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Light From Self-Luminous Tablet Computers Can Affect Evening Melatonin, Delaying Sleep
New LRC research can aid in the development of
“circadian-friendly” electronic devices
A new study from the Lighting Research Center (LRC) at
Rensselaer Polytechnic Institute shows that a two-hour exposure
to electronic devices with self-luminous “backlit” displays
causes melatonin suppression, which might lead to delayed
bedtimes, especially in teens.
The research team, led by
Mariana Figueiro, associate professor at Rensselaer and
director of the LRC’s Light
and Health Program, tested the effects of self-luminous
tablets on melatonin suppression. In order to simulate typical
usage of these devices, 13 individuals used self-luminous
tablets to read, play games, and watch movies. Results of the
study, titled “Light level and duration of exposure determine
the impact of self-luminous tablets on melatonin suppression,”
were recently published in the journal Applied
Ergonomics.
“Our study shows that a two-hour exposure to light from
self-luminous electronic displays can suppress melatonin by
about 22 percent. Stimulating the human circadian system to
this level may affect sleep in those using the devices prior to
bedtime,” said Figueiro.
The actual melatonin suppression values after 60 minutes
were very similar to those estimated using a predictive model
of human circadian phototransduction for one-hour light
exposures. “Based on these results, display manufacturers can
use our model to determine how their products could affect
circadian system regulation,” said Figueiro.
The results of this study, together with the LRC predictive
model of human circadian phototransduction, could urge
manufacturers to design more “circadian-friendly” electronic
devices that could either increase or decrease circadian
stimulation depending on the time of day—reducing circadian
stimulation in the evening for a better night’s sleep, and
increasing in the morning to encourage alertness. In the
future, manufacturers might be able to use data and predictive
models to design tablets for tailored daytime light exposures
that minimize symptoms of seasonal affective disorder, and
sleep disorders in seniors. Individuals would be able to
receive light treatments while playing games or watching
movies, making light therapy much more enjoyable than just
sitting in front of a light box.
Along with Figueiro, co-authors of the study are LRC
Director and Professor Mark S. Rea, LRC Research Specialist
Brittany Wood, and LRC Research Nurse Barbara Plitnick.
Melatonin is a hormone produced by the pineal gland at night
and under conditions of darkness in both diurnal and nocturnal
species. It is a “timing messenger,” signaling nighttime
information throughout the body. Exposure to light at night,
especially short-wavelength light, can slow or even cease
nocturnal melatonin production. Suppression of melatonin by
light at night resulting in circadian disruption has been
implicated in sleep disturbances, increased risk for diabetes
and obesity, as well as increased risk for more serious
diseases, such as breast cancer, if circadian disruption occurs
for many consecutive years, such as in nightshift workers.
“Technology developments have led to bigger and brighter
televisions, computer screens, and cell phones,” said Wood, who
used the study as the basis for her master’s thesis. “To
produce white light, these electronic devices must emit light
at short wavelengths, which makes them potential sources for
suppressing or delaying the onset of melatonin in the evening,
reducing sleep duration and disrupting sleep. This is
particularly worrisome in populations such as young adults and
adolescents, who already tend to be night owls.”
In the study, the participants were divided into three
groups. The first group viewed their tablets through a pair of
clear goggles fitted with 470-nm (blue) light from light
emitting diodes (LEDs). This was a “true positive” condition
because the blue light is known to be a strong stimulus for
suppressing melatonin. The second group viewed their tablets
through orange-tinted glasses, capable of filtering out the
short-wavelength radiation that can suppress melatonin; this
was the “dark control” condition. The third group did not wear
glasses or goggles. Each tablet was set to full brightness.
In order to accurately record personal light exposures
during the experiment, each subject wore a
Dimesimeter close to the eye. The Dimesimeter is a small
calibrated light meter device developed by the LRC that
continuously records circadian light and activity levels. Last
year, international magazine The Scientist named the
LRC’s Dimesimeter as one of the “Top 10 Innovations of
2011.”
The research team established that duration of exposure and
the distance between the eye and the display, which determines
the amount of light reaching the back of the eye, affects
melatonin levels. Melatonin suppression after a one-hour
exposure to the tablet was not significantly affected. However,
after a two-hour exposure there was significant
suppression.
The type of task being performed on the tablets also
determines how much light is delivered to the cornea and,
therefore, the impact on evening melatonin levels. As shown by
the team’s Dimesimeter measurements, the range of photopic
illuminance levels at the cornea from the tablets alone varied
from 5 lux, which is not likely to affect melatonin, to over 50
lux, which would result in measurable melatonin suppression
after a two-hour exposure. Therefore, before any
generalizations can be made, it is important to measure how
much light one is receiving from these self-luminous
devices.
Until manufacturers develop more “circadian-friendly”
electronic devices that increase or decrease light exposure
based on time of day, Figueiro has several recommendations to
reduce their effects on sleep. “We recommended dimming these
devices at night as much as possible in order to minimize
melatonin suppression, and limiting the amount of time spent
using these devices prior to bedtime.”
The study was funded by Sharp Laboratories of America.
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Published
August 27,
2012 |
Contact: Rebekah Mullaney
Phone: (518) 687-7118
E-mail: mullar2@rpi.edu |
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