Abstract
Purpose
68 Ga-DOTA-TOC uptake in the pancreas uncinate process is often found due to physiologic expression of somatostatin receptors (SSTR). We investigated the association of physiologic 68 Ga-DOTA-TOC uptake in the pancreas uncinate process with blood glucose level.
Methods
68 Ga-DOTA-TOC PET scans acquired from 44 patients (male:female = 20:24, age = 50.8 ± 14.8y [mean ± SD]) were retrospectively analyzed. The blood glucose level (BGL) was examined before 68 Ga-DOTA-TOC injection. Patients diagnosed with diabetes mellitus and patients with BGL over 200 mg/dl were excluded. 68 Ga-DOTA-TOC uptake was measured by the maximum standardized uptake values (SUVmax). Additionally, SSTR-positive volume (SV) in the pancreas uncinate process was measured with two different thresholds: by SUV cutoff of 2.5 (SV2.5) and 40% of SUVmax (SV40%). These measurements on 68 Ga-DOTA-TOC PET were correlated with BGL.
Results
The mean of SUVmax of the pancreas uncinate process was 6.51 ± 2.04. SV2.5 was 17.81 ± 7.14 cm3, and SV40% was 18.20 ± 8.83 cm3. A significant negative correlation was found between SUVmax of the pancreas uncinate process and BGL (r = -0.37, p = 0.01). The ratio between SUVmax of the pancreas uncinate process and SUVmean of the pancreas body also showed a significance negative correlation with BGL (r = -0.40, p = 0.01). SV2.5 (r = 0.27, p = 0.07) and SV40% (r = -0.151, p = 0.32) were not significantly correlated with BGL.
Conclusion
Physiologic 68 Ga-DOTA-TOC uptake in the pancreas uncinate process was negatively correlated with BGL. Our results suggested that glycemia could affect physiologic uptake of 68 Ga-DOTA-TOC.
Similar content being viewed by others
Data Availability
Please contact author for data requests.
References
Zhang H, Moroz MA, Serganova I, Ku T, Huang R, Vider J, et al. Imaging expression of the human somatostatin receptor subtype-2 reporter gene with 68Ga-DOTA-TOC. J Nucl Med. 2011;52:123–31.
Hennrich U, Benešová M. [68Ga]Ga-DOTA-TOC: the first FDA-approved 68Ga-radiopharmaceutical for PET imaging. Pharmaceuticals (Basel). 2020;13:38.
Jacobsson H, Larsson P, Jonsson C, Jussing E, Grybäck P. Normal uptake of 68Ga-DOTA-TOC by the pancreas uncinate process mimicking malignancy at somatostatin receptor PET. Clin Nucl Med. 2012;37:362–5.
Imperiale A, Meuter L, Pacak K, Taïeb D. Variants and pitfalls of PET/CT in neuroendocrine tumors. Semin Nucl Med. 2021;51:519–28.
Wang X, Zielinski MC, Misawa R, Wen P, Wang TY, Wang CZ, et al. Quantitative analysis of pancreatic polypeptide cell distribution in the human pancreas. PLoS One. 2013;8:e55501.
Rizza R, Go V, Cryer P, Verdonk C, Gerich J. Stimulation of human pancreatic polypeptide secretion by hypoglycemia is independent of adrenergic mechanisms. J Clin Endocrinol Metab. 1982;55:1234–6.
Veedfald S, Plamboeck A, Hartmann B, Svendsen LB, Vilsbøll T, Knop FK, et al. Pancreatic polypeptide responses to isoglycemic oral and intravenous glucose in humans with and without intact vagal innervation. Peptides. 2015;71:229–31.
Kim W, Fiori JL, Shin YK, Okun E, Kim JS, Rapp PR, et al. Pancreatic polypeptide inhibits somatostatin secretion. FEBS Lett. 2014;588:3233–9.
Portela-Gomes GM, Stridsberg M, Grimelius L, Oberg K, Janson ET. Expression of the five different somatostatin receptor subtypes in endocrine cells of the pancreas. Appl Immunohistochem Mol Morphol. 2000;8:126–32.
Ludvigsen E, Olsson R, Stridsberg M, Janson ET, Sandler S. Expression and distribution of somatostatin receptor subtypes in the pancreatic islets of mice and rats. J Histochem Cytochem. 2004;52:391–400.
Csaba Z, Peineau S, Dournaud P. Molecular mechanisms of somatostatin receptor trafficking. J Mol Endocrinol. 2012;48:R1-12.
Olsen C, Memarzadeh K, Ulu A, Carr HS, Bean AJ, Frost JA. Regulation of somatostatin receptor 2 trafficking by C-tail motifs and the retromer. Endocrinology. 2019;160:1031–43.
Funding
This work was supported by the Korea Medical Device Development Fund grant funded by the Korea government (the Ministry of Science and ICT, the Ministry of Trade, Industry and Energy, the Ministry of Health & Welfare, the Ministry of Food and Drug Safety) (Project Number: 202011A06).
Author information
Authors and Affiliations
Contributions
The study was designed by Dongkyu Oh and Hongyoon Choi. Material preparation and data collection and analysis were performed by Dongkyu Oh, Hongyoon Choi, and Jin Chul Paeng. The first draft of the manuscript was written by Dongkyu Oh. Review, editing and supervision were performed by Keon Wook Kang and Gi Jeong Cheon. All authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Competing Interests
Dongkyu Oh, Hongyoon Choi, Jin Chul Paeng, Keon Wook Kang, and Gi Jeong Cheon declare no conflict of interest.
Ethics Approval and Consent to Participate
The study design of the retrospective analysis and exemption of informed consent were approved by the Institutional Review Board of the Seoul National University Hospital (2108–072-1244). All procedures followed were performed in accordance with the ethical standards of the responsible committee on human experimentation and with the Helsinki Declaration of 1975, as revised in 2013. The institutional review board waived the need to obtain informed consent.
Consent for Publication
The institutional review board waived the need to obtain informed consent because of the anonymity and the retrospective nature of the study.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Oh, D., Choi, H., Paeng, J.C. et al. A Negative Correlation Between Blood Glucose Level and 68 Ga-DOTA-TOC Uptake in the Pancreas Uncinate Process. Nucl Med Mol Imaging 56, 52–58 (2022). https://doi.org/10.1007/s13139-021-00723-5
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s13139-021-00723-5