Association of obesity in shift workers with the minor allele of a single-nucleotide polymorphism (rs4851377) in the largest circadian clock gene (NPAS2)

被引:0
|
作者
Dorokhov, Vladimir B. [1 ]
Puchkova, Alexandra N. [1 ]
Arsen'ev, Gleb N. [1 ]
Slominsky, Petr A. [2 ]
Dementienko, Valeriy V. [3 ]
Sveshnikov, Dmitry S. [4 ]
Putilov, Arcady A. [1 ]
机构
[1] Russian Acad Sci, Inst Higher Nervous Act & Neurophysiol, Lab Sleep Wake Neurobiol, Moscow, Russia
[2] Russian Acad Sci, Inst Mol Genet, Lab Mol Genet Hereditary Dis, Moscow, Russia
[3] Russian Acad Sci, Kotelnikov Inst Radio Engn & Elect, Lab Med Elect, Moscow, Russia
[4] Peoples Friendship Univ Russia, Med Inst, Dept Normal Physiol, Moscow, Russia
关键词
Rotating shift; circadian disruption; metabolism; candidate gene; single nucleotide polymorphism; SOCIAL JETLAG; SLEEP DURATION; DISORDER; DIET; DISRUPTION; DEPRESSION; COMPONENTS; VARIANTS; PATTERNS; RHYTHMS;
D O I
10.1080/09291016.2018.1537558
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
A growing body of evidence has hinted at the involvement of the largest gene of the circadian clock family, NPAS2, in the regulatory mechanisms underlying the link between metabolic diseases and circadian rhythm disruption. We tested whether one of single-nucleotide polymorphisms in NPAS2 (rs4851377) is associated with obesity and alternations of sleep times in 126 male rotational shift workers (bus drivers). We confirmed positive association of Body Mass Index (BMI) with the difference between free and working days in sleep times, but this difference was smaller in the homozygotes for the minor allele. Moreover, BMI above 30 (obesity) was revealed in the majority of these homozygotes and in the minority of homozygotes for the major allele (11 of 21 or 52.4% and 3 of 40 or 7.5%, respectively). Further studies are required to replicate these results and to elucidate the mechanisms linking NPAS2MODIFIER LETTER PRIMEpolymorphism in with obesity in shift workers.
引用
收藏
页码:522 / 534
页数:13
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