Deep longitudinal multiomics profiling reveals two biological seasonal patterns in California

被引:33
作者
Sailani, M. Reza [1 ]
Metwally, Ahmed A. [1 ]
Zhou, Wenyu [1 ]
Rose, Sophia Miryam Schuessler-Fiorenza [1 ]
Ahadi, Sara [1 ]
Contrepois, Kevin [1 ]
Mishra, Tejaswini [1 ]
Zhang, Martin Jinye [2 ]
Kidzinski, Lukasz [3 ]
Chu, Theodore J. [4 ]
Snyder, Michael P. [1 ]
机构
[1] Stanford Univ, Dept Genet, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Elect Engn, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Pediat, Div Allergy & Immunol, Stanford, CA 94305 USA
基金
瑞士国家科学基金会;
关键词
INSULIN-RESISTANCE; GUT MICROBIOTA; BLOOD-PRESSURE; PHYSICAL-ACTIVITY; PROTEIN; HEMOGLOBIN; PER1; HIBERNATION; POPULATION; EXPRESSION;
D O I
10.1038/s41467-020-18758-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
The influence of seasons on biological processes is poorly understood. In order to identify biological seasonal patterns based on diverse molecular data, rather than calendar dates, we performed a deep longitudinal multiomics profiling of 105 individuals over 4 years. Here, we report more than 1000 seasonal variations in omics analytes and clinical measures. The different molecules group into two major seasonal patterns which correlate with peaks in late spring and late fall/early winter in California. The two patterns are enriched for molecules involved in human biological processes such as inflammation, immunity, cardiovascular health, as well as neurological and psychiatric conditions. Lastly, we identify molecules and microbes that demonstrate different seasonal patterns in insulin sensitive and insulin resistant individuals. The results of our study have important implications in healthcare and highlight the value of considering seasonality when assessing population wide health risk and management. Seasonal patterns of molecular markers in humans have not been extensively studied. Here, the authors combine host components (transcriptome, metabolome, proteome, immunome, clinical lab tests) and microbiome to profile 105 individuals, identifying over 1000 markers in two major seasonal patterns.
引用
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页数:12
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