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Partial Sleep Restriction Activates Immune Response-Related Gene Expression Pathways: Experimental and Epidemiological Studies in Humans

Overview of attention for article published in PLOS ONE, October 2013
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Title
Partial Sleep Restriction Activates Immune Response-Related Gene Expression Pathways: Experimental and Epidemiological Studies in Humans
Published in
PLOS ONE, October 2013
DOI 10.1371/journal.pone.0077184
Pubmed ID
Authors

Vilma Aho, Hanna M. Ollila, Ville Rantanen, Erkki Kronholm, Ida Surakka, Wessel M. A. van Leeuwen, Maili Lehto, Sampsa Matikainen, Samuli Ripatti, Mikko Härmä, Mikael Sallinen, Veikko Salomaa, Matti Jauhiainen, Harri Alenius, Tiina Paunio, Tarja Porkka-Heiskanen

Abstract

Epidemiological studies have shown that short or insufficient sleep is associated with increased risk for metabolic diseases and mortality. To elucidate mechanisms behind this connection, we aimed to identify genes and pathways affected by experimentally induced, partial sleep restriction and to verify their connection to insufficient sleep at population level. The experimental design simulated sleep restriction during a working week: sleep of healthy men (N = 9) was restricted to 4 h/night for five nights. The control subjects (N = 4) spent 8 h/night in bed. Leukocyte RNA expression was analyzed at baseline, after sleep restriction, and after recovery using whole genome microarrays complemented with pathway and transcription factor analysis. Expression levels of the ten most up-regulated and ten most down-regulated transcripts were correlated with subjective assessment of insufficient sleep in a population cohort (N = 472). Experimental sleep restriction altered the expression of 117 genes. Eight of the 25 most up-regulated transcripts were related to immune function. Accordingly, fifteen of the 25 most up-regulated Gene Ontology pathways were also related to immune function, including those for B cell activation, interleukin 8 production, and NF-κB signaling (P<0.005). Of the ten most up-regulated genes, expression of STX16 correlated negatively with self-reported insufficient sleep in a population sample, while three other genes showed tendency for positive correlation. Of the ten most down-regulated genes, TBX21 and LGR6 correlated negatively and TGFBR3 positively with insufficient sleep. Partial sleep restriction affects the regulation of signaling pathways related to the immune system. Some of these changes appear to be long-lasting and may at least partly explain how prolonged sleep restriction can contribute to inflammation-associated pathological states, such as cardiometabolic diseases.

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Geographical breakdown

Country Count As %
United States 2 2%
Portugal 1 <1%
Sweden 1 <1%
India 1 <1%
Finland 1 <1%
Japan 1 <1%
Singapore 1 <1%
Unknown 94 92%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 17 17%
Student > Bachelor 16 16%
Researcher 13 13%
Other 8 8%
Student > Master 7 7%
Other 15 15%
Unknown 26 25%
Readers by discipline Count As %
Medicine and Dentistry 16 16%
Agricultural and Biological Sciences 13 13%
Neuroscience 12 12%
Nursing and Health Professions 6 6%
Psychology 5 5%
Other 17 17%
Unknown 33 32%