4.6 Article

Poor sleep correlates with biomarkers of neurodegeneration in mild traumatic brain injury patients: a CENC study

期刊

SLEEP
卷 44, 期 6, 页码 -

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/sleep/zsaa272

关键词

traumatic brain injury; sleep disorders; military health; dementia; neurofilament; tau; amyloid

资金

  1. U.S. Army Medical Research and Material Command, Department of Defense, Chronic Effects of Neurotrauma Consortium (CENC) [W81XWH-13-2-0095]
  2. Department of Veterans Affairs CENC Award [I01 CX001135]
  3. VHA Central Office VA TBI Model Systems Program of Research/DHA Contracting Office (CO-NCR) [W91YTZ-13-C-0015/HT0014-19-C-0004, HT0014]

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This study found that poor sleep quality in patients with mild traumatic brain injury was associated with higher levels of neurodegeneration markers and lower cognitive function. Poor sleep quality may be related to the risk of obstructive sleep apnea.
Study Objectives: Sleep disorders affect over half of mild traumatic brain injury (mTBI) patients. Despite evidence linking sleep and neurodegeneration, longitudinal TBI-related dementia studies have not considered sleep. We hypothesized that poor sleepers with mTBI would have elevated markers of neurodegeneration and lower cognitive function compared to mTBI good sleepers and controls. Our objective was to compare biomarkers of neurodegeneration and cognitive function with sleep quality in warfighters with chronic mTBI. Methods: In an observational warfighters cohort (n = 138 mTBI, 44 controls), the Pittsburgh Sleep Quality Index (PSQI) was compared with plasma biomarkers of neurodegeneration and cognitive scores collected an average of 8 years after injury. Results: In the mTBI cohort, poor sleepers (PSQI >= 10, n = 86) had elevated plasma neurofilament light (NfL, (x) over bar = 11.86 vs 7.91 pg/mL, p = 0.0007, d = 0.63) and lower executive function scores by the categorical fluency ((x) over bar = 18.0 vs 21.0, p = 0.0005, d = -0.65) and stop-go tests ((x) over bar = 30.1 vs 31.1, p = 0.024, d = -0.37). These findings were not observed in controls (n = 44). PSQI predicted NfL (beta = 0.22, p = 0.00002) and tau (beta = 0.14, p = 0.007), but not amyloid beta 42. Poor sleepers showed higher obstructive sleep apnea (OSA) risk by STOP-BANG scores ((x) over bar = 3.8 vs 2.7, p = 0.0005), raising the possibility that the PSQI might be partly secondary to OSA. Conclusions: Poor sleep is linked to neurodegeneration and select measures of executive function in mTBI patients. This supports implementation of validated sleep measures in longitudinal studies investigating pathobiological mechanisms of TBI related neurodegeneration, which could have therapeutic implications.

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