TY - JOUR
T1 - MRI-visible perivascular space volumes, sleep duration and daytime dysfunction in adults with cerebrovascular disease
AU - Ondri Investigators
AU - Ramirez, Joel
AU - Holmes, Melissa F.
AU - Berezuk, Courtney
AU - Kwan, Donna
AU - Tan, Brian
AU - Beaton, Derek
AU - Scott, Christopher J.M.
AU - Ozzoude, Miracle
AU - Gao, Fuqiang
AU - Yu, Di
AU - Swardfager, Walter
AU - Lawrence-Dewar, Jane
AU - Dowlatshahi, Dar
AU - Saposnik, Gustavo
AU - Boulos, Mark I.
AU - Murray, Brian J.
AU - Symons, Sean
AU - Bartha, Robert
AU - Black, Sandra E.
AU - Swartz, Richard H.
AU - Strong, Michael
AU - Kleinstiver, Peter
AU - Rashkovan, Natalie
AU - Bronskill, Susan
AU - Borrie, Michael
AU - Finger, Elizabeth
AU - Fischer, Corinne
AU - Frank, Andrew
AU - Freedman, Morris
AU - Kumar, Sanjeev
AU - Pasternak, Stephen
AU - Pollock, Bruce
AU - Rajji, Tarek
AU - Seitz, Dallas
AU - Tang-Wai, David
AU - Tartaglia, Carmela
AU - Varriano, Brenda
AU - Abrahao, Agessandro
AU - Chum, Marvin
AU - Shoesmith, Christen
AU - Turnbull, John
AU - Zinman, Lorne
AU - Fraser, Julia
AU - McIlroy, Bill
AU - Cornish, Ben
AU - Van Ooteghem, Karen
AU - Faria, Frederico
AU - Montero-Odasso, Manuel
AU - Sarquis-Adamson, Yanina
AU - Roberts, Angela
N1 - Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/7
Y1 - 2021/7
N2 - Objectives: Recent studies suggest that interindividual genetic differences in glial-dependent CSF flow through the brain parenchyma, known as glymphatic flow, may trigger compensatory changes in human sleep physiology. In animal models, brain perivascular spaces are a critical conduit for glymphatic flow. We tested the hypothesis that MRI-visible PVS volumes, a putative marker of perivascular dysfunction, are associated with compensatory differences in real-world human sleep behavior. Methods: We analyzed data from 152 cerebrovascular disease patients from the Ontario Neurodegenerative Disease Research Initiative (ONDRI). PVS volumes were measured using 3T-MRI. Self-reported total sleep time, time in bed, and daytime dysfunction were extracted from the Pittsburgh Sleep Quality Index. Results: Individuals with greater PVS volumes reported longer time in bed (+0.85 h per log10 proportion of intracranial volume (ICV) occupied by PVS, SE = 0.30, p = 0.006) and longer total sleep times (+0.70 h per log10 proportion of ICV occupied by PVS volume, SE = 0.33, p = 0.04), independent of vascular risk factors, sleep apnea, nocturnal sleep disturbance, depression, and global cognitive status. Further analyses suggested that the positive association between PVS volumes and total sleep time was mediated by greater time in bed. Moreover, despite having on average greater total sleep times, individuals with greater basal ganglia PVS volumes were more likely to report daytime dysfunction (OR 5.63 per log10 proportion of ICV occupied by PVS, 95% CI: 1.38–22.26, p = 0.018). Conclusions: Individuals with greater PVS volumes spend more time in bed, resulting in greater total sleep time, which may represent a behavioral compensatory response to perivascular space dysfunction.
AB - Objectives: Recent studies suggest that interindividual genetic differences in glial-dependent CSF flow through the brain parenchyma, known as glymphatic flow, may trigger compensatory changes in human sleep physiology. In animal models, brain perivascular spaces are a critical conduit for glymphatic flow. We tested the hypothesis that MRI-visible PVS volumes, a putative marker of perivascular dysfunction, are associated with compensatory differences in real-world human sleep behavior. Methods: We analyzed data from 152 cerebrovascular disease patients from the Ontario Neurodegenerative Disease Research Initiative (ONDRI). PVS volumes were measured using 3T-MRI. Self-reported total sleep time, time in bed, and daytime dysfunction were extracted from the Pittsburgh Sleep Quality Index. Results: Individuals with greater PVS volumes reported longer time in bed (+0.85 h per log10 proportion of intracranial volume (ICV) occupied by PVS, SE = 0.30, p = 0.006) and longer total sleep times (+0.70 h per log10 proportion of ICV occupied by PVS volume, SE = 0.33, p = 0.04), independent of vascular risk factors, sleep apnea, nocturnal sleep disturbance, depression, and global cognitive status. Further analyses suggested that the positive association between PVS volumes and total sleep time was mediated by greater time in bed. Moreover, despite having on average greater total sleep times, individuals with greater basal ganglia PVS volumes were more likely to report daytime dysfunction (OR 5.63 per log10 proportion of ICV occupied by PVS, 95% CI: 1.38–22.26, p = 0.018). Conclusions: Individuals with greater PVS volumes spend more time in bed, resulting in greater total sleep time, which may represent a behavioral compensatory response to perivascular space dysfunction.
KW - Glymphatic system
KW - Perivascular spaces
KW - Sleep quality
KW - Small vessel disease
KW - Vascular cognitive impairment
KW - Virchow-Robin
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U2 - 10.1016/j.sleep.2021.03.043
DO - 10.1016/j.sleep.2021.03.043
M3 - Article
C2 - 33991894
AN - SCOPUS:85108303459
SN - 1389-9457
VL - 83
SP - 83
EP - 88
JO - Sleep Medicine
JF - Sleep Medicine
ER -