Regional Oncologic Centre, Uppsala University Hospital, Uppsala, Sweden.
Cancer Epidemiol Biomarkers Prev. 2010 Aug;19(8):2088-96. doi: 10.1158/1055-9965.EPI-10-0112. Epub 2010 Jul 20.
Associations between metabolic syndrome (MetS) components and prostate cancer development have not been studied comprehensively; results have been divergent. Using the National Cholesterol Education Program Adult Treatment panel III (NCEP) and International Diabetes Federation (IDF) definitions of the MetS, we investigated such associations taking competing risks of death into consideration.
In the prospective Uppsala Longitudinal Study of Adult Men of 2,322 Caucasian men with 34 years of follow-up baseline, MetS measurements at age 50 years were used. Cumulative incidence of prostate cancer and death with/without the MetS were calculated. Competing risk of dying was taken into account by calculating the conditional probability of prostate cancer with/without the MetS.
Two hundred and thirty-seven prostate cancers were identified. Prostate cancer probability by age 80 years with baseline MetS compared with without MetS was nonsignificantly higher [5.2 percent units (confidence interval (CI), -0.8% to 11.3%; NCEP); 2.7 percent units (CI, -2.7% to 8.0%; IDF)]; cumulative incidence proportions of death was significantly higher [19.3 percent units (CI, 13.4-25.3%; NCEP); 15.3 percent units (CI, 9.5-21.1%; IDF)]; and conditional probability of prostate cancer considering death from other causes was significantly higher [7.3 percent-units (CI, 0.2-14.5%); odds ratio of 1.64 (CI, 1.03-2.23; NCEP)] and nonsignificantly higher [5.0 percent-units (CI, -1.6% to 11.6%); odds ratio of 1.43 (CI, 0.89-1.90; IDF].
The MetS by the NCEP definition is associated with prostate cancer, taking the competing risk of early death from other causes into account.
The results further highlight the public health effect of the increasing prevalence of MetS and the importance of considering competing risks when studying risk factors for cancer.
代谢综合征(MetS)各组分与前列腺癌发展之间的关联尚未得到全面研究,研究结果存在差异。我们采用国家胆固醇教育计划成人治疗专家组 III(NCEP)和国际糖尿病联盟(IDF)的 MetS 定义,在考虑到死亡竞争风险的情况下,研究了这些关联。
在有 34 年随访基线的 2322 名白种人男性的前瞻性乌普萨拉男性成人纵向研究中,在 50 岁时测量 MetS 指标。计算了有/无 MetS 的前列腺癌累积发病率和死亡情况。通过计算有/无 MetS 的前列腺癌的条件概率,考虑了死亡竞争风险。
确定了 237 例前列腺癌。与无 MetS 相比,基线时存在 MetS 的患者在 80 岁时患前列腺癌的概率(NCEP:5.2 个百分点单位[置信区间(CI),-0.8%至 11.3%];IDF:2.7 个百分点单位[CI,-2.7%至 8.0%])无显著差异;死亡累积发生率显著更高(NCEP:19.3 个百分点单位[CI,13.4-25.3%];IDF:15.3 个百分点单位[CI,9.5-21.1%]);考虑到其他原因死亡的情况下,前列腺癌的条件概率也显著更高(NCEP:7.3 个百分点单位[CI,0.2-14.5%];比值比为 1.64[CI,1.03-2.23])和无显著差异(IDF:5.0 个百分点单位[CI,-1.6%至 11.6%];比值比为 1.43[CI,0.89-1.90])。
NCEP 定义的 MetS 与前列腺癌相关,考虑到其他原因导致的早期死亡竞争风险。
这些结果进一步强调了 MetS 患病率增加的公共卫生影响,以及在研究癌症危险因素时考虑竞争风险的重要性。