Wu Bechien U, Chen Qiaoling, Moon Becky H, Lustigova Eva, Nielsen Erin G, Alvarado Monica, Ahmed Syed A
Center for Pancreatic Care, Division of Gastroenterology, Kaiser Permanente Los Angeles Medical Center, Los Angeles, California, USA.
Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, California, USA.
Clin Transl Gastroenterol. 2024 Jan 1;15(1):e00650. doi: 10.14309/ctg.0000000000000650.
Screening for pancreatic cancer (PC) is suggested for high-risk individuals. Additional risk factors may enhance early detection in this population.
Retrospective cohort study among patients with germline variants and/or familial pancreatic cancer in an integrated healthcare system between 2003 and 2019. We calculated the incidence rate (IR) by risk category and performed a nested case-control study to evaluate the relationship between HbA1C and PC within 3 years before diagnosis (cases) or match date (controls). Cases were matched 1:4 by age, sex, and timing of HbA1c. Logistic regression was performed to assess an independent association with PC.
We identified 5,931 high-risk individuals: 1,175(19.8%) familial PC, 45(0.8%) high-risk germline variants ( STK11, CDKN2A ), 4,097(69.1%) had other germline variants ( ATM, BRCA 1, BRCA 2, CASR, CDKN2A, CFTR, EPCAM, MLH1, MSH2, MSH6, PALB2, PRSS1, STK11, and TP53 ), and 614(10.4%) had both germline variants and family history. Sixty-eight patients (1.1%) developed PC; 50% were metastatic at diagnosis. High-risk variant was associated with greatest risk of PC, IR = 85.1(95% confidence interval: 36.7-197.6)/10,000 person-years; other germline variants and first-degree relative had IR = 33 (18.4, 59.3), whereas IR among ≥2 first-degree relative alone was 10.7 (6.1, 18.8). HbA1c was significantly higher among cases vs controls (median = 7.0% vs 6.4%, P = 0.02). In multivariable analysis, every 1% increase in HbA1c was associated with 36% increase in odds of PC (odds ratio 1.36, 95% confidence interval: 1.08-1.72). Pancreatitis was independently associated with a risk of PC (odds ratio 3.93, 95% confidence limit 1.19, 12.91).
Risk of PC varies among high-risk individuals. HbA1c and history of pancreatitis may be useful additional markers for early detection in this patient population.
建议对高危个体进行胰腺癌(PC)筛查。其他风险因素可能有助于该人群的早期检测。
对2003年至2019年期间综合医疗系统中携带种系变异和/或家族性胰腺癌患者进行回顾性队列研究。我们按风险类别计算发病率(IR),并进行巢式病例对照研究,以评估诊断前3年内(病例组)或匹配日期(对照组)糖化血红蛋白(HbA1C)与胰腺癌之间的关系。病例组按年龄、性别和HbA1c检测时间与对照组以1:4进行匹配。采用逻辑回归分析评估与胰腺癌的独立关联。
我们共识别出5931名高危个体:1175例(19.8%)家族性胰腺癌,45例(0.8%)携带高危种系变异(STK11、CDKN2A),4097例(69.1%)携带其他种系变异(ATM、BRCA1、BRCA2、CASR、CDKN2A、CFTR、EPCAM、MLH1、MSH2、MSH6、PALB2、PRSS1、STK11和TP53),614例(10.4%)既携带种系变异又有家族史。68例患者(1.1%)发生胰腺癌;50%在诊断时已发生转移。高危变异与胰腺癌风险最高相关联,发病率为85.1(95%置信区间:36.7 - 197.6)/10000人年;其他种系变异和一级亲属的发病率为33(18.4,59.3)而仅≥2名一级亲属的发病率为10.7(6.1,18.8)。病例组的HbA1c显著高于对照组(中位数分别为7.0%和6.4%,P = 0.02)。在多变量分析中,HbA1c每升高1%,胰腺癌发生几率增加36%(优势比1.36,95%置信区间:1.08 - 1.72)。胰腺炎与胰腺癌风险独立相关(优势比3.93,95%置信区间1.19,12.91)。
胰腺癌风险在高危个体中各不相同。HbA1c和胰腺炎病史可能是该患者人群早期检测的有用附加标志物。