Disorientation effects, circulating small ribonucleic acid, and genetic susceptibility on static postural stability

Background: Motion Sickness increases risk of performance deficits and safety of flight concerns. The etiology of motion sickness is poorly understood. Here, we attempted to quantify the physiological effects of motion sickness on static balance and determine the genetic predictors associated with t...

Full description

Bibliographic Details
Main Authors: Ashley Turner, Michael Markey, Peter Le, Ali Reiter, Cyndy Cox, Stacy Simmons, M.B. Rao, Lorenna Altman, Kermit Davis, Dustin Huber, Jonathan S. Dufour, William Marras, Amit Bhattacharya
Format: Article
Language:English
Published: Elsevier 2023-03-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844023016201
_version_ 1797851755701075968
author Ashley Turner
Michael Markey
Peter Le
Ali Reiter
Cyndy Cox
Stacy Simmons
M.B. Rao
Lorenna Altman
Kermit Davis
Dustin Huber
Jonathan S. Dufour
William Marras
Amit Bhattacharya
author_facet Ashley Turner
Michael Markey
Peter Le
Ali Reiter
Cyndy Cox
Stacy Simmons
M.B. Rao
Lorenna Altman
Kermit Davis
Dustin Huber
Jonathan S. Dufour
William Marras
Amit Bhattacharya
author_sort Ashley Turner
collection DOAJ
description Background: Motion Sickness increases risk of performance deficits and safety of flight concerns. The etiology of motion sickness is poorly understood. Here, we attempted to quantify the physiological effects of motion sickness on static balance and determine the genetic predictors associated with these effects. Methods: 16 subjects underwent a disorientation stimulus to induce motion sickness. Motion sickness susceptibility was identified using the Motion Sickness Susceptibility Questionnaire. Postural balance outcomes were measured using two tasks, and small ribonucleic acid profiles were assessed with blood draws before motion sickness stimulus. Differences in postural sway before and after the stimulus as well as effect modification of susceptibility were assessed. A random forest followed by regression tree analysis was constructed for each postural sway variable to determine top genetic and covariate predictors. Findings: Significant differences existed in mean postural balance responses between before and after stimulus. Individuals with longer stimulus survival experienced a greater (but insignificant) perception of sway, even if not displaying increased sway for all conditions. Circulation small ribonucleic acids were differentially expressed between individuals with long and short stimulus survival, many of these microRNA have purported targets in genes related to vestibular disorders. Interpretation: We found motion sickness produces transient motor dysfunction in a healthy military population. Small ribonucleic acids were differentially expressed between subjects with long and short stimulus survival times.
first_indexed 2024-04-09T19:22:58Z
format Article
id doaj.art-04f13d17d65249a2957904693d36da15
institution Directory Open Access Journal
issn 2405-8440
language English
last_indexed 2024-04-09T19:22:58Z
publishDate 2023-03-01
publisher Elsevier
record_format Article
series Heliyon
spelling doaj.art-04f13d17d65249a2957904693d36da152023-04-05T08:25:22ZengElsevierHeliyon2405-84402023-03-0193e14413Disorientation effects, circulating small ribonucleic acid, and genetic susceptibility on static postural stabilityAshley Turner0Michael Markey1Peter Le2Ali Reiter3Cyndy Cox4Stacy Simmons5M.B. Rao6Lorenna Altman7Kermit Davis8Dustin Huber9Jonathan S. Dufour10William Marras11Amit Bhattacharya12Department of Environmental and Public Health Sciences, University of Cincinnati, Cincinnati, OH, USADepartment of Biochemistry and Molecular Biology, Wright State University, Dayton, OH, USA; Corresponding author. Center for Genomics Research, Department of Biochemistry and Molecular Biology, Wright State University, 3640 Colonel Glenn Hwy., Dayton, OH 45435-0001, USA.NAMRU-D and Air Force Research Laboratory, 711th Human Performance Wing, WPAFB, OH 45433, USADepartment of Biochemistry and Molecular Biology, Wright State University, Dayton, OH, USADepartment of Environmental and Public Health Sciences, University of Cincinnati, Cincinnati, OH, USADepartment of Biochemistry and Molecular Biology, Wright State University, Dayton, OH, USADepartment of Environmental and Public Health Sciences, University of Cincinnati, Cincinnati, OH, USADepartment of Environmental and Public Health Sciences, University of Cincinnati, Cincinnati, OH, USADepartment of Environmental and Public Health Sciences, University of Cincinnati, Cincinnati, OH, USANAMRU-D and Air Force Research Laboratory, 711th Human Performance Wing, WPAFB, OH 45433, USASpine Research Institute, The Ohio State University, Columbus, OH, USASpine Research Institute, The Ohio State University, Columbus, OH, USADepartment of Environmental and Public Health Sciences, University of Cincinnati, Cincinnati, OH, USABackground: Motion Sickness increases risk of performance deficits and safety of flight concerns. The etiology of motion sickness is poorly understood. Here, we attempted to quantify the physiological effects of motion sickness on static balance and determine the genetic predictors associated with these effects. Methods: 16 subjects underwent a disorientation stimulus to induce motion sickness. Motion sickness susceptibility was identified using the Motion Sickness Susceptibility Questionnaire. Postural balance outcomes were measured using two tasks, and small ribonucleic acid profiles were assessed with blood draws before motion sickness stimulus. Differences in postural sway before and after the stimulus as well as effect modification of susceptibility were assessed. A random forest followed by regression tree analysis was constructed for each postural sway variable to determine top genetic and covariate predictors. Findings: Significant differences existed in mean postural balance responses between before and after stimulus. Individuals with longer stimulus survival experienced a greater (but insignificant) perception of sway, even if not displaying increased sway for all conditions. Circulation small ribonucleic acids were differentially expressed between individuals with long and short stimulus survival, many of these microRNA have purported targets in genes related to vestibular disorders. Interpretation: We found motion sickness produces transient motor dysfunction in a healthy military population. Small ribonucleic acids were differentially expressed between subjects with long and short stimulus survival times.http://www.sciencedirect.com/science/article/pii/S2405844023016201Motion sicknessBalancemicroRNAMilitary
spellingShingle Ashley Turner
Michael Markey
Peter Le
Ali Reiter
Cyndy Cox
Stacy Simmons
M.B. Rao
Lorenna Altman
Kermit Davis
Dustin Huber
Jonathan S. Dufour
William Marras
Amit Bhattacharya
Disorientation effects, circulating small ribonucleic acid, and genetic susceptibility on static postural stability
Heliyon
Motion sickness
Balance
microRNA
Military
title Disorientation effects, circulating small ribonucleic acid, and genetic susceptibility on static postural stability
title_full Disorientation effects, circulating small ribonucleic acid, and genetic susceptibility on static postural stability
title_fullStr Disorientation effects, circulating small ribonucleic acid, and genetic susceptibility on static postural stability
title_full_unstemmed Disorientation effects, circulating small ribonucleic acid, and genetic susceptibility on static postural stability
title_short Disorientation effects, circulating small ribonucleic acid, and genetic susceptibility on static postural stability
title_sort disorientation effects circulating small ribonucleic acid and genetic susceptibility on static postural stability
topic Motion sickness
Balance
microRNA
Military
url http://www.sciencedirect.com/science/article/pii/S2405844023016201
work_keys_str_mv AT ashleyturner disorientationeffectscirculatingsmallribonucleicacidandgeneticsusceptibilityonstaticposturalstability
AT michaelmarkey disorientationeffectscirculatingsmallribonucleicacidandgeneticsusceptibilityonstaticposturalstability
AT peterle disorientationeffectscirculatingsmallribonucleicacidandgeneticsusceptibilityonstaticposturalstability
AT alireiter disorientationeffectscirculatingsmallribonucleicacidandgeneticsusceptibilityonstaticposturalstability
AT cyndycox disorientationeffectscirculatingsmallribonucleicacidandgeneticsusceptibilityonstaticposturalstability
AT stacysimmons disorientationeffectscirculatingsmallribonucleicacidandgeneticsusceptibilityonstaticposturalstability
AT mbrao disorientationeffectscirculatingsmallribonucleicacidandgeneticsusceptibilityonstaticposturalstability
AT lorennaaltman disorientationeffectscirculatingsmallribonucleicacidandgeneticsusceptibilityonstaticposturalstability
AT kermitdavis disorientationeffectscirculatingsmallribonucleicacidandgeneticsusceptibilityonstaticposturalstability
AT dustinhuber disorientationeffectscirculatingsmallribonucleicacidandgeneticsusceptibilityonstaticposturalstability
AT jonathansdufour disorientationeffectscirculatingsmallribonucleicacidandgeneticsusceptibilityonstaticposturalstability
AT williammarras disorientationeffectscirculatingsmallribonucleicacidandgeneticsusceptibilityonstaticposturalstability
AT amitbhattacharya disorientationeffectscirculatingsmallribonucleicacidandgeneticsusceptibilityonstaticposturalstability