Journal List > J Korean Ophthalmol Soc > v.51(1) > 1008742

Lee, Chang, and Ahn: Correlation Between Multifocal Electroretinography and Visual Acuity After Resolution of Diabetic Macular Edema

Abstract

Purpose

To evaluate the prognostic value of multifocal electroretinography (mfERG) after a decrease of retinal thickness in eyes with diabetic macular edema (DME).

Methods

Sixty patients (60 eyes) underwent intravitreal injection of triamcinolone acetonide or bevacizumab for diabetic macular edema. Eyes were divided into three groups, according to foveal thickness: Group A (<500 μ m, n=20 eyes), Group B (500 μ m≦ <800 μ m, n=20 eyes), and Group C (≧800 μ m, n=20 eyes). Best-corrected visual acuity (BCVA) and mfERG responses from the most central seven hexagons were analyzed both before and after treatment.

Results

The preinjection P1 amplitudes of mfERG correlated significantly with end-point BCVA in Groups A and B (p<0.05), but did not correlate with end-point BCVA (p>0.05) in Group C.

Conclusions

The level of P1 amplitudes of mfERG may be a useful tool to predict visual outcomes after a decrease of retinal thickness in patients with diabetic macular edema.

References

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Figure 1.
Stimulus array of 61 hexagonal elements; ring 1 (red) and ring 2 (blue) correspond to the fovea and parafovea, respectively.
jkos-51-29f1.tif
Figure 2.
The typical waveform of the primary multifocal ERG response is a biphasic wave with initial negative deflection followed by a positive peak. There may be a second negative deflection after the peak. The preferred designation is to label these three peaks respectively N1, P1, and N2.
jkos-51-29f2.tif
Figure 3.
Scattergram demonstrating the relation between preinjection P1 amplitudes and end point BCVA in three groups. Group A (r=-0.772, p<0.001) and B (r=-0.651, p=0.001) show that preinjection P1 amplitude significantly related to the end point BCVA, but in group C, no significant relation between preinjection P1 amplitude and end point BCVA.
jkos-51-29f3.tif
Figure 4.
Comparison of P1 amplitudes of Group A, B and C between preinjection and end point state. The box- and -whiskers plots include the 25 th, 50 th, and 75 th percentiles. The whiskers define the minimum and maximum values.
jkos-51-29f4.tif
Table 1.
Comparison of clinical data of three groups
Group A Group B Group C p-value
Number of eyes 20 20 20
Age (years) 58.4±8.2 60.5±11.1 59.9±10.8 0.916
Sex (male/female) 12/8 10/10 13/7 0.619
Injection drug (TA*/B) 18/2 17/3 19/1 0.574
Duration of ME (months) 5.1±3.2 6.3±4.9 8.3±4.7 0.102
Duration of F/U (weeks) 9.1±3.0 10.9±2.7 11.8±3.2 0.038
BCVA (logMAR)
   Preinjection 0.77±0.31 0.84±0.38 0.96±0.47 0.322
   End-point 0.39±0.28 0.57±0.35 0.79±0.43 0.002
Mean foveal thickness (μm)
   Preinjection 431.35±64.41 664.55±84.30 964.80±156.65 <0.001
   End-point 208.70±17.73 227.25±25.98 235.55±14.28 <0.001
P1 amplitude (nV/deg2)§
   Preinjection 54.96±23.04 40.08±19.89 28.52±14.93 0.001
   End-point 72.95±25.68 56.17±22.29 34.21±15.86 <0.001

ME=Macular edema; F/U = follow–up

* TA=triamcinolone acetate

B=bevacizumab

log MAR=log minimal angle of resolution

§ nanovolt/square degrees

Kruskall-Wallis test

chi-square test.

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