Department of Epidemiology, German Institute of Human Nutrition Potsdam-Rehbruecke, Nuthetal, Germany.
PLoS One. 2012;7(6):e38877. doi: 10.1371/journal.pone.0038877. Epub 2012 Jun 13.
Observational studies have shown that glycated haemoglobin (HbA(1c)) is related to mortality, but the shape of the association is less clear. Furthermore, disease duration and medication may modify this association. This observational study explored the association between HbA(1c) measured in stored erythrocytes and mortality. Secondly, it was assessed whether disease duration and medication use influenced the estimates or were independently associated with mortality.
Within the European Prospective Investigation into Cancer and Nutrition a cohort was analysed of 4,345 individuals with a confirmed diagnosis of diabetes at enrolment. HbA(1c) was measured in blood samples stored up to 19 years. Multivariable Cox proportional hazard regression models for all-cause mortality investigated HbA(1c) in quartiles as well as per 1% increment, diabetes medication in seven categories of insulin and oral hypoglycaemic agents, and disease duration in quartiles.
After a median follow-up of 9.3 years, 460 participants died. Higher HbA(1c) was associated with higher mortality: Hazard Ratio for 1%-increase was 1.11 (95% CI 1.06, 1.17). This association was linear (P-nonlinearity = 0.15) and persistent across categories of medication use, disease duration, and co-morbidities. Compared with metformin, other medication types were not associated with mortality. Longer disease duration was associated with mortality, but not after adjustment for HbA(1c) and medication.
This prospective study showed that persons with lower HbA(1c) had better survival than those with higher HbA(1c). The association was linear and independent of disease duration, type of medication use, and presence of co-morbidities. Any improvement of HbA(1c) appears to be associated with reduced mortality risk.
观察性研究表明,糖化血红蛋白(HbA(1c))与死亡率有关,但这种关联的形状不太清楚。此外,疾病持续时间和药物治疗可能会改变这种关联。本观察性研究探讨了储存红细胞中测量的 HbA(1c)与死亡率之间的关系。其次,评估了疾病持续时间和药物使用是否影响估计值或与死亡率独立相关。
在欧洲癌症前瞻性调查和营养研究中,对 4345 名在入组时确诊为糖尿病的个体进行了分析。HbA(1c)在储存长达 19 年的血液样本中进行测量。使用多变量 Cox 比例风险回归模型,对全因死亡率进行了分析,研究了 HbA(1c)在四分位数和每增加 1%的情况下,以及在胰岛素和口服降糖药的 7 个类别中的糖尿病药物治疗情况,以及四分位数中的疾病持续时间。
在中位数为 9.3 年的随访后,460 名参与者死亡。较高的 HbA(1c)与较高的死亡率相关:每增加 1%的危险比为 1.11(95%置信区间 1.06,1.17)。这种关联是线性的(P-非线性=0.15),并且在药物使用、疾病持续时间和合并症的类别中都存在。与二甲双胍相比,其他药物类型与死亡率无关。疾病持续时间较长与死亡率相关,但在调整了 HbA(1c)和药物治疗后则不然。
本前瞻性研究表明,HbA(1c)水平较低的患者比 HbA(1c)水平较高的患者生存更好。这种关联是线性的,与疾病持续时间、药物使用类型和合并症的存在无关。HbA(1c)的任何改善似乎都与降低死亡率风险有关。