GWAS IDs “Morning People”

In a large genome-wide association study, researchers from 23andMe locate 15 DNA regions associated with people’s preferences for early morning starts.

Written byCatherine Offord
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WIKIMEDIA, DAVID ECCLESA CBS poll in 2007 suggested that just over half of US citizens felt “at their best” in the hours before midday. But whether you’re more of a night owl or a morning lark, a recent analysis of nearly 90,000 genomes from the personal genomics company 23andMe suggests that your preferred schedule is at least partially determined by your DNA. The study was published earlier this week (February 2) in Nature Communications.

“We identify 15 significantly associated loci, including seven near established circadian genes,” the authors wrote in their paper.

Screening spit samples mailed in by more than 89,000 customers, the team at 23andMe conducted genome-wide, single-nucleotide polymorphism (SNP) analyses to match self-reported “morningness” with genetic variation.

Beyond finding specific loci associated with early risers, the researchers found evidence to link a preference for early mornings—which tended to be more commonly reported in women—to a reduced predisposition to insomnia and sleep apnea, though the team’s Mendelian randomization analysis did not reveal a causal relationship.

Of course, using self-reported preferences for mornings does not guarantee an accurate classification of participants’ “morningness,” Barbara Stranger of the University of Chicago, who was not involved in the study, told Wired. Some ...

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Meet the Author

  • After undergraduate research with spiders at the University of Oxford and graduate research with ants at Princeton University, Catherine left arthropods and academia to become a science journalist. She has worked in various guises at The Scientist since 2016. As Senior Editor, she wrote articles for the online and print publications, and edited the magazine’s Notebook, Careers, and Bio Business sections. She reports on subjects ranging from cellular and molecular biology to research misconduct and science policy. Find more of her work at her website.

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