Skip to Main Content
 

Global Search Box

 
 
 
 

ETD Abstract Container

Abstract Header

Understanding a Low Back Pain Pathway: Utilizing MRI and MRS to Link Pain Due to Muscle Inflammation to Changes in Brain Metabolites

Kotowski, Susan E.

Abstract Details

2009, PhD, University of Cincinnati, Medicine : Environmental Health.
Low back pain (LBP) has been described as one of the most prevalent and significant musculoskeletal problems, with upwards of 85% of the population experiencing LBP at some point in their life. Of those experiencing LBP, up to 85% will not receive a definitive diagnoses as to the cause of the pain. Although a number of known injury sites exist within the low back, because of the ongoing occurrence of LBP, other injury mechanisms must still exist. Complicating pain is the fact that there are several pain pathways as well as there are no objective measures of pain. Recently, it has been shown that exercise induced muscle inflammation, which causes pain, can be analyzed using magnetic resonance imaging (MRI). In addition, magnetic resonance spectroscopy (MRS) has been shown to be able to detect changes in the chemicals in the brain, which are known to respond to painful stimuli. Given these two factors, the goal of this study was to identify whether inflammation in the low back musculature (measured using MRI) could be linked with metabolite changes in the brain known to respond to pain (measured with MRS). Ten healthy subjects (5 males and 5 females) underwent baseline lumbar and brain scans and then completed a lifting and lowering designed to produce inflammation in the erector spinae muscles. Subjects were asked to lift a 9.1 kg carton 8 times per minute until they could no longer do so. Following completion of the lifting task, subjects underwent another lumbar and brain scan. Twenty-four hours later a final lumbar and brain scan series was completed. Subjective ratings of perceived exertion and pain levels were also collected at baseline, immediately following the lifting task, and 24-hours after completing the task. T2 maps were used to analyze muscle inflammation. In an unexpected finding, T2 relaxation times actually decreased significantly following the completion of the lifting task. Glutamate and glutamine, pain markers, were not elevated based on the MRS analysis even though subjective pain ratings were moderate at completion of the task. Twenty-four hours following the lifting task T2 relaxation times were significantly elevated above baseline values, which correlated with subjective pain ratings, which remained elevated. However, no significant changes MRS pain markers were detected. Limitations included a small sample size, limited ability to identify the temporal nature of inflammation and pain, and the use of only healthy subjects. While a definitive link between muscle inflammation and brain response could not be proven, the study did provided some interesting insights for future work.
Kermit Davis, PhD (Committee Chair)
Lisa Lemen, PhD (Committee Member)
Kim Cecil, PhD (Committee Member)
96 p.

Recommended Citations

Citations

  • Kotowski, S. E. (2009). Understanding a Low Back Pain Pathway: Utilizing MRI and MRS to Link Pain Due to Muscle Inflammation to Changes in Brain Metabolites [Doctoral dissertation, University of Cincinnati]. OhioLINK Electronic Theses and Dissertations Center. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1243367529

    APA Style (7th edition)

  • Kotowski, Susan. Understanding a Low Back Pain Pathway: Utilizing MRI and MRS to Link Pain Due to Muscle Inflammation to Changes in Brain Metabolites. 2009. University of Cincinnati, Doctoral dissertation. OhioLINK Electronic Theses and Dissertations Center, http://rave.ohiolink.edu/etdc/view?acc_num=ucin1243367529.

    MLA Style (8th edition)

  • Kotowski, Susan. "Understanding a Low Back Pain Pathway: Utilizing MRI and MRS to Link Pain Due to Muscle Inflammation to Changes in Brain Metabolites." Doctoral dissertation, University of Cincinnati, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1243367529

    Chicago Manual of Style (17th edition)