Abstract:Failed back surgery syndrome (FBSS), a chronic neuropathic pain condition, is a common indication for spinal cord stimulation (SCS). However, the mechanisms of SCS, especially its effects on supraspinal/brain functional connectivity, are still not fully understood. Resting state functional magnetic resonance imaging (rsfMRI) studies have shown characteristics in patients with chronic low back pain (cLBP). In this case study, we performed rsfMRI scanning (3.0 T) on an FBSS patient, who presented with chronic lo… Show more
“…16,19,23,27,29 However, in contrast to our previous study, 19 these studies have had several limitations such as 1) heterogenous populations of patients; 16 2) limited number of patients; 23 3) lack of analysis of subcortical regions; 23,27 4) lack of comparison to controls 16,23,27 or 5) lack of cross-network analysis. 16,23,27,29 Limitations/Future Directions…”
mentioning
confidence: 76%
“…7,20 However, these reports were based upon heterogeneous cLBP populations with different etiologies and pain phenotypes (neuropathic vs nociceptive; constant or intermittent). Several groups have also explored the supraspinal effects of spinal neuromodulation for pain, 16,[22][23][24][25][26][27][28][29][30] recently reviewed in 31 In addition, a few recent fcMRI studies on chronic pain patients with implanted SCS systems have been presented. 16,19,23,27,29 However, in contrast to our previous study, 19 these studies have had several limitations such as 1) heterogenous populations of patients; 16 2) limited number of patients; 23 3) lack of analysis of subcortical regions; 23,27 4) lack of comparison to controls 16,23,27 or 5) lack of cross-network analysis.…”
Background
Chronic low back pain (cLBP) has been associated with alterations in brain functional connectivity (FC) but based upon heterogeneous populations and single network analyses. Our goal is to study a more homogeneous cLBP population and focus on multiple cross-network (CN) connectivity analysis. We hypothesize that within this population: 1) altered CN FC, involving emotion and reward/aversion functions are related to their pain levels and 2) altered relationships are dependent upon pain phenotype (constant neuropathic vs intermittent pain).
Methods
In this case series, resting state fcMRI scans were obtained over a study duration of 60 months from 23 patients (13 constant neuropathic and 10 intermittent pain) with Persistent Spinal Pain Syndrome (PSPS Type 2) being considered for spinal cord stimulation (SCS) therapy at a single academic center. Images were acquired using a Discovery MR750 GE scanner. During the resting state acquisitions, they were asked to close their eyes and relax. The CN analysis was performed on 7 brain networks and compared to age-matched controls. Linear regression was used to test the correlation between CN connectivity and pain scores.
Results
CN FC involving emotion networks (STM: striatum network index) was significantly lower than controls in all patients, regardless of pain phenotype (P < 0.003). Pain levels were positively correlated with emotional FC for intermittent pain but negatively correlated for constant pain.
Conclusion
This is the first report of 1) altered CN FC involving emotion/reward brain circuitry in 2) a homogeneous population of cLBP patients with 3) two different pain phenotypes (constant vs intermittent) in PSPS Type 2 patients being considered for SCS. FC patterns were altered in cLBP patients as compared to controls and were characteristic for each pain phenotype. These data support fcMRI as a potential and objective tool in assessing pain levels in cLBP patients with different pain phenotypes.
“…16,19,23,27,29 However, in contrast to our previous study, 19 these studies have had several limitations such as 1) heterogenous populations of patients; 16 2) limited number of patients; 23 3) lack of analysis of subcortical regions; 23,27 4) lack of comparison to controls 16,23,27 or 5) lack of cross-network analysis. 16,23,27,29 Limitations/Future Directions…”
mentioning
confidence: 76%
“…7,20 However, these reports were based upon heterogeneous cLBP populations with different etiologies and pain phenotypes (neuropathic vs nociceptive; constant or intermittent). Several groups have also explored the supraspinal effects of spinal neuromodulation for pain, 16,[22][23][24][25][26][27][28][29][30] recently reviewed in 31 In addition, a few recent fcMRI studies on chronic pain patients with implanted SCS systems have been presented. 16,19,23,27,29 However, in contrast to our previous study, 19 these studies have had several limitations such as 1) heterogenous populations of patients; 16 2) limited number of patients; 23 3) lack of analysis of subcortical regions; 23,27 4) lack of comparison to controls 16,23,27 or 5) lack of cross-network analysis.…”
Background
Chronic low back pain (cLBP) has been associated with alterations in brain functional connectivity (FC) but based upon heterogeneous populations and single network analyses. Our goal is to study a more homogeneous cLBP population and focus on multiple cross-network (CN) connectivity analysis. We hypothesize that within this population: 1) altered CN FC, involving emotion and reward/aversion functions are related to their pain levels and 2) altered relationships are dependent upon pain phenotype (constant neuropathic vs intermittent pain).
Methods
In this case series, resting state fcMRI scans were obtained over a study duration of 60 months from 23 patients (13 constant neuropathic and 10 intermittent pain) with Persistent Spinal Pain Syndrome (PSPS Type 2) being considered for spinal cord stimulation (SCS) therapy at a single academic center. Images were acquired using a Discovery MR750 GE scanner. During the resting state acquisitions, they were asked to close their eyes and relax. The CN analysis was performed on 7 brain networks and compared to age-matched controls. Linear regression was used to test the correlation between CN connectivity and pain scores.
Results
CN FC involving emotion networks (STM: striatum network index) was significantly lower than controls in all patients, regardless of pain phenotype (P < 0.003). Pain levels were positively correlated with emotional FC for intermittent pain but negatively correlated for constant pain.
Conclusion
This is the first report of 1) altered CN FC involving emotion/reward brain circuitry in 2) a homogeneous population of cLBP patients with 3) two different pain phenotypes (constant vs intermittent) in PSPS Type 2 patients being considered for SCS. FC patterns were altered in cLBP patients as compared to controls and were characteristic for each pain phenotype. These data support fcMRI as a potential and objective tool in assessing pain levels in cLBP patients with different pain phenotypes.
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