Research

A preliminary fMRI study of analgesic treatment in chronic back pain and knee osteoarthritis

Marwan N Baliki¹ , Paul Y Geha¹ , Rami Jabakhanji¹ , Norm Harden² , Thomas J Schnitzer and A Vania Apkarian^1,3

¹  Department of Physiology, Northwestern University, Feinberg School of Medicine, 303 East Chicago Ave, Chicago IL, 60611, USA

²  Rehabilitation Institute of Chicago, Northwestern University, Feinberg School of Medicine, 303 East Chicago Ave, Chicago IL, 60611, USA

³  Departments of Anesthesia, Surgery, and Lurie Cancer Center, Northwestern University, Feinberg School of Medicine, 303 East Chicago Ave, Chicago IL, 60611, USA

author email corresponding author email

Molecular Pain 2008, 4:47doi:10.1186/1744-8069-4-47

Published:	25 October 2008

Abstract

The effects of an analgesic treatment (lidocaine patches) on brain activity in chronic low back pain (CBP) and in knee osteoarthritis (OA) were investigated using serial fMRI (contrasting fMRI between before and after two weeks of treatment). Prior to treatment brain activity was distinct between the two groups: CBP spontaneous pain was associated mainly with activity in medial prefrontal cortex, while OA painful mechanical knee stimulation was associated with bilateral activity in the thalamus, secondary somatosensory, insular, and cingulate cortices, and unilateral activity in the putamen and amygdala. After 5% lidocaine patches were applied to the painful body part for two weeks, CBP patients exhibited a significant decrease in clinical pain measures, while in OA clinical questionnaire based outcomes showed no treatment effect but stimulus evoked pain showed a borderline decrease. The lidocaine treatment resulted in significantly decreased brain activity in both patient groups with distinct brain regions responding in each group, and sub-regions within these areas were correlated with pain ratings specifically for each group (medial prefrontal cortex in CBP and thalamus in OA). We conclude that the two chronic pain conditions involve distinct brain regions, with OA pain engaging many brain regions commonly observed in acute pain. Moreover, lidocaine patch treatment modulates distinct brain circuitry in each condition, yet in OA we observe divergent results with fMRI and with questionnaire based instruments.