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诊断前血糖水平、糖尿病与胶质瘤之间的关联。

Associations between prediagnostic blood glucose levels, diabetes, and glioma.

机构信息

Division of Epidemiology, College of Public Health, Ohio State University, Columbus, Ohio, 43210, United States of America.

Comprehensive Cancer Center, Ohio State University, Columbus, Ohio, 43210, United States of America.

出版信息

Sci Rep. 2017 May 3;7(1):1436. doi: 10.1038/s41598-017-01553-2.

Abstract

Previous literature indicates that pre-diagnostic diabetes and blood glucose levels are inversely related to glioma risk. To replicate these findings and determine whether they could be attributed to excess glucose consumption by the preclinical tumour, we used data from the Apolipoprotein MOrtality RISk (AMORIS) (n = 528,580) and the Metabolic syndrome and Cancer project (Me-Can) cohorts (n = 269,365). We identified individuals who were followed for a maximum of 15 years after their first blood glucose test until glioma diagnosis, death, emigration or the end of follow-up. Hazard ratios (HRs), 95% confidence intervals (CIs) and their interactions with time were estimated using Cox time-dependent regression. As expected, pre-diagnostic blood glucose levels were inversely related to glioma risk (AMORIS, P  = 0.002; Me-Can, P  = 0.04) and pre-diagnostic diabetes (AMORIS, HR = 0.30, 95% CI 0.17 to 0.53). During the year before diagnosis, blood glucose was inversely associated with glioma in the AMORIS (HR = 0.78, 95% CI 0.66 to 0.93) but not the Me-Can cohort (HR = 0.99, 95% CI 0.63 to 1.56). This AMORIS result is consistent with our hypothesis that excess glucose consumption by the preclinical tumour accounts for the inverse association between blood glucose and glioma. We discuss additional hypothetical mechanisms that may explain our paradoxical findings.

摘要

先前的文献表明,糖尿病前期和血糖水平与胶质瘤风险呈负相关。为了复制这些发现,并确定它们是否归因于临床前肿瘤过量消耗葡萄糖,我们使用了载脂蛋白 M 死亡率风险(AMORIS)(n=528580)和代谢综合征和癌症项目(Me-Can)队列(n=269365)的数据。我们确定了在首次血糖测试后最多随访 15 年的个体,直到胶质瘤诊断、死亡、移民或随访结束。使用 Cox 时间依赖性回归估计风险比(HR)、95%置信区间(CI)及其与时间的交互作用。正如预期的那样,糖尿病前期血糖水平与胶质瘤风险呈负相关(AMORIS,P=0.002;Me-Can,P=0.04)和糖尿病前期(AMORIS,HR=0.30,95%CI0.17 至 0.53)。在诊断前一年,血糖与 AMORIS 中的胶质瘤呈负相关(HR=0.78,95%CI0.66 至 0.93),但在 Me-Can 队列中无相关性(HR=0.99,95%CI0.63 至 1.56)。AMORIS 的这一结果与我们的假设一致,即临床前肿瘤过量消耗葡萄糖解释了血糖与胶质瘤之间的反比关系。我们讨论了可能解释我们矛盾发现的其他假设机制。

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