Hu Yao, Zhong Yuan, Hu Yuxiao
Department of PET/CT Center, Jiangsu Cancer Hospital and Jiangsu Institute of Cancer Research and the Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China.
School of Psychology, Nanjing Normal University, Nanjing, Jiangsu, China.
Front Oncol. 2025 Jun 26;15:1598911. doi: 10.3389/fonc.2025.1598911. eCollection 2025.
The purpose of this study was to explore brain metabolic correlates of peripheral inflammatory markers in patients with cervical cancer (CC).
Cervical cancer (CC) patients (267) without treatments who underwent [18F] Fluorodeoxyglucose ([18F]FDG) positron-emission tomography (PET)/computed tomography (CT) were retrospectively studied. All CC patients were grouped into the International Federation of Gynecology and Obstetrics (FIGO) stage II (n=16), the FIGO stage III (n=160), and the FIGO stage IV (n=91) according to the FIGO stage. According to the median of metabolic tumor volume (MTV) or total lesion glycolysis (TLG) for primary tumor in different FIGO stage, CC patients in different FIGO stage were grouped into the Low_MTV (TLG) group (<median) and High_MTV (TLG) group (≥median). Regression analysis were used to explore the relationships between regional brain glucose metabolism and peripheral inflammatory markers [including Neutrophil-to-Lymphocyte ratio (NLR), Platelet-to-Lymphocyte ratio (PLR), Monocyte-to-Lymphocyte ratio (MLR), and systemic immune-inflammation index (SII)] in whole group, subgroups in different FIGO stage.
The MTV and TLG for primary tumor positively correlated with SII ( =0.402, =0.000; =0.397, =0.000), PLR ( =0.317, =0.000; =0.323, =0.000), NLR ( =0.311, =0.000; =0.328, =0.000), MLR ( =0.255, =0.001; =0.275, =0.000) in FIGO stage III, and they positively correlated with SII ( =0.223, =0.033; =0.291, =0.005), NLR ( =0.220, =0.036) in FIGO stage IV, but didn't significantly correlate with MLR, or PLR in FIGO stage IV or with all peripheral inflammatory markers in FIGO stage II (P>0.05). The SII and NLR had significantly negative correlations with the glucose metabolism mainly in the bilateral dorsolateral prefrontal cortex (dlPFC) in CC patients with FIGO stage III ( < 0.05) and those regions negatively correlated with SII were mainly located in the right dlPFC in CC patients with FIGO stage IV ( < 0.05). Compared with patients with the Low_MTV (TLG) group in FIGO stage III, those with High_MTV (TLG) group showed stronger relationships between the glucose metabolism of dlPFC and peripheral inflammatory markers (SII, or NLR), while the relationships in FIGO stage IV weakened or even disappeared.
The glucose metabolism in the dlPFC negatively correlated with peripheral inflammatory markers in CC patients with FIGO stage III or IV may be relevant in the disease severity and vary depending on the disease severity.
本研究旨在探讨宫颈癌(CC)患者外周炎症标志物与脑代谢的相关性。
回顾性研究267例未经治疗的宫颈癌(CC)患者,这些患者均接受了[18F]氟脱氧葡萄糖([18F]FDG)正电子发射断层扫描(PET)/计算机断层扫描(CT)检查。根据国际妇产科联盟(FIGO)分期,所有CC患者被分为FIGO II期(n = 16)、FIGO III期(n = 160)和FIGO IV期(n = 91)。根据不同FIGO分期中原发肿瘤的代谢肿瘤体积(MTV)或总病变糖酵解(TLG)的中位数,将不同FIGO分期的CC患者分为低MTV(TLG)组(<中位数)和高MTV(TLG)组(≥中位数)。采用回归分析探讨全组、不同FIGO分期亚组中脑区葡萄糖代谢与外周炎症标志物[包括中性粒细胞与淋巴细胞比值(NLR)、血小板与淋巴细胞比值(PLR)、单核细胞与淋巴细胞比值(MLR)和全身免疫炎症指数(SII)]之间的关系。
FIGO III期中,原发肿瘤的MTV和TLG与SII(r = 0.402,P = 0.000;r = 0.397,P = 0.000)、PLR(r = 0.317,P = 0.000;r = 0.323,P = 0.000)、NLR(r = 0.311,P = 0.000;r = 0.328,P = 0.000)、MLR(r = 0.255,P = 0.001;r = 0.275,P = 0.000)呈正相关;在FIGO IV期中,它们与SII(r = 0.223,P = 0.033;r = 0.291,P = 0.005)、NLR(r = 0.220,P = 0.036)呈正相关,但与FIGO IV期的MLR或PLR以及FIGO II期的所有外周炎症标志物均无显著相关性(P>0.05)。SII和NLR与FIGO III期CC患者双侧背外侧前额叶皮质(dlPFC)的葡萄糖代谢呈显著负相关(P<0.05),与SII呈负相关的区域主要位于FIGO IV期CC患者的右侧dlPFC(P<0.05)。与FIGO III期低MTV(TLG)组患者相比,高MTV(TLG)组患者dlPFC的葡萄糖代谢与外周炎症标志物(SII或NLR)之间的关系更强,而FIGO IV期的这种关系则减弱甚至消失。
FIGO III期或IV期CC患者dlPFC的葡萄糖代谢与外周炎症标志物呈负相关,这可能与疾病严重程度相关,且因疾病严重程度而异。