It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
Humans are exposed to extreme environmental stressors during spaceflight and return with alterations in brain structure and shifts in intracranial fluids. To date, no studies have evaluated the effects of spaceflight on perivascular spaces (PVSs) within the brain, which are believed to facilitate fluid drainage and brain homeostasis. Here, we examined how the number and morphology of magnetic resonance imaging (MRI)-visible PVSs are affected by spaceflight, including prior spaceflight experience. Fifteen astronauts underwent six T1-weighted 3 T MRI scans, twice prior to launch and four times following their return to Earth after ~ 6-month missions to the International Space Station. White matter MRI-visible PVS number and morphology were calculated using an established, automated segmentation algorithm. We validated our automated segmentation algorithm by comparing algorithm PVS counts with those identified by two trained raters in 50 randomly selected slices from this cohort; the automated algorithm performed similarly to visual ratings (r(48) = 0.77, p < 0.001). In addition, we found high reliability for four of five PVS metrics across the two pre-flight time points and across the four control time points (ICC(3,k) > 0.50). Among the astronaut cohort, we found that novice astronauts showed an increase in total PVS volume from pre- to post-flight, whereas experienced crewmembers did not (p = 0.020), suggesting that experienced astronauts may exhibit holdover effects from prior spaceflight(s). Greater pre-flight PVS load was associated with more prior flight experience (r = 0.60–0.71), though these relationships did not reach statistical significance (p > 0.05). Pre- to post-flight changes in ventricular volume were not significantly associated with changes in PVS characteristics, and the presence of spaceflight associated neuro-ocular syndrome (SANS) was not associated with PVS number or morphology. Together, these findings demonstrate that PVSs can be consistently identified on T1-weighted MRI scans, and that spaceflight is associated with PVS changes. Specifically, prior spaceflight experience may be an important factor in determining PVS characteristics.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
1 University of Florida, Department of Applied Physiology and Kinesiology, Gainesville, USA (GRID:grid.15276.37) (ISNI:0000 0004 1936 8091)
2 Oregon Health and Science University, Layton-NIA Oregon Aging and Alzheimer’s Disease Research Center, Department of Neurology, Portland, USA (GRID:grid.5288.7) (ISNI:0000 0000 9758 5690); Oregon Health and Science University, Advanced Imaging Research Center, Portland, USA (GRID:grid.5288.7) (ISNI:0000 0000 9758 5690)
3 Oregon Health and Science University, Division of Child Neurology, Department of Pediatrics, Doernbecher Children’s Hospital, Portland, USA (GRID:grid.5288.7) (ISNI:0000 0000 9758 5690)
4 KBR, Houston, USA (GRID:grid.481680.3) (ISNI:0000 0004 0634 8729)
5 University of Texas Health Science Center at Houston, Department of Diagnostic and Interventional Imaging, Houston, USA (GRID:grid.267308.8) (ISNI:0000 0000 9206 2401)
6 NASA Johnson Space Center, Houston, USA (GRID:grid.419085.1) (ISNI:0000 0004 0613 2864)
7 Oregon Health and Science University, Layton-NIA Oregon Aging and Alzheimer’s Disease Research Center, Department of Neurology, Portland, USA (GRID:grid.5288.7) (ISNI:0000 0000 9758 5690); Veteran’s Affairs Portland Health Care System, Neurology, Portland, USA (GRID:grid.484322.b)
8 University of Washington School of Medicine, Department of Psychiatry and Behavioral Sciences, Seattle, USA (GRID:grid.34477.33) (ISNI:0000000122986657); University of Washington School of Medicine, Department of Neurology, Seattle, USA (GRID:grid.34477.33) (ISNI:0000000122986657); VA Puget Sound Health Care System, VISN 20 Mental Illness Research, Education and Clinical Center (MIRECC), Seattle, USA (GRID:grid.413919.7) (ISNI:0000 0004 0420 6540)
9 University of Florida, Department of Applied Physiology and Kinesiology, Gainesville, USA (GRID:grid.15276.37) (ISNI:0000 0004 1936 8091); University of Florida, Norman Fixel Institute for Neurological Diseases, Gainesville, USA (GRID:grid.15276.37) (ISNI:0000 0004 1936 8091)




