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Retinal nerve fiber layer sector-specific compromise in relapsing and remitting multiple sclerosis
eNeurologicalSci, Volume 1, Issue 2, June 2015, Pages 30 - 37
To evaluate quadrant and sector retinal nerve fiber layer (RNFL) thickness and total macular volume (TMV) in relapsing–remitting multiple sclerosis (RR-MS) patients.
Optical coherence tomography measures of RNFL and TMV were studied in 321 eyes without prior optic neuritis (ON) (MS unaffected), 151 eyes with prior ON (MS affected), and 148 healthy control eyes.
Mean RNFL thickness was significantly lower in the MS affected and MS unaffected groups relative to the control group (p < 0.0001). RNFL thicknesses in the superior, inferior, and temporal quadrants were significantly reduced in MS unaffected (113 ± 15 μm, 119 ± 17 μm, 63 ± 13 μm) (p < 0.001) and MS affected groups (99 ± 19 μm, 103 ± 21 μm, 51 ± 13 μm) (p < 0.0001) compared with that in controls (120 ± 14 μm, 128 ± 15 μm, 69 ± 8 μm, respectively). TMV was significantly reduced in both the MS affected and MS unaffected groups compared with that in the controls (p < 0.0001).
Quadrant, sector, and PMB RNFL thicknesses are significant individual measures in RR-MS for both affected and unaffected eyes and may prove valuable in future investigations including biomarker and outcomes research.
- We detailed RNFL quadrant and sector segmentation analysis in multiple sclerosis.
- RNFL sector thicknesses were lower in 2 affected eyes relative to 1 affected eye.
- PMB thickness distinguishes MS affected and MS unaffected groups from controls.
- TMV thickness distinguishes MS affected and MS unaffected groups from controls.
- EDSS correlated with RNFL for unaffected group and TMV for affected group.
Keywords: Axonal loss, Multiple sclerosis, Optic neuritis, Optical coherence tomography, Retinal nerve fiber layer, Total macular volume.
Multiple sclerosis (MS) is a chronic inflammatory disease that affects the central nervous system (CNS)  and is a leading cause of neurological disability affecting young adults . MS leads to progressive axonal loss and degeneration of neurons , and often result in permanent disability . Optic neuritis (ON)  is the first demyelinating event in approximately 20% of MS patients, and 30–70% of MS patients experience ON during the course of the disease . ON results in thinning of the retinal nerve fiber layer (RNFL) and compromise of the total macular volume (TMV)  and . These detrimental retinal changes result from both axonal thinning with associated loss of neurofilament phosphorylation and subsequent axonal transection with retrograde degeneration  and . Visual problems in MS can result from a range of pathologies, including inflammation, degeneration, demyelination, and axonal loss in the anterior visual pathway (retina, optic nerves, chiasm and tracts) . Alterations in the visual system can be important indicators of CNS neurodegeneration and potential impact of neuroprotective therapy . Optic atrophy and compromise of the RNFL are common findings on ophthalmologic examinations of patients with MS , and RNFL thinning in MS patients has been linked to brain atrophy  and volumetric changes in the white matter as assessed by magnetic resonance imaging . Other studies found that RNFL and ganglion cell layer (GCL) associated with normalized brain volume, white matter volume and gray matter volume in relapsing and remitting (RR)-MS patients with previous ON , whereas Saidha et al. found the strongest relationship between GCL and whole-brain atrophy in progressive MS . RNFL decrease and optic nerve atrophy are more prevalent in those with a prior history of ON  and , but can also occur throughout the natural progression of MS in the absence of ON .
Optical coherence tomography (OCT) is a non-invasive imaging technique that can quantify RNFL thickness in vivo . Initially, OCT was used to not only examine retinal axonal loss in glaucoma  and , but also to demonstrate RNFL loss in the eyes of MS patients with  and  and without previous ON  and .
Our objective was to use spectral-domain (SD) OCT to examine the RNFL thickness with special attention to analyses of RNFL quadrants and sectors as well as TMV. These measurements were completed in patients diagnosed with RR-MS (with or without a prior history of ON) and compared to results obtained with healthy controls to determine the significance of the measurements, their distribution and their suitability as biomarkers for disease state. We hypothesized that when compared to controls, the thickness of the RNFL quadrants and the RNFL sectors may be selectively compromised in MS patients both with and without ON. Here we describe the injury to the RNFL in more detail through quadrant and sector analysis.
2. Materials and methods
2.1. Study design and patient population
A total of 236 patients from the University of Utah with clinically definite RR-MS (ages 49 ± 12 years) according to the revised 2005 McDonald criteria  and 74 healthy controls (ages 47 ± 12 years) participated in this cross-sectional study. MS sub-type classification was based on the clinical course and determined by the treating physician (JWR), and the ON attacks were documented in our medical records and determined by the treating physician (JWR). All MS patients underwent a fundoscopic eye exam and a visual acuity test at the time of the clinic visit. Patients with a history of eye disease that may affect OCT measures (e.g. glaucoma, retinal disease, age-related macular degeneration, diabetes, neuromyelitis optica (NMO), Alzheimer's disease or Parkinson's disease) were excluded. Patients had to be free of relapse and ON for at least six months prior to the OCT assessment. None of the patients were taking Gilenya® (fingolimod) at the time of the study.
One goal of this study was also to assess whether there were RNFL differences between the MS patients that had 2 affected eyes compared with 1 affected eye, and similarly, examine potential differences between MS patients with 2 affected eyes compared with 2 unaffected eyes. The rationale behind this partitioned approach is based on evidence from previous studies that suggest a more frequent thinning of the RNFL in eyes with a prior history of ON  and , but this can also occur through the natural progression of MS in the absence of ON . Even if the clinical burden of MS is low, a subclinical loss of RNFL in MS patients without prior ON has been suggested .
These investigations were approved by the Institutional Review Board of the University of Utah, and all participants provided written informed consent prior to their participation in accordance with the ethical standards of the 1964 Declaration of Helsinki.
2.3. Spectral-domain optical coherence tomography
The subjects in this study underwent SD-OCT examination using the Heidelberg Engineering Spectralis SD-OCT (Heidelberg Engineering, Heidelberg, Germany, Spectralis software version 188.8.131.52, Eye Explorer Software 184.108.40.206). This SD-OCT utilizes a scanning superluminescence diode to emit a scan beam with a wavelength of 870 nm to acquire 40,000 A scans/s with a depth resolution of 7 μm, from which various retinal layers can be identified, and objectively and precisely assessed  (Fig. 1). The OCT device also combines OCT and confocal infrared laser ophthalmoscope, which provides a reference infrared fundus image . The combination of eye tracking (TruTrac) and high-speed scanning reduce noise caused by natural eye movement . In addition, TMV scan (30° × 25°, 61 B-scans (121 μm distance between B-scans), ART 9; 768 A-scans each) was centered over the macula after the TruTrac was activated. The following OCT parameters were calculated: global mean RNFL thickness around the optic nerve head from nasal, inferior, temporal, superior to nasal (NITSN) quadrant, and further RNFL sector thicknesses (temporal–inferior; TI, temporal–superior; TS, nasal–inferior; NI, nasal–superior; NS and peripapillary macular bundle (PMB)). The mean retinal thickness was measured in μm per quadrant of the peripapillary area whereas the macular scan provided volume data (mm3). All scans were performed by an experienced operator (ASL-F). The images were subsequently reviewed for acceptable signal strength (> 25), correct placement of the scan ring and appropriate beam placement.
2.5. Data analyses
For our studies we have examined the eyes of patients and healthy controls by status as unaffected or affected by ON. Group 1 and group 2 together are labeled the ‘MS unaffected group’. Group 3 and group 4 together are labeled the ‘MS Affected group’. In more detail: The MS unaffected group consists of patients with 2 eyes not affected by optic neuritis (number of eyes = 256) in addition to the patients that have unilateral optic neuritis (number of eyes = 65), where the non-optic neuritis eyes are included in the ‘MS unaffected group’ (Total number of eyes = 321) (Table 1). The same grouping procedures were applied when creating the ‘MS Affected group’ (Total number of eyes = 151). Here we included the eyes of patients with bilateral optic neuritis (number of eyes = 86) and the eyes that were affected in the unilateral optic neuritis group (number of eyes = 65). These five groups of eyes are summarized as;
|1. MS eyes without ON (n = 256)||MS unaffected group (n = 321)|
|2. MS eyes unaffected by unilateral ON (n = 65)|
|3. MS eyes affected by unilateral ON (n = 65)||MS affected group (n = 151)|
|4. MS eyes affected by bilateral ON (n = 86)|
|5. Healthy control eyes (n = 148)|
MS; multiple sclerosis, ON; optic neuritis, n; number of eyes.
Here we compare the eyes in the MS unaffected (no prior optic neuritis) and MS affected (prior optic neuritis) groups with the healthy control group. Further, the MS patients that had 2 affected eyes and the MS patients that had 2 unaffected eyes were also compared with the healthy control eyes. Similarly, the MS patients that had 1 affected eye and 1 unaffected eye were compared with the control eyes. In addition, the MS patients that had either 2 affected or 2 unaffected eyes were compared with those MS patients that had only 1 affected or 1 unaffected eye. Only MS patients and healthy controls with complete data for both eyes were included in the analyses.
2.6. Statistical analyses
This was a cross-sectional exploratory study design, where no adjustments for multiple comparisons were made. Kolmogorov and Smirnov test was performed on all dependent variables to test for assumption of normality. Mann–Whitney U-tests were performed to examine significant differences in age between the groups. Partial correlation analyses, adjusted for disease duration, were used to examine the relationships between EDSS and OCT parameters in the MS groups. Statistical differences of the various OCT variables between the groups were calculated with a linear model using generalized estimating equations (GEE) with compound symmetry correlation structure to account for gender and within-subject inter-eye differences. Statistical analyses were performed using commercially available software (SPSS 17.0, SPSS Inc., Chicago, IL and Graphpad Software InStat 3.0, La Jolla, CA). All of the data are expressed as mean ± SD. Statistical significance was set as p ≤ 0.05.
3.1. Patient population
We enrolled 310 subjects including 74 healthy controls and 236 patients with relapsing and remitting multiple sclerosis. The RR-MS group included patients without ON, with unilateral ON, and with bilateral ON. The subject demographics are presented in Table 2. There were no significant differences in age between individuals in the MS group as a whole and the control group, or between the MS patients with optic neuritis and the MS patients without optic neuritis (p > 0.05). There was a 3.1:1 ratio of women to men in the MS group and a 1.1:1 ratio of women to men in the control group. Average disease duration was 14 ± 8 years (range 1–45 years). There were no gender differences in RNFL values in the control group or in the MS affected group. However, the males in the MS unaffected group had slightly lower mean RNFL values compared with the females (p < 0.05) (data not shown).
|Characteristics||Controls (n = 74)||MS patients (n = 236)|
|Age (yrs)||47 ± 12||49 ± 12|
|Age range (yrs)||27–73||20–82|
|Male, n (%)||34 (46)||54 (23)|
|Female, n (%)||40 (54)||182 (77)|
|Bilateral unaffected eyes, n (%)||148 (100)||256 (54)|
|Bilateral affected eyes, n (%)||n/a||86 (18)|
|Unilateral unaffected eyes, n (%)||n/a||65 (14)|
|Unilateral affected eyes, n (%)||n/a||65 (14)|
|Disease duration (yrs)||n/a||14 ± 8|
|DMT, n (%)||n/a||214 (90)|
|EDSS||n/a||1.7 ± 1.7|
|EDSS range (median)||n/a||0–7 (3)|
Mean ± SD, ON; optic neuritis, DMT; disease-modifying therapies, EDSS; expanded disability status scale.
3.2. RNFL thickness and TMV in MS affected and MS unaffected groups and controls
Mean RNFL thickness was significantly reduced in the MS affected and the MS unaffected groups relative to the healthy controls (p < 0.0001). The MS affected group had a lower RNFL in comparison to the MS unaffected group (p < 0.0001). Mean TMV was lower in both MS affected and MS unaffected groups compared to that in the control group (p < 0.0001). The MS affected group had a reduced TMV relative to the MS unaffected group (p < 0.0001) (Fig. 2A & B).
3.3. RNFL quadrants and PMB thicknesses in MS affected and MS unaffected groups and controls
RNFL thickness in the superior (S), inferior (I) and temporal (T) quadrants was reduced in the MS unaffected group compared to that in the control group (p ≤ 0.001), and different across all four quadrants (S, I, N (nasal), T) relative to the MS affected group (p < 0.0001). RNFL thickness for all four quadrants was also significantly lower in the MS affected group compared to that in the MS unaffected group (p < 0.0001). The PMB thickness was reduced in the MS affected and MS unaffected groups relative to the control group (p < 0.0001), and lower in the MS affected group compared to that in the MS unaffected group (p < 0.0001) (Fig. 3).
3.4. RNFL quadrant and RNFL sector thicknesses in the MS eyes and control eyes
When MS patients' eyes as a pooled cohort were compared to the healthy control eyes, both the RNFL quadrants and the RNFL sectors (TS, NS, NI and TI) were significantly reduced (p ≤ 0.001). Similar results were observed when comparing MS 2 affected eyes (p ≤ 0.03) and MS 1 affected eye (p ≤ 0.01) to healthy controls. The MS 2 unaffected eyes scored significantly lower compared with the control group for mean RNFL, superior, and temporal quadrants (p ≤ 0.02), in addition to NI, TS, TI and PMB RNFL sectors (p ≤ 0.05). Further, only the inferior quadrant showed significance when comparing MS patients with 2 affected eyes to MS patients with 1 affected eye (p = 0.04). Patients with 2 affected eyes showed significantly lower RNFL quadrant and RNFL sector scores compared with MS 2 unaffected eyes (p ≤ 0.01), with the exception of the inferior quadrant (p = 0.2). The MS patients with 1 affected eye showed significantly lower scores for all RNFL quadrants and RNFL sectors relative to MS patients with 1 unaffected eye (p ≤ 0.003). Thus, the PMB seems to have a selective vulnerability from a more distinct region of the RNFL (Table 3).
|RNFL quadrants & sectors||Control eyes (n = 148)||All MS eyes (n = 472)||MS 2 unaffected eyes (n = 256)||MS 1 unaffected eye (n = 65)||MS 2 affected eyes (n = 86)||MS 1 affected eye (n = 65)||Control vs. all MS P-value||Control vs. MS 2 unaffected P-value||Control vs. MS 2 affected P-value||Control vs. MS 1 unaffected P-value||Control vs. MS 1 affected P-value||MS 2 affected vs. MS 1 affected P-value||MS 2 affected vs. MS 2 unaffected P-value||MS 2 affected vs. MS 1 unaffected P-value||MS 1 affected vs. MS 1 unaffected P-value|
|RNFL (μm)||98 ± 9||87 ± 13||93 ± 10||89 ± 12||77 ± 14||80 ± 13||0.0001||0.004||0.0001||0.0001||0.0001||0.8||0.0001||0.001||0.0001|
|Superior (μm)||120 ± 14||108 ± 18||115 ± 14||110 ± 15||97 ± 19||101 ± 19||0.0001||0.02||0.0001||0.0001||0.0001||0.3||0.0001||0.0001||0.0001|
|Inferior (μm)||128 ± 15||113 ± 20||121 ± 15||116 ± 19||101 ± 20||105 ± 22||0.0001||0.3||0.03||0.04||0.01||0.04||0.2||0.3||0.0001|
|Nasal (μm)||74 ± 13||68 ± 16||71 ± 13||70 ± 17||61 ± 17||64 ± 16||0.001||0.4||0.004||0.06||0.0001||0.9||0.005||0.2||0.0001|
|Temporal (μm)||69 ± 8||58 ± 14||64 ± 13||60 ± 14||51 ± 12||51 ± 13||0.0001||0.001||0.0001||0.0001||0.0001||0.8||0.0001||0.0001||0.0001|
|Nasal–superior (μm)||104 ± 17||95 ± 19||101 ± 17||97 ± 17||84 ± 20||89 ± 21||0.001||0.3||0.0001||0.02||0.0001||0.3||0.0001||0.001||0.003|
|Nasal–inferior (μm)||112 ± 21||101 ± 22||105 ± 20||106 ± 23||90 ± 23||97 ± 22||0.0001||0.05||0.0001||0.09||0.0001||0.5||0.01||0.02||0.0001|
|Temporal–superior (μm)||136 ± 14||121 ± 21||128 ± 16||123 ± 18||109 ± 22||113 ± 23||0.0001||0.001||0.0001||0.0001||0.0001||0.5||0.0001||0.001||0.0001|
|Temporal–inferior (μm)||145 ± 15||125 ± 25||136 ± 19||125 ± 23||111 ± 23||114 ± 29||0.0001||0.001||0.0001||0.0001||0.0001||0.2||0.0001||0.001||0.0001|
|PMB (μm)||53 ± 6||45 ± 11||49 ± 9||45 ± 11||38 ± 9||40 ± 10||0.0001||0.0001||0.0001||0.0001||0.0001||0.2||0.0001||0.0001||0.0001|
|TMV (mm3)||8.6 ± 0.5||8.3 ± 0.5||8.4 ± 0.4||8.3 ± 0.5||8.1 ± 0.4||8.1 ± 0.5||0.0001||0.009||0.0001||0.0001||0.0001||1||0.002||0.6||0.1|
Mean ± SD, MS; multiple sclerosis, RNFL; retinal nerve fiber layer, TMV; total macular volume. (n); number of eyes, significant values are depicted in bold italics. p ≤ 0.05.
3.5. Expanded disability status scale correlates
There was no difference in EDSS scores between the MS unaffected and the MS affected group (p > 0.05). However, when comparing the patients with 1 affected eye (1.9 ± 1.8), EDSS score was significantly lower in the MS patients with 2 affected ON eyes (1.5 ± 1.4) (p ≤ 0.01), and in patients with 2 unaffected eyes (1.6 ± 1.6) (p ≤ 0.0001). EDSS correlated with mean TMV (r = − 0.33, p = 0.001) and temporal quadrant (r = − 0.25, p = 0.01) in the MS affected group, while correlations with mean RNFL (r = − 0.16, p = 0.03), superior quadrant (r = − 0.15, p = 0.04), inferior quadrant (r = − 0.15, p = 0.04), and NI RNFL sector (r = − 0.22, p = 0.003) were significant in the MS unaffected group. EDSS correlated with the temporal quadrant (r = − 0.28, p = 0.03) and TMV (r = − 0.26, p = 0.05) in the MS group with 1 unaffected eye and with TMV in the group with 1 affected eye (r = − 0.31, p = 0.02) (data not shown).
The goal of our study was to examine OCT measurements of the retinal nerve fiber layer in RR-MS patients. The basic investigations of RNFL and TMV in our patient population demonstrated that: 1) there was significant RNFL thinning of 12% in our RR-MS patients regardless of ON status compared to that in healthy controls, 2) there was significant RNFL thinning of about 15% in the MS affected group compared to that in the MS unaffected group, and 3) there was a significant decrease in TMV in the MS patients as a group of about 4% compared to that in healthy controls and a 3% decrease in the MS affected group vs. the MS unaffected group. In our patient population there was significant loss in RNFL thickness and TMV in the eyes with a clinical history of ON compared with that in the unaffected eyes and healthy control eyes which are similar to previous studies  and . These results confirm previous investigations and demonstrate reproducibility of these measurements among comparable patient populations.
4.1. RNFL measures by quadrants and sectors in MS patients and healthy controls
Our study revealed a thinning of the mean RNFL, the RNFL quadrants, PMB and RNFL sectors in MS patients compared to that in the control group. In addition, the MS patients with prior ON showed greater thinning than the MS patients with no history of ON. Our results agree with studies by Oberwahrenbrock et al. , Bock et al. , and Lange et al.  who found a pronounced thinning of the RNFL and reduction of TMV  in the MS eyes compared to that in the healthy control eyes, and in MS affected eyes compared to that in MS unaffected eyes. However, in contrast to Oberwahrenbrock et al.  who only reported the mean RNFL and TMV, our study examined the RNFL quadrants, PMB and sectors of the RNFL in detail. We have identified that the temporal quadrant seems to be a more vulnerable area within the RNFL in MS patients, which is in agreement with the findings of Winges et al. . The temporal quadrant contains fibers of the PMB  and  which appeared to be a compromised area with clear distinction between the controls, MS unaffected and MS affected groups.
The temporal quadrant followed by the superior and inferior quadrants in our study demonstrated similar involvement, but in contrast, the nasal quadrant was less impacted. The TS and TI RNFL sectors were the most significant in relationship to controls vs. the MS unaffected group, whereas all quadrants and RNFL sectors were reduced in the MS affected group compared with that in the controls. These results are similar to that of Serbecic et al.  who also examined RNFL sector measurements in MS patients with and without previous ON and found a reduced RNFL globally in all MS groups compared to that in controls. In addition, the temporal quadrant, TI and TS RNFL sectors were reduced in the MS group with prior ON, whereas the MS group without previous ON only showed a significant reduction in TS. Garcia-Martin et al.  found a decrease in average RNFL, SN (superior–nasal), IN (inferior–nasal), IT (inferior–temporal), ST (superior–temporal) sectors, and temporal quadrant in the MS eyes compared with the healthy control eyes. However, when they compared the MS eyes with ON to the MS eyes without ON, only the temporal quadrant reached statistical significance. The lack of significance in other areas may be a result of the relatively small number of eyes studied. They only studied 75 eyes without prior ON and 25 eyes with previous ON, whereas our study examined 321 unaffected eyes and 151 affected eyes.
Previous studies have shown that RNFL thickness was 46% lower in the MS eyes with prior ON compared to that in ‘healthy’ control eyes, 26% reduced RNFL in unaffected MS eyes compared with that in control eyes, and 28% lower RNFL in affected eyes compared to that in the unaffected eye of the same patient  and . A retrospective study by Winges et al. found a 34% and 25% reduction in RNFL and TMV, respectively in RR-MS patients that scored less than 5th percentile of normal limits . During the inflammatory process of ON, the optic nerve can swell secondary to inflammation, and in the months following an acute event, the swelling subsides and subsequently the optic nerve decreases in size. It has also been suggested that RNFL thinning becomes more prominent in the 3–6 months following an inflammatory event , which is why the patients with ON in the 6 months preceding the measurements were excluded from our study.
4.2. TMV in MS patients and healthy controls
Total macular volume includes all the neuronal layers of the retina  and reflects the number of retinal ganglion cell bodies and axons, which have shown to be decreased in the ON eyes . In agreement with other studies  and , our study revealed a reduced volume in MS patients compared to that in the control group, and the MS patients with prior ON displayed even lower volumes than the MS patients with no history of ON. In agreement with our results, Henderson et al. showed a lower baseline TMV in their MS patients compared with that in healthy controls. In addition, the same study found no difference in TMV reduction over time between healthy controls and progressive MS patients, though, the small number of subjects in their study and the use of time-domain OCT are limitations. However, these results make us question if TMV changes are more related to normal aging rather than disease changes , and if it is appropriate to use TMV as a measurement of neuronal degeneration. It has been suggested that early in the disease course there may be some underlying micro-inflammatory disease activity , and the use of disease-modifying therapies  may explain why there was no difference in TMV between MS patients with 2 affected eyes and MS patients with 1 affected eye in our study. We will be looking to examine this issue as we divide the MS eyes into 4 groups. This analysis may suggest that the TMV becomes equally compromised both with bilateral and unilateral ON.
4.3. RNFL quadrants and sectors in MS affected and MS unaffected eyes
After separating the MS group according to the number of eyes affected with and without ON, we observed that MS patients with 2 affected eyes had decreased thickness in several RNFL quadrants and in all RNFL sectors compared to MS patients with 2 unaffected eyes. Significant differences in RNFL quadrant and sector values between the patients with 1 affected eye relative to the MS patients with 1 unaffected eye were detected. Although, we observed a trend with lower RNFL scores in the patients with 2 affected eyes compared to the MS patients that had 1 affected eye, only the inferior quadrant reached statistical significance.
4.4. Expanded disability status score correlates
We found significant correlations between EDSS and mean RNFL, inferior quadrant, superior quadrant, and NI RNFL sector in the MS unaffected group. Also, EDSS significantly correlated with the temporal quadrant and TMV in the MS affected group. In addition, the MS group with 1 unaffected eye showed correlations between EDSS and the temporal quadrant and TMV, and the MS group with 1 affected eye revealed a correlation between EDSS and TMV. EDSS scores have previously been shown to be associated with decreased RNFL and TMV in MS patients with and without prior ON , which is similar to our findings, while another study reported a correlation between EDSS and RNFL in untreated MS patients . TMV seems to be the best correlate with EDSS in our patient population. Although, several of the comparisons in our study displayed low r values, suggesting a weak association that remained statistically significant after we adjusted for disease duration, was attributed to the large sample size in our study.
4.5. Sex-specific differences in RNFL
There were no significant differences in RNFL between men and women in the control group or in the MS affected group. However, we found that the males had slightly lower RNFL values compared to the females in the MS unaffected group. Costello et al. showed that baseline RNFL values did not differ in the ON eyes between men and women, but found that male MS patients displayed greater RNFL thinning 6 months following ON compared to women, suggesting that there may be a difference in visual recovery following episodes of ON . Men often show worse clinical outcomes and faster disease progression relative to women , and this difference may be attributed to sex hormones , specifically estrogen  and .
There are some limitations in our study that should be noted. The control group (74 subjects) was relatively small compared to the MS group (236 subjects), and the male proportion was particularly smaller than the women in the MS group. However, this reflects the higher incidence of MS in women, but it is possible that our results were affected, hence we adjusted for gender in the analyses (GEE model). This study was confined to only RR-MS patients, so the results should not be generalized to other MS sub-types. Also, this was a cross-sectional exploratory study design, and cannot infer cause and effect, but this issue will be addressed with a longitudinal study which is currently underway.
As OCT begins to emerge as a valuable tool for assessing disease severity, it is important to understand its potential strengths and limitations with respect to sensitivity and fidelity in measuring degeneration in MS patients. This is particularly important for comparing results between different MS centers. Our results demonstrate that OCT measurements can be comparable to those at other institutions. Our study is unique in that we also focused on the various quadrant thicknesses, the PMB and RNFL sector thicknesses, to identify regional differences in contrast to the majority of studies that have primarily focused on mean RNFL thickness. In addition, we validated the results with our patient population compared to other studies and we found similar results for mean RNFL and TMV showing uniformity of this measurement between centers. We also detailed RNFL sector segmentation analysis showing that the nasal quadrant was least affected for significant changes in our MS patients, while other studies have found the nasal quadrant to be more sensitive to change in NMO patients with ON compared with MS ON patients by using the ratio of nasal to temporal RNFL thickness for comparing quadrant-wise thinning . Also, a review study by Bennett et al. showed that NMO patients without a history of ON had normal RNFL thicknesses . Future OCT studies may be important in examining if there are different RNFL injury patterns between NMO and MS patients with ON, and if nasal quadrant injury is more common in NMO and temporal quadrant damage is more prominent in MS. In addition, our study demonstrated that RNFL thickness in the PMB distinguishes MS affected and MS unaffected eyes from controls as well as differentiating MS affected eyes from MS unaffected eyes.
Identifying reproducible and significant measures of neurodegeneration in MS would allow for biomarker development with the potential to assist with diagnosis, ongoing disease course evaluation and pharmacologic disease management . Future studies including large multicenter studies may focus on RNFL changes in quadrants and sectors for investigation of early MS, secondary progressive MS and primary progressive MS, natural history, clinical trials and biomarker correlations.
VA Merit Review (JWR).
Conflict of interest
The authors have no conflict of interest.
The authors thank
Sonja and Kent Davis for their support of the OCT,
Alice and Kevin Steiner for research support, and
James Burns MD, for the review of the manuscript.
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a Department of Neurology, University of Utah, 729 Arapeen Drive, Salt Lake City, UT 84108, USA
b Neurovirology Research, VA SLC HCS, GRECC, 500 Foothill Drive, Salt Lake City, UT 84148, USA
c Department of Neurobiology & Anatomy, University of Utah, 20 North 1900 East, Salt Lake City, UT 84132 USA
d Department of Pediatrics, University of Utah, 295 Chipeta Way, Salt Lake City, UT 84108, USA
⁎ Corresponding author at: Department of Neurology, University of Utah, Imaging & Neuroscience Center, 729 Arapeen Drive, Salt Lake City, UT 84108, USA.
© 2015 Published by Elsevier B.V.