Chou Chu-Lin, Juan Shu-Hui, Li Ching-Hao, Chen Hsi-Hsien, Kao Chih-Chin, Chen Li-Ying, Chien Li-Nien, Fang Te-Chao
Division of Nephrology, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan.
Division of Nephrology, Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Front Oncol. 2022 May 6;12:840142. doi: 10.3389/fonc.2022.840142. eCollection 2022.
Plasma dipeptidyl peptidase-4 (DPP4) levels were significantly lower in patients with colorectal and liver cancers, and animal studies also showed DPP4 inhibitors (DPP4is) have procarcinogenic effects in colorectal cancer. Until now, whether DPP4is therapy affects the progression of liver cancer and colorectal cancer in patients with T2DM has not been well investigated. We investigated the association between cumulative defined daily dose (cDDD) of DPP4is exposure and risks of liver and colorectal cancers in patients with type 2 diabetes.
We identified 268,520 patients with diabetes receiving DPP4is as second-line agents between March 1, 2009, and December 31, 2013, from Taiwan's National Health Insurance Research Database, Taiwan Cancer Registry, and National Death Registry of Taiwan. The amount of DPP4is were divided into three groups (low, medium, and high) based on the interquartile range of the cDDD of the DPP4is.
The data showed that the low cDDD of DPP-4is was associated with a reducing risk of colorectal cancer [adjusted odds ratio (OR), 0.49; 95% CI, 0.32-0.75; P=0.001]. However, the high cDDD of DPP-4is was associated with an increasing risk of colorectal cancer (adjusted OR, 1.86; 95% CI, 1.32-2.61; P<0.001). No association between DPP4is use and liver cancer risk was observed.
This nested case study revealed a J-shaped association between the cDDD of DPP-4is and colorectal cancer risk, but not liver cancer risk. Therefore, the effects of long-term DPP4is use on colorectal cancer risk warrant further study.
结直肠癌和肝癌患者的血浆二肽基肽酶4(DPP4)水平显著降低,动物研究也表明DPP4抑制剂(DPP4is)在结直肠癌中有促癌作用。迄今为止,DPP4is治疗是否会影响2型糖尿病(T2DM)患者的肝癌和结直肠癌进展尚未得到充分研究。我们调查了DPP4is暴露的累积限定日剂量(cDDD)与2型糖尿病患者肝癌和结直肠癌风险之间的关联。
我们从台湾国民健康保险研究数据库、台湾癌症登记处和台湾国家死亡登记处中,识别出2009年3月1日至2013年12月31日期间接受DPP4is作为二线药物治疗的268520例糖尿病患者。根据DPP4is的cDDD四分位数间距,将DPP4is的用量分为三组(低、中、高)。
数据显示,DPP-4is的低cDDD与结直肠癌风险降低相关[调整后的优势比(OR)为0.49;95%置信区间(CI)为0.32-0.75;P=0.001]。然而,DPP-4is的高cDDD与结直肠癌风险增加相关(调整后的OR为1.86;95%CI为1.32-2.61;P<0.001)。未观察到使用DPP4is与肝癌风险之间存在关联。
这项巢式病例研究揭示了DPP-4is的cDDD与结直肠癌风险之间呈J形关联,但与肝癌风险无关。因此,长期使用DPP4is对结直肠癌风险的影响值得进一步研究。