Correlation of structure and function of the macula in patients with retinitis pigmentosa

Abstract

Purpose

To correlate the structure of the macula, as measured by spectral-domain optical coherence tomography (SD-OCT) and function, as measured by microperimetry (MAIA) in patients with retinitis pigmentosa (RP) and relatively good visual acuity.

Design

Prospective, cross-sectional, non-intervention study.

Subjects

Patients with RP.

Methods

Thirty patients with RP and good central visual acuity were identified. Each patient underwent SD-OCT of the macula and microperimetry. The images were overlaid using the custom-designed software. The retinal sensitivity by microperimetry was correlated with corresponding retinal thickness, as measured by the SD-OCT. ELM, COST, and IS/OS junction were scored as intact, disrupted, or absent.

Main outcome measures

Comparing the retinal sensitivity on the MAIA with various measurements on the SD-OCT.

Results

The retinal sensitivity on the MAIA showed a significant correlation with total retinal thickness and outer retinal thickness on the SD-OCT. There was no association with either the inner retinal thickness or the choroidal thickness. ORT showed a statistically significant correlation with the anatomical classification of ELM (r=−0.76, P<0.001), IS/OS (r=−0.800, P<0.001), and COST (r=−0.733, P<0.001).

Conclusion

This study determined that there was a high correlation of the structure and function of the central macula in patients with RP. These studies are important to establish surrogate markers that can be used as end points for various tests in future therapeutic clinical trials.

Introduction

Retinitis pigmentosa (RP) is the most common type of inherited retinal degenerative disease characterized by loss of photoreceptors, night blindness, bone spicule-like pigmentary changes in the midperiphery and decreased or undetectable responses on an electroretinogram.^{1, 2} RP is a spectrum of diseases characterized by progressive peripheral visual field constriction that can eventually involve the macula with loss of central visual acuity. There is no effective intervention, although several clinical trials are underway to either slow down or arrest the progression of the disease.^{3, 4, 5, 6, 7} Progression in RP has traditionally been monitored in the past by assessing visual fields and full-field electroretinography. Although Goldmann visual field testing was the gold standard, more recently static perimetry using the Humphrey Field Analyzer (HFA) (programs 30-2 and 10-2) has been used for this purpose. With the advent of spectral-domain optical coherence tomography (SD-OCT), it has become standard practice to monitor the progression in the structure of the retina, more specifically, the outer retina.

Microperimetry, or fundus-related perimetry, is a technique that involves visual field testing while observing the retina simultaneously. This allows observation of the point on the retina that is being stimulated. This is an especially useful method to assess visual fields in patients with unstable or eccentric fixation caused by macular pathologies.⁸ Literature suggests that retinal sensitivity, and not visual acuity, is related to quality of life and has shown to be sensitive to change of function in a trial in RP patients in contrast to HFA 10-2.^{9, 10, 11}

SD-OCT can show cross-sectional images of the retina with an axial resolution of up to 5 μm.¹² This resolution enhances visualization of the various retinal layers, particularly at the level of the external limiting membrane (ELM) and photoreceptor inner segment/outer segment (IS/OS) junction.¹³ Several studies have highlighted the importance of the IS/OS layer integrity in studying the progression of RP.^{13, 14, 15} Studies have also shown the gradual reduction in the IS/OS layer assessed by the fundus autofluorescence (FAF) ring.¹⁶

In a study in 2011, Lupo et al¹⁷ studied the relation between SD-OCT and microperimetry in RP. Lenassi et al investigated the ultrastructural details on the SD-OCT and compared them with the function of the macula, as measured by the microperimetry in these patients.¹⁸ The purpose of the current study was to perform a structure-function correlation of the retinal sensitivity on the MAIA to thickness of retinal layers and structural changes in the IS/OS, COST layer, and ELM on the SD-OCT.

Materials and methods

The study was a prospective case series, approved by the ethics committee of Narayana Nethralaya, Bangalore, India. All the patients consented for the study, and for publication of their data and procedures adhered to the tenets of Declaration of Helsinki. Thirty-four eyes of 34 patients diagnosed with non-syndromic RP based on clinical examination, visual field measurements, and electrophysiology were enrolled into the study. The visual acuity in each eye was measured using the Snellen's visual acuity chart. The eye with the better central visual acuity was selected; if both were the same, the right eye was selected. Patients with vision less than 6/36 on the Snellen chart, macular lesions, or macular edema on fundus examination or SD-OCT were excluded to ensure a stable fixation during microperimetry and to exclude lower microperimetry values due to macular edema. Thirty eyes were used for statistical analysis.

All patients underwent microperimetry on the MAIA (CenterVue, Padova, Italy) using a predefined pattern that covered the central 10°. The Macular Integrity Assessment or MAIA microperimeter uses a scanning laser to perform retinal imaging and an LED light as a stimulus. The eye tracking system on the MAIA was used to ascertain a stable fixation during the entire study. Points corresponding to the foveal center and the horizontal and vertical lines were used for statistical analysis. Patients who could not maintain a steady fixation underwent a repeat testing, and the second test was used for analysis if fixation was stable. Fixation was considered stable if the reliability index was >60%. If there was no fixation in the fovea, patients were excluded.

SD-OCT was performed with the Spectralis (Heidelberg Engineering, Heidelberg, Germany). The simultaneous confocal scanning laser ophthalmoscope (cSLO) on the Spectralis allowed precise localization of the anatomical landmarks. The eye tracking system ensured a stable fixation during the entire test. Multiple single scans were averaged at the same location to obtain an increased signal-to-noise ratio. A 100-ART vertical and horizontal scan centered on the fovea was obtained on the SD-OCT for each patient within an area of central 30°. Enhanced-depth imaging scans were obtained to assess the choroidal thickness.

An overlay was prepared using a customized software. The MAIA images were overlaid on the cSLO images of the OCT and matched using blood vessels as a co-registration marker. Structural details on the SD-OCT corresponding to the retinal sensitivity at the central (foveal), 1°, 3° and 5° horizontal and vertical lines on the MAIA were compared (Figure 1).

Figure 1.

The MAIA of the right eye of a subject overlaid on the cSLO image of the SD-OCT (100 ART horizontal scan) with co-registration of the blood vessels using a customized software. The point measured corresponds to the 5° temporal location on the MAIA (white arrow) and the corresponding measurement on the SD-OCT (yellow arrow).

The inner and outer retinal thickness and the choroidal thickness on the SD-OCT were assessed at each point corresponding to the central and six horizontal and vertical points within the central 10° on the MAIA. Two observers (RB, AK) made the measurements independent of each other. The mean values were calculated and used in the analyses. In case there was a difference of 20 μm or more between the two observers, the patient was excluded (n=4). On the SD-OCT the ELM, COST layer and IS/OS were assessed and classified as intact, interrupted or absent according to the methods used by others.¹⁸

The outer retinal thickness (ORT) was measured between the outer border of the retinal pigment epithelium and the inner border of the outer plexiform layer (OPL), to include the inner segments, outer segments and the outer nuclear layer; the inner retinal thickness (IRT) was measured between the vitreoretinal interface and the inner border of the OPL.¹⁹ Submacular choroidal thickness (CT) was measured manually from the inner border of the sclera to the outer border of the RPE vertically using the calipers of the Heidelberg reader software.²⁰

Statistical analysis

For statistical analysis Snellen visual acuity was converted to LogMAR units. To determine the relation between retinal sensitivity on the microperimetry and the retinal thickness at corresponding locations on the SD-OCT, the IRT, ORT, the choroidal thickness, ELM, IS/OS and COST abnormalities at different eccentricities were measured. A linear mixed models (LMM) analysis was performed with subject ID as a grouping factor, retinal sensitivity as an independent variable, and SD-OCT values, eccentricity, and site (foveal, inferior, superior, nasal, and temporal) as covariates, as well as their interaction terms. All data were analyzed using the statistical software package SPSS version 22.0 (IBM Corporation, New York City, NY, USA).

Results

Thirty eyes of 30 patients were studied, 23 males and 7 females. Mean age was 32±12 years (range 12–63) and mean LogMAR visual acuity was 0.19±0.17. There was no statistical difference between males and females either in age or LogMAR visual acuity.

On the MAIA, the average reliability index was 94.23% (range 67–100%). The average duration to perform the test was 6'52” (range 4'12”–18'51”). The average macular integrity was 90.35 (range 44.3–100). The average threshold was 17.58 dB (range 2.8–30.1 dB). The mean fixation stabilities were 77.63% (P1) and 89.80% (P2). The fixation plot showed that the average bivariate contour ellipse area at 63% was 2.41^{0 2} and at 95% was 14.55⁰.² There was a negative correlation between LogMAR values and sensitivity at the fovea (r=−0.52, P=0.004); the lower the visual acuity, the worse was the retinal sensitivity.

On the SD-OCT, the mean total foveal thickness was 211 μm (range 97–281 μm), the average inner retinal thickness being 122 μm (range 62–201 μm) and outer retinal thickness being 93 μm (range 27–119 μm). The mean choroidal thickness in the subfoveal area was 232 μm (range 83–439 μm).

Figure 2 shows the relation between retinal sensitivity and ORT; for all different sites and eccentricities we found a significant correlation. Figure 3 shows the mean ORT for different sites and eccentricities. LMM analyses revealed a significant association between retinal sensitivity and ORT. This association was different for the different sites and eccentricities, that is, showing significant interaction terms.

Figure 2.

Scatter plot showing the relation between MAIA values of ORT for the different sites (f-fovea, i-inferior, n-nasal, s-superior, t- temporal) shown in different rows and eccentricities (columns). The correlation coefficients included are all significant (P<0.005).

Figure 3.

Mean ORT for the different sites. Different lines represent different eccentricities. Similar graphs were drawn for the IRT and EDI (f-fovea, i-inferior, n-nasal, s-superior, t-temporal).

ELM, COST, and IS/OS junction were scored as intact, disrupted or absent. Analysis of retinal sensitivities by location yielded us a total of 390 locations. We found that the ELM was intact in 206, disrupted in 74, and absent in 110 locations.

Similar analysis for IS/OS gave 182, 74, and 134, respectively, and analysis of COST gave 88, 68, and 234, respectively. All three layers were intact in 86, disrupted in 1, and absent in 90 locations. ORT showed a statistically significant correlation with the anatomical classification of ELM (r=−0.76, P<0.001), IS/OS (r=−0.800, P<0.001), and COST (r=−0.733, P<0.001).

Sensitivity values at different locations and eccentricities were grouped according to the above anatomical integrity classification, and we found highest mean sensitivities in the intact group, lower for the disrupted group, and lowest for the absent group for all three layers (Table 1).

Table 1. Summary of the mean retinal sensitivities using MAIA at different locations and eccentricities grouped by the anatomical status of the outer retinal layers on SD-OCT.

Location	Eccentricitya	IS/OS				COST				ELM
		Intact	Disrupted	Absent	P-valueb	Intact	Disrupted	Absent	P-valueb	Intact	Disrupted	Absent	P-valueb
Foveal	0	24.43	17.63	23.00	<0.001	25.93	17.86	21.00	0.004	24.39	20.20	7.50	<0.001
Inferior	1	24.48	17.17	3.63	<0.001	26.23	20.56	12.75	<0.001	24.14	14.33	5.50	<0.001
	3	25.78	14.00	18.00	0.58	27.67	25.00	18.00	0.176	25.00	18.11	16.09	0.100
	5	24.50	21.00	7.96	<0.001	26.67	18.00	9.46	0.016	21.29	11.00	7.95	0.010
Superior	1	25.78	12.60	12.50	<0.001	27.55	23.22	16.90	0.002	25.73	15.67	10.50	<0.001
	3	28.00	18.43	10.07	<0.001	29.67	28.50	13.87	0.004	25.75	17.13	7.60	<0.001
	5	26.80	14.00	7.53	<0.001	27.00	26.00	9.77	0.007	23.67	10.00	6.35	<0.001
Nasal	1	26.48	12.00	8.50	<0.001	27.60	23.30	17.70	0.025	25.52	16.33	12.50	0.003
	3	26.50	6.20	14.43	<0.001	28.50	25.80	16.26	0.018	26.17	10.86	12.40	<0.001
	5	23.88	12.00	10.42	0.003	27.67	21.00	11.63	0.011	20.69	11.00	8.62	0.004
Temporal	1	25.71	17.13	19.00	0.021	27.64	24.57	18.33	0.010	25.00	22.20	11.67	0.015
	3	26.46	20.14	14.00	0.002	30.60	27.00	16.32	<0.010	26.12	19.29	7.67	<0.001
	5	26.29	15.33	7.65	<0.001	29.67	20.33	10.67	0.004	25.38	15.33	6.94	<0.001

Abbreviations: COST, cone outer segment tips; ELM, external limiting membrane; IS/OS, inner segment outer segment junction.

^aEccentricity measured in degrees from fovea.

^bComparison of means—One-way ANOVA.

Bivariate correlation showed that MAIA correlated significantly with sex (P<0.001), spherical equivalent (P<0.001), TRT (P<0.001), outer retinal thickness (P<0.001), ELM (P<0.001), IS/OS (P<0.027), COST (P<0.001), location (P=0.032), and eccentricity (P<0.001).

Using the above data we performed a multivariate regression (Table 2) keeping the retinal sensitivity as the dependent variable and age, sex, spherical equivalent, ORT, IRT, TRT, anatomy of the ELM, IS/OS, and COST, and location and eccentricity of measurement. We found that sex, ORT, and the anatomical integrity of ELM and IS/OS had an important role in the retinal sensitivity value.

Table 2. Multivariate linear regression model for dependent variable: retinal sensitivity in db measured with the MAIA (Model R ²=0.607).

Parameter	Beta	Standardized Beta	P-value
Intercept	25.15		<0.001
Age (years)	−0.05	−0.059	0.112
Sex (male, female)	−4.64	−0.192	<0.001
Sph Eq (in diopters)	−0.162	−0.042	0.251
TRT (μm)	−0.050	−0.266	0.542
ORT (μm)	0.175	0.467	0.043
IRT (μm)	0.070	0.372	0.393
ELMa	−2.909	−0.248	<0.001
ISOSa	−1.942	−0.170	0.006
COSTa	−0.490	−0.040	0.442
EDIa	−0.004	−0.033	0.385
Locationb	−0.052	−0.006	0.856
Eccentricityc	−0.663	−0.062	0.252

Abbreviations: COST, cone outer segment tips; EDI, extended depth imaging of the choroid; ELM, external limiting membrane; IRT, inner retinal thickness; ISOS, inner segment outer segment junction; ORT, outer retinal thickness; Sph Eq, spherical equivalent; TRT, total retinal thickness.

^aIntact—1, disrupted—2, absent—3.

^bFovea—1, temporal—2, nasal—3, superior—4, inferior—5.

^c1°—1, 3°—2, 5°—3. Bold indicates statistically significant.

Discussion

Lupo et al¹⁷ studied the relationship between retinal thickness and retinal function in RP. They, however, only compared the central retinal thickness with the retinal sensitivity on the microperimetry and did not look at the structural details. A study by Lenassi et al assessed the correlation of visual function measured by both static and kinetic fundus-related perimetry with structural changes in the inner and outer retina evaluated with SD-OCT and with molecular changes in the RPE visualized with FAF.¹⁸ Mitamura et al²¹ found a significant correlation between the length of the IS/OS line and the retinal sensitivity using the MP-1 microperimeter.

Studies to establish the structure-function correlation in retinal degenerative diseases are essential as more and more treatment modalities become available. We developed a custom-made software to assess the structure-function correlation between fundus-related microperimetry and SD-OCT. We found that the retinal sensitivity correlated with the outer retinal structure and an intact ELM and IS/OS junction but not with the inner retinal thickness, choroidal thickness, or the COST layer.

Microperimeters allow for registration of fundus photos with the other imaging modalities and make it possible to compare retinal morphology with visual function.²² Retinal sensitivity assessed using microperimetry has been advocated as a potential outcome measure of macular function for clinical trials involving patients with RP.²³ Cideciyan et al²³ have established repeatability of microperimetry in patients with RP. In their cohort of patients with ABCA4-associated retinopathy that included RP, they showed that the repeated microperimetry tests showed reasonable concordance and the test-retest variance was not significant. Changes on the SD-OCT have been used in several studies to study the disease progression,^{13, 14, 15, 16} and by the same measure may be useful in monitoring response to therapy.

RP is a heterogeneous group of diseases; mutations in more than 50 genes are known to cause non-syndromic RP and more than 3100 mutations have been identified in these genes.^{24, 25} The gene products involve multiple metabolic pathways localized to mostly rods, or rods and cones, or the retinal pigment epithelium.² These include proteins of rod visual transduction, photoreceptor differentiation, proteins of the cytoskeleton, protein transportation, and retinol metabolism among others.² Mutations in any of the biochemical cycles that alter the phototransduction cascade, including renewal and shedding of the photoreceptor outer segments, visual transduction, and/or retinol metabolism may cause retinitis pigmentosa.²⁶

Our study showed that the retinal sensitivity in the macula correlated well with the outer retinal thickness mainly, which included the inner and outer segments of the photoreceptors. It is not surprising that many important biochemical processes occur in the outer retinal layers, and structural preservation of these layers corresponds to a functional preservation.

Issa et al²⁷ showed that in one patient with Usher's syndrome, there was a significant relationship between outer retinal thickness and retinal sensitivity. They demonstrated that good functional preservation was associated with outer retinal thickness >50 μm in spite of extensive disruption of the inner retina.

The study by Lenassi et al¹⁸ found a high correlation between retinal sensitivity and outer retinal thickness, than overall retinal thickness in patients with RP. We found that the retinal sensitivity correlates well with both outer and total retinal thickness and not inner retinal thickness or the choroidal thickness. Changes in the choroid are probably secondary to changes that occur in the retinal layers, and therefore choroidal thickness may vary in patients with RP.

In addition to the IS/OS line, the integrity of the ELM and COST layers has been described as potential indicators of retinal function; a relation between intact ELM/COST layer and good visual acuity has been described in degenerative eye diseases like age-related macular degeneration, macular hole, and epiretinal membrane.^{28, 29, 30, 31}

We found that the presence of intact ELM and an intact IS/OS correlated significantly with the retinal sensitivity. Oishi et al²⁹ found a strong correlation between ELM status and visual acuity that was higher than that with the IS/OS in a cohort of patients with age-related macular degeneration (AMD). The status of the ELM was the most important factor for visual acuity. In RP, it is possible that, in addition to the IS/OS, the ELM is a marker of photoreceptor integrity. Progressive degeneration of photoreceptors may lead to loss of inner retinal structures, and loss of ELM may indicate a severe degree of damage.

In a similar study, Itoh et al^{28, 30} found a significant correlation between the presence of an intact COST line and visual recovery in patients who underwent surgery for macular hole. In an earlier study, Srinivasan et al³² had shown that the cone outer segment lengths were greatest in the foveola and decreased with increasing eccentricity. We did not find a significant association between the COST layer and the retinal sensitivity.

Functional mapping of the macula is essential in retinal degenerative diseases. It allows us a window of opportunity to treat before permanent structural damage occurs. It also helps select patients with early functional loss in whom there are better chances of success with an experimental therapy and help efficient monitoring of the effectiveness of any therapy in RP. Although visual acuity is considered to be the standard primary end point in clinical trials of retinal diseases, it is important that other end points be considered in diseases like RP. This study is one such an attempt to identify surrogate end points, which may be useful to monitor future therapies. Sugawara et al⁹ have established that macular sensitivity determined by microperimetry may be a good predictor of quality of life in RP patients with relatively good vision. Quality of life needs to be an important consideration when future clinical trials and pharmaceutical regulations are considered.

Studies like this help us understand better the structural changes that occur in RP. It would be interesting to study the natural course of the disease and assess the rate of functional loss vis-à-vis the morphological changes in the structure. This may be an important consideration for pharmaceutical interventions. Our study is an attempt to establish the markers that may help identify early structural damage before functional loss is noted. This may further help us understand how soon we need to intervene in the course of the disease for it to prevent irretrievable visual loss. Identifying these markers is important in formulating the inclusion and exclusion criterla for clinical trials in RP.

It is hard to predict whether functional changes precede structural changes in RP. A co-registration of the MAIA and SD-OCT shows the early functional changes associated with micro-structural alterations. Issa et al²⁷ suggested that micro-structural alterations precede functional loss, and high-resolution retinal imaging can detect this. If structural changes do precede functional loss, and it is possible to detect these changes on a high-definition imaging device, this would be of vital importance in patients with RP, as it would mean that therapy can be offered to these patients before they notice a functional visual loss. Adaptive optics may be one such imaging device that may pick up ultrafine structural changes.³³ A structure function correlation between adaptive optics and microperimetry may be useful to detect the earliest structural changes in RP and other such degenerative retinal disorders.

Our study has limitations. The sample size was small, and it was a cross-sectional study. We did not have the results of genetic studies of these patients.

There is a continuous need to detect degenerative diseases like RP in its earliest stage, when therapy may be most useful and before irreversible damage has occurred. Studies like ours try to identify surrogate end points to monitor response to clinical trials before true functional loss has occurred.

The authors declare no conflict of interest.