Abstract
purpose. To examine the effect of myopia, occasionally associated with
glaucomatous eyes, on the results obtained by frequency-doubling
perimetry (FDP).
methods. Sixty emmetropic or myopic normal volunteers (mean age, 26.2 ±
0.35 years, mean ± SEM; range, 19–34) with good visual acuity
and without glaucoma were divided into three groups. The groups were
emmetropia to low-myopia (mean refractive error, −1.16 ± 0.23
D), intermediate-myopia (−4.95 ± 0.17 D), and high-myopia
(−8.12 ± 0.36 D; n = 20 each). All subjects
were tested on the FDP full-threshold C-20 program and the Humphrey
Field Analyzer (HFA; Humphrey, Dublin, CA) full-threshold program on
one randomly selected eye. FDP and the HFA test were conducted with the
subjects wearing their full distance correction and with their distance
correction with appropriate additional correction for near,
respectively. The calculated mean sensitivity (MS), mean deviation
(MD), pattern standard deviation (PSD), and test durations for FDP and
the HFA test for the three groups were compared using one-way analysis
of variance. The relationship between the refractive error and MS, MD,
or PSD was also analyzed by simple regression analysis.
results. The MS and MD for the fields determined by the HFA decreased
significantly as the refractive errors increased, but there were no
significant differences in the MS, MD, and PSD for FDP between the
three groups. There were no significant differences in the test
durations between the three groups for both FDP and HFA testing. The
refractive error was correlated with both MS and MD only for the fields
determined by the HFA.
conclusions. The results showed that lens-corrected myopia does not alter the visual
fields obtained by FDP, and FDP can therefore be used regardless of the
presence of myopia.
The recent interest in frequency-doubling technology (Welch
Allyn, Skaneateles Falls, NY) was applied to develop a commercial
frequency-doubling perimeter (Humphrey Systems, Dublin, CA). This
perimetric technique has been reported to detect early glaucomatous
visual field loss.
1 2 3
There is evidence that different retinal functions can be selectively
altered by myopia. We have found a loss of sensitivity of the
short-wavelength–sensitive cones in myopic eyes by electroretinography
(ERG),
4 by blue-on-yellow perimetry,
5 and by
visually evoked cortical potentials.
6 We have also found a
reduction of the amplitude and a delay of the implicit times of each
wave of the multifocal ERG in myopic eyes.
7
It is well known that myopia is often associated with glaucomatous
eyes. Thus, with increasing levels of intraocular pressure (IOP), an
increasing degree of myopia has been detected,
8 and there
is a strong relationship between myopia and glaucoma.
9 In
a country with a high incidence of myopia as in Japan,
10 it is especially important to distinguish the changes in retinal
sensitivity induced by glaucoma from that caused by myopia. However, it
has not been determined whether the visual fields determined by
frequency-doubling perimetry (FDP) are altered by myopia.
In this study, we investigated the influence of myopia on the results
of FDP. These data were compared with the results obtained by the
conventional automated Humphrey Field Analyzer model 750 (HFA;
Humphrey, Dublin, CA).
Sixty emmetropic or myopic normal volunteers with good corrected
visual acuity (20/20 or better) with a mean refractive error of−
4.62 ± 0.40 D (mean ± SEM; range, 0.00 to −12.00 D) were
tested. The subjects were divided into three groups according to their
refractive error measured by an autorefractometer (RK-90; Topcon,
Tokyo, Japan). The three groups were emmetropia to low-myopia
(refractive error, −1.16 ± 0.23 D), intermediate-myopia
(−4.95 ± 0.17 D), and high-myopia (−8.12 ± 0.36 D;
n = 20 each;
Table 1 The mean age of the subjects was 26.2 ± 0.35 years
(range, 19–34). The age differences in the three groups were not
significant (
P = 0.13). All subjects had normal IOP
(<20 mm Hg), normal-appearing optic discs, and no family history of
glaucoma. This study was conducted in conformity with the tenets of the
Declaration of Helsinki. The procedures were fully explained to all
subjects, and informed consent was obtained in all cases before the
tests.
Two types of perimetric visual fields were determined in all the
subjects. Only one eye, randomly selected, was tested.
The first perimetric test was performed with the FDP full-threshold
C-20 program with 17 test areas located 20° from the fovea (four
10° square targets per quadrant and a central 5° circular target).
Each test area was made up of black and white sinusoidal grating (0.25
cyc/deg) that flickered at 25 Hz. The contrast between dark and light
phases of the vertical stripes in each stimulus pattern was changed
automatically according to the response of the subjects. The contrast
sensitivity was determined at each location from the log contrast
sensitivity and expressed on a decibel scale. The tests were performed
with the subjects wearing their distance glasses or contact lenses.
The second test was a white-on-white perimetric test using the HFA
full-threshold program with 76 test points in the central 30° field.
The threshold sensitivity was determined at each test point. The
subjects wore their distance refraction combined with appropriate
additional correction for near.
All subjects had been tested on the two perimetric tests at least once,
and the second or later results were used for the analysis. The two
tests were performed on different days but within a month. Results with
more than 20% false positive or false negative readings or fixation
losses were excluded. The left eye data were converted to the right eye
format, and the two blind-spot locations from the HFA test were
removed.
To evaluate the variation of the mean sensitivity (MS) with
eccentricity, the FDP and HFA fields were divided into three zones: R1,
the central zone; R2, the paracentral zone; and R3, the midperipheral
zone.
11 The variation of the MS was also evaluated for the
four quadrants (superior-temporal, inferior-temporal, superior-nasal,
and inferior-nasal).
The mean deviation (MD, a measure of the average departure of
sensitivity at each test location from the age-corrected normal value),
the pattern SD (PSD, a measure of the degree to which the shape of the
measured field departed from the age-corrected normal reference field),
and the test durations were obtained automatically from a printout from
FDP and the HFA.
The significance of the differences in the MS, MD, PSD, and the test
durations was analyzed for the three groups using a one-way analysis of
variance (ANOVA). ANOVA with post hoc comparison using Fisher’s
protected least-significant difference (PLSD) correction of probability
was performed for multiple comparison (statistically significant level, P < 0.05). In addition, the relationship between the
refraction and the MS, MD, or PSD was analyzed with a simple regression
analysis (statistically significant level, P < 0.05).
Although blue-on-yellow perimetry with the HFA has been shown to
detect early glaucomatous damage,
12 it is also affected by
myopia.
5 Relevant to this study, even the HFA
full-threshold program white-on-white perimetry has been shown to be
affected by myopia
5 as was found in this study. Thus, the
effect of myopia must be taken into account when interpreting the
fields obtained by the HFA.
FDP has been developed only recently, and, unfortunately, studies have
not been reported on the effect of myopia on FDP. In this study, the
MS, MD, and PSD of FDP were analyzed and were found not to differ
significantly for the fields of the three different refractive error
groups. Thus, FDP can be used regardless of the presence of myopia.
The user’s guide states that FDP may be performed with or without the
patient’s correction for refractive errors of less than 7.00 D.
Although a sinusoidal pattern stimulus is less affected by refractive
defocus than a square-wave pattern stimulus, we corrected the
refractive error for both FDP and the HFA to eliminate the effect of
retinal blur on the sensitivity.
13 In FDP, the size of the
stimulus is a 10° square, whereas that for the HFA is a point of less
than 1° of visual angle. Thus, the large size of the stimulus for FDP
may be more easily seen than that in the HFA.
A fatigue effect in myopic eyes may be responsible for the poorer
results of myopic eyes with conventional perimetry, but the two
perimetric tests were performed on different days but within 1 month.
We also analyzed the test duration on these two testing methods and
determined that there was no significant difference in the test
durations for both perimetric tests among the three different groups.
Thus, we conclude that there was no fatigue effect on the myopic eyes.
The MS on differential light sensitivity (DLS) testing, such as that
with the HFA, decreased with increasing myopia, indicating that the
total deviations increase with higher levels of myopia. Because PSD
remained unchanged, this indicates that the PSDs were not altered by
myopia. It is interesting that there was a generalized, not localized,
diffuse depression effect with increasing myopia on DLS testing. It
should be noted, however, that we did not find a generalized diffuse
depression effect on FDP results in this study.
In summary, there was no decrease in contrast MS, MD, and PSD in FDP in
corrected myopic eyes. These results indicate that the effects of
myopia up to −12.0 D can be ignored when using FDP.
Supported in part by Grant in-aid for Scientific Research 10357015 from the Ministry of Education, Science, Sports and Culture, Japan.
Submitted for publication August 10, 2000; revised November 27, 2000; accepted December 8, 2000.
Commercial relationships policy: N.
Corresponding author: Akira Ito, Department of Ophthalmology, Chiba University School of Medicine, Inohana 1-8-1 Chuo-ku, Chiba 260-8670, Japan.
[email protected]
| Refraction* | Number of Eyes, † | Age (y) | Test Duration, ‡ | |
| | | | FDT | HFA |
Emmetropia (∼ −3 D) | −1.16 ± 0.23 | 20 (12:8) | 27.1 ± 0.6 | 273 ± 4.2 | 764 ± 15.1 |
Intermediate myopia (−3 D ∼−6 D) | −4.59 ± 0.17 | 20 (8:12) | 26.2 ± 0.6 | 270 ± 2.3 | 805 ± 22.8 |
High myopia (−6 D ∼−12 D) | −8.12 ± 0.36 | 20 (10:10) | 25.4 ± 0.6 | 267 ± 3.1 | 792 ± 12.6 |
Total | −4.62 ± 0.40 | 60 (30:30) | 26.2 ± 0.4 | 270 ± 1.9 | 787 ± 10.3 |
The authors thank Duco Hamasaki for helpful comments and support in
manuscript preparation.
Johnson CA, Samuels SJ. Screening for glaucomatous visual field loss with frequency-doubling perimetry. Invest Ophthalmol Vis Sci
. 1997;38:413–425.
[PubMed]Quigley HA. Identification of glaucoma-related visual field abnormality with the screening protocol of frequency doubling technology. Am J Ophthalmol
. 1998;125:819–829.
[CrossRef] [PubMed]Sponsel WE, Arango S, Trigo Y, Mensah J. Clinical classification of glaucomatous visual field loss by frequency doubling perimetry. Am J Ophthalmol
. 1998;125:830–836.
[CrossRef] [PubMed]Kawabata H, Murayama K, Adachi–Usami E. Sensitivity loss in short wavelength sensitive cones in myopic eyes. J Jpn Ophthalmol Soc. 1996;100:868–876.
Kawabata H, Fujimoto N, Adachi–Usami E. Sensitivity loss of short wavelength sensitivity cones in myopic eyes by blue on yellow perimetry. J Jpn Ophthalmol Soc. 1997;101:648–655.
Adachi–Usami E, Kawabata H. Short wavelength sensitivity measured in myopia by visually evoked cortical potentials. Lin LL-K Shih Y-F Hung PT eds. Myopia Updates II. 2000;77–79. Springer–Verlag Tokyo.
Kawabata H, Adachi–Usami E. Multifocal electroretinogram in myopia. Invest Ophthalmol Vis Sci
. 1997;38:2844–2851.
[PubMed]Shiose Y, Kitazawa Y, Tsukahara S, et al. Epidemiology of glaucoma in Japan: a nationwide glaucoma survey. Jpn J Ophthalmol
. 1991;35:133–155.
[PubMed]Mitchell P, Hourihan F, Sandbach J, Wang JJ. The relationship between glaucoma and myopia: the Blue Mountains Eye Study. Ophthalmology
. 1999;106:2010–2015.
[CrossRef] [PubMed]Hosaka A. Population studies: myopia experience in Japan. Acta Ophthalmol (Suppl)
. 1988;185:37–40.
[PubMed]Fujimoto N, Adachi–Usami E. Frequent doubling perimetry in resolved optic neuritis. Invest Ophthalmol Vis Sci
. 2000;41:2558–2560.
[PubMed]Johnson CA, Adams AJ, Casson EJ, Brandt JD. Blue-on-yellow perimetry can predict the development of glaucomatous visual field loss. Arch Ophthalmol
. 1993;111:645–650.
[CrossRef] [PubMed]Anderson DR. The basis of perimetry. Anderson DR eds. Perimetry with and without Automation. 1987;330–344. CV Mosby St. Louis.