Clinical imaging with optical coherence tomography.

Recent advances in optical fiber and wave-guide technologies have led to the availability of clinically viable optical coherence tomography (OCT) systems. OCT provides cross-sectional images of tissue with a resolution of approximately 10 m. Its relatively shallow depth of penetration (approximately 2–3 mm) requires the use of fiberoptic catheters and endoscopes for accessing internal organs, but flexible, narrow-diameter OCT probes are readily constructed with standard telecommunications optical fiber (diameter, 250 m). Recent studies have described the use of OCT for imaging in several human organ systems. This article reviews the current technology and provides an overview of recent OCT studies in gastroenterology and cardiology. Imaging techniques such as radiography, computed tomography, magnetic resonance (MR) imaging, and ultrasound (US) allow noninvasive investigation of largescale structures in the human body, with resolutions ranging from 100 m to 1 mm. For many disease processes, however, including cancer in its early stages, higher resolution is necessary for accurate diagnosis. In addition, some clinical screening procedures, such as random biopsies for the detection of high-grade dysplasia in Barrett esophagus, could be improved by the use of a high-resolution, noninvasive imaging technique to determine which biopsy site corresponds to the most severe disease. Finally, in locations where biopsies cannot be performed because the results would be catastrophic (eg, the coronary arteries), high-resolution, noninvasive imaging is necessary for diagnosis. To address these and other clinical problems in situ requires a noninvasive imaging technology with a resolution approaching that used in conventional histologic studies. OCT, first introduced in 1991 (1), is a cross-sectional optical imaging technique that can obtain images with an axial (depth) resolution of 10 m. OCT measures the path length traveled by the interrogating beam incident on the tissue sample by using an optical technique known as interferometry (1,2). This process is commonly accomplished by dividing the source light into two identical beams with a Michelson interferometer and directing one beam to the sample and the other to a reference mirror with a known location. When light returns from both the sample and the reference mirror it is recombined at a detector, and the interference between the two beams is registered. The use of temporally incoherent light allows the distance traveled by the sample beam to be determined, since interference can occur only when light from both beams arrives at the detector simultaneously. The axial or depth resolution of the OCT system is determined by the property of light referred to as the coherence length. With advanced femtosecond laser systems, OCT resolution can be as low as a few micrometers (3–5). A single line or axial scan in an OCT image is obtained by changing the delay in the reference arm and recording the interference modulation amplitude as a function of reference arm delay. Transverse scanning of the sample arm beam across the specimen during recording of the axial data for each lateral location allows an entire two-dimensional OCT image to be formed. OCT, performed with a source center wavelength of 850 nm, was first used to image posterior and anterior Acad Radiol 2002; 9:942–953

[1]  B E Bouma,et al.  Images in cardiovascular medicine. Catheter-based optical imaging of a human coronary artery. , 1996, Circulation.

[2]  J G Fujimoto,et al.  High-resolution optical coherence tomographic imaging using a mode-locked Ti:Al(2)O(3) laser source. , 1995, Optics letters.

[3]  S E Nissen,et al.  Intravascular ultrasound of the coronary arteries: current applications and future directions. , 1992, The American journal of cardiology.

[4]  David F. Cruess,et al.  Barrett's esophagus: A prevalent, occult complication of gastroesophageal reflux disease , 1987 .

[5]  K. I. Pravdenko,et al.  High-spatial-resolution optical-coherence tomography of human skin and mucous membranes , 1995 .

[6]  M. Leon,et al.  Early lumen loss after treatment of in-stent restenosis: an intravascular ultrasound study. , 1998, Circulation.

[7]  P. Fitzgerald,et al.  Intravascular ultrasound: state of the art and future directions. , 1998, The American journal of cardiology.

[8]  W. Bechstein,et al.  Extended resections for hilar cholangiocarcinoma. , 1999, Annals of surgery.

[9]  J. Tobis,et al.  Morphological Effects of Coronary Balloon Angioplasty In Vivo Assessed by Intravascular Ultrasound Imaging , 1992, Circulation.

[10]  A. Weyman,et al.  Intravascular ultrasound: basic principles and role in assessing arterial morphology and function. , 1992, American journal of cardiac imaging.

[11]  Hubert W. Vliegen,et al.  Magnetic Resonance Imaging in Coronary Artery Disease , 1991, Developments in Cardiovascular Medicine.

[12]  J. Isner,et al.  Gene therapy for the vulnerable plaque. , 1995, Journal of the American College of Cardiology.

[13]  Y. Uchida,et al.  Prediction of acute coronary syndromes by percutaneous coronary angioscopy in patients with stable angina. , 1995, American heart journal.

[14]  B E Bouma,et al.  Imaging of coronary artery microstructure (in vitro) with optical coherence tomography. , 1996, The American journal of cardiology.

[15]  J. Fujimoto,et al.  High-speed optical coherence domain reflectometry. , 1992, Optics letters.

[16]  B. Bouma,et al.  Power-efficient nonreciprocal interferometer and linear-scanning fiber-optic catheter for optical coherence tomography. , 1999, Optics letters.

[17]  B E Bouma,et al.  High resolution imaging of normal and osteoarthritic cartilage with optical coherence tomography. , 1999, The Journal of rheumatology.

[18]  R Birngruber,et al.  Optical coherence tomography of the human skin. , 1997, Journal of the American Academy of Dermatology.

[19]  R. R. Smith,et al.  Prevalence and characteristics of Barrett esophagus in patients with adenocarcinoma of the esophagus or esophagogastric junction. , 1988, Human pathology.

[20]  R. Jenkins,et al.  Aggressive surgical resection for cholangiocarcinoma. , 1995, Archives of surgery.

[21]  J. Peters,et al.  Is Barrett's metaplasia the source of adenocarcinomas of the cardia? , 1994, Archives of surgery.

[22]  J. Izatt,et al.  Optical coherence microscopy in gastrointestinal tissues , 1996, Summaries of papers presented at the Conference on Lasers and Electro-Optics.

[23]  M. Makuuchi,et al.  Improved surgical results for hilar cholangiocarcinoma with procedures including major hepatic resection. , 1999, Annals of surgery.

[24]  Brett E Bouma,et al.  Optical coherence tomography of the biliary tree during ERCP. , 2002, Gastrointestinal endoscopy.

[25]  J. Fujimoto,et al.  High-speed phase- and group-delay scanning with a grating-based phase control delay line. , 1997, Optics letters.

[26]  J. Schmitt,et al.  Optical-coherence tomography of a dense tissue: statistics of attenuation and backscattering. , 1994, Physics in medicine and biology.

[27]  Bridget Wilcken,et al.  Pathogenesis of coronary artery disease , 1969 .

[28]  M. Jochims,et al.  MRI assessment of coronary artery disease. , 1999, Rays.

[29]  J. Fujimoto,et al.  Micron‐resolution ranging of cornea anterior chamber by optical reflectometry , 1991, Lasers in surgery and medicine.

[30]  K. Seung,et al.  Visualization of coronary atherosclerotic plaques in patients using optical coherence tomography: comparison with intravascular ultrasound. , 2002, Journal of the American College of Cardiology.

[31]  C. Compton,et al.  High-resolution imaging of the human esophagus and stomach in vivo using optical coherence tomography. , 2000, Gastrointestinal endoscopy.

[32]  E. Falk Why do plaques rupture? , 1992, Circulation.

[33]  B E Bouma,et al.  Porcine coronary imaging in vivo by optical coherence tomography. , 2000, Acta cardiologica.

[34]  J. G. Fujimoto,et al.  Optical Biopsy in Human Pancreatobiliary Tissue Using Optical Coherence Tomography , 1998, Digestive Diseases and Sciences.

[35]  P. Pairolero,et al.  Barrett's disease: pathophysiology of metaplasia and adenocarcinoma. , 1993, The Annals of thoracic surgery.

[36]  James G. Fujimoto,et al.  Optical Coherence Tomography of Ocular Diseases , 1995 .

[37]  R A Schatz,et al.  Catheter-based radiotherapy to inhibit restenosis after coronary stenting. , 1997, The New England journal of medicine.

[38]  P. Libby,et al.  Pathogenic mechanisms of atherosclerosis: effect of lipid lowering on the biology of atherosclerosis. , 1996, The American journal of medicine.

[39]  J. Fujimoto,et al.  Optical Coherence Tomography , 1991 .

[40]  G Tearney,et al.  Visualization of tissue prolapse between coronary stent struts by optical coherence tomography: comparison with intravascular ultrasound. , 2001, Circulation.

[41]  J. Duker,et al.  Imaging of macular diseases with optical coherence tomography. , 1995, Ophthalmology.

[42]  J. Fujimoto,et al.  High resolution imaging of the upper respiratory tract with optical coherence tomography: a feasibility study. , 1998, American journal of respiratory and critical care medicine.

[43]  B E Bouma,et al.  Diagnosis of specialized intestinal metaplasia by optical coherence tomography. , 2001, Gastroenterology.

[44]  K. Seung,et al.  Long-term angiographic and clinical outcome after percutaneous transluminal coronary angioplasty and intracoronary radiation therapy in humans. , 1997, Circulation.

[45]  J. G. Fujimoto,et al.  Assessing atherosclerotic plaque morphology: comparison of optical coherence tomography and high frequency intravascular ultrasound. , 1997, Heart.

[46]  J. Fujimoto,et al.  Optical biopsy in human urologic tissue using optical coherence tomography. , 1997, The Journal of urology.

[47]  Patricia L. Blount,et al.  An endoscopic biopsy protocol can differentiate high-grade dysplasia from early adenocarcinoma in Barrett's esophagus. , 1993, Gastroenterology.

[48]  V. Fuster,et al.  The pathogenesis of coronary artery disease and the acute coronary syndromes (2). , 1992, The New England journal of medicine.

[49]  J. Cameron,et al.  Management of proximal cholangiocarcinomas by surgical resection and radiotherapy. , 1990, American journal of surgery.

[50]  B E Bouma,et al.  Self-phase-modulated Kerr-lens mode-locked Cr:forsterite laser source for optical coherence tomography. , 1996, Optics letters.

[51]  J M Schmitt,et al.  Subsurface imaging of living skin with optical coherence microscopy. , 1995, Dermatology.

[52]  P Hall,et al.  Intracoronary stenting without anticoagulation accomplished with intravascular ultrasound guidance. , 1995, Circulation.

[53]  J. Fujimoto,et al.  In vivo endoscopic optical biopsy with optical coherence tomography. , 1997, Science.

[54]  S A Boppart,et al.  High-resolution imaging of gynecologic neoplasms using optical coherence tomography. , 1999, Obstetrics and gynecology.

[55]  B E Bouma,et al.  Optical biopsy in human gastrointestinal tissue using optical coherence tomography. , 1997, The American journal of gastroenterology.

[56]  J. Izatt,et al.  High-resolution cross-sectional imaging of the gastrointestinal tract using optical coherence tomography: preliminary results. , 1998, Gastrointestinal endoscopy.

[57]  J. Fujimoto,et al.  Optical biopsy and imaging using optical coherence tomography , 1995, Nature Medicine.

[58]  R Birngruber,et al.  Optical coherence tomography of the skin. , 1998, Current problems in dermatology.

[59]  G. Gelikonov,et al.  In vivo endoscopic OCT imaging of precancer and cancer states of human mucosa. , 1997, Optics express.

[60]  P. Libby,et al.  The unstable atheroma. , 1997, Arteriosclerosis, thrombosis, and vascular biology.

[61]  G. Gores,et al.  Biliary tract cancers. , 1999, The New England journal of medicine.

[62]  J. Fujimoto,et al.  Optical coherence tomography for optical biopsy. Properties and demonstration of vascular pathology. , 1996, Circulation.