Diabetes, metformin and cancer risk in myotonic dystrophy type I

被引:12
作者
Alsaggaf, Rotana [1 ,2 ]
Pfeiffer, Ruth M. [3 ]
Wang, Youjin [1 ]
St George, Diane Marie M. [2 ]
Zhan, Min [2 ]
Wagner, Kathryn R. [4 ,5 ,6 ]
Amr, Sania [2 ,7 ]
Greene, Mark H. [1 ]
Gadalla, Shahinaz M. [1 ]
机构
[1] NCI, Clin Genet Branch, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[2] Univ Maryland, Dept Epidemiol & Publ Hlth, Baltimore, MD 21201 USA
[3] NCI, Biostat Branch, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[4] Kennedy Krieger Inst, Hugo W Moser Res Inst, Baltimore, MD USA
[5] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[6] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[7] Univ Maryland, Marlene & Stuart Greenebaum Comprehens Canc Ctr, Baltimore, MD 21201 USA
基金
美国国家卫生研究院;
关键词
myotonic dystrophy; diabetes; cancer; metformin; CPRD; INSULIN-RECEPTOR; CTG REPEAT; MORTALITY; VALIDITY; DATABASE; BIASES; RNA; DM1; UK;
D O I
10.1002/ijc.32801
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Myotonic dystrophy type I (DM1) is an autosomal dominant multisystem disorder characterized by myotonia and muscle weakness. Type 2 diabetes (T2D) and cancer have been shown to be part of the DM1 phenotype. Metformin, a well-established agent for the management of T2D, is thought to have cancer-preventive effects in the general population. In our study, we aimed to assess the association between T2D, metformin use and the risk of cancer in DM1 patients. We identified a cohort of 913 DM1 patients and an age-, sex- and clinic-matched cohort of 12,318 DM1-free controls from the UK Clinical Practice Research Datalink, a large primary care records database. We used Cox regression models to assess cancer risk in T2D patients who were metformin users or nonusers compared to patients without T2D. Separate analyses were conducted for DM1 patients and controls. T2D was more prevalent in DM1 than in controls (8% vs. 3%, p < 0.0001). DM1 patients with T2D, compared to those without T2D, were more likely to develop cancer (hazard ratio [HR] = 3.60, 95% confidence interval [CI] = 1.18-10.97; p = 0.02), but not if they were treated with metformin (HR = 0.43, 95% CI = 0.06-3.35; p = 0.42). Among controls, we observed no significant associations between T2D and cancer risk in either users or nonusers of Metformin (HR = 1.28, 95% CI = 0.91-1.79; p = 0.16 and HR = 1.13, 95% CI = 0.72-1.79; p = 0.59, respectively). These results show an association between T2D and cancer risk in DM1 patients and may provide new insights into the possible benefits of Metformin use in DM1.
引用
收藏
页码:785 / 792
页数:8
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