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    Coloured filters, worn in spectacle frames or used as overlays, have been used in the

    treatment ofdyslexia, migraine and photosensitive epilepsy (Fowleret al, 1992; Wilkins

    et al. 1999; Wilkins et al, 2002). Recently, 'blue-blocking' coloured filters have also been

    shown to modulate the circadian pattern of melatonin output and sleep-cycle variables

    (Sasseville et al, 2006; Sasseville et al, 2010).

    Oxford Blue Filters (OBF) (Fig. 1) have been used in the treatment of Dyslexia in Oxford for

    twenty years, although understanding of their mechanism of action has remained illusive.

    Joe A Taylor and John F Stein. Department of Physiology, Anatomy and Genetics, The University of Oxford

    Current applications of coloured filters OBF impact sleep quality and altertness Discussion and conclusions

    Implications and further research

    To determine the effects of daytime OBF use over sleep quality and continuity, we asked

    eleven healthy adult volunteers to wear OBF filters for one-hour immediately after waking

    each morning over a period of thirty days. In a randomised order, they also wore 'yellow'

    filters, with an opposite transmission profile, for thirty days.

    Each morning, participants completed visual analogue scales (VAS) to indicate their

    perceived alertness on waking and the quality of their previous nights' sleep. They also

    recorded the number of times they had woken during the night. Repeated measures

    comparisons were made of responses between the period during which OBF were worn

    and that during 'yellow' filter use against a thirty-day baseline period without filter use.

    During the period of OBF use, participants reported improved sleep quality (p = 0.05) and

    felt more alert when they woke (p = 0.05) (Fig. 3). No change was observed during 'yellow'

    filter use.

    Seasonal affective disorder (SAD)Fowler et al. Lancet. 1992;340:724. Sasseville et al. J Pineal Res. 2006;4(9):73.

    Sasseville et al. Prog Neuropsychopharmacol Biol Psychiatry. 2010;34(7):1236. Wilkins

    et al. Seizure. 1999;8(8):444. Wilkins. Cephalalgia. 2002;22:711-19.

    This work is supported by the Dyslexia Research Trust and Medical Research Council.

    Further research employing objective measures of sleep quality and consolidation,

    including electroencephalography and actigraphy, are warranted on the basis of these

    initial findings.

    There are a large number of neurological conditions subject to circadian variation in

    expression of their symptoms and associated with sleep disturbance. These includeAlzheimer's Disease (AD), Diffuse Lewy Body Disease (DLBD), Parkinson's Disease (PD)

    and depression. In addition, there are many well-characterised disorders of sleep

    regulation. We expect that OBF will improve sleep quality in a range of disorders and may

    prove a means of influencing the pattern of primary symptom expression in some

    neurological conditions.

    Further research should initially focus on the effects of filter use in conditions known to

    involve dysfunction of the SCN:

    Cluster headache

    Sleep disorders

    Jetlag

    One hour wearing blue filters in the morning improves sleep quality

    Fig. 1: OBF are worn in spectacle frames

    OBF influence retinohypothalamic driveOBF block the transmission of longer-wavelengths of light. In addition, we previously

    demonstrated that OBF use results in pupil dilation sufficient to increase the energy of short

    wavelength (WL) light reaching the retina (Fig. 2). On the basis of these changes, we have

    calculated that OBF use increases retinohypothalamic (RHT) drive by more than 35%.

    The RHT is dominated by short-wavelength sensitive ipRGCs and projects to the

    suprachiasmatic nucleus (SCN), which is the central circadian pacemaker. The SCN

    projects to the medial preoptic area (MPA) and the ventrolateral preoptic area (VLPo), both

    important in the regulation of sleep. It is via the RHT that light exposure influences the

    sleep-wake cycle and circadian patterns of alertness.

    Although not statistically significant, participants tended to wake less frequently in the night

    (p = 0.08) during the period of OBF use, whilst no such trend was evident with the use of

    'yellow' filters (Fig 4).

    Fig. 2: OBF increase short WL light incident at retina

    Fig. 3: VAS scores at baseline against OBF use period

    Fig. 4: Sleep continuity at baseline against OBF use period

    The findings reported in Figures 3 and 4 support our hypothesis that OBF increase photic

    influence over the SCN, and thereby improve sleep quality via the connections of the SCN

    (Fig. 5).

    The failure to reach significance for influence of OBF over the frequency of nighttime

    waking may reflect either the low incidence of nocturnal waking in our healthy participant

    group or the failure of participants to accurately recall each occurrence of waking.

    The improvement in subjective sleep quality and alertness on wearing OBF for a short

    period, raises the prospect that they may of use in the general population.

    0

    Baseline

    0.2

    0.4

    0.6

    0.8

    1.0

    OBF

    'Very alert'

    'Very sleepy' 0

    Baseline

    0.2

    0.4

    0.6

    0.8

    1.0

    OBF

    'Very goodquality'

    'Very poorquality'

    Fig. 5: Pathways subject to modulation by OBF

    0

    Baseline

    0.4

    0.8

    1.2

    1.6

    2.0

    OBF

    Meannumberofnocturnalawakenings

    duringperiod

    Excitator y inp ut Inhibitory input Endocrine output

    VLPo

    RETINA

    SCN PN

    PPC

    SC

    DMN LC

    PVN

    IML SCG PIN aMT

    aMT Melatonin

    DMH Dorsomedial nucleus

    IML

    LC

    PIN

    PN

    PPC

    PVN

    SC

    SCG

    SCN

    VLPo

    Intermediolateral column of the spinal cord

    Locus coeruleus

    Pineal gland

    Pulvinar nucleus

    Posterior parietal cortex

    Paraventricular nucleus

    Superior colliculus

    Superior cervical ganglia

    Suprachiasmatic nucleus

    Ventrolateral preoptic nucleus