Nogueira Leticia M, Newton Christina C, Pollak Michael, Silverman Debra T, Albanes Demetrius, Männistö Satu, Weinstein Stephanie J, Jacobs Eric J, Stolzenberg-Solomon Rachael Z
Texas Cancer Registry, Department of State Health Services, Austin, Texas.
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Rockville, Rockville, Maryland.
Cancer Epidemiol Biomarkers Prev. 2017 Jun;26(6):914-922. doi: 10.1158/1055-9965.EPI-16-0891. Epub 2017 Jan 17.
Studies examining associations between circulating concentrations of C-peptide and total adiponectin, two biomarkers related to obesity and insulin secretion and sensitivity and pancreatic ductal adenocarcinoma (PDA) risk have shown inconsistent results and included limited numbers of smokers. We examined associations of these biomarkers and high molecular weight (HMW) adiponectin with PDA, overall, and by smoking status. We conducted a pooled nested case-control analysis in 3 cohorts (Prostate, Lung, Colorectal, and Ovarian Cancer Trial, Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study, and Cancer Prevention Study-II), with 758 cases (435 current smokers) and 1,052 controls (531 smokers) matched by cohort, age, sex, race, blood draw date and follow-up time. We used conditional logistic regression adjusted for age, smoking, diabetes, and body mass index to calculate ORs and 95% confidence intervals (CI). Circulating C-peptide concentration was not associated with PDA in never or former smokers, but was inversely associated with PDA in current smokers (per SD OR = 0.67; 95% CI, 0.54-0.84; = 0.005). HMW adiponectin was inversely associated with PDA in never smokers (OR = 0.43; 95% CI, 0.23-0.81), not associated in former smokers, and positively associated in smokers (OR = 1.23; 95% CI, 1.04-1.45; = 0.009). Total adiponectin was not associated with PDA in nonsmokers or current smokers. Associations of biomarkers of insulin secretion and sensitivity with PDA differ by smoking status. Smoking-induced pancreatic damage may explain the associations in smokers while mechanisms related to insulin resistance associations in nonsmokers. Future studies of these biomarkers and PDA should examine results by smoking status. .
研究检测了与肥胖、胰岛素分泌及敏感性以及胰腺导管腺癌(PDA)风险相关的两种生物标志物——循环C肽浓度与总脂联素之间的关联,结果并不一致,且纳入的吸烟者数量有限。我们研究了这些生物标志物以及高分子量(HMW)脂联素与PDA总体的关联,并按吸烟状况进行了分析。我们在3个队列(前列腺、肺、结肠直肠癌和卵巢癌试验、α-生育酚、β-胡萝卜素癌症预防研究以及癌症预防研究-II)中进行了一项汇总巢式病例对照分析,有758例病例(435例当前吸烟者)和1052例对照(531例吸烟者),按队列、年龄、性别、种族、采血日期和随访时间进行匹配。我们使用经年龄、吸烟、糖尿病和体重指数调整的条件逻辑回归来计算比值比(OR)和95%置信区间(CI)。循环C肽浓度在从不吸烟者或既往吸烟者中与PDA无关,但在当前吸烟者中与PDA呈负相关(每标准差OR = 0.67;95% CI,0.54 - 0.84;P = 0.005)。HMW脂联素在从不吸烟者中与PDA呈负相关(OR = 0.43;95% CI,0.23 - 0.81),在既往吸烟者中无关联,而在吸烟者中呈正相关(OR = 1.23;95% CI,1.04 - 1.45;P = 0.009)。总脂联素在非吸烟者或当前吸烟者中与PDA均无关联。胰岛素分泌和敏感性生物标志物与PDA的关联因吸烟状况而异。吸烟引起的胰腺损伤可能解释了吸烟者中的关联,而非吸烟者中的关联可能与胰岛素抵抗机制有关。未来关于这些生物标志物与PDA的研究应按吸烟状况检查结果。