An innovative instrument
for the psychophysical measurement of macular pigment optical density
using a CRT display
P. West, Cambridge Research Systems Ltd, Rochester, Kent, UK
J. Mellerio,
Rayne Institute of Ophthalmology, Kings College, London, UK
Abstract
We describe a new instrument for psychophysical measurement of Macular Pigment
Optical Density (MPOD) designed to overcome many of the difficulties
usually encountered when performing subjective photometry on
naïve
subjects.
The system employs a CRT monitor for stimulus presentation and incorporates
an optical filter that overcomes the usual limitations of the phosphors of
a CRT monitor. Part of the broad spectral emission of each of the three CRT
phosphors is absorbed by the macular pigment. Therefore when employed as
a stimulus for heterochromatic flicker or motion nulling photometry there
is a systematic and significant underestimate in MPOD. To overcome this limitation
we have designed a band blocking filter that blocks light between 460-640
nm. When viewed through the filter the spectra of the red and blue phosphors
do not overlap and the blue component is absorbed by the MP whilst the red
is not. Thus the subjective photometric measurements made using this configuration
are close to those made with monochromatic lights.
Test Stimuli are consecutively presented in concentric arcs between 0 and
8 degrees, with central fixation, thus allowing a MPOD profile to be measured.
The design brief was that the instrument should measure MPOD in large groups
of subjects, for example for screening or drug trials. Therefore we have
incorporated two further novel features that improve subject performance
and measurement robustness.
We employ the motion nulling grating method of Cavanagh and Anstis (1983).
A chromatic blue-red grating is displayed sequentially with a luminance
grating. The gratings appear to drift either up or down. The direction
of drift is
dependent upon the relative perceived luminance of the red and blue
component. This stimulus is easy to see and setting luminance for a
motion null is easily
to perform: it is ideally suited to the forced choice staircase psychophysical
paradigm that we employ.
The quality of any psychophysical MPOD estimate relies on knowing the exact
retinal eccentricity that is being measured. We use a video based gaze tracking
system to ensure that correct central fixation is maintained. The stimulus
presentation sequence is inhibited unless the subject is accurately maintaining
central fixation. Subject feed back is provided by a visual cue when fixation
is correct.
We report MPOD profile measurements made with the device and compare them
to results in the literature using near-monochromatic lights (Mellerio, et
al, 2002; Moreland et al, 2004).
References
Anstis, S. & Cavanagh, P. (1983) A minimum motion technique
for judging equiluminance.
Mellerio, J., Ahmadi-Lari, S., van Kuijk, F. J. G. M.,Pauleikhoff,
D., Bird, A. C. & Marshall, J. (2002) A portable instrument for measuring
macular pigment with central fixation. Cur. Eye Res. 25:37–47
Moreland, J.D. Macular pigment assessment by motion photometry. (2004)
Archives of Biochemistry and Biophysics. 430:143–148
Metropsis MPOD test incorporates
three key innovations: a unique optical filter that eliminates
CRT phosphor problems, an undemanding test stimulus that radically
improves test performance and measurement repeatability, and
integrated eye
tracking that ensures
that the correct retinal locations are tested.