rs10736683 - P2RX3
Magnitude 2.2 · 1 study on file
Reported associations
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Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways. - Nature genetics (2022) · Watanabe K, Jansen PR, Savage JE, Nandakumar P, Wang X, Hinds DA, Gelernter J, Levey DF, Polimanti R, Stein MB, Van Someren EJW, Smit AB, Posthuma D · PubMed 35835914
Insomnia is a heritable, highly prevalent sleep disorder for which no sufficient treatment currently exists. Previous genome-wide association studies with up to 1.3 million subjects identified over 200 associated loci. This extreme polygenicity suggested that many more loci remain to be discovered. The current study almost doubled the sample size to 593,724 cases and 1,771,286 controls, thereby increasing statistical power, and identified 554 risk loci (including 364 novel loci). To capitalize on this large number of loci, we propose a novel strategy to prioritize genes using external biological resources and functional interactions between genes across risk loci. Of all 3,898 genes naively implicated from the risk loci, we prioritize 289 and find brain-tissue expression spec
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Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Diet
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late-day caffeine intake Moderate
Caffeine intake in afternoon and evening may exacerbate insomnia risk in carriers of genetic susceptibility variants
avoid caffeine after 2 PM; limit total daily intake to less than 200 mg
Lifestyle
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consistent sleep schedule Moderate
Regular sleep timing supports circadian stability and may reduce insomnia severity in genetically predisposed individuals
maintain consistent bedtime and wake time within 1 hour, seven days per week
Screening
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sleep quality and insomnia symptoms Moderate
T allele at rs10736683 associated with significantly increased insomnia prevalence in genome-wide study of 1.2 million individuals
track sleep duration, quality, and daytime function; discuss persistent sleep problems with physician