Brain Structure and Function of Chronic Low Back Pain Patients on Long-Term Opioid Analgesic Treatment: A Preliminary Study

Author:

Murray Kyle1ORCID,Lin Yezhe2ORCID,Makary Meena M3456ORCID,Whang Peter G7,Geha Paul234ORCID

Affiliation:

1. Department of Physics and Astronomy, University of Rochester, Rochester, NY, USA

2. Department of Psychiatry, School of Medicine and Dentistry, University of Rochester, Rochester, NY, USA

3. The John B. Pierce Laboratory, New Haven, CT, USA

4. Department of Psychiatry, Yale School of Medicine, Yale University, New Haven, CT, USA

5. Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, USA

6. Systems and Biomedical Engineering Department, Faculty of Engineering, Cairo University, Giza, Egypt

7. Department of Orthopaedics and Rehabilitation, Yale School of Medicine, New Haven, CT, USA

Abstract

Chronic low back pain (CLBP) is often treated with opioid analgesics (OA), a class of medications associated with a significant risk of misuse. However, little is known about how treatment with OA affect the brain in chronic pain patients. Gaining this knowledge is a necessary first step towards understanding OA associated analgesia and elucidating long-term risk of OA misuse. Here we study CLBP patients chronically medicated with opioids without any evidence of misuse and compare them to CLBP patients not on opioids and to healthy controls using structural and functional brain imaging. CLBP patients medicated with OA showed loss of volume in the nucleus accumbens and thalamus, and an overall significant decrease in signal to noise ratio in their sub-cortical areas. Power spectral density analysis (PSD) of frequency content in the accumbens’ resting state activity revealed that both medicated and unmedicated patients showed loss of PSD within the slow-5 frequency band (0.01–0.027 Hz) while only CLBP patients on OA showed additional density loss within the slow-4 frequency band (0.027–0.073 Hz). We conclude that chronic treatment with OA is associated with altered brain structure and function within sensory limbic areas.

Funder

National Institute on Drug Abuse

Publisher

SAGE Publications

Subject

Anesthesiology and Pain Medicine,Cellular and Molecular Neuroscience,Molecular Medicine

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