A teljes test rezgésének munkavégzési expozíciója az Egyesült Államok katonai veteránjai körében: akut és krónikus hozzájárulás az izületi és mozgásszervi rendellenességekhez és a gerincközelben jelentkező fájdalomhoz

Musculoskeletal (MSK) disorders and spine-related pain are major health concerns among veterans. Low back pain is the most common chronic pain condition among Veterans, contributing significantly to healthcare utilization and rising treatment costs within the Veteran's Health Administration (VHA). As VHA community care expenditures more than doubled between 2017 and 2021, the growing demand for chronic pain services underscores the need for improved understanding of the mechanisms that contribute to spine degeneration in this population. There is evidence that occupational exposure to whole body vibration (WBV) is associated with an increased risk for a multitude of negative health outcomes, including MSK pain in the back and neck. However, despite extensive research on low back pain etiology and disc degeneration, major gaps persist around early detection of endplate degeneration and the impact of acute or chronic WBV exposure on IVD health.

The ubiquitous nature of low back pain in the general public but especially in veterans shows that there is a strong medical need for better understanding of the biomechanics of spine health. This study can help clinical practice by identifying early detection biomarkers with non-invasive MRI techniques and to investigate hydration as a protective mechanism.

The problem of low back pain and spine health is especially relevant within veterans because while service members are generally healthier than the typical U.S. adult of similar age at the time they enter service (because of rigorous physical and mental screening requirements to join the military, continued fitness standards, and access to comprehensive healthcare), research has shown that Veterans have poorer overall health-related quality of life than nonveterans and a high prevalence of back pain-related conditions. Veterans have often been exposed to WBV during their military career while in armored or heavy vehicles or in aircraft. Many veterans also continue to be exposed to WBV in their post-military careers with 28.5% working in natural resources, construction and maintenance or production, transportation and material moving. These jobs and many others may expose workers to WBV while operating vehicles (trucks, construction and heavy machinery), or operating tools where the vibrational amplitude is large enough to transmit to the body. These WBV exposures during their military career and post military career carries an increased risk of negative health outcomes including MSK pain in the back and neck.

While we know that many veterans are exposed to these conditions and they are associated with an increased risk of MSK pain, understanding the biomechanics will help understand how to prevent and treat those long term or chronic injuries. These are knowledge gaps that we have identified in relation to intervertebral disc health and exposure to WBV:

1. Segment- and region-specific disc fluid dynamics under WBV are poorly understood.

   While diurnal disc fluid migration patterns have been documented, the impact of acute or chronic WBV on nucleus pulposus and annulus fibrosis fluid distribution, especially across lumbar levels, remains unknown.

2. Early endplate degeneration cannot currently be detected noninvasively. Modic bone marrow changes observable with MRI lack sensitivity and reflect late-stage pathology. No clinical imaging method reliably identifies early degenerative alterations of the cartilaginous or bony endplates.

3. The relationship between endplate health and disc fluid transport under WBV exposure is unclear.

   Endplate degeneration likely disrupts regional fluid exchange and may drive segment-dependent susceptibility to WBV-induced disc injury.

4. No prior studies have integrated advanced quantitative MRI techniques to evaluate endplate perfusion, disc fluid movement, and WBV response.

Although dynamic contrast-enhanced MRI can measure endplate perfusion, concerns about gadolinium retention limit its use. Non-contrast alternatives such as arterial spin labeling (ASL) have not been applied to endplate assessment.

This study will address those gaps by combining multi-parametric MRI and groups selected for both acute and longitudinal occupational exposure to WBV to evaluate IVD fluid transport and endplate health. By addressing these gaps, this study will advance understanding of the biomechanical and physiological impacts of WBV on spine health.

We seek to understand the connection between WBV exposure and spine health by comparing groups of veterans with history of or ongoing exposure to WBV and using advanced MRI techniques to study intervertebral disc (IVD) and vertebral endplate health. We also seek to study the acute changes in IVD and vertebral endplate biology before and after exposure to WBV and whether individual hydration state influences IVD water dynamics.

The specific aims are:

Aim 1: Determine the impact of acute and longitudinal WBV on lumbar spine endplate health.

Aim 2: Determine how segmental lumbar and regional IVD fluid distribution and transport are acutely affected by WBV and determine if there are correlations with endplate health.

Aim 3: Determine whether individual hydration state influences IVD water dynamics following acute vibrational exposure.

We hypothesize the following

Specific Aim 1 Hypothesis 1: Multi-parametric MRI will reveal Veterans with previous military WBV exposure have more degenerative endplate markers when compared to Veterans with no occupational WBV exposure.

Hypothesis 2: Multi-parametric MRI in Veterans with current occupational exposure to WBV, but with no previous military WBV exposure, will have earlier expression of degenerative endplate markers when compared to Veterans with no WBV exposure.

Hypothesis 3: The rate of change for degenerative endplate markers over the four-year duration of the study will be greater for Veterans with current occupational WBV exposure than for Veterans that had previous military occupational WBV exposure.

Specific Aim 2 Hypothesis 1: Veterans who routinely experience occupational WBV will exhibit less IVD regional fluid distribution before and after experimental WBV, while those without daily WBV will have greater changes in IVD regional fluid distribution following experimental WBV, with water moving from the NP into the AF or out of the disc.

Hypothesis 2: Veterans who routinely experience occupational WBV will exhibit a cranial to caudal decrease in water transport as well as a decrease in baseline water distribution.

Hypothesis 3: Degenerative endplate health will be correlated with decreased lumbar spine water distribution and transport.

Specific Aim 3 Hypothesis 1: Participants in a low-hydration state will exhibit a larger reduction in intervertebral disc (IVD) water content and altered fluid-transport metrics after 30 minutes of controlled seated vibration than participants in a normal/high-hydration state.

This research is relevant to the VA due to approximately 50% of veterans experiencing chronic pain with lower back pain being the most common type of chronic pain. This is one of the most common reasons for seeking care within the VHA and this creates a significant financial burden on the Veterans Health Administration. There is also data that shows despite service members being generally healthier than the typical U.S. adult when entering service, there is a high incidence of lower back pain among service members and that veterans have poorer overall health related quality of life than non-veterans. Occupational exposure to vibration is associated with an increased risk for a multitude of negative health outcomes, including MSK pain in the back and neck.

Study Design:

This study will investigate acute and chronic effects of occupational whole-body vibration on the health of lumbar spine endplates and intervertebral discs by studying Veterans that had occupational exposure to WBV in their military occupation and Veterans with current civilian occupations that involve WBV. The approximate study timeline, as outlined in the grant proposal, is shown below. Lumbar spine endplate characteristics and intervertebral disc perfusion and hydration in both study groups will be compared to age- and sex-matched Veteran controls with no history of occupational WBV. The volunteer population will be chosen to represent the ethnic and sex distribution of the Zablocki Veterans Affairs Medical Center patient population. Current and military occupations will be selected to maximize consistency in WBV characteristics. For example, the ZVAMC patient population includes both truck drivers and heavy equipment operators. However, given that the WBV characteristics (e.g., frequency and magnitude of vibration) between those occupations are different, which will likely have different acute and chronic effects on the spine, preference in the research population be given to maximize consistency in the WBV environment across the research subject population. We will follow a similar procedure for choosing Veterans with military occupational WBV. Occupations unique to the military, such as helicopter aircrew, will be given priority although other occupations such as truck drivers, etc. will be targeted if we are not able to enroll Veterans with previous military helicopter occupation in sufficient numbers. The initial questionnaire will also include the Oswestry Disability Index (ODI), which will provide information on the impact of low back pain for each prospective subject's daily activities and function. The ODI will also be used in the selection of subjects for the MRI arm of the study to ensure a consistent sample. All interested Veterans will be consented and enrolled into the study prior to the pre-screening interview and Veterans that fit into the selected groups for the MRI study will receive a separate invitation to participate in that arm of the study. The five groups of Veterans that will be required to complete this study are described below.

• Current WBV Group (Group 1) will consist of Veterans with no history of active duty occupational WBV exposure, but with civilian occupational WBV exposure as a Veteran. These individuals will be less than 45 years old and have less than 5 years of civilian occupational WBV exposure. This group will demonstrate the effects of civilian occupational WBV exposure on endplate degeneration, IVD fluid dynamics, and spine structural degeneration metrics. Three multi-parametric MRI scans obtained over the course of this four-year protocol (aim 1) will allow for tracking of endplate health and identification of progressive changes in spine structural characteristics such as lumbar Cobb angle, disc/foraminal dimensions, endplate degeneration, and intervertebral disc perfusion and hydration. These changes will be correlated with WBV logs maintained by each enrolled subject that will provide weekly estimates of the type and duration of occupational exposure over the duration of the study. An experimental acute WBV protocol (aim 2) will outline the acute response of the lumbar spine endplates and intervertebral discs to WBV This protocol will consist of a baseline upright MRI scan in the morning, 30 minutes of experimental WBV, and a second post-WBV upright MRI scan in the afternoon. Subjects will be selected for participation in the MRI arm of the study to ensure consistency in occupational WBV characteristics (e.g., heavy equipment operators versus long haul truck drivers) and duration of occupation to reduce the variability in ongoing occupational WBV that may influence the current spine health at the time of enrollment
• Military WBV Group (Group 2) will consist of Veterans with at least 6 years of active duty WBV exposure (ex. heavy equipment operators, helicopter pilots, small watercraft operators). These individuals will be less than 45 years old and have no civilian occupational exposure to WBV. This group will undergo two series of supine multi-parametric MRI scans at the beginning and end of the study (aim 1) and the experimental acute WBV protocol as described above (aim 2). Our pre-screening process will allow us to select a group of individuals that had similar active duty WBV characteristics in terms of type and duration of occupation. Subjects will be selected for participation in the MRI arm of the study to ensure consistency in Military WBV characteristics (e.g., helicopter pilots versus fast boat drivers) and duration of military occupation to reduce the variability in WBV history that may influence the current spine health at the time of enrollment.
• No WBV Group (Control Group) (Group 3) will consist of Veterans with no history of active duty or civilian occupational exposure to WBV. These individuals will be age and sex matched with Current WBV and Military WBV Groups and will not experience any fluid restriction. This group will undergo the same procedures as the Current WBV Group, including three multi-parametric MRI scans (aim 1) and one exposure to the acute WBV protocol (aim 2).
• Hydrated Group (Group 4). The No WBV Group from aims 1 and 2 of the study will participate in aim 3, participating in multi-parametric MRI scans in both a well hydrated state and a dehydrated state. A 3-day fluid log will be maintained following consent to provide a fluid intake baseline. The 3 days prior to their arrival participants will be asked to consume at least 2.7 liters (11 cups) of fluids per day for female participants, and at least 3.7 liters (16 cups) for male participants. Hydration status will be confirmed with measurements of urine specific gravity values less than 1.010. The day prior to multi-parametric MRI scanning, participants will be asked to refrain from rigorous exercise. This group will participate in the Hydrated MRI protocol during Year 3 of the study.
• Dehydrated Group (Group 5). The No WBV Group from aims 1 and 2 of the study will participate in aim 3, participating in multi-parametric MRI scans in both a well hydrated state and a dehydrated state. A 3-day fluid log will be maintained following consent to provide a fluid intake baseline. The 3 days prior to their arrival participants will be asked to consume about 1.3 liters (5.5 cups) of fluids per day for female participants, and about 1.8 liters (8 cups) for male participants. Hydration status will be confirmed with measurements of urine specific gravity values greater than 1.020. The day prior to multi-parametric MRI scanning, participants will be asked to refrain from rigorous exercise. This group will participate in the Dehydrated MRI protocol during Year 4 of the study.

Veterans selected for the MRI arm of the study will be informed of this decision via a letter that will describe their study group, the MRI procedures in which they will be asked to participate, their study-specific subject number, and their stipend for participation. They must then agree to participate by signing and returning an included consent form to the study team. After they have agreed to participate in the MRI arm of the study, a study team member will work with them to schedule their MRI scan(s) at either MCW Center for Imaging Research (supine scans) or Upright MRI of Deerfield (Upright scans), depending on their study group. Veterans will then be provided with information on the date/time of their scan, when to arrive, facility and parking locations (including map), how long the scan will take, what they should wear, and any fluid restrictions if necessary. They will be informed that a study team member will meet them at the scan location, prior to their scan, and will guide them through the process. Veterans will also be informed that they have been given a study-specific de-identified subject number to ensure their privacy and that they can use that number to identify themselves the study team member and the MRI facility upon arrival.

Veterans will be responsible for their own transport to the MRI facility. Upon arrival, they will be met at the facility by a study team member. The study team member will confirm their study-specific subject number, describe the procedures that will occur, how long the entire process will take, and answer any questions that the Veteran may have. Veterans will be asked to arrive at the MRI facility approximately 30 minutes prior to their MRI scan time. If the Veteran is not wearing MRI appropriate clothing, they will be guided to a changing room where they can change into scrubs provided by the facility. Prior to scanning, Veterans will be asked to fill out an MRI screening form that will ask MRI-relevant questions regarding implants and medical conditions. The MRI screening form is included as a part of this IRB submission.

Each MRI scan will last no more than 60 minutes. Participation in Aim 1 will include a total of three MRI scans; the first MRI scan in Year 1 of the study, the second in Years 2 or 3, and the third in year 4. Participation in Aims 2 and 3 will include 2 MRI scans and one whole body vibration protocol on the same day. The whole body vibration protocol will consist of the following. Acute whole body vibration will be delivered through a low backed chair mounted on a controlled vibrating platform. Participants will experience a 30-minute vertical vibration session of 5 Hz with a peak-to-peak amplitude of 3 mm, and a peak acceleration of 2 m/s2. This exposure was used previously, determined to be safe for participants, and was shown to have a measurable effect on diurnal height changes [Sullivan Spine 1990].

Urine samples will be collected prior to MRI scans for Hydrated and Dehydrated groups in Aim 3. Upon arrival at the MRI facility, each subject will be provided with a urine collection container by the Study Team member, who will describe the "clean-catch" method for collection. That method involves starting to urinate, stopping, collecting urine mid-stream in the container, then finishing urination in the toilet. The subject will then give the contained back to the Study Team member, who will place it in a refrigerated container. Following the MRI scan, the Study Team member will return the same to our labs at the ZVAMC and analyze specific gravity of the sample using a refractometer.

Recruitment Aim 1 has a total of 3 experimental groups (Current WBV, Military WBV, and No WBV), and three MRIs per subject. 39 subjects (13 per group) are required, who will undergo a total of 117 supine MRIs.

Aim 2 has a total of 3 experimental groups (Current WBV, Military WBV, and No WBV), and two upright MRIs per subject. 39 subjects (13 per group) are required, for a total of 78 upright MRIs. However we feel that the effect size for this experiment will be higher than the effect size in the preliminary data since the proposed experiment will measure acute mechanically-induced changes in disc hydration following WBV, whereas groupwise differences in our preliminary data were the result of chronic degenerative changes in disc hydration.

Therefore, we anticipate having the ability to detect statistically significant and appropriately powered groupwise differences during this experiment, even with smaller group sizes.

Aim 3 has a total of 2 experimental groups (hydrated and dehydrated), and two MRIs per subject. 34 subjects (17 per group) are required, who will undergo a total of 68 MRIs.

Potential research subjects will be identified using VA Informatics and Computing Infrastructure (VINCI). All potential subjects will be notified via letter that they meet the preliminary requirements for inclusion in a research study being conducted by Investigators at the ZVAMC. They will be asked to respond via telephone or email if interested and notified that we will follow up with a phone call approximately two weeks after the date of the letter to confirm whether they would like to participate. This protocol is common for other human studies at ZVAMC and has been in use by our Translational Research Unit (TRU) for years. All interested Veterans will be interviewed at a time of their choosing via telephone or in person interviews to determine their suitability for inclusion in this study.

Veterans that consent for initial enrollment will be provided with baseline questionnaires about military service, current and prior whole body vibration exposure, pain intensity, pain-related disability, and modifiers of pain, using the questionnaires listed below. Study team members will review the list of Veterans that have agreed to the initial enrollment on an ongoing basis. We will stop enrolling new subjects when we have obtained a sufficient number for matched cohorts for each experimental group based on similarity in age, whole body vibration characteristics, and pain profile.

Subjects from each matched cohort will be asked to participate in Aims 1 and 2 (Groups 1, 2, and 3) or Aim 3 (additional Group 3 enrollment). Aims 1 and 2 will enroll 39 subjects (13 per group for Groups 1, 2, and 3) that will receive a total of 5 MRI scans (3 at MCW and 2 at Upright MRI of Deerfield). Aim 3 will enroll an additional 34 subjects (17 per group x 2 groups) that will each receive 2 MRI scans at MCW. This will result in a minimum of 73 ZVAMC Veterans (13 per group x 3 groups for Aims 1 and 2; 17 per group x 2 groups for Aim 3) enrolled in the study. However, we anticipate that some subjects may not be willing to participate in multiple arms of the study. Since each Aim includes repeated measurements so that subjects can be used as their own controls, the study protocol will allow for separate cohorts of Veterans to be enrolled in each Aim. Therefore, the maximum enrollment for the study, if we had separate cohorts for each Aim, would be 112 Veterans (39 for Aim 1, 39 for Aim 2, 34 for Aim 3).