Metcalf Patricia Anne, Kyle Cam, Kenealy Tim, Jackson Rod T
Department of Epidemiology & Biostatistics, School of Population Health, University of Auckland; Department of Statistics, University of Auckland.
LabPlus, Auckland City Hospital, and Department of Molecular Medicine, University, of Auckland, Private Bag 92019, Auckland Mail Center, Auckland 1010, New Zealand.
J Diabetes Complications. 2017 May;31(5):814-823. doi: 10.1016/j.jdiacomp.2017.02.007. Epub 2017 Feb 21.
We compared the utility of glycated hemoglobin (HbA) and oral glucose tolerance (oGTT) in non-diabetic patients for identifying incident diabetes; all-cause mortality; cardiovascular disease (CVD) mortality; CVD, coronary heart disease (CHD), and ischemic stroke events; and diabetes microvascular complications.
Data from a New Zealand community setting were prospectively linked to hospitalization, mortality, pharmaceutical and laboratory test results data. After applying exclusion criteria (prior laboratory diagnosis or history of drug treatment for diabetes or hospitalization for diabetes or CVD event), there were 31,148 adults who had an HbA and 2-h 75g oGTT. HbA was measured by ion-exchange high-performance liquid chromatography, and glucose using a commercial enzymatic method. We compared glycemic measures and outcomes using multivariable Cox proportional hazards regression.
The median follow-up time was 4years (range 0 to 13). The mean age was 57·6years and 53·0% were male. After adjusting for other glycemic measures (fasting glucose, 2-h glucose and/or HbA where relevant) in addition to age, sex, ethnicity and smoking habit, the hazard ratios for incident diabetes and diabetes complications of retinopathy and nephropathy were highest for 2-h glucose levels, followed by HbA and lastly by fasting glucose. However, all-cause mortality and CHD were significantly associated with HbA concentrations only, and ischemic stroke and CVD events with 2-h glucose only. Circulatory complications showed a stronger association with HbA.
Apart from neuropathy, HbA showed stronger associations with outcomes compared to fasting glucose and provides a convenient alternative to an oGTT.
我们比较了糖化血红蛋白(HbA)和口服葡萄糖耐量试验(oGTT)在非糖尿病患者中用于识别新发糖尿病、全因死亡率、心血管疾病(CVD)死亡率、CVD、冠心病(CHD)和缺血性中风事件以及糖尿病微血管并发症的效用。
来自新西兰社区的数据前瞻性地与住院、死亡率、药物治疗和实验室检查结果数据相关联。在应用排除标准(先前的实验室诊断或糖尿病药物治疗史或因糖尿病或CVD事件住院)后,有31148名成年人进行了HbA和2小时75g口服葡萄糖耐量试验。HbA通过离子交换高效液相色谱法测量,葡萄糖使用商业酶法测量。我们使用多变量Cox比例风险回归比较了血糖测量指标和结局。
中位随访时间为4年(范围0至13年)。平均年龄为57.6岁,男性占53.0%。在调整了除年龄、性别、种族和吸烟习惯外的其他血糖测量指标(空腹血糖、2小时血糖和/或相关时的HbA)后,2小时血糖水平发生新发糖尿病以及糖尿病视网膜病变和肾病并发症的风险比最高,其次是HbA,最后是空腹血糖。然而,全因死亡率和冠心病仅与HbA浓度显著相关,缺血性中风和CVD事件仅与2小时血糖相关。循环系统并发症与HbA的关联更强。
除神经病变外,与空腹血糖相比,HbA与结局的关联更强,并且是oGTT的便捷替代方法。