/LCI device during clinical measurements. SB, EC, CGZ and MP were responsible for study coordination. NJS, RDM, ESD & BFO scanned patients in the clinic during endoscopy procedures. AB, JRG, DT & JTW provided histological evaluation of tissue biopsies. JG performed statistical analysis. NGT, YZ & AW were responsible for design and construction of the a/LCI instrument, acquiring and analyzing data. NJS & AW were responsible for study design. NGT, YZ, NJS & AW were responsible for drafting this manuscript. |
ISSN: | 0016-5085 1528-0012 |
DOI: | 10.1053/j.gastro.2010.09.008 |