Purpose
To compare optical coherence tomography (OCT) and histology of outer retinal
tubulation (ORT) secondary to advanced age-related macular degeneration (AMD) in
patients and in post-mortem specimens, with particular attention to the basis of the
hyper-reflective border of ORT.
Method
A private referral practice (imaging) and an academic research laboratory
(histology) collaborated on two retrospective case series. High-resolution OCT raster
scans of 43 eyes (34 patients) manifesting ORT secondary to advanced AMD were compared
to high-resolution histological sections through the fovea and superior perifovea of
donor eyes (13 atrophic AMD and 40 neovascular AMD) preserved ≤4 hours after
death.
Results
ORT seen on OCT corresponded to histologic findings of tubular structures
comprised largely of cones lacking outer segments (OS) and lacking inner segments (IS).
Four phases of cone degeneration were histologically distinguishable in ORT lumenal
walls, nascent, mature, degenerate, and end-stage (IS and OS; IS only; no IS; no
photoreceptors and only Müller cells forming external limiting membrane, ELM,
respectively). Mitochondria, which are normally long and bundled within IS ellipsoids,
were small and scattered within shrunken IS and cell bodies of surviving cones. A
lumenal border was delimited by an ELM. ORT observed in closed and open configurations
were distinguishable from cysts and photoreceptor islands on both OCT and histology.
Hyper-reflective lumenal material seen on OCT represents trapped retinal pigment
epithelium (RPE) and non-RPE cells.
Conclusions
The defining OCT features of ORT are location in the outer nuclear layer (ONL),
a hyper-reflective band differentiating it from cysts, and RPE that is either dysmorphic
or absent. ORT histologic and OCT findings corresponded in regard to composition,
location, shape, and stages of formation. The reflectivity of ORT lumenal walls on OCT
apparently does not require an OS or an IS/OS junction, indicating an independent
reflectivity source, possibly mitochondria, in the IS.
In AMD, macula cones exhibit loss of detectable myoid due to IS shortening in addition to OS loss, as described. Mitochondria shrink and translocate toward the nucleus. As reflectivity sources, translocating mitochondria may be detectable using in vivo imaging to monitor photoreceptor degeneration in retinal disorders. These results improve the knowledge basis for interpreting high-resolution clinical retinal imaging.
Citation: Georgiou M, Litts KM, Kalitzeos A, et al. Adaptive optics retinal imaging in CNGA3-associated achromatopsia: retinal characterization, interocular symmetry, and intrafamilial variability. Invest Ophthalmol Vis Sci. 2019;60:383-396. https://doi.org/ 10.1167/iovs.18-25880 PURPOSE. To investigate retinal structure in subjects with CNGA3-associated achromatopsia and evaluate disease symmetry and intrafamilial variability.METHODS. Thirty-eight molecularly confirmed subjects underwent ocular examination, optical coherence tomography (OCT), and nonconfocal split-detection adaptive optics scanning light ophthalmoscopy (AOSLO). OCT scans were used for evaluating foveal hypoplasia, grading foveal ellipsoid zone (EZ) disruption, and measuring outer nuclear layer (ONL) thickness. AOSLO images were used to quantify peak foveal cone density, intercell distance (ICD), and the coefficient of variation (CV) of ICD.RESULTS. Mean (6SD) age was 25.9 (613.1) years. Mean (6 SD) best corrected visual acuity (BCVA) was 0.87 (60.14) logarithm of the minimum angle of resolution. Examination with OCT showed variable disruption or loss of the EZ. Seven subjects were evaluated for disease symmetry, with peak foveal cone density, ICD, CV, ONL thickness, and BCVA not differing significantly between eyes. A cross-sectional evaluation of AOSLO imaging showed a mean (6SD) peak foveal cone density of 19,844 (613,046) cones/mm 2 . There was a weak negative association between age and peak foveal cone density (r ¼ À0.397, P ¼ 0.102), as well as between EZ grade and age (P ¼ 0.086).CONCLUSIONS. The remnant cone mosaics were irregular and variably disrupted, with significantly lower peak foveal cone density than unaffected individuals. Variability was also seen among subjects with identical mutations. Therefore, subjects should be considered on an individual basis for stratification in clinical trials. Interocular symmetry suggests that both eyes have comparable therapeutic potential and the fellow eye can serve as a valid control. Longitudinal studies are needed, to further examine the weak negative association between age and foveal cone structure observed here.
PurposeTo characterize sources of inter- and intrasubject variability in quantitative foveal avascular zone (FAZ) metrics.MethodsTwo 3×3-mm optical coherence tomography angiography scans (centered on the fovea) were acquired in both eyes of 175 subjects. An image of the superficial plexus was extracted from each scan and segmented twice by a single observer. Four quantitative FAZ morphology metrics (area, axis ratio, acircularity, major horizontal axis angle) were calculated, and a variance components analysis was performed.ResultsMean (±SD) age was 27.9 ± 11.9 years, and 55% were female. Area had the largest amount of variance resulting from intersubject differences (93.1%). In contrast, there was large interocular variance for axis ratio, acircularity, and major horizontal axis angle (55.0%, 53.7%, 70.7%, respectively), though only axis ratio showed significant asymmetry between fellow eyes (P < 0.05). Neither repeated images from the same eye nor repeated segmentation on the same image were significant sources of variance.ConclusionsMetrics of FAZ morphology show excellent repeatability and reliability. Excluding FAZ area, there was a high amount of variance attributed to interocular differences for the other FAZ metrics; therefore, the fellow eye should not be considered a control for FAZ studies when using these metrics.Translational RelevanceVision scientists must be prudent when choosing FAZ metrics, as they display varying degrees of within-subject differences relative to between-subject differences. It seems likely that different metrics will be best suited for different tasks, such as monitoring small changes over time within a single subject or assessing whether a given FAZ is abnormal.
Purpose: We examine the interocular symmetry of foveal outer nuclear layer (ONL) thickness measurements in subjects with achromatopsia (ACHM). Methods: Images from 76 subjects with CNGA3-or CNGB3-associated ACHM and 42 control subjects were included in the study. Line or volume scans through the fovea of each eye were acquired using optical coherence tomography (OCT). Image quality was assessed for each image included in the analysis using a previously-described maximum tissue contrast index (mTCI) metric. Three foveal ONL thickness measurements were made by a single observer and interocular symmetry was assessed using the average of the three measurements for each eye. Results: Mean (6 standard deviation) foveal ONL thickness for subjects with ACHM was 79.7 6 18.3 lm (right eye) and 79.2 6 18.7 lm (left eye) compared to 112.9 6 15.2 (right eye) and 112.1 6 13.9 lm (left eye) for controls. Foveal ONL thickness did not differ between eyes for ACHM (P ¼ 0.636) or control subjects (P ¼ 0.434). No significant relationship between mTCI and observer repeatability was observed for either control (P ¼ 0.140) or ACHM (P ¼ 0.351) images. Conclusions: While foveal ONL thickness is reduced in ACHM compared to controls, the high interocular symmetry indicates that contralateral ONL measurements could be used as a negative control in early-phase monocular treatment trials. Translational Relevance: Foveal ONL thickness can be measured using OCT images over a wide range of image quality. The interocular symmetry of foveal ONL thickness in ACHM and control populations supports the use of the non-study eye as a control for clinical trial purposes.
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