就诊间糖化血红蛋白变异性与糖尿病患者晚期癌症发展相关

Yuki Saito, H. Noto, O. Takahashi, D. Kobayashi
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引用次数: 10

摘要

目的近年来的研究表明,糖尿病患者发生肿瘤的风险较高。然而,血糖变异性对糖尿病患者肿瘤发生的影响尚未得到很好的研究。因此,我们进行了一项回顾性队列研究,以分析每次就诊时血红蛋白A1c (HbA1c)变异性与恶性肿瘤晚发的影响。方法本研究纳入2640例50岁以上的糖尿病患者。为了分析每次就诊的血糖活动,我们计算了所有记录的HbA1c的个人SD,并使用SD-HbA1c作为血糖变异性的衡量标准。由于个体就诊次数不同,我们将SD-HbA1c除以就诊次数,以调整个体间就诊时差的潜在影响。根据患者的HbA1c变异性将患者分为四分位数,并使用Cox回归模型评估血糖变异性与肿瘤发生晚发性之间的关系。结果随访期间发生恶性肿瘤330例,占12.5%。中位随访期为1511天(4.1年;四分位数间距为2487.5天)。相对于血糖变异性最低的组(第一个四分位数),血糖变异性较高的组与肿瘤发生呈剂量依赖关系。第二、第三和第四四分位数的比值比分别为1.20(95%可信区间为0.88-1.65)、1.43(1.02-2.00)和2.19(1.52-3.17)。平均HbA1c和糖尿病病程与肿瘤发生无显著相关性。当限制协变量的数量时,这一结果是一致的。这些结果表明,每次就诊的HbA1c变异性是晚期肿瘤发生的潜在危险因素。这种关联可能是由氧化应激或激素变异介导的。对于血糖控制不稳定的糖尿病患者,建议进行常规癌症筛查。
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Visit-to-Visit Hemoglobin A1c Variability Is Associated With Later Cancer Development in Patients With Diabetes Mellitus
Purpose Recent studies have shown that patients with diabetes mellitus have a higher risk of tumorigenesis. However, the effect of glycemic variability on tumorigenesis among diabetic patients has not been well investigated. Hence, we performed a retrospective cohort study to analyze the effect of visit-to-visit hemoglobin A1c (HbA1c) variability and later onset of malignancies. Methods This study included 2640 patients with diabetes mellitus 50 years or older. To analyze visit-to-visit glycemic activity, we calculated intrapersonal SD of all recorded HbA1c and used SD-HbA1c as a measure of glycemic variability. Because the number of individual visits varied, we divided SD-HbA1c by visit times in order to adjust for the potential influence of visit time difference between individuals. Patients were divided into quartiles according to their HbA1c variability, and Cox regression models were used to evaluate the association between glycemic variability and later onset of tumorigenesis. Results Three hundred thirty patients (12.5%) developed malignancy during follow-up. The median follow-up period was 1511 days (4.1 years; interquartile range, 2487.5 days). Relative to the group with the lowest glycemic variability (first quartile), the groups with higher glycemic variability showed a dose-dependent association with tumorigenesis. The odds ratios for the second, third, and fourth quartiles were 1.20 (95% confidence interval, 0.88–1.65), 1.43 (1.02–2.00), and 2.19 (1.52–3.17), respectively. The mean HbA1c and diabetes mellitus duration periods were not significantly associated with tumorigenesis. This result was consistent when limiting the number of covariates. Conclusions These results demonstrated that visit-to-visit HbA1c variability is a potential risk factor for later tumorigenesis. The association may be mediated by oxidative stress or hormone variability. Routine cancer screening may be suggested for diabetic patients with unstable glycemic control.
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