Xu Sheng, Zhang Gui-Ming, Guan Feng-Ju, Dong Da-Hai, Luo Lei, Li Bin, Ma Xiao-Cheng, Zhao Jun, Sun Li-Jiang
Department of Urology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Department of Surgery, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
World J Surg Oncol. 2015 Aug 7;13:236. doi: 10.1186/s12957-015-0631-5.
Evidence of the association of metabolic syndrome (MetS) with cancer risk is accumulating. However, uncertainties still exist as to the link of MetS with bladder cancer. This study aimed to assess the relationship between MetS and the risk of urothelial carcinoma of the bladder (UC) in a Chinese population.
We retrospectively analyzed clinicopathological data of 972 newly diagnosed UC patients and 1098 cancer-free controls matched to the cases by age and gender. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using unconditional logistic regression in both unadjusted and adjusted models.
MetS was not significantly associated with the overall UC risk (p=0.08). However, a significant association of MetS with UC was observed in female patients (p=0.006). Diabetes mellitus (crude OR 1.339, 95% CI 1.079-1.662, p=0.008; adjusted OR 1.767, 95% CI 1.308-2.386, p<0.001) and hypertriglyceridemia (crude OR 1.245, 95% CI 1.018-1.522, p=0.033; adjusted OR 1.254, 95% CI 1.020-1.542, p=0.032) were significantly associated with UC risk. As the number of MetS components increased, the UC risk was elevated. Having three or more (versus zero) components of MetS was significantly related to risk of overall UC (OR 1.315; 95% CI 1.006-1.719; p=0.045) and non-muscle invasive bladder cancer (OR 1.354; 95% CI 1.019-1.798; p=0.037).
The present study indicated a marginal association between MetS and UC risk, and a significant association with UC risk in female patients. The results need to be evaluated in large-scale prospective cohorts.
代谢综合征(MetS)与癌症风险之间关联的证据正在不断积累。然而,关于MetS与膀胱癌之间的联系仍存在不确定性。本研究旨在评估中国人群中MetS与膀胱尿路上皮癌(UC)风险之间的关系。
我们回顾性分析了972例新诊断的UC患者以及1098例按年龄和性别匹配的无癌对照者的临床病理数据。使用无条件逻辑回归在未调整和调整模型中计算比值比(OR)和95%置信区间(CI)。
MetS与总体UC风险无显著关联(p = 0.08)。然而,在女性患者中观察到MetS与UC存在显著关联(p = 0.006)。糖尿病(粗OR 1.339,95% CI 1.079 - 1.662,p = 0.008;调整后OR 1.767,95% CI 1.308 - 2.386,p < 0.001)和高甘油三酯血症(粗OR 1.245,95% CI 1.018 - 1.522,p = 0.033;调整后OR 1.254,95% CI 1.020 - 1.542,p = 0.