TY - JOUR
T1 - The Bidirectional Link Between Sleep Disturbances and Traumatic Brain Injury Symptoms
T2 - A Role for Glymphatic Dysfunction?
AU - Piantino, Juan A.
AU - Iliff, Jeffrey J.
AU - Lim, Miranda M.
N1 - Funding Information:
These studies were supported by funding from the National Institutes of Health (NIH) National Heart, Lung and Blood Institute (Grant No. K23HL150217-01 [to JAP]); NIH National Institute on Aging (Grant Nos. AG054456 and AG066509 [to JJI]); NIH National Institute of Neurological Disorders and Stroke (Grant No. 089709 [to JJI]); Veterans Affairs Clinical Science Research and Development (Grant No. CX002022 [to MML]); the Department of Defense (Grant No. PT160162 [to MML]); and the Center for Neuroscience & Regenerative Medicine Award (to MML).
Funding Information:
These studies were supported by funding from the National Institutes of Health (NIH) National Heart, Lung and Blood Institute (Grant No. K23HL150217-01 [to JAP]); NIH National Institute on Aging (Grant Nos. AG054456 and AG066509 [to JJI]); NIH National Institute of Neurological Disorders and Stroke (Grant No. 089709 [to JJI]); Veterans Affairs Clinical Science Research and Development (Grant No. CX002022 [to MML]); the Department of Defense (Grant No. PT160162 [to MML]); and the Center for Neuroscience & Regenerative Medicine Award (to MML). This material is the result of work supported with resources and the use of facilities at the VA Puget Sound Health Care System and the VA Portland Health Care System. Interpretations and conclusions are those of the authors and do not represent the views of the U.S. Department of Veterans Affairs or the United States Government. We would like to thank members of the DISECT-TBI (Defining Imaging, Sleep, and Exchange of CSF in TBI) Consortium for their collaborations and input on TBI, biomarkers, and sleep, including Drs Jessica Gill, Christine MacDonald, Swati Rane Levendowsky, Jonathan Elliott, Sara Mithani, Vivian Guedes, Nadir Balba, and Molly Braun. We would also like to thank Drs Lisa Silbert and Randy Woltjer at Oregon Health & Science University for scientific discussions about PVSs. Finally, we would like to express our sincere gratitude for the participants in our research studies. The authors report no biomedical financial interests or potential conflicts of interest.
Publisher Copyright:
© 2021
PY - 2022/3/1
Y1 - 2022/3/1
N2 - Mild traumatic brain injury (mTBI), often referred to as concussion, is a major cause of morbidity and mortality worldwide. Sleep disturbances are common after mTBI. Moreover, subjects who develop subjective sleep complaints after mTBI also report more severe somatic, mental health, and cognitive impairment and take longer to recover from mTBI sequelae. Despite many previous studies addressing the role of sleep in post-mTBI morbidity, the mechanisms linking sleep to recovery after mTBI remain poorly understood. The glymphatic system is a brainwide network that supports fluid movement through the cerebral parenchyma and the clearance of interstitial solutes and wastes from the brain. Notably, the glymphatic system is active primarily during sleep. Clearance of cellular byproducts related to somatic, mental health, and neurodegenerative processes (e.g., amyloid-β and tau, among others) depends in part on intact glymphatic function, which becomes impaired after mTBI. In this viewpoint, we review the current knowledge regarding the association between sleep disturbances and post-mTBI symptoms. We also discuss the role of glymphatic dysfunction as a potential link between mTBI, sleep disruption, and posttraumatic morbidity. We outline a model where glymphatic dysfunction and sleep disruption caused by mTBI may have an additive effect on waste clearance, leading to cerebral dysfunction and impaired recovery. Finally, we review the novel techniques being developed to examine glymphatic function in humans and explore potential interventions to alter glymphatic exchange that may offer a novel therapeutic approach to those experiencing poor sleep and prolonged symptoms after mTBI.
AB - Mild traumatic brain injury (mTBI), often referred to as concussion, is a major cause of morbidity and mortality worldwide. Sleep disturbances are common after mTBI. Moreover, subjects who develop subjective sleep complaints after mTBI also report more severe somatic, mental health, and cognitive impairment and take longer to recover from mTBI sequelae. Despite many previous studies addressing the role of sleep in post-mTBI morbidity, the mechanisms linking sleep to recovery after mTBI remain poorly understood. The glymphatic system is a brainwide network that supports fluid movement through the cerebral parenchyma and the clearance of interstitial solutes and wastes from the brain. Notably, the glymphatic system is active primarily during sleep. Clearance of cellular byproducts related to somatic, mental health, and neurodegenerative processes (e.g., amyloid-β and tau, among others) depends in part on intact glymphatic function, which becomes impaired after mTBI. In this viewpoint, we review the current knowledge regarding the association between sleep disturbances and post-mTBI symptoms. We also discuss the role of glymphatic dysfunction as a potential link between mTBI, sleep disruption, and posttraumatic morbidity. We outline a model where glymphatic dysfunction and sleep disruption caused by mTBI may have an additive effect on waste clearance, leading to cerebral dysfunction and impaired recovery. Finally, we review the novel techniques being developed to examine glymphatic function in humans and explore potential interventions to alter glymphatic exchange that may offer a novel therapeutic approach to those experiencing poor sleep and prolonged symptoms after mTBI.
KW - Glymphatic system
KW - Perivascular spaces
KW - Sleep
KW - Traumatic brain injury
KW - Virchow-Robin spaces
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UR - http://www.scopus.com/inward/citedby.url?scp=85114153772&partnerID=8YFLogxK
U2 - 10.1016/j.biopsych.2021.06.025
DO - 10.1016/j.biopsych.2021.06.025
M3 - Review article
C2 - 34481662
AN - SCOPUS:85114153772
SN - 0006-3223
VL - 91
SP - 478
EP - 487
JO - Biological Psychiatry
JF - Biological Psychiatry
IS - 5
ER -