Chonnam Med J.  2013 Apr;49(1):38-42. 10.4068/cmj.2013.49.1.38.

Changes in 18F-Fluorodeoxyglucose Uptake in the Spinal Cord in a Healthy Population on Serial Positron Emission Tomography/Computed Tomography

Affiliations
  • 1Department of Nuclear Medicine, Chosun University Hospital, School of Medicine, Chosun University, Gwangju, Korea.
  • 2Department of Nuclear Medicine, Chonnam National University Hospital, Gwangju, Korea. songhc@jnu.ac.kr
  • 3Department of Nuclear Medicine, Chonnam National University Hwasun Hospital, Hwasun, Korea.
  • 4Department of Neurosurgery, Chonnam National University Hospital, Chonnam National University Medical School, Gwangju, Korea.

Abstract

We aimed to determine the changes in 18F-fluorodeoxyglucose (FDG) uptake in the spinal cord on two serial positron emission tomography/computed tomography (PET/CT) scans in a healthy population. We retrospectively enrolled healthy people who underwent PET/CT twice for cancer screening. We excluded those who had degenerative vertebral disease, neurologic disease, or a history of a vertebral operation. The standardized uptake value (SUVmax) of the spinal cord of each mid-vertebral body was obtained by drawing a region of interest on an axial image of PET/CT. For analysis, the cord-to-background ratio (CTB) was used (CTB=SUVmax of each level/SUVmax of L5 level). Differences in pattern, sex, age, and intervals of the two serial PET/CT scans were analyzed. A total of 60 PET/CT images of 30 people were analyzed. The mean interval between the two PET/CT imaging studies was 2.80+/-0.94 years. On the follow-up PET/CT, significant change was shown only at the level of the C6 and T10 vertebrae (p<0.005). Mean CTB showed a decreasing pattern from cervical to lumbar vertebrae. There were two peaks at the lower cervical level (C4-6) and at the lower thoracic level (T12). Neither sex nor age significantly affected CTB. The FDG uptake of the spinal cord changed significantly on follow-up PET/CT only at the level of the C6 and T10 vertebrae. This finding is valuable as a baseline reference in the follow-up of metabolic changes in the spinal cord.

Keyword

Spinal cord; Fluorodeoxyglucose F18; Positron-emission tomography and computed tomography

MeSH Terms

Early Detection of Cancer
Electrons
Fluorodeoxyglucose F18
Follow-Up Studies
Lumbar Vertebrae
Positron-Emission Tomography and Computed Tomography
Retrospective Studies
Spinal Cord
Spine
Fluorodeoxyglucose F18

Figure

  • FIG. 1 Demonstration of a drawing of the region-of-interest for FDG uptake in the spinal cord at each vertebral body level. (A) Fused PET/CT image in sagittal view. (B) Sagittal PET image. (C) Sagittal CT image. (D) Axial view of fused PET/CT image at the level of the yellow cross mark of the image. (E) Axial view of the CT image at the same level as in D. First, we placed a cursor at the level of the specific vertebra (at the middle height of the vertebral body). Then, Advanced Workstation 3.4 automatically showed axial views of each PET, CT, and fusion PET/CT images at the same level. Using the fused image, we drew the region-of-interest (ROI) in the spinal canal. The SUVmax of the ROI was obtained. We repeated the same process at all vertebral levels in every subject.

  • FIG. 2 Changes of mean 18F-FDG uptake in the spinal cord of 30 healthy people between the first and follow-up PET/CT. FDG uptake is shown as the cord-to-background ratio (CTB, cord SUVmax to L5 SUVmax). The graph shows the mean CTB of each vertebral level of the spinal cord of 30 healthy people (white circle mark). It shows a decreasing pattern along the spinal cord from the cervical to lumbar vertebrae. There are two peaks at the lower cervical level (C4-7) and at the lower thoracic level (T12). The follow-up FDG PET/CT (rectangular mark) was done after more than a year (2.80±0.94 years). The cervical peak was not prominent in the follow-up PET/CT. Moreover, the mean CTB of each level was lower in the second PET. However, the Wilcoxon signed rank test showed that there was no significant change in FDG uptake in the spinal cord at each vertebral level between the first and second PET/CT with the significance level of p<0.001 (Also see Table 1). Note: Error bars represent the 9% confidence interval (CI) of each mean value.


Reference

1. Zhang N, Wimmer J, Qian SJ, Chen WS. Stem cells: current approach and future prospects in spinal cord injury repair. Anat Rec (Hoboken). 2010. 293:519–530.
Article
2. Saporta S, Makoui AS, Willing AE, Daadi M, Cahill DW, Sanberg PR. Functional recovery after complete contusion injury to the spinal cord and transplantation of human neuroteratocarcinoma neurons in rats. J Neurosurg. 2002. 97:1 Suppl. 63–68.
Article
3. Coutts M, Keirstead HS. Stem cells for the treatment of spinal cord injury. Exp Neurol. 2008. 209:368–377.
Article
4. Frangioni JV, Hajjar RJ. In vivo tracking of stem cells for clinical trials in cardiovascular disease. Circulation. 2004. 110:3378–3383.
Article
5. Amin A, Rosenbaum SJ, Bockisch A. Physiological 18F-FDG uptake by the spinal cord: is it a point of consideration for cancer patients? J Neurooncol. 2012. 107:609–615.
Article
6. Do BH, Mari C, Tseng JR, Quon A, Rosenberg J, Biswal S. Pattern of 18F-FDG uptake in the spinal cord in patients with non-central nervous system malignancy. Spine (Phila Pa 1976). 2011. 36:E1395–E1401.
Article
7. McCarville MB, Monu N, Smeltzer MP, Li CS, Laningham FH, Morris EB, et al. PET-CT of the normal spinal cord in children. Acad Radiol. 2009. 16:881–885.
Article
8. Esik O, Emri M, Szakáll S Jr, Herzog H, Sáfrány G, Lengyel E, et al. PET identifies transitional metabolic change in the spinal cord following a subthreshold dose of irradiation. Pathol Oncol Res. 2004. 10:42–46.
Article
9. Esik O, Csere T, Stefanits K, Szakáll S Jr, Lengyel Z, Sáfrány G, et al. Increased metabolic activity in the spinal cord of patients with long-standing Lhermitte's sign. Strahlenther Onkol. 2003. 179:690–693.
10. Chamroonrat W, Posteraro A, El-Haddad G, Zhuang H, Alavi A. Radiation myelopathy visualized as increased FDG uptake on positron emission tomography. Clin Nucl Med. 2005. 30:560.
Article
11. Esik O, Emri M, Csornai M, Kásler M, Gödény M, Trón L. Radiation myelopathy with partial functional recovery: PET evidence of long-term increased metabolic activity of the spinal cord. J Neurol Sci. 1999. 163:39–43.
Article
12. Esik O, Lengyel Z, Sáfrány G, Vönöczky K, Agoston P, Székely J, et al. A PET study on the characterization of partially reversible radiogenic lower motor neurone disease. Spinal Cord. 2002. 40:468–473.
Article
13. Komori T, Delbeke D. Leptomeningeal carcinomatosis and intramedullary spinal cord metastases from lung cancer: detection with FDG positron emission tomography. Clin Nucl Med. 2001. 26:905–907.
Article
14. Jeon MJ, Kim TY, Han JM, Yim JH, Rhim SC, Kim WB, et al. Intramedullary spinal cord metastasis from papillary thyroid carcinoma. Thyroid. 2011. 21:1269–1271.
Article
15. Ota K, Tsunemi T, Saito K, Yamanami F, Watanabe M, Irioka T, et al. 18F-FDG PET successfully detects spinal cord sarcoidosis. J Neurol. 2009. 256:1943–1946.
Article
16. Sakushima K, Yabe I, Shiga T, Yashima-Yamada M, Tsuji-Akimoto S, Terae S, et al. FDG-PET SUV can distinguish between spinal sarcoidosis and myelopathy with canal stenosis. J Neurol. 2011. 258:227–230.
Article
17. Floeth FW, Stoffels G, Herdmann J, Jansen P, Meyer W, Steiger HJ, et al. Regional impairment of 18F-FDG uptake in the cervical spinal cord in patients with monosegmental chronic cervical myelopathy. Eur Radiol. 2010. 20:2925–2932.
Article
18. Uchida K, Nakajima H, Yayama T, Kobayashi S, Shimada S, Tsuchida T, et al. High-resolution magnetic resonance imaging and 18FDG-PET findings of the cervical spinal cord before and after decompressive surgery in patients with compressive myelopathy. Spine (Phila Pa 1976). 2009. 34:1185–1191.
Article
19. Baba H, Uchida K, Sadato N, Yonekura Y, Kamoto Y, Maezawa Y, et al. Potential usefulness of 18F-2-fluoro-deoxy-D-glucose positron emission tomography in cervical compressive myelopathy. Spine (Phila Pa 1976). 1999. 24:1449–1454.
Article
20. Gray H. William PL, editor. Gray's anatomy. Spinal Medulla or Cord. 1989. 37th ed. New York: Churchill Livingstone;922.
21. Kameyama T, Hashizume Y, Sobue G. Morphologic features of the normal human cadaveric spinal cord. Spine (Phila Pa 1976). 1996. 21:1285–1290.
Article
22. Schafer EA. Quain J, Schafer EA, Thane GD, editors. Quain's elements of anatomy. The Spinal Cord. 1900. 10th ed. London: Longmans, Green and Co.;1–219.
23. Cahill CM, Stroman PW. Mapping of neural activity produced by thermal pain in the healthy human spinal cord and brain stem: a functional magnetic resonance imaging study. Magn Reson Imaging. 2011. 29:342–352.
Article
24. Stroman PW, Coe BC, Munoz DP. Influence of attention focus on neural activity in the human spinal cord during thermal sensory stimulation. Magn Reson Imaging. 2011. 29:9–18.
Article
25. Chen YY, Shih YY, Chien CN, Chou TW, Lee TW, Jaw FS. MicroPET study of brain neuronal metabolism under electrical and mechanical stimulation of the rat tail. Nucl Med Commun. 2009. 30:188–193.
Article
26. Chen YY, Shih YY, Lo YC, Lu PL, Tsang S, Jaw FS, et al. MicroPET imaging of noxious thermal stimuli in the conscious rat brain. Somatosens Mot Res. 2010. 27:69–81.
Article
27. Fehm HL, Kern W, Peters A. The selfish brain: competition for energy resources. Prog Brain Res. 2006. 153:129–140.
Article
28. Mapp PI, Terenghi G, Walsh DA, Chen ST, Cruwys SC, Garrett N, et al. Monoarthritis in the rat knee induces bilateral and time-dependent changes in substance P and calcitonin gene-related peptide immunoreactivity in the spinal cord. Neuroscience. 1993. 57:1091–1096.
Article
Full Text Links
  • CMJ
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr