June 2021
Volume 62, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2021
Determination of Quantitative Light Discomfort Thresholds in a Large Healthy Human Sample
Author Affiliations & Notes
  • Sarah Marie
    R&P Light & Life Science, Essilor International, Paris, Île-de-France, France
  • Robert Montés-Micó
    Department of Optics and Optometry and Vision Sciences, Optometry Research Group (GIO), University of Valencia, Valencia, Spain
  • Alejandro Cerviño
    Department of Optics and Optometry and Vision Sciences, Optometry Research Group (GIO), University of Valencia, Valencia, Spain
  • Noelia Martínez-Albert
    Department of Optics and Optometry and Vision Sciences, Optometry Research Group (GIO), University of Valencia, Valencia, Spain
  • José Vicente García-Marqués
    Department of Optics and Optometry and Vision Sciences, Optometry Research Group (GIO), University of Valencia, Valencia, Spain
  • Footnotes
    Commercial Relationships   Sarah Marie, Essilor International (E); Robert Montés-Micó, Essilor International (F); Alejandro Cerviño, Essilor International (F); Noelia Martínez-Albert, Essilor International (F); José Vicente García-Marqués, Essilor International (F)
  • Footnotes
    Support  Essilor research grant to the University of Valencia
Investigative Ophthalmology & Visual Science June 2021, Vol.62, 495. doi:
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      Sarah Marie, Robert Montés-Micó, Alejandro Cerviño, Noelia Martínez-Albert, José Vicente García-Marqués; Determination of Quantitative Light Discomfort Thresholds in a Large Healthy Human Sample. Invest. Ophthalmol. Vis. Sci. 2021;62(8):495.

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Abstract

Purpose : To determine light discomfort thresholds quantitatively using a new clinical device on a large sample of healthy adult humans, reliability and relationship with biometric and optical parameters.

Methods : A total of 489 healthy subjects with ages ranging from 20 to 70 years (241 men, 248 women), were examined with the LUMIZ™ 100 (Essilor Intl., France), a new handheld, portable, clinical device for the determination of light discomfort thresholds. Instructions were given by means of a recorded video to ensure homogeneity in the explanations. A mock-up test was carried out prior to measurement. Two thresholds, “just perceptible” and “really disturbing” discomfort, were determined for three light presentation protocols (Continuous warm, Continuous cold, and flashing warm), using two different LED sources (Warm:4000°K, and Cold:6500°K). Iris color and skin pigmentation level were classified, and subjective manifest refraction was also determined.

Results : Discomfort thresholds are well distributed across the range of intensities. Intrasession intraclass correlation coefficients were higher than 0.80 for all thresholds. First measurement was representative of the median of three. There was no effect of age on discomfort thresholds (r2<0.1, p=0.30), nor affected reliability of the measurements (p=0.368). For the considered population, women have lower discomfort thresholds than men (p<0.001). Subjects with high self-perceived light sensitivity tend to have lower discomfort threshold and vice versa (p<0.001). No effect on discomfort thresholds was found for ametropia (p=0.45), nor was any link with pupil size, axial length or wavefront aberrations in this sample. There was no significant representation of iris color or skin tone to allow for statistical significance of the effect, although a trend for green eyes to have lower thresholds was observed.

Conclusions : The new device is reliable for the clinical determination of light discomfort thresholds on healthy subjects. Nor age, refractive error, or biometric parameters seem to have an effect on discomfort thresholds. Women tend to have lower thresholds than men. The new device is useful for the quantitative determination of light discomfort in healthy subjects. Applications in diseased eyes and filter treatments are to be explored.

This is a 2021 ARVO Annual Meeting abstract.

 

Lumiz 100 device

Lumiz 100 device

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