rs10819613 - NCS1
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.
Discuss with your doctor
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sleep assessment and management strategies Moderate
rs10819613 T allele is associated with increased insomnia risk
Discuss genetic predisposition and consider evaluation for sleep disorders; explore behavioral and treatment options
Lifestyle
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optimize sleep hygiene practices Moderate
rs10819613 T allele is associated with increased insomnia risk; behavioral sleep optimization may help mitigate predisposition
Consistent sleep schedule, dark and cool bedroom environment, avoid screens 1-2 hours before bed
Screening
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sleep quality and sleep duration Moderate
rs10819613 T allele is associated with increased insomnia risk; monitoring helps detect problems early
Track sleep quality and duration weekly; discuss persistent issues with healthcare provider