Risk of cancer in patients on insulin glargine and other insulin analogues in comparison with those on human insulin: results from a large population-based follow-up study

被引:89
作者
Ruiter, R. [1 ,2 ]
Visser, L. E. [1 ,3 ,4 ]
van Herk-Sukel, M. P. P. [5 ]
Coebergh, J. W. W. [6 ]
Haak, H. R. [7 ]
Geelhoed-Duijvestijn, P. H. [8 ]
Straus, S. M. J. M. [9 ,10 ]
Herings, R. M. C. [5 ,11 ]
Stricker, B. H. Ch [1 ,2 ,4 ,10 ]
机构
[1] Erasmus MC, Dept Epidemiol, NL-3000 CA Rotterdam, Netherlands
[2] Inspectorate Hlth Care, Drug Safety Unit, The Hague, Netherlands
[3] Erasmus MC, Dept Hosp Pharm, NL-3000 CA Rotterdam, Netherlands
[4] Erasmus MC, Dept Internal Med, NL-3000 CA Rotterdam, Netherlands
[5] PHARMO Inst Drug Outcomes Res, Utrecht, Netherlands
[6] Erasmus MC, Dept Publ Hlth, NL-3000 CA Rotterdam, Netherlands
[7] Maxima Med Ctr, Dept Internal Med, Eindhoven, Netherlands
[8] Med Ctr Haaglanden, Dept Internal Med, The Hague, Netherlands
[9] Dutch Med Evaluat Board, The Hague, Netherlands
[10] Erasmus MC, Dept Med Informat, NL-3000 CA Rotterdam, Netherlands
[11] Erasmus MC, Dept Hlth Policy & Management, NL-3000 CA Rotterdam, Netherlands
关键词
Breast cancer; Cancer; Insulin; Insulin analogues; Insulin glargine; DIABETES-MELLITUS; COLORECTAL-CANCER; RESEARCH NETWORK; BREAST-CANCER; MALIGNANCIES; METAANALYSIS; MORTALITY; THERAPY; COHORT;
D O I
10.1007/s00125-011-2312-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Several publications suggest an association between certain types of insulin and cancer, but with conflicting results. We investigated whether insulin glargine (A21Gly,B31Arg,B32Arg human insulin) is associated with an increased risk of cancer in a large population-based cohort study. Data for this study were obtained from dispensing records from community pharmacies individually linked to hospital discharge records from 2.5 million individuals in the Netherlands. In a cohort of incident users of insulin, the association between insulin glargine and other insulin analogues, respectively, and cancer was analysed in comparison with human insulin using Cox proportional hazard models with cumulative duration of drug use as a time-varying determinant. The first hospital admission with a primary diagnosis of cancer was considered as the main outcome; secondary analyses were performed with specific cancers as outcomes. Of the 19,337 incident insulin users enrolled, 878 developed cancer. Use of insulin glargine was associated with a lower risk of malignancies in general in comparison with human insulin (HR 0.75, 95% CI 0.71, 0.80). In contrast, an increased risk was found for breast cancer (HR 1.58, 95% CI 1.22, 2.05). Dose-response relationships could not be identified. Users of insulin glargine and users of other insulin analogues had a lower risk of cancer in general than those using human insulin. Both associations might be a consequence of residual confounding, lack of adherence or competing risk. However, as in previous studies, we demonstrated an increased risk of breast cancer in users of insulin glargine in comparison with users of human insulin.
引用
收藏
页码:51 / 62
页数:12
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