Kalkanis Alexandros, Kalkanis Dimitrios, Drougas Dimitrios, Vavougios George D, Datseris Ioannis, Judson Marc A, Georgiou Evangelos
aDepartment of Pulmonary Medicine, Division of Pulmonary and Critical Care Medicine, 401 Military and VA Hospital bDepartment of Nuclear Medicine, 251 General Airforce and VA Hospital cDepartment of Nuclear Medicine and PET/CT, Evangelismos Hospital dDepartment of Medicine, Medical Physics Laboratory Simulation Centre, University of Athens, Athens eDepartment of Respiratory Medicine, University of Thessaly, Larisa, Greece fDepartment of Medicine, Albany Medical College, Albany, New York, USA.
Nucl Med Commun. 2016 Mar;37(3):273-7. doi: 10.1097/MNM.0000000000000431.
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.
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.
A statistically significant linear dependence was detected between sIL-2R and log-transformed spleen-average standard uptake value (SUV avg) (R2=0.488, P<0.0001) and log-transformed spleen-maximum standard uptake value (SUV max) (R2=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.
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.
我们研究的目的是评估脾脏 F-18-氟脱氧葡萄糖(18F-FDG)摄取与结节病活动的其他既定生化标志物之间的可能关系。
30 例初治结节病患者前瞻性纳入本研究。他们接受了生化实验室检查,包括血清白细胞介素-2 受体(sIL-2R)、血清 C 反应蛋白、血清血管紧张素-I 转换酶和 24 小时尿钙水平,并作为我们研究所正在进行的一项研究的一部分进行了全身 18F-FDG 正电子发射断层扫描/计算机断层扫描(PET/CT)。对这些患者的这些生物标志物进行了统计学比较。
在 sIL-2R 与对数转换后的脾脏平均标准摄取值(SUV avg)(R2 = 0.488,P < 0.0001)和对数转换后的脾脏最大标准摄取值(SUV max)(R2 = 0.490,P < 0.0001)之间检测到统计学上显著的线性相关性。sIL-2R 水平与脾脏大小呈线性相关(Pearson 相关系数 r = 0.373,P = 0.042)。多变量线性回归分析显示,在调整年龄和性别后,这种相关性仍然显著(β = 0.001,标准误 = 0.001,P = 0.024)。在(a)任何两种血清生物标志物之间或(b)脾脏 SUV 测量值与除 sIL-2R 之外的任何血清生物标志物之间未检测到统计学上显著的关联。
我们的分析揭示了 sIL-2R 水平与脾脏 18F-FDG 摄取及大小之间的关联,而所有其他血清生物标志物彼此之间或与 PET 18F-FDG 摄取均无显著关联。我们的结果表明,脾脏炎症可能与结节病中的全身炎症反应相关,这可能与 sIL-2R 水平升高有关。