PER3 gene polymorphisms have been associated with differences in human sleep-wake phenotypes, and sensitivity to light. The aims of this study were to assess: i) the frequency of allelic variants at two PER3 polymorphic sites (rs57875989 length polymorphism: PER3 , PER3 ; rs228697 SNP: PER3 , PER3 ) in relation to sleep-wake timing; ii) the effect of morning light on behavioural/circadian variables in PER3 /PER3 and PER3 /PER3 homozygotes. 786 Caucasian subjects living in Northern Italy donated buccal DNA and completed diurnal preference, sleep quality/timing and sleepiness/mood questionnaires. 19 PER3 /PER3 and 11 PER3 /PER3 homozygotes underwent morning light administration, whilst monitoring sleep-wake patterns and the urinary 6-sulphatoxymelatonin (aMT6s) rhythm. No significant relationship was observed between the length polymorphism and diurnal preference. By contrast, a significant association was observed between the PER3 variant and morningness (OR = 2.10), and between the PER3 -PER3 haplotype and morningness (OR = 2.19), for which a mechanistic hypothesis is suggested. No significant differences were observed in sleep timing/aMT6s rhythms between PER3 /PER3 and PER3 /PER3 subjects at baseline. After light administration, PER3 /PER3 subjects advanced their aMT6s acrophase (p < 0.05), and showed a trend of advanced sleep-wake timing. In conclusion, significant associations were observed between PER3 polymorphic variants/their combinations and both diurnal preference and the response to light.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537342 | PMC |
http://dx.doi.org/10.1038/s41598-017-06769-w | DOI Listing |
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