rs11648222 - GNAO1-DT
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.
Lifestyle
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Cognitive behavioral therapy for insomnia (CBT-I) Moderate
rs11648222 T allele increases insomnia risk through altered GNAO1 neuronal signaling.
Discuss CBT-I with healthcare provider; typically 6-8 weekly sessions for insomnia
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Consistent sleep-wake schedule Moderate
Genetic predisposition to insomnia; consistent circadian rhythm mitigates expression.
Maintain consistent bedtime and wake time within 30 minutes daily
Screening
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Sleep disorder evaluation Moderate
Genetic association with insomnia risk warrants clinical assessment for sleep disorders.