Oxford Pain and Inflammation Helped by Spinal Manipulation

Pain and inflammation are known companions. Spinal manipulation has been used to decrease spine pain, back pain, neck pain, arm pain, and leg pain. New studies show that the effect of spinal manipulation may go beyond the spine to potentially mediate inflammation and its influence on spine pain. Satterwhite Chiropractic sees improvement in our spine pain patients on many fronts: pain reduction, function improvement, etc. The roles of inflammation in back pain and of spinal manipulation in decreasing that pain is core to the Oxford chiropractic treatment plan.

BIOMARKERS

Biomarkers are quantifiable indicators of body function via tests like blood pressure, urine testing, blood testing, imaging, etc. Biomarkers can signify normal and abnormal processes occurring in the body. In the area of back pain, researchers have been scrutinizing blood testable biomarkers like tumor necrosis factor (TNFα), interleukin-1 β (IL-1β), IL-6, IL-2, interferon (IFN), IL-1 receptor antagonist (IL-1RA), TNF soluble receptor type 2 (sTNFR2) and IL-10 to tell the story.  A recent biomarker test is brain imaging. What makes brain imaging interesting? Researchers recognize that chronic back pain surely changes the spine and suggest that it changes the brain structure. Brain imaging is a non-invasive biomarker capable of producing brain resting-state functional connectivity to analyze such alterations. (1) Researchers keep thinking up new tests! Satterwhite Chiropractic is observing these biomarker findings carefully.

BIOMARKER TESTING FOR BACK PAIN

As low back pain keeps dominating healthcare as one of the most significant contributors to disability around the globe, researchers are studying biomarkers and their role in low back pain. Researchers wanted to know if there was a contrast in the inflammatory profiles of nonspecific acute and chronic low back pain sufferers. They found a distinct difference in that there was a difference between pro-inflammatory and anti-inflammatory mediator levels leaning toward an overproduction of proinflammatory components in both types of patients. (2) Another report found that C-reactive protein in patients with acute non-specific low back pain and TNF-α in chronic non-specific low back pain patients were elevated. (3) These kinds of tests may help your Oxford chiropractor observe your back pain in a new way.

BIOMARKER TESTING OF BACK PAIN RESPONSE TO SPINAL MANIPULATION

The chiropractic treatment plan at Satterwhite Chiropractic currently heavily relies on gentle spinal manipulation to reduce pain. A blood test study for biomarkers taken at the beginning of and 2 weeks after such spinal manipulative treatment found significant (though limited and diverse) changes in the production of several biomarkers in acute and chronic back pain patients. Pain and disability scores dropped too. (4) These are encouraging findings for the implementation of spinal manipulation for back pain. Satterwhite Chiropractic is excited to see more information about biomarker-level changes with Oxford spinal manipulation!

CONTACT Satterwhite Chiropractic

Listen to this PODCAST with Dr. James Cox on The Back Doctors Podcast with Dr. Michael Johnson as he describes how use of chiropractic spinal manipulation and Cox® Technic Flexion Distraction may well go beyond pain relief.

Set up your Oxford chiropractic appointment today. Every day, pain and inflammation come to our clinic together. Our treatment helps decrease their influence on the lives of our Oxford chiropractic patients.

 
Satterwhite Chiropractic presents encouraging news about the influence of spinal manipulation may be shown via blood test biomarkers. 
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"This information and website content is not intended to diagnose, guarantee results, or recommend specific treatment or activity. It is designed to educate and inform only. Please consult your physician for a thorough examination leading to a diagnosis and well-planned treatment strategy. See more details on the DISCLAIMER page. Content is reviewed by Dr. James M. Cox I."