Visual Electrophysiology




(1)
University of Sydney, Sydney, Australia

 




Overview






  • Visual electrophysiology is the recording of electrical signals produced by the visual system.


  • It allows assessment of the entire visual pathway, from RPE cells to the visual cortex.


  • Most electrophysiology tests are evoked potentials.


  • An abnormality at a proximal location along the visual pathway usually gives abnormal signal proximally as well as distally.


  • Hence, tests should be evaluated in the context of a full clinical history, examination, and other structural and visual electrophysiology investigations, and not interpreted in isolation.


  • Signal averaging involves recording and averaging several similar traces [1]. It increases signal to noise ratio, important in distinguishing small signals (e.g., the pattern ERG) from background activity [2].


Common Visual Electrophysiology Tests






  • Different testing strategies are used to assess separate parts of the visual pathway (Fig. 10.1).

    A347009_1_En_10_Fig1_HTML.gif


    Fig. 10.1
    Origin of the electroretinogram components and other electrophysiology studies


  • These include:

    (i)

    Electrooculogram

     

    (ii)

    Electroretinogram (ERG)

    (a)

    Full field

     

    (b)

    Focal

     

    (c)

    Pattern

     

    (d)

    Multifocal

     

     

    (iii)

    Visual evoked potentials

    (a)

    Pattern

     

    (b)

    Flash

     

    (c)

    Multifocal

     

     


The Electrooculogram






  • The electrooculogram (EOG) is a recording of the slow change in resting potential (voltage) of the retinal pigment epithelium (RPE) from a dark-adapted to a light-adapted state.


  • The resting potential is measured as the difference in voltage between the front (positive) and the back (negative) of the eye.


  • It is used as a measure of RPE function.


1.

Origin of the retinal pigment epithelium resting potential



  • RPE cells have a barrier layer of adjoining tight junctions near their apical surface (see Chap. 9, The Retinal Pigment Epithelium).


  • This separates the cell apical and basal membranes, causing a standing potential difference (voltage) across the RPE layer that is positive apically.


  • This results in the back of the eye (basal RPE layer) being negatively charged relative to the front of eye (cornea) (Fig. 10.2a).

    A347009_1_En_10_Fig2_HTML.gif


    Fig. 10.2
    (a) Origin of the ocular resting potential. (b, c) The electrooculogram test procedure


  • Dark adaptation results in a slow reduction in the RPE resting potential.


  • Light induces a slow rise in the RPE resting potential, due to intracellular calcium flux or bestrophin-controlled changes in ionic channels in the basal RPE membrane [35].

 

2.

Electrooculogram test procedure [5]



  • The test is performed binocularly, with the pupils dilated.


  • The electrode placement is outlined in Table 10.1 and Fig. 10.2b.


    Table 10.1
    Electrode placement for the electrooculogram



















    Electrode

    Site

    Active (+)

    Inner canthi

    Reference (−)

    Outer canthi

    Earth

    Forehead, above the respective eyebrows


  • The patient shifts gaze repeatedly from left to right (Fig. 10.2c).

 

3.

Electrooculogram recording



  • The shifts in voltage on alternating gaze are recorded (Fig. 10.3).

    A347009_1_En_10_Fig3_HTML.gif


    Fig. 10.3
    Recording the electrooculogram. (a) Shifts in voltage on alternating gaze change in dark and light conditions. (b) This change can be plotted over time


  • The test is performed under light and dark adaptation states.


  • The dark trough is the minimal voltage amplitude in the dark.


  • The light peak is the maximal voltage amplitude in the light.


  • The Arden ratio is calculated:



    • Arden ratio = dark trough to light peak


  • The Arden ratio is normally >1.85


  • Values <1.85 are subnormal, and <1.3 are severely subnormal or extinguished.

 

4.

Electrooculogram: uses and limitations



  • The EOG depends on the function of both the RPE and the overlying photoreceptors [6].


  • Hence, it is most specific for the RPE when other tests of retinal function are normal.

 


The Full-Field Electroretinogram






  • The full-field ERG (ffERG) is a mass retinal potential evoked by a brief flash of light.


  • It is important in diagnosing retinal dystrophies or degenerations and can be used to evaluate global retinal dysfunction due to trauma or drug toxicity.


1.

Electroretinogram test procedure [7]



  • The test is performed monocularly with the subject’s pupils dilated.


  • Brief light flashes are presented full field to the retina, dispersed using a Ganzfeld bowl.


  • The bowl surface allows light to diffuse uniformly, stimulating the whole retina (Fig. 10.4).

    A347009_1_En_10_Fig4_HTML.gif


    Fig. 10.4
    The Ganzfeld bowl


  • A fixation point is incorporated into the bowl.


  • The electrodes placed on the face are outlined in Table 10.2.


    Table 10.2
    Common electrodes used in electroretinogram measurement [7]






























    Electrode

    Site

    Function

    Active (+)

    Contact lens (provides the most accurate and reproducible results) OR

    Measurement of retinal electrical activity

    Lower fornix, OR

    Skin over eyelid (suboptimal trace)

    Reference (–)

    Incorporated into speculum (contacting the conjunctiva), OR

    A baseline for measurement

    Close to lateral canthus

    Earth

    Distant to the eyes

    Elimination of electrical interference

 

2.

Recording the electroretinogram [7]



  • Recordings are usually made in two retinal adaptation states:

    (a)

    Scotopic trace: after 20 min of dark adaptation.

     

    (b)

    Photopic trace: after 10 min of light adaptation.

     


  • Recording the ERG in these two states helps separate the rod and cone system responses.

 

3.

Components of the electroretinogram (Fig. 10.5)

A347009_1_En_10_Fig5_HTML.gif


Fig. 10.5
Waveforms of standardized electroretinogram responses




  • In general, the ERG is characterized by:

    (a)

    An a-wave (negative waveform), followed by

     

    (b)

    A b-wave (positive waveform), followed by

     

    (c)

    A c-wave (positive waveform)

    (i)

    The a-wave



    • The a-wave is generated by light-induced photoreceptor hyperpolarization, with some postreceptoral contributions from OFF bipolar cells [811].


    • In the dark, cationic nucleotide-gated (CNG) channels are open resulting in the dark current (see Chap. 8, The Retina).


    • Light stimulation halts this cationic transfer, resulting in photoreceptor hyperpolarization.


    • Cones respond more quickly than rods, so cone hyperpolarization gives earlier negative deflection.

     

    (ii)

    The b-wave



    • The b-wave is generated by light-induced membrane potential change in ON (depolarizing) bipolar and Müller cells [12, 13].

     

    (iii)

    The c-wave



    • The c-wave is an additional waveform reflecting RPE and Müller cell activity [13, 14].


    • It is seen only in dark-adapted eyes and can be difficult to record clinically.

     

    (iv)

    Electroretinogram duration



    • The duration of the response is usually <150 ms.


    • The implicit time (τ) is from stimulus onset to the trough of the a-wave or peak of the b-wave.

     

     

 

4.

Standardized electroretinogram responses



  • Recording the ERG along international standards allows consistent and reproducible results [15].


  • 5 standard ERG responses are typically recorded (Table 10.3 and Fig. 10.5).


    Table 10.3
    Standardized electroretinogram tests (flash strength in candela seconds per square meter) [7]














    Test

    Former name

    Response

    Dark-adapted 0.01 ERG

    Only gold members can continue reading. Log In or Register to continue

    Stay updated, free articles. Join our Telegram channel

    Oct 28, 2016 | Posted by in OPHTHALMOLOGY | Comments Off on Visual Electrophysiology

    Full access? Get Clinical Tree

    Get Clinical Tree app for offline access