Skip to main content
Log in

Alteration of regional cerebral blood flow in patients with chronic pain —Evaluation before and after epidural spinal cord stimulation—

  • Original Article
  • Published:
Annals of Nuclear Medicine Aims and scope Submit manuscript

Abstract

Background

Chronic pain is defined as intractable pain caused by abnormal pain transmission or impairment of the pain control system per se. Alteration of regional cerebral blood flow (rCBF) is known to occur under the presence of pain stimulation. Epidural spinal cord stimulation (SCS) is occasionally effective in relieving the symptom.

Objective

The aim of the current study is to investigate the alteration of rCBF in baseline condition and to find the association between the rCBF change and the efficacy of SCS in chronic pain.

Methods

A total of 18 patients underwent Tc-99m-HMPAO SPECT before and after SCS. Analysis with three-dimensional stereo-tactic surface projections (3D-SSP) with stereo-tactic extraction estimation (SEE) software was adopted to evaluate the rCBF. We assessed the extent score of the abnormal region in each segment (rate of the coordinates with a Z-value that exceeds three kinds of threshold value 2.0, 2.5 and 3.0 in all coordinates within a segment). According to the therapeutic response defined by visual analogue scale, we categorized patients into two groups, the good responder (GR) group (n = 12) and poor responder (PR) group (n = 6). In the analysis, we compared the extent score in the following two conditions. (1)Comparison between the PR group and normal control group under both baseline condition and after SCS. (2)Comparison between the GR group and normal control group under both baseline condition and after SCS.

Results

(1)In the PR group, increased rCBF was observed in left thalamus, bilateral precuneus and bilateral cerebellum under the baseline condition. After SCS, the range of these increased rCBF areas localized but remained. Decrease of rCBF was noted in bilateral subcallosal gyrus, superior temporal gyrus (STG) and bilateral anterior cingulate gyrus (ACG). They localized after SCS, but remained. (2)In the GR group, increased rCBF areas were noted in bilateral precuneus and bilateral cerebellum under the baseline condition. After SCS, they localized in bilateral precuneus but those of bilateral cerebellum remained. Decreased rCBF area was noted in bilateral subcallosal gyrus, STG and bilateral ACG under the baseline. After SCS, they localized in bilateral subcallosal gyrus and bilateral STG. In contrast, they enlarged in bilateral ACG.

Conclusion

Chronic pain patients demonstrated abnormal rCBF distribution on both baseline and post SCS conditions. Increased rCBF of thalamus and precuneus under both conditions in the PR group and decreased rCBF of ACG under post SCS conditions in the GR group were characteristic patterns. Tc-99m-HMPAO SPECT with 3D-SSP and SEE analysis is likely objective and effective in monitoring and evaluating therapeutic outcome by SCS in chronic pain. In addition, it provides information that is useful in the selection of SCS candidates.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Devor M, Seltzer Z. Pathophysiology of damaged nerves in relation to chronic pain. In: Wall PD, Melzack R.Textbook of pain. 4th ed. Edinburgh; Churchill Livingstone, 1999: 129–164.

    Google Scholar 

  2. Lewin GR, Mendell LM. Nerve growth factor and nociceptin.Trends Neurosci 1993; 16: 353–359.

    Article  PubMed  CAS  Google Scholar 

  3. Woolf CJ, Shortlamd P, Coggeshall RE. Peripheral nerve injury triggers central sprouting of myelinated afferents.Nature 1992; 355: 75–77.

    Article  PubMed  CAS  Google Scholar 

  4. Melzack R. Phantom limb pain: Implications for treatment of pathologic pain.Anesthesiology 1971; 35: 409–419.

    Article  PubMed  CAS  Google Scholar 

  5. Lewandowski W. Psychological factors in chronic pain: a worthwhile undertaking for nursing?Arch Psychiatr Nurs 2004; 18 (3): 97–105.

    Article  PubMed  Google Scholar 

  6. Estlander AM, Takala EP, Verkasalo M. Assessment of depression in chronic musculoskeletal pain patients.Clin J Pain 1995; 11: 194–200.

    Article  PubMed  CAS  Google Scholar 

  7. Love AW, Peck DL. The MMPI and psychological factors in chronic low back pain: A review.Pain 1987; 28: 1–12.

    Article  PubMed  CAS  Google Scholar 

  8. Doan BD, Wadden NP. Relationship between depressive symptoms and descriptions of chronic pain.Pain 1989; 36: 75–84.

    Article  PubMed  CAS  Google Scholar 

  9. Yakhnitsa V, Linderoth B, Meyerson BA. Spinal cord stimulation attenuates dorsal horn neuronal hyperexcitabil-ity in a rat model of mononeuropathy.Pain 1999; 79: 223–233.

    Article  PubMed  CAS  Google Scholar 

  10. Shealy CN, Mortimer JT, Reswick JB. Electrical inhibition of pain by stimulation of dorsal columns: Preliminary clinical report.Anesth Analg 1967; 46: 489–491.

    PubMed  CAS  Google Scholar 

  11. Melzack R, Wall PD. Pain mechanism: A new theory.Science 1965; 150: 971–979.

    Article  PubMed  CAS  Google Scholar 

  12. Yakhnitsa V, Linderoth B, Meyerson BA. Spinal cord stimulation attenuates dorsal horn neuronal hyperexcitabil-ity in rat model of mononeuropathy.Pain 1999; 79: 223–233.

    Article  PubMed  CAS  Google Scholar 

  13. Roberts MHT, Rees H. Physiological basis of spinal cord stimulation.Pain Rev 1994; 1: 184–191.

    Google Scholar 

  14. Nakabeppu Y, Nakajo M, Gushiken T, Tsuchimochi S, Tani A, Kanmura Y. Decreased perfusion of the bilateral thalami in patients with chronic pain detected by Tc-99m-ECD SPECT with statistical parametric mapping.Ann Nucl Med 2001; 15: 459–463.

    PubMed  CAS  Google Scholar 

  15. Peyron R, Laurent B, Garcia-Larrea L. Functional imaging of brain responses to pain. A review and meta-analysis (2000).Neurophysiol Clin 2000; 30: 263–288.

    Article  PubMed  CAS  Google Scholar 

  16. Barker RA, Barasi A, Neal MJ.Neuroscience at a glance.First Japanese Edition. Tokyo; Medical Science International, 2000: 42–81.

    Google Scholar 

  17. Garcia-Larrea L, Peyron R, Mertens P, Gregoire MC, Lavenne F, Le Bars D, et al. Electrical stimulation of motor cortex for pain control: a combined PET-scan and electro-physiological study.Pain1999; 83: 259–273.

    Article  PubMed  CAS  Google Scholar 

  18. Davis KD, Taub E, Duffner F, Lozano AM, Tasker RR, Houle S, et al. Activation of the anterior cingulate cortex by thalamic stimulation in patients with chronic pain: a positron emission tomography study.J Neurosurg 2000; 92: 64–69.

    PubMed  CAS  Google Scholar 

  19. Mailis-Gagnon A, Giannoylis I, Downar J, Kwan CL, Mikulis DJ, Crawley AP, et al. Altered central somatosen-sory processing in chronic pain patients with “hysterical” anesthesia.Neurology 2003; 60: 1501–1507.

    PubMed  CAS  Google Scholar 

  20. Peyron R, Frot M, Schneider F, Garcia-Larrea L, Mertens P, Barrai FG, et al. Role of operculoinsular cortices in human pain processing: converging evidence from PET, fMRI, dipole modeling, and intracerebral recordings of evoked potentials.Neuroimage 2002; 17: 1336–1346.

    Article  PubMed  CAS  Google Scholar 

  21. Minoshima S, Frey KA, Koeppe RA, Foster NL, Kuhl DE. A diagnostic approach in Alzheimer’s disease using three dimensional stereotactic surface projections of fluorine 18-FDG PET.J Nucl Med 1995; 36: 1238–1248.

    PubMed  CAS  Google Scholar 

  22. Fristen KJ, Holmes AP, Worsley KJ, Poline JB, Frith CD, Frackowiak RSJ. Statistical parametric maps in functional imaging: A general approach.Hum Brain Mapp 1995; 2: 189–210.

    Article  Google Scholar 

  23. Mizumura S, Kumita S, Cho K, Ishihara M, Nakajo H, Toba M, et al. Development of quantitative analysis method for stereotactic brain image: Assessment of reduced accumulation in extent and severity using anatomical segmentation.Ann Nucl Med 2003; 17: 289–295.

    Article  PubMed  Google Scholar 

  24. Kunitake A, Iwasaki T, Hidaka N, Nagamachi S, Katsuki H, Uno T, et al. The effects of spinal cord stimulation on the neuronal activity of the brain in patients with chronic neuropathic pain.Pain Research 2005; 20: 117–125.

    Google Scholar 

  25. Whaley L, Wong D.Nursing Care of infants and children, 3rd ed. St. Louis; Mosby, 1987: 1070.

    Google Scholar 

  26. Chapman CR, Gavrin J. Suffering: The contribution of persistent pain.Lancet 1999; 353: 2233–2237.

    Article  PubMed  CAS  Google Scholar 

  27. Petrovic P, Ingvar M, Stone-Elander S, Petersson KM, Hansson P. A PET activation study of dynamic mechanical allodynia in patients with mononeuropathy.Pain 1999; 83: 459–470.

    Article  PubMed  CAS  Google Scholar 

  28. Iadarola MJ, Berman KF, Zeffiro TA, Byassmith MG, Gracely RH, Max AB, et al. Neural activation during acute capsaicin-evoked pain and allodynia assessed with PET.Brain 1998; 121:931–947.

    Article  PubMed  Google Scholar 

  29. Middleton FA, Strick PL. Cerebellar projections to the prefrontal cortex of the primate.J Neurosci 2001; 21: 700–712.

    PubMed  CAS  Google Scholar 

  30. Seminowicz DA, Mikulis DJ, Davis KD. Cognitive modulation of pain-related brain responses depends on behavioral strategy.Pain 2004; 112: 48–58.

    Article  PubMed  CAS  Google Scholar 

  31. Qiu Y, Inui K, Wang X, Nguyen BT, Tran TD, Kakigi R. Effects of distraction on magnetoencephalographic responses ascending through C-fibers in humans.Clin Neurophysiol 2004; 115: 636–646.

    Article  PubMed  Google Scholar 

  32. Osaka N, Osaka M, Kondo H, Morishita M, Fukuyama H, Shibasaki H. The neural basis of executive function in working memory: an fMRI study based on individual differences.Neuroimage 2004; 21: 623–631.

    Article  PubMed  Google Scholar 

  33. Goldman-Rakic PS. Working memory and the mind.Sci Am 1992; 267: 110–117.

    Article  PubMed  CAS  Google Scholar 

  34. Kimberg DY, Farah MJ. A unified account of cognitive impairments following frontal lobe damage: the role of working memory in complex, organized behavior.J Exp Psychol Gen 1993; 122: 411–428.

    Article  PubMed  CAS  Google Scholar 

  35. Apkarian AV, Thomas PS, Krauss BR, Szeverenyi NM. Prefrontal cortical hyperactivity in patients with sympathetically mediated chronic pain.Neurosci Lett 2001; 311: 193–197.

    Article  PubMed  CAS  Google Scholar 

  36. Kupers RC, Gybels JM, Gjedde A. Positron emission tomography study of a chronic pain patient successfully treated with somatosensory thalamic stimulation.Pain 2000; 87: 295–302.

    Article  PubMed  CAS  Google Scholar 

  37. Ikemoto T, Ushida T, Taniguchi S, Tani T, Morio K, Sasaki T, et al. Brain cortical activation is altered with improvement of pain.Pain Research 2005; 20: 111–115.

    Google Scholar 

  38. Kretschmann HJ, Weinrich W.Computertomographie und Magnetresonanztomographie.Japanese edition, Tokyo; Igaku-Shoin Ltd., 1995: 332–333.

    Google Scholar 

  39. Kitamura Y, Kakigi R, Hoshiyama M, Koyama S, Shimojo M, Watanabe S. Pain-related somatosensory evoked magnetic fields.Electroencephalogr Clin Neurophysiol 1995; 95: 463–474.

    Article  PubMed  CAS  Google Scholar 

  40. Yamasaki H, Kakigi R, Naka D. Effects of attention on pain perception: Magnet- and electro-encephalographic studies.Brain Res Cogn Brain Res 1999; 8: 73–76.

    Article  PubMed  CAS  Google Scholar 

  41. Tran TD, Inui K, Hoshiyama M, Lam K, Qiu Y, Kakigi R. Cerebral activation by the signals ascending through unmy-elinated C-fibers in humans: a magnetoencephalographic study.Neuroscience 2002; 113: 375–386.

    Article  PubMed  CAS  Google Scholar 

  42. Kakigi R, Tran TD, Qiu Y, Wang X, Nguyen TB, Inui K, et al. Cerebral responses following stimulation of unmy-elinated C-fibers in humans: electro- and magnetoencephalographic study.Neurosci Res 2003; 45: 255–275.

    Article  PubMed  Google Scholar 

  43. Videbech P. PET measurements of brain glucose metabolism and blood flow in major depressive order: a critical review.Ada Psychiatr Scand 2000; 101: 11–20.

    Article  CAS  Google Scholar 

  44. Drevets WC, Price JL, Simpson Jr JR, Todd RD, Reich T, Vannier M, et al. Subgenual prefrontal cortex abnormalities in mood disorders.Nature 1997; 386: 824–827.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Shigeki Nagamachi.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nagamachi, S., Fujita, S., Nishii, R. et al. Alteration of regional cerebral blood flow in patients with chronic pain —Evaluation before and after epidural spinal cord stimulation—. Ann Nucl Med 20, 303–310 (2006). https://doi.org/10.1007/BF02984647

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02984647

Key words

Navigation