NREM delta power and AD-relevant tauopathy are associated with shared cortical gene networks

Abstract Reduced NREM sleep in humans is associated with AD neuropathology. Recent work has demonstrated a reduction in NREM sleep in preclinical AD, pointing to its potential utility as an early marker of dementia. We test the hypothesis that reduced NREM delta power and increased tauopathy are ass...

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Main Authors: Joseph R. Scarpa, Peng Jiang, Vance D. Gao, Martha H. Vitaterna, Fred W. Turek, Andrew Kasarskis
Format: Article
Language:English
Published: Nature Publishing Group 2021-04-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-86255-6
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spelling doaj-fcfae50e25be41e6bc8196f655c447ac2021-04-11T11:32:17ZengNature Publishing GroupScientific Reports2045-23222021-04-0111111110.1038/s41598-021-86255-6NREM delta power and AD-relevant tauopathy are associated with shared cortical gene networksJoseph R. Scarpa0Peng Jiang1Vance D. Gao2Martha H. Vitaterna3Fred W. Turek4Andrew Kasarskis5Department of Anesthesiology, Weill Cornell MedicineCenter for Sleep and Circadian Biology, Department of Neurobiology, Northwestern UniversityCenter for Sleep and Circadian Biology, Department of Neurobiology, Northwestern UniversityCenter for Sleep and Circadian Biology, Department of Neurobiology, Northwestern UniversityCenter for Sleep and Circadian Biology, Department of Neurobiology, Northwestern UniversityIcahn Institute for Genomics and Multiscale Biology, Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount SinaiAbstract Reduced NREM sleep in humans is associated with AD neuropathology. Recent work has demonstrated a reduction in NREM sleep in preclinical AD, pointing to its potential utility as an early marker of dementia. We test the hypothesis that reduced NREM delta power and increased tauopathy are associated with shared underlying cortical molecular networks in preclinical AD. We integrate multi-omics data from two extensive public resources, a human Alzheimer’s disease cohort from the Mount Sinai Brain Bank (N = 125) reflecting AD progression and a (C57BL/6J × 129S1/SvImJ) F2 mouse population in which NREM delta power was measured (N = 98). Two cortical gene networks, including a CLOCK-dependent circadian network, are associated with NREM delta power and AD tauopathy progression. These networks were validated in independent mouse and human cohorts. Identifying gene networks related to preclinical AD elucidate possible mechanisms associated with the early disease phase and potential targets to alter the disease course.https://doi.org/10.1038/s41598-021-86255-6
collection DOAJ
language English
format Article
sources DOAJ
author Joseph R. Scarpa
Peng Jiang
Vance D. Gao
Martha H. Vitaterna
Fred W. Turek
Andrew Kasarskis
spellingShingle Joseph R. Scarpa
Peng Jiang
Vance D. Gao
Martha H. Vitaterna
Fred W. Turek
Andrew Kasarskis
NREM delta power and AD-relevant tauopathy are associated with shared cortical gene networks
Scientific Reports
author_facet Joseph R. Scarpa
Peng Jiang
Vance D. Gao
Martha H. Vitaterna
Fred W. Turek
Andrew Kasarskis
author_sort Joseph R. Scarpa
title NREM delta power and AD-relevant tauopathy are associated with shared cortical gene networks
title_short NREM delta power and AD-relevant tauopathy are associated with shared cortical gene networks
title_full NREM delta power and AD-relevant tauopathy are associated with shared cortical gene networks
title_fullStr NREM delta power and AD-relevant tauopathy are associated with shared cortical gene networks
title_full_unstemmed NREM delta power and AD-relevant tauopathy are associated with shared cortical gene networks
title_sort nrem delta power and ad-relevant tauopathy are associated with shared cortical gene networks
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-04-01
description Abstract Reduced NREM sleep in humans is associated with AD neuropathology. Recent work has demonstrated a reduction in NREM sleep in preclinical AD, pointing to its potential utility as an early marker of dementia. We test the hypothesis that reduced NREM delta power and increased tauopathy are associated with shared underlying cortical molecular networks in preclinical AD. We integrate multi-omics data from two extensive public resources, a human Alzheimer’s disease cohort from the Mount Sinai Brain Bank (N = 125) reflecting AD progression and a (C57BL/6J × 129S1/SvImJ) F2 mouse population in which NREM delta power was measured (N = 98). Two cortical gene networks, including a CLOCK-dependent circadian network, are associated with NREM delta power and AD tauopathy progression. These networks were validated in independent mouse and human cohorts. Identifying gene networks related to preclinical AD elucidate possible mechanisms associated with the early disease phase and potential targets to alter the disease course.
url https://doi.org/10.1038/s41598-021-86255-6
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