e Electro-Oculography | RPC Rounds Ophthalmology Blog

Electro-Oculography

Last updated: September 2026

Electro-oculography (EOG) tests a completely different part of the visual system than the ERG does — it's the test to reach for specifically when Best disease is on your differential, since the ERG in that condition is often deceptively normal.

What it actually measures

EOG records the standing electrical potential between the cornea and Bruch's membrane/RPE — not a light-evoked response like the ERG, but a resting potential that changes predictably with light and dark adaptation. Skin electrodes are placed near the outer and inner canthus of each eye, and the patient makes fixed-angle horizontal saccades between alternating lights; each eye movement produces a measurable deflection proportional to this standing potential.

The Arden ratio (now formally the "light peak:dark trough ratio")

  • During dark adaptation, the resting potential dips to a minimum — the dark trough (Dt)
  • When the light comes on, the potential rises substantially — the light peak (Lp) — then declines again as the retina adapts
  • Arden ratio = Lp / Dt
  • ≥1.80 — normal  |  1.65-1.80 — subnormal  |  <1.65 — significantly subnormal

The current international testing protocol is set by ISCEV (International Society for Clinical Electrophysiology of Vision); the 2017 standard formally renamed "Arden ratio" to "light peak:dark trough ratio," though "Arden ratio" remains the term most commonly used in everyday clinical conversation and older literature.

Why EOG matters: the classic exam pearl

In Best vitelliform macular dystrophy, the full-field ERG is typically normal, while the EOG light rise is severely reduced or absent — this dissociation (normal ERG + abnormal EOG) is itself the diagnostic clue, and is what distinguishes Best disease from other autosomal dominant maculopathies with similar fundus appearance, including some cases of adult vitelliform dystrophy and pattern dystrophy.

Recent genotype-confirmed data adds an important nuance: EOG severity in Best disease is more variable than classically taught — in one large cohort of BEST1-confirmed patients, roughly 27% had a completely absent light rise, 65% had intermediate reduction, and a small minority (8%) had only mild reduction. The takeaway: a mildly reduced or borderline EOG does not exclude Best disease in a patient with a compatible phenotype.

Other conditions with an abnormal EOG

  • Stargardt macular dystrophy (typically only in advanced stages)
  • Pattern dystrophies (usually only mildly-to-moderately subnormal)
  • Retinitis pigmentosa and rod-cone dystrophies
  • Acquired cone and cone-rod dystrophies
  • Oguchi disease
  • Certain toxic retinopathies, when RPE function is disproportionately affected relative to the ERG

A useful discriminating pattern: in autosomal recessive bestrophinopathy and adult-onset vitelliform disease, the ERG itself is often already abnormal, but the EOG is disproportionately more abnormal than the ERG reduction alone would predict — this relative dissociation, not just an isolated abnormal number, is what points toward RPE-specific pathology.

Key references: ISCEV Standard for Clinical Electro-oculography (2017 update). Doc Ophthalmol.  |  Electrooculogram, EyeWiki.  |  Genotype-phenotype variability of EOG in Best disease and ARB, UCL.

📘 Want the exam-ready deep dive? This topic, and much more is covered in Ophthalmology Explorer (A High-Yield Clinical Reference for Ophthalmology Residents, Fellows & Board Exams) — available on Kindle. See all my books.

Written by Dr. Dhaval Patel, MD (Ophthalmology, AIIMS New Delhi)

Consultant, Cataract & Refractive Surgery — among a small number of AIIMS-trained ophthalmologists practicing in Gujarat. Read full credentials & experience or view his 28 publications on ResearchGate.

📚 Also the author of high-yield ophthalmology exam-prep books used by residents and PG aspirants.

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