Abstract
purpose. To describe the characteristics of the optic nerve head (ONH) in patients with nonarteritic anterior ischemic optic neuropathy (NAION) and compare them with control subjects by using optical coherence tomography (OCT).
methods. Patients with NAION underwent a complete ophthalmic examination, including OCT scanning of the ONH at diagnosis. The examination was repeated 1.5, 3, and 6 months later. Age- and sex-matched control subjects with no ocular disease underwent a similar evaluation. Data were obtained by using the ONH analysis protocol of the StratusOCT (Carl Zeiss Meditec, Dublin, CA).
results. Twenty-three patients and 23 control subjects were included. In eyes with NAION, the vertical integrated rim area decreased significantly (P < 0.01) from the acute phase to the 6-month visit. The cup-to-disc (C/D) area ratio increased significantly (P = 0.002) from the acute examination to the 3-month visit. There was a significant difference between the NAION fellow eyes and the control eyes in C/D ratio, evaluated by slit lamp funduscopy (P < 0.001), and in the C/D area ratio (P = 0.001). The vertical integrated rim area was significantly (P = 0.001) greater in NAION fellow eyes than in control eyes. There was no significant difference in optic disc area or vertical disc diameter among the control eyes, NAION-affected eyes, and NAION fellow eyes.
conclusions. Although patients with NAION have lower C/D ratios than does the normal population, with a higher level of nerve fiber crowding, there was no difference in optic disc size between patients with NAION and control subjects. After the development of NAION, 47.8% of eyes had a C/D ratio that differed from that in the fellow eye by more than 0.1.
Nonarteritic anterior ischemic neuropathy (NAION) is believed to result from transient hypoperfusion or nonperfusion in a so-called disc at risk.
1 2 These discs have been described as having a small or nonexistent physiologic cup, with crowding of the retinal nerve fibers.
3 4 5 6 Studies performed with the Heidelberg Retina Tomograph (HRT; Heidelberg Engineering, Heidelberg, Germany) have confirmed the presence of a smaller physiologic cup in patients with NAION but reported no difference in the size of the optic nerve head (ONH).
7 8 However, no studies have analyzed the characteristics of the ONH in patients with NAION with optical coherence tomography (OCT), an imaging method that has been used extensively to measure the retinal nerve fiber layer (RNFL) thickness and to study the ONH in patients with glaucoma.
9 10 11 12 13 14 Although its applications in neuro-ophthalmology have been more limited, OCT also may be a useful tool in this field.
15 16 17 18 19 20
The purpose of this study was to describe the characteristics of the ONH in patients with NAION and to use OCT to compare them with those in subjects with no known ocular diseases.
All patients with NAION diagnosed in our center between April 1, 2004, and March 31, 2006, were considered for inclusion. These patients had been evaluated prospectively as part of a larger observational study. They were evaluated within 3 days of diagnosis by one of the authors (IC, SN, or GR). Diagnosis of NAION was based on sudden loss of visual acuity (VA); disc edema on fundus ophthalmoscopy; visual field defects consistent with NAION; erythrocyte sedimentation rate and reactive protein C levels within normal values, with no signs or symptoms suggestive of giant cell arteritis; and resolution of disc edema in 2 months. Exclusion criteria were visual loss of more than 2 weeks' duration, the presence of an ocular disease other than NAION, and the presence of systemic diseases that precluded adequate follow-up and examination. Cataract surgery in the affected eye was not an exclusion criterion. All participants provided informed consent to be included in the study according to the Declaration of Helsinki. The study was approved by the ethics committee.
Patients underwent a complete ophthalmic examination, including Snellen VA, Goldmann applanation tonometry, slit lamp evaluation of the anterior and posterior poles (including estimation of the vertical cup-to-disc [C/D] ratio), standard automated perimetry with the SITA (Swedish Interactive Threshold Algorithm) 24-2 strategy, and OCT scanning of the ONH. This examination was repeated at 6 weeks and 3 and 6 months after the acute episode.
Age- and sex-matched control subjects were recruited from among the workers at our center and the relatives of patients. They underwent the same tests as the patients. Exclusion criteria were Snellen VA worse than 20/40 or the detection of an ocular disease.
OCT scanning was performed with StratusOCT (Carl Zeiss Meditec, Dublin, CA) by two of the authors (IC, SN) after pharmacologic mydriasis. Image acquisition was performed with the Fast RNFL (3.4) and the Fast Optic Disc protocols. Good-quality scans (signal score of 4 or higher) were saved as soon as they appeared. The RNFL thickness was obtained with the StratusOCT RNFL Thickness Average analysis protocol and the ONH parameters with the Optic Nerve Head Analysis protocol. Before recording these values, one author (IC) checked that the OCT software had correctly identified the limits of the optic nerve and manually reset them when necessary
(Fig. 1) . The ONH analysis protocol searches for the limits of the retinal pigment epithelium (RPE)/choriocapillaris layer and sets the disc margins at its ends. A straight line connects the edges of the RPE/choriocapillaris layer, and a second line is drawn 150 μm anterior and parallel to the first one
(Fig. 1) . Structures below this last line are defined as the disc cup and above this line as the neuroretinal rim. For the C/D ratio, the OCT software assigns a value of 1.0 in the absence of a physiologic cup
(Fig. 1) ; in these cases, the C/D ratio was recorded as 0.0. The values recorded were the vertical disc diameter, the vertical integrated rim area (VIRA), the disc area, the C/D area ratio, the C/D horizontal ratio, and the C/D vertical ratio. The VIRA is an estimate of the total volume of RNFL tissue in the rim, calculated by multiplying the average individual rim area times the circumference of the disc.
Statistical analysis was performed with commercial software (SPSS, ver. 12.0; SPSS, Chicago, IL). Given the small sample size, we used nonparametric tests. Since multiple comparisons were performed according to the Bonferroni correction method, the final level of significance was set to 0.002 (two-sided).
Twenty-seven patients (14 men, 13 women) with NAION were evaluated. Mean age was 66.7 years (SD, 9.7). Mean time from onset to initial examination was 5.0 days (SD, 4.7). Three patients had had an episode of NAION in the fellow eye and were excluded from statistical analysis, as was one patient with pathologic myopia. Three patients had undergone cataract surgery between 5 and 14 days before the onset of NAION. Approximately 40% of the ONH scans had to have the limits of the RPE manually redefined.
Twenty-three age- and sex-matched control subjects were recruited. A comparison between ONH parameters and overall RNFL thickness between the right and left eyes of this control group did not show any significant difference (data not shown). In patients with NAION, the values of the ONH parameters at the time of the initial evaluation and at the 3- and 6-month visits are shown in
Table 1 .
On slit lamp funduscopy, 81.5% of the fellow eyes of patients with NAION had a vertical C/D ratio of 0.1 or less, with 40.7% of these having no physiologic cup. The mean vertical C/D ratio on funduscopy was 0.10 (SD, 0.13). In the control group, the mean vertical C/D ratio was 0.29 (SD, 0.1) and 95.6% of patients had a difference in the C/D ratio between the right and left eyes that was equal to or lower than 0.1.
In the NAION-affected eye, the VIRA, disc area, and diameter decreased significantly (
P < 0.001,
P < 0.002, and
P < 0.002, respectively, Wilcoxon test) and C/D area ratio increased significantly (
P = 0.002) from the acute phase to the 3-month visit, with no significant change between the 3- and 6-month visits. The ONH parameters (except the C/D area ratio) were all significantly different between the NAION-affected and fellow eyes at the initial examination; from then on, there were no significant differences between both eyes at any time point
(Table 1) .
To compare the characteristics of the ONH between patients with NAION and the control group, one eye was randomly selected from each subject in the control group to be included in the analysis. Data from the 3-month visit of patients with NAION of the affected and fellow eyes were compared with the eyes in the control group. There was a significant difference between the NAION fellow eye and the control eye in the C/D vertical ratio, as evaluated by slit lamp funduscopy, and in the C/D area ratio and C/D vertical ratio, with lower values for all these parameters in the NAION fellow eye
(Table 2) . There were no significant differences in the parameters between control eyes and NAION-affected eyes or between NAION-affected and fellow eyes.
At the 3-month visit, 47.8% of eyes with NAION had a C/D area ratio that differed from the fellow eye by more than 0.1. The mean C/D area ratio was 50% higher in the affected eye than in the fellow eye. The VIRA was significantly higher in NAION fellow eyes than in control eyes (Mann-Whitney test, P = 0.001).
There was no significant difference in the optic disc area and vertical disc diameter between the three groups at the 3-month visit. Mean RNFL thickness decreased in the NAION affected eye compared with fellow and control eyes (Mann-Whitney test,
P < 0.001 for both comparisons;
Table 2 ). In the NAION fellow eyes, mean RNFL thickness did not correlate with disc area or vertical disc diameter (
r = 0.11 and
r = 0.311;
P = 0.618 and
P = 0.148, respectively). Nor did mean RNFL thickness correlate with disc area (
r = 0.190,
P = 0.168), or vertical disc diameter (
r = 0.102,
P = 0.461) in control eyes.