Grewe Steven, Jördens Markus S, Roderburg Christoph, Leyh Catherine, Labuhn Simon, Luedde Tom, Krieg Sarah, Krieg Andreas, Loosen Sven H, Kostev Karel
Department of Gastroenterology, Hepatology and Infectious Diseases, University Hospital Düsseldorf, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstrasse 5, 40225 Düsseldorf, Germany.
Department of Inclusive Medicine, University Hospital Ostwestfalen-Lippe, Bielefeld University, 33617 Bielefeld, Germany.
J Clin Med. 2024 Sep 20;13(18):5584. doi: 10.3390/jcm13185584.
The early diagnosis of pancreatic cancer (ICD-10 C25) can improve the patient's prognosis. The association between pancreatic cancer and type 2 diabetes (T2D) is known, but not yet fully understood. It is, therefore, necessary to investigate the impact of hemoglobin A1c (HbA1c) serum levels on pancreatic cancer development and the potential intervention options. In the case-control study, patients from the German IQVIA Disease Analyzer database aged ≥18 years with a diagnosis of pancreatic cancer (ICD-10 C25) and a diagnosis of T2D (ICD-10: E11) were included. The patients' propensity score matched 1:5 with individuals without pancreatic cancer. Logistic regression models were used to estimate odds ratios (ORs) with 95% confidence intervals (95% CI). An elevated serum HbA1c prior to the index date was found to be significantly associated with an increased risk of a subsequent pancreatic cancer diagnosis for the mean HbA1c values of 6.5-8.4% (OR: 1.38; 95% CI: 1.22-1.57) as well as for mean HbA1c values ≥8.5% (OR: 1.41; 95% CI: 1.16-1.73). The only antihyperglycemic agent negatively associated with the subsequent pancreatic cancer diagnosis was the sodium-glucose cotransporter-2 (SGLT-2) inhibitor, with an odds ratio of 0.80 (95% confidence interval: 0.74-0.87 per year of therapy). This correlation was observed in both age- and sex-stratified subgroups. The data indicate that elevated serum HbA1c levels in patients with T2D are associated with an increased risk of pancreatic cancer development. It is possible that SGLT2 therapy may prove an effective means of reducing the risk of pancreatic cancer, thereby offering a potential avenue for the future reduction in pancreatic cancer incidence in patients with T2D.
胰腺癌(ICD - 10 C25)的早期诊断可改善患者预后。胰腺癌与2型糖尿病(T2D)之间的关联已为人所知,但尚未完全明晰。因此,有必要研究糖化血红蛋白(HbA1c)血清水平对胰腺癌发展的影响以及潜在的干预措施。在这项病例对照研究中,纳入了来自德国IQVIA疾病分析仪数据库、年龄≥18岁、诊断为胰腺癌(ICD - 10 C25)且诊断为T2D(ICD - 10:E11)的患者。患者的倾向得分与无胰腺癌的个体按1:5进行匹配。采用逻辑回归模型估计比值比(OR)及95%置信区间(95%CI)。结果发现,在索引日期之前血清HbA1c升高与后续胰腺癌诊断风险增加显著相关,平均HbA1c值为6.5 - 8.4%时(OR:1.38;95%CI:1.22 - 1.57)以及平均HbA1c值≥8.5%时(OR:1.41;95%CI:1.16 - 1.73)均如此。唯一与后续胰腺癌诊断呈负相关的降糖药物是钠 - 葡萄糖协同转运蛋白2(SGLT - 2)抑制剂,治疗每年的比值比为0.80(95%置信区间:0.74 - 0.87)。在年龄和性别分层的亚组中均观察到这种相关性。数据表明,T2D患者血清HbA1c水平升高与胰腺癌发生风险增加相关。SGLT2治疗可能是降低胰腺癌风险的有效手段,从而为未来降低T2D患者胰腺癌发病率提供了一条潜在途径。