Diabetic Retinopathy (DR)

Early screening opportunities for diabetic retinopathy

The early stages of DR are often asymptomatic, with many patients experiencing no noticeable changes in their vision. Some individuals may temporarily struggle with reading or seeing distant objects, but these issues tend to be intermittent. As DR progresses, more severe symptoms can appear, including the growth of new blood vessels in the retina. These vessels may leak or bleed, causing dark spots or cobweb-like streaks in the field of vision. Without timely treatment, this bleeding can lead to retinal scarring, detachment, and eventually permanent vision loss.

Visual electrophysiology for diabetic retinopathy 

ISCEV guidelines recommend using the ERG to test retinal ischemic conditions. Recent advancements in understanding DR emphasize the importance of tracking retinal neural dysfunction particularly in the disease’s early stages. A variety of tests can aid in identifying these neural changes: 

  • Multifocal Electroretinogram (mfERG) and Full-Field Electroretinogram (ERG): These tests detect changes in retinal electrical activity, revealing dysfunction before vascular damage occurs. Loss of oscillatory potentials (OPs) and delayed responses are common in diabetes. MfERG results in patients with early DR may highlight localized areas of concern, predicting where new lesions could develop based on changes in response times. 
  • Full-Field Flicker ERG: Abnormalities, especially at high flicker rates, have been found in patients with early-stage DR. A reduced flicker ERG amplitude and delayed responses indicate retinal dysfunction. 
  • Photopic Negative Response (PhNR): This ERG component, which is linked to retinal ganglion cells (RGC), may be reduced in patients with DR. This reduction can signal the presence of early retinal ganglion cell dysfunction. 

References

Han Y, Bearse MA Jr, Schneck ME, Barez S, Jacobsen CH, Adams AJ. Multifocal electroretinogram delays predict sites of subsequent diabetic retinopathy. Invest Ophthalmol Vis Sci. 2004 Mar;45(3):948-54. doi: 10.1167/iovs.03-1101. PMID: 14985316.

Harrison WW, Bearse MA Jr, Ng JS, Jewell NP, Barez S, Burger D, Schneck ME, Adams AJ. Multifocal electroretinograms predict onset of diabetic retinopathy in adult patients with diabetes. Invest Ophthalmol Vis Sci. 2011 Feb 9;52(2):772-7. doi: 10.1167/iovs.10-5931. PMID: 20926810; PMCID: PMC3053106.

McAnany JJ, Park JC. Cone Photoreceptor Dysfunction in Early-Stage Diabetic Retinopathy: Association Between the Activation Phase of Cone Phototransduction and the Flicker Electroretinogram. Invest Ophthalmol Vis Sci. 2019 Jan 2;60(1):64-72. doi: 10.1167/iovs.18-25946. PMID: 30640972; PMCID: PMC6333111.

Park JC, Chau FY, Lim JI, McAnany JJ. Electrophysiological and pupillometric measures of inner retina function in nonproliferative diabetic retinopathy. Doc Ophthalmol. 2019 Oct;139(2):99-111. doi: 10.1007/s10633-019-09699-2. Epub 2019 Apr 23. PMID: 31016437; PMCID: PMC6742572.

Tzekov R, Arden GB. The electroretinogram in diabetic retinopathy. Surv Ophthalmol. 1999 Jul-Aug;44(1):53-60. doi: 10.1016/s0039-6257(99)00063-6. PMID: 10466588.