Insulin glargine use and cancer risk among patients with type 2 diabetes mellitus: a real-world study in Shanghai, China

被引:1
作者
Qi, Jiying [1 ,2 ]
He, Ping [3 ]
Yao, Huayan [4 ]
Sun, Wen [5 ]
Lu, Ping [5 ]
Zhang, Zizheng [1 ,2 ]
Cui, Bin [1 ,2 ]
Ning, Guang [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Ruijin Hosp, Shanghai Inst Endocrine & Metab Dis, Dept Endocrine & Metab Dis,Sch Med, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Natl Clin Res Ctr Metab Dis, Key Lab Endocrine & Metab Dis Natl Hlth Commiss PR, Shanghai Key Lab Endocrine Tumor,State Key Lab Med, Shanghai, Peoples R China
[3] Shanghai Hosp Dev Ctr, Link Healthcare Engn & Informat Dept, Shanghai, Peoples R China
[4] Shanghai Jiao Tong Univ, Ruijin Hosp, Comp Net Ctr, Sch Med, Shanghai, Peoples R China
[5] Wonders Informat Co Ltd, Shanghai, Peoples R China
关键词
Insulin glargine; NPH insulin; Cancer; Type 2 diabetes mellitus; Real-world study; SHORT-TERM INCIDENCE; LONG-ACTING INSULIN; BREAST-CANCER; BASAL INSULIN; ANALOGS; MALIGNANCIES; COHORT; TIME; PROSTATE;
D O I
10.1007/s13410-023-01230-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectiveThe association of insulin glargine with overall and site-specific cancer risk remains uncertain. This study aims to provide relevant evidence from mainland China.MethodsBased on the Shanghai Link Healthcare Database, patients newly treated with insulin glargine or neutral protamine Hagedorn (NPH) insulin between January 1, 2013 and December 31, 2020 were identified and followed up until December 31, 2021. In addition to the original cohort, we created a 1:1 propensity score-matched cohort with balanced baseline characteristics. Cox proportional hazards models were used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for incident cancers, comparing insulin glargine with NPH insulin.ResultsA total of 26,810 insulin glargine users and 47,765 NPH insulin users were enrolled in the final analysis. During a median follow-up of 4.18 years, 3903 patients developed cancer. Including a 1-year lag period, insulin glargine use was not associated with increased cancer risk compared to NPH insulin use in both the original cohort (HR 1.02, 95% CI 0.95-1.10) and the propensity score-matched cohort (HR 1.01, 95% CI 0.94-1.09). In stratified analyses by sex, age, and cancer site, as well as in sensitivity analyses at different lag periods, the estimated cancer risk, although fluctuating, remained uncorrelated without any substantial change.ConclusionInsulin glargine is not associated with the risk of overall and site-specific cancers compared to NPH insulin among patients with type 2 diabetes mellitus.
引用
收藏
页码:137 / 144
页数:8
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