Oct.
23, 2013 — Population-level studies have indicated that insufficient sleep
increases the risk of cardiovascular diseases and type 2 diabetes. These
diseases are known to be linked to inflammatory responses in the body. University
of Helsinki researchers have now shown what kinds of biological mechanisms
related to sleep loss affect the immune system and trigger an inflammatory
response. They identified the genes which are most susceptible to sleep
deprivation and examined whether these genes are involved in the regulation of
the immune system. The study was published in the journal PLOS ONE on 23
October 2013.
Conducted
at the sleep laboratory of the Finnish Institute of Occupational Health, the
study restricted the amount of sleep of a group of healthy young men to four
hours per night for five days, imitating the schedule of a normal working week.
Blood samples were taken before and after the sleep deprivation test. White
blood cells were isolated from the samples, and the expression of all genes at
the time of the sampling was examined using microarrays. The results were
compared with samples from healthy men of comparable age who had been sleeping
eight hours per night for the week.
"We
compared the gene expression before and after the sleep deprivation period, and
focused on the genes whose behaviour was most strongly altered," explains
researcher Vilma Aho. "The expression of many genes and gene pathways
related to the functions of the immune system was increased during the sleep
deprivation. There was an increase in activity of B cells which are responsible
for producing antigens that contribute to the body's defensive reactions, but
also to allergic reactions and asthma. This may explain the previous
observations of increased asthmatic symptoms in a state of sleep
deprivation."
The
amount of certain interleukins, or signalling molecules which promote
inflammation, increased, as did the amount of associated receptors such as
Toll-like receptors (TLR). On the gene level, this was apparent in the
higher-than-normal expression of the TLR4 gene after sleep loss. CRP level was
also elevated, indicating inflammation.
The
researchers also wanted to examine the impact that long-term sleep deprivation
could have on the immune system. For this follow-up study, they used material
from the national FINRISKI health survey. Participants in this population study
underwent blood tests but also answered questions about their health, for
example whether they were getting enough sleep.
The
researchers compared participants who believed they were sleeping sufficiently
with those who felt that they were not sleeping enough. Some of the gene-level
changes observed in the experimental working week sleep restriction study were
repeated in the population sample. These results may help explain the
connection between shorter sleep and the development of inflammatory diseases,
such as cardiovascular disease and diabetes, which has been established in
epidemiological studies.
"These
results corroborate the idea that sleep does not only impact brain function,
but also interacts with our immune system and metabolism. Sleep loss causes
changes to the system that regulates our immune defence. Some of these changes
appear to be long-term, and may contribute to the development of diseases that
have been linked to sleep deprivation in epidemiological research," Aho
states.
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