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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Correlation of spleen metabolism assessed by 18F-FDG PET with serum interleukin-2 receptor levels and other biomarkers in patients with untreated sarcoidosis

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Συγγραφέας
Kalkanis A., Kalkanis D., Drougas D., Vavougios G.D., Datseris I., Judson M.A., Georgiou E.
Ημερομηνία
2016
Γλώσσα
en
DOI
10.1097/MNM.0000000000000431
Λέξη-κλειδί
biological marker
C reactive protein
calcium
dipeptidyl carboxypeptidase
fluorodeoxyglucose f 18
interleukin 2 receptor
biological marker
fluorodeoxyglucose f 18
interleukin 2 receptor
adult
Article
calcium urine level
chemical parameters
clinical article
computer assisted emission tomography
controlled study
drug uptake
female
human
male
PET-CT scanner
prospective study
protein blood level
sarcoidosis
spleen
spleen function
spleen metabolism
splenomegaly
standard uptake value
tissue metabolism
whole body scintiscanning
blood
diagnostic imaging
metabolism
positron emission tomography
sarcoidosis
spleen
transport at the cellular level
Adult
Biological Transport
Biomarkers
Female
Fluorodeoxyglucose F18
Humans
Male
Positron-Emission Tomography
Receptors, Interleukin-2
Sarcoidosis
Spleen
Lippincott Williams and Wilkins
Εμφάνιση Μεταδεδομένων
Επιτομή
Background The objective of our study was to assess the possible relationship between splenic F-18-fluorodeoxyglucose (18F-FDG) uptake and other established biochemical markers of sarcoidosis activity. Patients and methods Thirty treatment-naive sarcoidosis patients were prospectively enrolled in this study. They underwent biochemical laboratory tests, including serum interleukin-2 receptor (sIL-2R), serum C-reactive protein, serum angiotensin-I converting enzyme, and 24-h urine calcium levels, and a whole-body combined 18F-FDG PET/computed tomography (PET/CT) scan as a part of an ongoing study at our institute. These biomarkers were statistically compared in these patients. Results A statistically significant linear dependence was detected between sIL-2R and log-transformed spleen-average standard uptake value (SUV avg) (R 2 =0.488, P<0.0001) and log-transformed spleen-maximum standard uptake value (SUV max) (R 2 =0.490, P<0.0001). sIL-2R levels and splenic size correlated linearly (Pearson's r=0.373, P=0.042). Multivariate linear regression analysis revealed that this correlation remained significant after age and sex adjustment (β=0.001, SE=0.001, P=0.024). No statistically significant associations were detected between (a) any two serum biomarkers or (b) between spleen-SUV measurements and any serum biomarker other than sIL-2R. Conclusion Our analysis revealed an association between sIL-2R levels and spleen 18F-FDG uptake and size, whereas all other serum biomarkers were not significantly associated with each other or with PET 18F-FDG uptake. Our results suggest that splenic inflammation may be related to the systemic inflammatory response in sarcoidosis that may be associated with elevated sIL-2R levels. © 2016 Wolters Kluwer Health, Inc. All rights reserved.
URI
http://hdl.handle.net/11615/74177
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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