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患者就诊间糖化血红蛋白变异性与糖尿病患者后期癌症发生相关。

Visit-to-Visit Hemoglobin A1c Variability Is Associated With Later Cancer Development in Patients With Diabetes Mellitus.

机构信息

From the Department of Gastroenterology, Keio University School of Medicine.

Department of Endocrinology.

出版信息

Cancer J. 2019 Jul/Aug;25(4):237-240. doi: 10.1097/PPO.0000000000000387.

Abstract

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.

摘要

目的

最近的研究表明,糖尿病患者的肿瘤发生风险更高。然而,血糖变异性对糖尿病患者肿瘤发生的影响尚未得到充分研究。因此,我们进行了一项回顾性队列研究,分析了随访间糖化血红蛋白(HbA1c)变异性与恶性肿瘤发生时间的关系。

方法

本研究纳入了 2640 名年龄在 50 岁及以上的糖尿病患者。为了分析随访间血糖变化,我们计算了所有记录的 HbA1c 的个体内标准差,并将 HbA1c 标准差(SD-HbA1c)作为血糖变异性的衡量指标。由于个体的随访次数不同,我们将 SD-HbA1c 除以随访次数,以调整个体间随访时间差异的潜在影响。根据 HbA1c 变异性将患者分为四分位组,采用 Cox 回归模型评估血糖变异性与肿瘤发生时间的关系。

结果

330 例(12.5%)患者在随访期间发生恶性肿瘤。中位随访时间为 1511 天(4.1 年;四分位间距为 2487.5 天)。与血糖变异性最低的(四分位 1 组)患者相比,血糖变异性较高的患者发生肿瘤的风险呈剂量依赖性增加。四分位 2、3 和 4 组的比值比分别为 1.20(95%置信区间为 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均无显著相关性。当限制协变量数量时,该结果仍然一致。

结论

这些结果表明,随访间 HbA1c 变异性是肿瘤发生的潜在危险因素。这种相关性可能是由氧化应激或激素变异性介导的。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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