Menu

 

The NASA Task Book
Advanced Search     

Project Title:  Potential Subclinical Neurologic Changes in Astronauts Due to Repeated Hypobaric Exposures Reduce
Fiscal Year: FY 2015 
Division: Human Research 
Research Discipline/Element:
HRP HHC:Human Health Countermeasures
Start Date: 09/20/2014  
End Date: 07/31/2015  
Task Last Updated: 05/24/2016 
Download report in PDF pdf
Principal Investigator/Affiliation:   Sherman, Paul  M.D. / United States Air Force 
Address:  Director of Neuroimaging Research at USAF School of Aerospace Medicine 
2200 Bergquist Drive, Ste 1 
Lackland AFB , TX 78236 
Email: paul.sherman@us.af.mil 
Phone: (210) 292-0494  
Congressional District: 20 
Web:  
Organization Type: GOVERNMENT 
Organization Name: United States Air Force 
Joint Agency:  
Comments:  
Co-Investigator(s)
Affiliation: 
McGuire, Steven  M.D. United States Air Force 
Norcross, Jason  M.S. Wyle Science, Technology and Engineering Group 
Project Information: Grant/Contract No. Directed Research 
Responsible Center: NASA JSC 
Grant Monitor: Norsk, Peter  
Center Contact:  
Peter.norsk@nasa.gov 
Unique ID: 10389 
Solicitation / Funding Source: Directed Research 
Grant/Contract No.: Directed Research 
Project Type: GROUND 
Flight Program:  
TechPort: No 
No. of Post Docs:  
No. of PhD Candidates:  
No. of Master's Candidates:  
No. of Bachelor's Candidates:  
No. of PhD Degrees:  
No. of Master's Degrees:  
No. of Bachelor's Degrees:  
Human Research Program Elements: (1) HHC:Human Health Countermeasures
Human Research Program Risks: (1) DCS:Risk of Decompression Sickness [inactive]
Human Research Program Gaps: (1) DCS7:We have not validated procedures to adequately treat DCS in the spaceflight environment should it occur.
Flight Assignment/Project Notes: NOTE: Change in start date to reflect start of the project, per CoI J. Norcross (Ed., 5/23/16)

Task Description: Recent evidence has revealed that neurologic changes occur due to repeated hypobaric exposures. Specifically, the US Air Force (USAF) has reported an increased number and increased total volume of white matter hyperintensities (WMH) on MRI (magnetic resonance imaging) in high-altitude pilots. This is important because WMH on MRI are indicators of neurocognitive changes including decreased cognitive speed and dementia. These pilots are exposed to similar occupational environmental conditions as astronauts and those who display these WMH changes also suffer from acute neurocognitive deficits as a result of hypobaric conditions. WMH changes and neurocognitive deficits in USAF pilots have been found to be independent of clinical symptoms. Pilots with an increased number of WMH on MRI and neurocognitive deficits due to hypobaric exposure have been found in both those who deny any clinical symptoms of decompression sickness (DCS) as well as those pilots with DCS.

The goal of this data mining effort is to identify if any evidence of this potential risk exists in the NASA astronaut population. Our central hypothesis is that NASA has successfully mitigated this potential threat of subclinical neurologic DCS linked to WMH and neurocognitive deficits in past and present missions but may encounter it in the future. We have based this hypothesis on the fact that NASA has no reported incidents of DCS during operational EVAs (extravehicular activity) and no apparent signs of neurocognitive deficits amongst its astronauts. However, NASA plans on increasing the number of hypobaric exposures of its astronauts by several orders of magnitude in the future. Successful completion of this data mining effort will enable NASA to make an informed decision on the need for proper mission monitoring and occupational surveillance for past, present, and future astronauts.

Aims:

Aim #1: Determine if cumulative hypobaric exposures including EVAs are a risk factor for WMH increase on MRI amongst NASA astronauts during past operations. Hypothesis: NASA's risk-mitigation measures sufficiently minimize the risk of DCS over repeated hypobaric exposures. We will execute a retrospective study on existing MRIs of astronauts' brains compared with those of USAF U-2 pilots, hypobaric technicians, and an age-, health-, and intelligence-matched control population.

Aim #2: Develop new measures to estimate the future risk of DCS for astronauts and missions based on newly revealed data of subclinical neurologic DCS. Hypothesis: NASA is underestimating the risk of subclinical DCS for future astronauts and missions because of the paucity of clinical DCS during past operations. We will estimate the risk of subclinical DCS effects based on the current evidence, the anticipated increase in projected number, time, and frequency of EVAs per astronaut and a prolonged hypobaric exposure based on the ambient environment of future expeditionary space vehicles.

Rationale for HRP Directed Research: This study is highly constrained research that is needed near term to help quantify the potential risk to the astronaut population and to ensure proper surveillance is initiated to quantify the risk in the future. This is a joint effort with the United States Air Force ensuring cost sharing of resources and neuroimaging analysis performed by the same personnel.

Research Impact/Earth Benefits: This study provides the first look into the presence of white matter hyperintensities in astronauts. Results of this study also indicate that hypobaric exposure may not be the only type of exposure that increases the likelihood of developing WMH on MRI.

Task Progress & Bibliography Information FY2015 
Task Progress: This feasibility study is complete. Results were presented internally within the Human Health and Performance Directorate and follow up work starting with a review of the pre-flight MRI has been initiated.

Initial incidence of WMH in astronauts was higher than other subjects groups including military high altitude pilots, military hypobaric chamber technicians, and an advanced degreed control group. This study only reviewed the last available post-flight MRI in a convenience sample of astronauts. Initial results do not indicate that EVA exposure is a primary explanatory variable for the presence of WMH on MRI.

Follow-up work will evaluate the pre-flight MRI and if evidence of an increase in WMH is linked to spaceflight exposure; then future data mining efforts looking for contributory variables will be explored. Also, determination of a functional consequence related to WMH on MRI will be explored.

Bibliography: Description: (Last Updated: 05/24/2016) 

Show Cumulative Bibliography
 
Abstracts for Journals and Proceedings Sherman, PM, McGuire S. "Subcortical white matter hyperintensity burden in astronauts." 86th Annual Scientific Meeting, Aerospace Medical Association, Lake Buena Vista, FL, May 10-14, 2015.

Aerospace Medicine and Human Performance. 2015 Mar;86(3):476. , Mar-2015

Project Title:  Potential Subclinical Neurologic Changes in Astronauts Due to Repeated Hypobaric Exposures Reduce
Fiscal Year: FY 2014 
Division: Human Research 
Research Discipline/Element:
HRP HHC:Human Health Countermeasures
Start Date: 09/20/2014  
End Date: 07/31/2015  
Task Last Updated: 07/06/2015 
Download report in PDF pdf
Principal Investigator/Affiliation:   Sherman, Paul  M.D. / United States Air Force 
Address:  Director of Neuroimaging Research at USAF School of Aerospace Medicine 
2200 Bergquist Drive, Ste 1 
Lackland AFB , TX 78236 
Email: paul.sherman@us.af.mil 
Phone: (210) 292-0494  
Congressional District: 20 
Web:  
Organization Type: GOVERNMENT 
Organization Name: United States Air Force 
Joint Agency:  
Comments:  
Co-Investigator(s)
Affiliation: 
McGuire, Steven  M.D. United States Air Force 
Norcross, Jason  M.S. Wyle Science, Technology and Engineering Group 
Project Information: Grant/Contract No. Directed Research 
Responsible Center: NASA JSC 
Grant Monitor: Norsk, Peter  
Center Contact:  
Peter.norsk@nasa.gov 
Unique ID: 10389 
Solicitation / Funding Source: Directed Research 
Grant/Contract No.: Directed Research 
Project Type: GROUND 
Flight Program:  
TechPort: No 
No. of Post Docs:  
No. of PhD Candidates:  
No. of Master's Candidates:  
No. of Bachelor's Candidates:  
No. of PhD Degrees:  
No. of Master's Degrees:  
No. of Bachelor's Degrees:  
Human Research Program Elements: (1) HHC:Human Health Countermeasures
Human Research Program Risks: (1) DCS:Risk of Decompression Sickness [inactive]
Human Research Program Gaps: (1) DCS7:We have not validated procedures to adequately treat DCS in the spaceflight environment should it occur.
Flight Assignment/Project Notes: NOTE: Change in start date to reflect start of the project, per CoI J. Norcross (Ed., 5/23/16)

Task Description: Recent evidence has revealed that neurologic changes occur due to repeated hypobaric exposures. Specifically, the US Air Force (USAF) has reported an increased number and increased total volume of white matter hyperintensities (WMH) on MRI (magnetic resonance imaging) in high-altitude pilots. This is important because WMH on MRI are indicators of neurocognitive changes including decreased cognitive speed and dementia. These pilots are exposed to similar occupational environmental conditions as astronauts and those who display these WMH changes also suffer from acute neurocognitive deficits as a result of hypobaric conditions. WMH changes and neurocognitive deficits in USAF pilots have been found to be independent of clinical symptoms. Pilots with an increased number of WMH on MRI and neurocognitive deficits due to hypobaric exposure have been found in both those who deny any clinical symptoms of decompression sickness (DCS) as well as those pilots with DCS.

The goal of this data mining effort is to identify if any evidence of this potential risk exists in the NASA astronaut population. Our central hypothesis is that NASA has successfully mitigated this potential threat of subclinical neurologic DCS linked to WMH and neurocognitive deficits in past and present missions but may encounter it in the future. We have based this hypothesis on the fact that NASA has no reported incidents of DCS during operational EVAs (extravehicular activity) and no apparent signs of neurocognitive deficits amongst its astronauts. However, NASA plans on increasing the number of hypobaric exposures of its astronauts by several orders of magnitude in the future. Successful completion of this data mining effort will enable NASA to make an informed decision on the need for proper mission monitoring and occupational surveillance for past, present, and future astronauts.

Aims:

Aim #1: Determine if cumulative hypobaric exposures including EVAs are a risk factor for WMH increase on MRI amongst NASA astronauts during past operations. Hypothesis: NASA's risk-mitigation measures sufficiently minimize the risk of DCS over repeated hypobaric exposures. We will execute a retrospective study on existing MRIs of astronauts' brains compared with those of USAF U-2 pilots, hypobaric technicians, and an age-, health-, and intelligence-matched control population.

Aim #2: Develop new measures to estimate the future risk of DCS for astronauts and missions based on newly revealed data of subclinical neurologic DCS. Hypothesis: NASA is underestimating the risk of subclinical DCS for future astronauts and missions because of the paucity of clinical DCS during past operations. We will estimate the risk of subclinical DCS effects based on the current evidence, the anticipated increase in projected number, time, and frequency of EVAs per astronaut and a prolonged hypobaric exposure based on the ambient environment of future expeditionary space vehicles.

Rationale for HRP Directed Research: This study is highly constrained research that is needed near term to help quantify the potential risk to the astronaut population and to ensure proper surveillance is initiated to quantify the risk in the future. This is a joint effort with the United States Air Force ensuring cost sharing of resources and neuroimaging analysis performed by the same personnel.

Research Impact/Earth Benefits:

Task Progress & Bibliography Information FY2014 
Task Progress: New project for FY2015.

Bibliography: Description: (Last Updated: 05/24/2016) 

Show Cumulative Bibliography
 
 None in FY 2014