rs10875606 - KCTD16
Magnitude 2.2 · 1 study on file
Reported associations
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Genetic determinants of daytime napping and effects on cardiometabolic health - Unknown journal (n.d.) · Unknown authors · PubMed 33568662
ABSTRACT: Daytime napping is a common, heritable behavior, but its genetic basis and causal relationship with cardiometabolic health remain unclear. Here, we perform a genome-wide association study of self-reported daytime napping in the UK Biobank (n = 452,633) and identify 123 loci of which 61 replicate in the 23andMe research cohort (n = 541,333). Findings include missense variants in established drug targets for sleep disorders (HCRTR1, HCRTR2), genes with roles in arousal (TRPC6, PNOC), and genes suggesting an obesity-hypersomnolence pathway (PNOC, PATJ). Association signals are concordant with accelerometer-measured daytime inactivity duration and 33 loci colocalize with loci for other sleep phenotypes. Cluster analysis identifies three distinct clusters of nap-promoting mech
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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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daytime napping patterns and sleep quality Moderate
Genetic KCTD16 variants increase napping susceptibility; habitual napping causally increases hypertension and adiposity.
Lifestyle
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limit daytime napping frequency and duration Moderate
Daytime napping causally increases blood pressure and central adiposity; KCTD16 variants increase napping propensity.
Aim to avoid naps; if needed, limit to under 20 minutes. Prioritize 7-9 hours nighttime sleep.
Screening
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blood pressure annually Moderate
KCTD16 variants increase daytime napping frequency; daytime napping causally increases blood pressure; genetic risk requires monitoring.
Establish baseline BP; repeat annually or per provider guidance
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waist circumference and BMI Moderate
Daytime napping causally associates with increased abdominal adiposity; KCTD16 variants increase napping frequency.
Measure annually and assess trend; discuss with provider if rising