Aging of non-visual spectral sensitivity to light in humans: compensatory mechanisms?

PLoS One. 2014 Jan 23;9(1):e85837. doi: 10.1371/journal.pone.0085837. eCollection 2014.

Abstract

The deterioration of sleep in the older population is a prevalent feature that contributes to a decrease in quality of life. Inappropriate entrainment of the circadian clock by light is considered to contribute to the alteration of sleep structure and circadian rhythms in the elderly. The present study investigates the effects of aging on non-visual spectral sensitivity to light and tests the hypothesis that circadian disturbances are related to a decreased light transmittance. In a within-subject design, eight aged and five young subjects were exposed at night to 60 minute monochromatic light stimulations at 9 different wavelengths (420-620 nm). Individual sensitivity spectra were derived from measures of melatonin suppression. Lens density was assessed using a validated psychophysical technique. Although lens transmittance was decreased for short wavelength light in the older participants, melatonin suppression was not reduced. Peak of non-visual sensitivity was, however, shifted to longer wavelengths in the aged participants (494 nm) compared to young (484 nm). Our results indicate that increased lens filtering does not necessarily lead to a decreased non-visual sensitivity to light. The lack of age-related decrease in non-visual sensitivity to light may involve as yet undefined adaptive mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aging*
  • Circadian Clocks
  • Circadian Rhythm
  • Female
  • Humans
  • Lens, Crystalline / physiology
  • Light*
  • Male
  • Melatonin / blood
  • Middle Aged
  • Sleep*
  • Young Adult

Substances

  • Melatonin

Grants and funding

RPN was funded by “Ministère de l'Enseignement Supérieur et de la Recherche Français” and “Fédération des Aveugles et Handicapés Visuels de France”. CC was funded by Fondation de France (Berthe Fouassier grant). This work was supported by grants from FP6-EUCLOCK, ANR-09-MNPS-040, ANR 12-TECS-0013-01, GIS-Vieillissement, Rhône-Alpes Cible, Rhône-Alpes Cluster HVN, and Retina France. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.