Quantification of Ellipsoid Zone Changes in Retinitis Pigmentosa Using en Face Spectral Domain-Optical Coherence Tomography.

IMPORTANCE New methods are needed to quantify the change in the outer retinal structures in retinitis pigmentosa (RP). OBJECTIVE To implement an alternate method for tracking ellipsoid zone (EZ) changes in RP by quantifying the EZ area on en face spectral domain-optical coherence tomographic (SD-OCT) images. DESIGN, SETTING, AND PARTICIPANTS Data for this observational case study were collected at the Department of Ophthalmology, University of California, Los Angeles, from May 1 to July 30, 2015, and included SD-OCT images of a subset of patients from the Trial of Oral Valproic Acid for Retinitis Pigmentosa. To be eligible for the en face OCT subanalysis, the preserved EZ area was required to be limited to the SD-OCT scanning field. Cases in which the EZ band extended to the margins of any B-scan or the most superior or inferior B-scan were excluded. The SD-OCT images of all included cases were imported into the manufacturer's software to generate en face images at the level of the EZ. Two certified SD-OCT graders independently delineated the boundaries of the preserved EZ on the en face images. MAIN OUTCOMES AND MEASURES Comparison of the 2 masked gradings of the generated en face images of patients with RP for agreement between the graders and the validity of the method. RESULTS Of the 43 available patients with volume SD-OCT data, 45 eyes of 24 patients met the eligibility criteria and were included in this subanalysis. Every patient had 2 visits that were 1 year apart, which included a total of 90 en face OCT images that were graded. The mean (SD) absolute difference and percentage difference between the 2 independent graders for each visit were 0.08 (0.10) mm2 and 4.5% (5.9%), respectively. The EZ area determined by the 2 graders showed excellent agreement with an intraclass correlation coefficient of 0.996 (95% CI, 0.995-0.997; P < .001). CONCLUSIONS AND RELEVANCE Quantification of the preserved EZ area on en face SD-OCT images of patients with RP is a valid and reproducible method. En face SD-OCT quantification may be a useful tool for monitoring the EZ changes of patients with advanced RP and a useful outcome measurement variable in therapeutic trials.

[1]  F. Parmeggiani,et al.  Therapeutic Challenges to Retinitis Pigmentosa: From Neuroprotection to Gene Therapy , 2011, Current genomics.

[2]  D. Hood,et al.  Relationships among multifocal electroretinogram amplitude, visual field sensitivity, and SD-OCT receptor layer thicknesses in patients with retinitis pigmentosa. , 2012, Investigative ophthalmology & visual science.

[3]  R. Carr,et al.  Rates of change differ among measures of visual function in patients with retinitis pigmentosa. , 1996, Ophthalmology.

[4]  Donald C Hood,et al.  A Comparison of Methods for Tracking Progression in X-Linked Retinitis Pigmentosa Using Frequency Domain OCT. , 2013, Translational vision science & technology.

[5]  William J Feuer,et al.  Square root transformation of geographic atrophy area measurements to eliminate dependence of growth rates on baseline lesion measurements: a reanalysis of age-related eye disease study report no. 26. , 2013, JAMA ophthalmology.

[6]  Wolzt,et al.  World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects. , 2003, The Journal of the American College of Dentists.

[7]  Xian Zhang,et al.  Thickness of receptor and post-receptor retinal layers in patients with retinitis pigmentosa measured with frequency-domain optical coherence tomography. , 2009, Investigative ophthalmology & visual science.

[8]  Wolfgang Drexler,et al.  Ultra-high resolution optical coherence tomography assessment of photoreceptors in retinitis pigmentosa and related diseases. , 2006, American journal of ophthalmology.

[9]  D. Hood,et al.  Spectral-domain optical coherence tomography measures of outer segment layer progression in patients with X-linked retinitis pigmentosa. , 2013, JAMA ophthalmology.

[10]  J M Bland,et al.  Statistical methods for assessing agreement between two methods of clinical measurement , 1986 .

[11]  Neil M Bressler,et al.  DESIGNING CLINICAL TRIALS FOR AGE-RELATED GEOGRAPHIC ATROPHY OF THE MACULA: Enrollment Data From the Geographic Atrophy Natural History Study , 2006, Retina.

[12]  Donald C Hood,et al.  A comparison of visual field sensitivity to photoreceptor thickness in retinitis pigmentosa. , 2010, Investigative ophthalmology & visual science.

[13]  P. Gehlbach,et al.  RETINOCHOROIDAL MORPHOLOGY DESCRIBED BY WIDE-FIELD MONTAGE IMAGING OF SPECTRAL DOMAIN OPTICAL COHERENCE TOMOGRAPHY , 2016, Retina.

[14]  Eyal Margalit,et al.  The long-term natural history of geographic atrophy from age-related macular degeneration: enlargement of atrophy and implications for interventional clinical trials. , 2007, Ophthalmology.

[15]  B Rosner,et al.  Natural course of retinitis pigmentosa over a three-year interval. , 1985, American journal of ophthalmology.

[16]  C. Curcio,et al.  ANATOMICAL CORRELATES TO THE BANDS SEEN IN THE OUTER RETINA BY OPTICAL COHERENCE TOMOGRAPHY: Literature Review and Model , 2011, Retina.

[17]  S. Tsang,et al.  Multimodal Imaging of Central Retinal Disease Progression in a 2-Year Mean Follow-up of Retinitis Pigmentosa. , 2015, American journal of ophthalmology.