Bian Zilong, Xu Luopiao, Wang Yuting, Tsai Min-Kuang, Chu David Ta-Wei, Tu Huakang, Wen Chi-Pang, Wu Xifeng
Department of Big Data in Health Science School of Public Health, and Center of Clinical Big Data and Analytics of The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Institute of Population Health Sciences, National Health Research Institutes, Zhunan, Taiwan.
Front Oncol. 2024 Sep 9;14:1400893. doi: 10.3389/fonc.2024.1400893. eCollection 2024.
To investigate the specific role of inflammation in the connection between obesity and the overall incidence of cancer.
A total of 356,554 participants in MJ cohort study were included. Systemic inflammation markers from blood samples and anthropometric measurements were determined using professional instruments. The Cox model was adopted to evaluate the association.
Over a median follow-up of 8.2 years, 9,048 cancer cases were identified. For individual systemic inflammation biomarkers, the overall cancer risk significantly escalated as blood C-reactive protein (CRP) (hazard ratio (HR)=1.036 (1.017-1.054)) and globulin (GLO) (HR=1.128 (1.105-1.152)) levels increased, and as hemoglobin (HEMO) (HR=0.863 (0.842-0.884)), albumin (ALB) (HR=0.846 (0.829-0.863)) and platelets (PLA) (HR=0.842 (0.827-0.858)) levels decreased. For composite indicators, most of them existed a significant relationship to the overall cancer risk. Most indicators were correlated with the overall cancer and obesity-related cancer risk, but there was a reduction of association with non-obesity related cancer risk. Most of indicators mediated the association between anthropometric measurements and overall cancer risk.
Systemic inflammatory state was significantly associated with increased risks of cancer risk. Inflammation biomarkers were found to partly mediate the association between obesity and cancer risk.
探讨炎症在肥胖与癌症总体发病率之间的联系中所起的具体作用。
纳入MJ队列研究中的356,554名参与者。使用专业仪器测定血样中的全身炎症标志物和人体测量数据。采用Cox模型评估关联性。
在中位随访8.2年期间,共确诊9,048例癌症病例。对于个体全身炎症生物标志物,随着血C反应蛋白(CRP)(风险比(HR)=1.036(1.017 - 1.054))和球蛋白(GLO)(HR = 1.128(1.105 - 1.152))水平升高,以及血红蛋白(HEMO)(HR = 0.863(0.842 - 0.884))、白蛋白(ALB)(HR = 0.846(0.829 - 0.863))和血小板(PLA)(HR = 0.842(0.827 - 0.858))水平降低,总体癌症风险显著升高。对于综合指标,大多数与总体癌症风险存在显著关系。大多数指标与总体癌症及肥胖相关癌症风险相关,但与非肥胖相关癌症风险的关联性降低。大多数指标介导了人体测量数据与总体癌症风险之间的关联。
全身炎症状态与癌症风险增加显著相关。发现炎症生物标志物部分介导了肥胖与癌症风险之间的关联。