{"title":"青少年早期睡眠脑电图纺锤波活动与丘脑体积的联合遗传力。","authors":"Andjela Markovic,Duco Veen,Christoph Hamann,Kristina Adorjan,Michael Kaess,Ruth Tuura O'Gorman,Leila Tarokh","doi":"10.1523/jneurosci.1138-24.2025","DOIUrl":null,"url":null,"abstract":"Sleep spindles, transient bursts of rhythmic activity during non-rapid eye movement (NREM) sleep, are generated by the thalamocortical network through an intricate interplay between the thalamus and the cortex. Emerging research has shed light on the role of sleep spindles in cognitive function, memory consolidation, and overall brain health. Using a behavioral genetics approach in female and male adolescent humans, this study examined the degree to which sleep spindles (measured via high-density sleep EEG) and thalamic volume (measured via MRI) are driven by common genetic and environmental factors. Here we show a strong correlation between thalamic volume and sleep spindle amplitude and density. Bayesian structural equation modelling estimated that over posterior regions genetic factors accounted for approximately half of the covariance between sleep spindle activity and thalamic volume. Our findings demonstrate that genetic factors play a role in shaping the structural and functional integrity of the thalamocortical network, with implications for understanding how these processes contribute to neurodevelopmental outcomes.Significance statement Sleep spindles, oscillatory activity generated in the thalamus, are crucial for cognitive functions and brain health. This study investigated the joint genetic and environmental influences on sleep spindles and thalamic volume in adolescents. Our findings suggest a significant overlap in genetic factors influencing thalamic volume and spindle amplitude over posterior brain regions. Given that sleep spindle activity is altered in several brain disorders involving the thalamocortical system, this work not only enhances our understanding of the biological phenomena underlying the neuroanatomical substrates of the sleep EEG but also offers crucial insights for developing targeted interventions in neurodevelopmental disorders.","PeriodicalId":50114,"journal":{"name":"Journal of Neuroscience","volume":"39 1","pages":""},"PeriodicalIF":4.4000,"publicationDate":"2025-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Joint Heritability of Sleep EEG Spindle Activity and Thalamic Volume in Early Adolescence.\",\"authors\":\"Andjela Markovic,Duco Veen,Christoph Hamann,Kristina Adorjan,Michael Kaess,Ruth Tuura O'Gorman,Leila Tarokh\",\"doi\":\"10.1523/jneurosci.1138-24.2025\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Sleep spindles, transient bursts of rhythmic activity during non-rapid eye movement (NREM) sleep, are generated by the thalamocortical network through an intricate interplay between the thalamus and the cortex. Emerging research has shed light on the role of sleep spindles in cognitive function, memory consolidation, and overall brain health. Using a behavioral genetics approach in female and male adolescent humans, this study examined the degree to which sleep spindles (measured via high-density sleep EEG) and thalamic volume (measured via MRI) are driven by common genetic and environmental factors. Here we show a strong correlation between thalamic volume and sleep spindle amplitude and density. Bayesian structural equation modelling estimated that over posterior regions genetic factors accounted for approximately half of the covariance between sleep spindle activity and thalamic volume. Our findings demonstrate that genetic factors play a role in shaping the structural and functional integrity of the thalamocortical network, with implications for understanding how these processes contribute to neurodevelopmental outcomes.Significance statement Sleep spindles, oscillatory activity generated in the thalamus, are crucial for cognitive functions and brain health. This study investigated the joint genetic and environmental influences on sleep spindles and thalamic volume in adolescents. Our findings suggest a significant overlap in genetic factors influencing thalamic volume and spindle amplitude over posterior brain regions. Given that sleep spindle activity is altered in several brain disorders involving the thalamocortical system, this work not only enhances our understanding of the biological phenomena underlying the neuroanatomical substrates of the sleep EEG but also offers crucial insights for developing targeted interventions in neurodevelopmental disorders.\",\"PeriodicalId\":50114,\"journal\":{\"name\":\"Journal of Neuroscience\",\"volume\":\"39 1\",\"pages\":\"\"},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2025-04-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Neuroscience\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1523/jneurosci.1138-24.2025\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1523/jneurosci.1138-24.2025","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
Joint Heritability of Sleep EEG Spindle Activity and Thalamic Volume in Early Adolescence.
Sleep spindles, transient bursts of rhythmic activity during non-rapid eye movement (NREM) sleep, are generated by the thalamocortical network through an intricate interplay between the thalamus and the cortex. Emerging research has shed light on the role of sleep spindles in cognitive function, memory consolidation, and overall brain health. Using a behavioral genetics approach in female and male adolescent humans, this study examined the degree to which sleep spindles (measured via high-density sleep EEG) and thalamic volume (measured via MRI) are driven by common genetic and environmental factors. Here we show a strong correlation between thalamic volume and sleep spindle amplitude and density. Bayesian structural equation modelling estimated that over posterior regions genetic factors accounted for approximately half of the covariance between sleep spindle activity and thalamic volume. Our findings demonstrate that genetic factors play a role in shaping the structural and functional integrity of the thalamocortical network, with implications for understanding how these processes contribute to neurodevelopmental outcomes.Significance statement Sleep spindles, oscillatory activity generated in the thalamus, are crucial for cognitive functions and brain health. This study investigated the joint genetic and environmental influences on sleep spindles and thalamic volume in adolescents. Our findings suggest a significant overlap in genetic factors influencing thalamic volume and spindle amplitude over posterior brain regions. Given that sleep spindle activity is altered in several brain disorders involving the thalamocortical system, this work not only enhances our understanding of the biological phenomena underlying the neuroanatomical substrates of the sleep EEG but also offers crucial insights for developing targeted interventions in neurodevelopmental disorders.
期刊介绍:
JNeurosci (ISSN 0270-6474) is an official journal of the Society for Neuroscience. It is published weekly by the Society, fifty weeks a year, one volume a year. JNeurosci publishes papers on a broad range of topics of general interest to those working on the nervous system. Authors now have an Open Choice option for their published articles