Blood transcriptome based biomarkers for human circadian phase

被引:99
作者
Laing, Emma E. [1 ]
Moeller-Levet, Carla S. [2 ]
Poh, Norman [3 ]
Santhi, Nayantara [4 ]
Archer, Simon N. [4 ]
Dijk, Derk-Jan [4 ]
机构
[1] Univ Surrey, Fac Med & Hlth Sci, Sch Biosci & Med, Dept Microbial Sci, Guildford, Surrey, England
[2] Univ Surrey, Fac Med & Hlth Sci, Bioinformat Core Facil, Guildford, Surrey, England
[3] Univ Surrey, Fac Engn & Phys Sci, Dept Comp Sci, Guildford, Surrey, England
[4] Univ Surrey, Fac Med & Hlth Sci, Sch Biosci & Med, Surrey Sleep Res Ctr, Guildford, Surrey, England
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
TOTALLY BLIND PEOPLE; GENE-EXPRESSION; PERIPHERAL-BLOOD; RHYTHM DISORDERS; MTORC1; REPRESSOR; SKELETAL-MUSCLE; BODY TIME; SLEEP; MELATONIN; RECEPTOR;
D O I
10.7554/eLife.20214
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Diagnosis and treatment of circadian rhythm sleep-wake disorders both require assessment of circadian phase of the brain's circadian pacemaker. The gold-standard univariate method is based on collection of a 24-hr time series of plasma melatonin, a suprachiasmatic nucleus-driven pineal hormone. We developed and validated a multivariate whole-blood mRNA-based predictor of melatonin phase which requires few samples. Transcriptome data were collected under normal, sleep-deprivation and abnormal sleep-timing conditions to assess robustness of the predictor. Partial least square regression (PLSR), applied to the transcriptome, identified a set of 100 biomarkers primarily related to glucocorticoid signaling and immune function. Validation showed that PLSR-based predictors outperform published blood-derived circadian phase predictors. When given one sample as input, the R-2 of predicted vs observed phase was 0.74, whereas for two samples taken 12 hr apart, R-2 was 0.90. This blood transcriptome-based model enables assessment of circadian phase from a few samples.
引用
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页数:26
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