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基于肠促胰岛素的药物与2型糖尿病患者胆管癌风险之间的关联:一项基于人群的大型匹配队列研究。

Association between incretin-based drugs and risk of cholangiocarcinoma among patients with type 2 diabetes: A large population-based matched cohort study.

作者信息

Krishnan Arunkumar, Schneider Carolin V, Arkenau Hendrik-Tobias, Mauro Ezequiel Matias, Forner Alejandro, Scott Butsch W, Walsh Declan, Alqahtani Saleh A

机构信息

Department of Supportive Oncology, Atrium Health Levine Cancer, Charlotte, NC, USA.

Department of Medicine, Section of Hematology and Oncology, Wake Forest University School of Medicine, Winston Salem, NC, USA.

出版信息

J Clin Transl Endocrinol. 2024 Sep 18;38:100370. doi: 10.1016/j.jcte.2024.100370. eCollection 2024 Dec.

Abstract

AIM

To examine the association between the use of incretin-based drugs [glucagon-like peptide-1 receptor agonists (GLP-1RAs), dipeptidyl peptidase-4 inhibitors (DPP-4Is)] and the risk of cholangiocarcinoma (CCA) in the United States.

METHODS

This large population-based, retrospective cohort study using the TriNetX datasets included adult patients with type 2 diabetes mellitus (T2DM) who were new users of GLP-1RAs, DPP-4Is, or other second- or third-line antidiabetic drugs between 2010 and 2021. The primary outcome was the incidence of CCA.

RESULTS

A total of 3,816,071 patients were included (mean age, 61.4 years, female, 49.3 %). A 51 % and 23 % risk reduction in CCA after 1 year of exposure to GLP-1RAs (hazard ratio 0.49; 95 % CI 0.40-0.60) and DPP4Is (0.77, 95 % CI 0.67-0.90), respectively compared to new second-or third-line users. Results were consistent at 3, 5, and 7 years of follow-up (0.66, 0.71, and 0.72 for GLP-1RAs and 0.84, 0.87, and 0.85 for DPP-4Is, respectively). Compared to new metformin users, GLP-1RA users were associated with a 42 % lower risk of developing CCA, whereas DPP-4I group was not associated with an increased risk.

CONCLUSIONS

GLP-1RAs and DPP-4Is were not associated with a significantly increased risk of CCA. GLP-1RAs even showed a reduced risk of CCA development. They can be considered as safe and effective treatment options for patients with T2DM at risk of CCA.

摘要

目的

研究在美国使用基于肠促胰岛素的药物[胰高血糖素样肽-1受体激动剂(GLP-1RAs)、二肽基肽酶-4抑制剂(DPP-4Is)]与胆管癌(CCA)风险之间的关联。

方法

这项基于人群的大型回顾性队列研究使用TriNetX数据集,纳入了2010年至2021年间新使用GLP-1RAs、DPP-4Is或其他二线或三线抗糖尿病药物的2型糖尿病(T2DM)成年患者。主要结局是CCA的发病率。

结果

共纳入3816071例患者(平均年龄61.4岁,女性占49.3%)。与新使用二线或三线药物的患者相比,使用GLP-1RAs(风险比0.49;95%置信区间0.40-0.60)和DPP-4Is(0.77,95%置信区间0.67-0.90)1年后,CCA风险分别降低了51%和23%。在3年、5年和7年的随访中结果一致(GLP-1RAs分别为0.66,0.71和0.72,DPP-4Is分别为0.84,0.87和0.85)。与新使用二甲双胍的患者相比,使用GLP-1RAs的患者发生CCA的风险降低42%,而DPP-4I组与风险增加无关。

结论

GLP-1RAs和DPP-4Is与CCA风险显著增加无关。GLP-1RAs甚至显示出降低CCA发生风险的作用。对于有CCA风险的T2DM患者,它们可被视为安全有效的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f043/11460491/67c68cb31452/gr1.jpg

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