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Biology subjects

Zee, P.

Publications and source records attributed to Zee, P..

3 recordsLinked to original sources

Active Bed Microclimate Regulation Modulates Sleep Architecture, Autonomic, and Central Nervous System Activity during Sleep

Skin temperature and bed microclimate are established modulators of human sleep, but most prior work has relied on passive thermal materials. We used a smart bed capable of heating or cooling the microclimate to investigate how six temperature settings affect sleep architecture, autonomic activity, and electroencephalographic (EEG) activity. Eighteen adults (9 male, 9 female; mean age 44.5 years) completed two overnight polysomnography sessions with bed temperature assigned via Latin-square counterbalancing across three-hour segments of high cooling, medium cooling, low cooling, off, low heating, and medium heating. Mixed-effects regression models evaluated manipulation checks on induced thermal changes, the probability of sleep versus wake, and the probability of each sleep stage (N1, N2, N3, REM), while secondary analyses assessed sleep deepening, heart rate, and EEG spectral power. Temperature manipulations significantly affected sleep and physiological outcomes. All five active settings shifted sleep toward greater depth, increasing the odds of slow-wave sleep (odds ratios 1.21 to 3.65, largest for high cooling) and reducing the odds of light non-rapid eye movement sleep relative to off. Heating accelerated early sleep deepening relative to cooling without significantly altering sleep onset latency, whereas cooling produced a graded reduction in heart rate. EEG analyses revealed distinct cortical signatures for heating and cooling conditions. These findings demonstrate that active bed microclimate regulation modulates sleep architecture, autonomic activity, and cortical activity during sleep. The nonlinear pattern of effects suggests thermal "sweet spots" that may vary across the night and individuals, supporting the development of individualized programmable temperature-regulation strategies for sleep optimization.

physiology↗

Multi-ancestry genome-wide analysis identifies common genetic variants for self-reported sleep duration and shared genetic effects

Both short and long sleep duration are associated with increased risk of chronic diseases, but the genetic determinants of sleep duration are largely unknown outside of European populations. Here we report transferability of a polygenic score of 78 European ancestry sleep duration SNPs to an African (n=7,288; p=0.003), a South Asian (n=7,485; p=0.025), and a Japanese (n=13,618; p=6x10-4) cohort, but not to a cohort of Hispanic/Latino (n- XXX; p=0.71) participants. Furthermore, in a pan-ancestry (N = 483,235) meta-analysis of genome-wide association studies (GWAS) for habitual sleep duration, 5 novel and 68 known loci are associated with genome-wide significance. For the novel loci, sleep duration signals colocalize with expression-QTLs for PRR12 and COG5 in brain tissues, and pleiotropic associations are observed with cardiovascular and neuropsychiatric traits. Overall, our results suggest that the genetic basis of sleep duration is at least partially shared across diverse ancestry groups.

genomics↗

Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

Long and short sleep duration are associated with elevated blood pressure (BP), possibly through effects on molecular pathways that influence neuroendocrine and vascular systems. To gain new insights into the genetic basis of sleep-related BP variation, we performed genome-wide gene by short or long sleep duration interaction analyses on four BP traits (systolic BP, diastolic BP, mean arterial pressure, and pulse pressure) across five ancestry groups using 1 degree of freedom (1df) interaction and 2df joint tests. Primary multi-ancestry analyses in 62,969 individuals in stage 1 identified 3 novel loci that were replicated in an additional 59,296 individuals in stage 2, including rs7955964 (FIGNL2/ANKRD33) showing significant 1df interactions with long sleep duration and rs73493041 (SNORA26/C9orf170) and rs10406644 (KCTD15/LSM14A) showing significant 1df interactions with short sleep duration (Pint < 5x10-8). Secondary ancestry-specific two-stage analyses and combined stage 1 and 2 analyses additionally identified 23 novel loci that need external replication, including 3 and 5 loci showing significant 1df interactions with long and short sleep duration, respectively (Pint < 5x10-8). Multiple genes mapped to our 26 novel loci have known functions in sleep-wake regulation, nervous and cardiometabolic systems. We also identified new gene by long sleep interactions near five known BP loci ([&le;]1Mb) including NME7, FAM208A, MKLN1, CEP164, and RGL3/ELAVL3 (Pint < 5x10-8). This study indicates that sleep and primary mechanisms regulating BP may interact to elevate BP level, suggesting novel insights into sleep-related BP regulation.

genomics↗