In experienced hands, gonioscopy is an effective technique for assessing the anterior chamber angle. There are limitations, however, to its use for the diagnosis of and research on angle closure. First, gonioscopy requires technical skill and an excellent knowledge of the anatomy of the angle. Second, the technique is not quantitative. Third, it does not allow for the assessment of structural volume.
Robert Feldman, MD, is involved in research on the usefulness of anterior segment imaging as a diagnostic and research tool for assessing the angle. He summarizes the current state of this research in this month's edition of the “Peer Review” column.
Barbara Smit, MD, PhD, section editor
Angle-closure glaucoma (ACG) affects an estimated 16 million people worldwide, with 4 million bilaterally blind from the disease1 The global presence of ACG is approximately one-third that of open-angle glaucoma (OAG), yet the number of people blind due to ACG (3.9 million) is nearly equal to that blinded by OAG (4.5 million). Those figures are projected to be equal by 2020.2
Unlike with OAG, the angle's anatomy plays a major role in the etiology and progression of ACG. This spectrum disease is defined by the extent of angle closure and vision loss.3 Gonioscopy is the gold standard for evaluating angle anatomy, but the test is often difficult to perform and cannot provide reliable quantitative measurements. Although gonioscopy is unlikely ever to be replaced in clinical evaluation, imaging is becoming ever more important to the diagnosis and treatment of angle closure. Several techniques now available offer excellent reproducibility and quality in their detection of angle anatomy, and in some cases, they provide quantitative measurements of the angle, thereby furthering research into the relationship between angle anatomy and angle-closure disease.
ULTRASOUND BIOMICROSCOPY
UBM uses sound waves to image the anterior chamber.4 The advantage of UBM is its ability to image behind the iris to the ciliary body and sulcus (Figure 1). UBM is especially useful for diagnosing plateau iris, because it can visualize the anterior rotation of the ciliary body that causes anterior displacement of the iris in this mechanism of angle closure.
One disadvantage of UBM is its limited resolution, 50µm laterally and 25µm axially5 which is lower than that of anterior segment optical coherence tomography (AS-OCT). Additionally, UBM is a contact-dependent technique that must be performed by a skilled and experienced technician. The ocular structures may be distorted depending on the angle of the probe and the amount of pressure applied to the eye. Although quantitative studies have been performed using UBM6,7 other techniques provide better, more reproducible measurements for clinical use.
SCHEIMPFLUG IMAGING
Scheimpflug imaging uses light scattering to measure the anterior chamber.5,8 Despite its high resolutionresolution (4 μm laterally and 1 μm axially for the Galilei Dual Scheimpflug Analyzer [Ziemer Ophthalmic Systems AG]), the technology's usefulness for angle closure is limited by its inability to adequately image the angle recess.
ANTERIOR SEGMENT OPTICAL COHERENCE TOMOGRAPHY
AS-OCT recently emerged as the go-to method for obtaining high-resolution, quantitative images of the angle, including the angle recess. Not only is the technology advantageous for the diagnosis of angle closure, but it is another tool with which to research the disease.
Dedicated AS-OCT differs from posterior retinal OCT in that the former uses 1,310-nm light instead of 820-nm light to visualize the anterior chamber.5 The former wavelength allows for better visualization of the angle, cornea, iris, and lens, because the light infiltrates farther through tissues that scatter light such as the sclera and limbus. AS-OCT has a high resolution (10 μm axially and 30 μm transversally for the CASIA SS-1000 [Tomey Corporation]). Unlike UBM, AS-OCT is noncontact and does not require a highly skilled technician. The acquisition of images is rapid (30,000 A-scans/sec, with horizontal and vertical planes scanned simultaneously in 0.2 seconds for the CASIA SS-1000). As a result, many images can be obtained in one session. Three-dimensional reconstruction of the angle for 360º is also possible.
AS-OCT permits the quantitative, reproducible measurement of angle parameters. Common parameters in the literature are TISA, AOD, and angle recess area, usually 500 to 750 μm away from the scleral spur (Figure 2). The measurement of these distances requires the identification of the scleral spur, which may not always be visible, and, at this point, must always be performed manually. Recent research by my group has shown that the reproducible identification of a specified landmark using predetermined criteria (scleral spur landmark) is possible and results in the reproducible measurement of TISA750 and AOD750 (Figure 2).9
Additional parameters being investigated include iris volume and thickness, the trabecular meshwork, 10 and trabecular iris circumference volume11 Imaging artifacts such as shadows are also being investigated to determine if there is any clinical correlation with the artifacts seen,12 as evident with macular thickness and pathology on retinal OCT.13,14
In addition to imaging angle parameters, AS-OCT has been able to quantify opening of the angle after laser peripheral iridotomy and after cataract extraction.15-18 AS-OCT cannot visualize the ciliary body, however, and therefore cannot delineate plateau iris.
CONCLUSION
Although investigators and clinicians are just beginning to understand the capabilities of anterior segment imaging, this tool is already becoming valuable for diagnosing, treating, and conducting research on angle closure. Future studies will provide more insight into this disease and how best to treat it.
Section Editor Barbara Smit, MD, PhD, is a glaucoma consultant at the Spokane Eye Clinic and a clinical instructor at the University of Washington School of Medicine in Spokane, Washington. Dr. Smit may be reached at (509) 456-0107; bsmit@spokaneeye.com.
Robert M. Feldman, MD, is the Richard S. Ruiz, MD distinguished university chair, professor, and chairman of the Ruiz Department of Ophthalmology and Visual Science, The University of Texas Medical School at Houston and Robert Cizik Eye Clinic, Houston. He has been loaned a CASIA SS-1000 by Tomey Corporation. Dr. Feldman may be reached at (713) 559-5239; rfeldman@cizikeye.org.
- Quigley HA. Angle-closure glaucoma simpler answers to complex mechanisms: LXVI Edward Jackson Memorial Lecture. Am J Ophthalmol. 2009;148(5):657-669 e651.
- Quigley HA, Broman AT. The number of people with glaucoma worldwide in 2010 and 2020. Br J Ophthalmol. 2006;90(3):262-267.
- Feldman RM, Tanna AP. Understanding angle-closure glaucoma. Glaucoma Today. September/October 2012;10(5):32-34. http://bmctoday.net/glaucomatoday/2012/10/article.asp?f=understanding-angle-closureglaucoma. Accessed September 10, 2013.
- See JL. Imaging of the anterior segment in glaucoma. Clin Experiment Ophthalmol. 2009;37(5):506-513.
- Konstantopoulos A, Hossain P, Anderson DF. Recent advances in ophthalmic anterior segment imaging: a new era for ophthalmic diagnosis? Br J Ophthalmol. 2007;91(4):551-557.
- Henzan IM, Tomidokoro A, Uejo C, et al. Comparison of ultrasound biomicroscopic configurations among primary angle closure, its suspects, and nonoccludable angles: the Kumejima Study. Am J Ophthalmol. 2011;151(6):1065-1073 e1061.
- Dada T, Mohan S, Bali SJ, et al. Ultrasound biomicroscopic assessment of angle parameters in patients with primary angle closure glaucoma undergoing phacoemulsification. Eur J Ophthalmol. 2011;21(5):559-565.
- Wegener A, Laser-Junga H. Photography of the anterior eye segment according to Scheimpflug's principle: options and limitations—a review. Clin Experiment Ophthalmol. 2009;37(1):144-154. 9. Cumba RJ, Radhakrishnan S, Bell NP, et al.
- Cumba RJ, Radhakrishnan S, Bell NP, et al. Reproducibility of scleral spur identification and angle measurements using fourier domain anterior segment optical coherence tomography. J Ophthalmol. 2012;2012:487309.
- Usui T, Tomidokoro A, Mishima K, et al. Identification of Schlemm's canal and its surrounding tissues by anterior segment fourier domain optical coherence tomography. Invest Ophthalmol Vis Sci. 2011;52(9):6934-6939.
- Nguyen D, Bell N, Blieden L, et al. Effect of laser peripheral iridotomy on trabecular-iris surface area over 360 degrees in primary angle closure. Invest Ophthalmol Vis Sci. 2013;54:e-abstract 4812.
- Gold ME, Kansara S, Nagi KS, et al. Age-related changes in trabecular meshwork imaging. Biomed Res Int. In press.
- Costa RA, Skaf M, Melo LA Jr, et al. Retinal assessment using optical coherence tomography. Prog Retin Eye Res. 2006;25(3):325-353.
- Jaffe GJ, Caprioli J. Optical coherence tomography to detect and manage retinal disease and glaucoma. Am J Ophthalmol. 2004;137(1):156-169.
- Lee KS, Sung KR, Shon K, et al. Longitudinal changes in anterior segment parameters after laser peripheral iridotomy assessed by anterior segment optical coherence tomography. Invest Ophthalmol Vis Sci. 2013;54(5):3166- 3170.
- Zheng C, Guzman CP, Cheung CY, et al. Analysis of anterior segment dynamics using anterior segment optical coherence tomography before and after laser peripheral iridotomy. JAMA Ophthalmol. 2013;131(1):44-49.
- Kim M, Park KH, Kim TW, et al. Anterior chamber configuration changes after cataract surgery in eyes with glaucoma. Korean J Ophthalmol. 2012;26(2):97-103.
- Nolan WP, See JL, Aung T, et al. Changes in angle configuration after phacoemulsification measured by anterior segment optical coherence tomography. J Glaucoma. 2008;17(6):455-459.
