Department of Medical Statistics, Informatics and Health Economics, Innsbruck Medical University, Innsbruck, Austria.
PLoS One. 2013;8(1):e54242. doi: 10.1371/journal.pone.0054242. Epub 2013 Jan 23.
To investigate the association between total serum cholesterol (TSC) and cancer incidence in the Metabolic syndrome and Cancer project (Me-Can).
Me-Can consists of seven cohorts from Norway, Austria, and Sweden including 289,273 male and 288,057 female participants prospectively followed up for cancer incidence (n = 38,978) with a mean follow-up of 11.7 years. Cox regression models with age as the underlying time metric were used to estimate hazard ratios (HR) and their 95% confidence intervals (CI) for quintiles of cholesterol levels and per 1 mmol/l, adjusting for age at first measurement, body mass index (BMI), and smoking status. Estimates were corrected for regression dilution bias. Furthermore, we performed lag time analyses, excluding different times of follow-up, in order to check for reverse causation.
In men, compared with the 1st quintile, TSC concentrations in the 5th quintile were borderline significantly associated with decreasing risk of total cancer (HR = 0.94; 95%CI: 0.88, 1.00). Significant inverse associations were observed for cancers of the liver/intrahepatic bile duct (HR = 0.14; 95%CI: 0.07, 0.29), pancreas cancer (HR = 0.52, 95% CI: 0.33, 0.81), non-melanoma of skin (HR = 0.67; 95%CI: 0.46, 0.95), and cancers of the lymph-/hematopoietic tissue (HR = 0.68, 95%CI: 0.54, 0.87). In women, hazard ratios for the 5th quintile were associated with decreasing risk of total cancer (HR = 0.86, 95%CI: 0.79, 0.93) and for cancers of the gallbladder (HR = 0.23, 95%CI: 0.08, 0.62), breast (HR = 0.70, 95%CI: 0.61, 0.81), melanoma of skin (HR = 0.61, 95%CI: 0.42, 0.88), and cancers of the lymph-/hematopoietic tissue (HR = 0.61, 95%CI: 0.44, 0.83).
TSC was negatively associated with risk of cancer overall in females and risk of cancer at several sites in both males and females. In lag time analyses some associations persisted, suggesting that for these cancer sites reverse causation did not apply.
在代谢综合征与癌症项目(Me-Can)中,研究总血清胆固醇(TSC)与癌症发病率之间的关联。
Me-Can 由来自挪威、奥地利和瑞典的七个队列组成,共包括 289273 名男性和 288057 名女性参与者,前瞻性随访癌症发病率(n=38978),平均随访时间为 11.7 年。使用 Cox 回归模型,以年龄为基础时间指标,估计胆固醇水平五分位数和每 1mmol/l 的风险比(HR)及其 95%置信区间(CI),并调整首次测量时的年龄、体重指数(BMI)和吸烟状况。估计值校正了回归稀释偏差。此外,我们进行了滞后时间分析,排除了不同的随访时间,以检查反向因果关系。
在男性中,与第 1 五分位相比,第 5 五分位的 TSC 浓度与总癌症风险降低呈边缘显著相关(HR=0.94;95%CI:0.88,1.00)。观察到与肝癌/肝内胆管(HR=0.14;95%CI:0.07,0.29)、胰腺癌(HR=0.52,95%CI:0.33,0.81)、非黑素瘤皮肤癌(HR=0.67;95%CI:0.46,0.95)和淋巴/造血组织癌(HR=0.68,95%CI:0.54,0.87)呈显著负相关。在女性中,第 5 五分位的 HR 与总癌症风险降低相关(HR=0.86,95%CI:0.79,0.93)和胆囊癌(HR=0.23,95%CI:0.08,0.62)、乳腺癌(HR=0.70,95%CI:0.61,0.81)、黑色素瘤皮肤癌(HR=0.61,95%CI:0.42,0.88)和淋巴/造血组织癌(HR=0.61,95%CI:0.44,0.83)。
TSC 与女性的总体癌症风险和男性及女性多个部位的癌症风险呈负相关。在滞后时间分析中,一些关联仍然存在,这表明对于这些癌症部位,反向因果关系并不适用。