Wen Chi Pang, Cheng Ting Yuan David, Tsai Shan Pou, Hsu Hui Ling, Wang Shu Li
Division of Health Policy Research, National Health Research Institutes, Taiwan, ROC.
Diabetes Care. 2005 Nov;28(11):2756-61. doi: 10.2337/diacare.28.11.2756.
The objective of this article was to assess mortality risks at different levels of fasting blood glucose (FBG) in Taiwan, with particular attention to those pre-diabetic subjects with impaired fasting glucose (IFG).
Governmental employees and schoolteachers were followed up for an average of 11 years. With the use of Cox regression analyses, mortality risks were calculated for 36,386 subjects, aged 40-69.
FBG > or =110 mg/dl was associated with increased mortality risks for all causes, cardiovascular diseases (CVD), and diabetes. IFG, when defined as 110-125 mg/dl, was associated with a significant increase for CVD and/or diabetes mortality. These mortality risks remained elevated when known CVD risk factors were adjusted for. The IFG group shared risk factor characteristics more with the FBG > or =126 mg/dl group than with the FBG <110 mg/dl group. When IFG was defined as 100-125 mg/dl, the number of subjects quadrupled, but mortality risks diminished substantially because of the inclusion of 100-109 mg/dl group. The lowest FBG group, 50-75 mg/dl, had a significant 2-fold risk from all causes.
There was an overall J-shaped relationship between all-cause mortality and FBG. IFG, when defined as 110-125 mg/dl, is an independent risk factor and should be aggressively treated as a disease because its subsequent mortality risks for CVD and diabetes were significantly increased. The newly defined IFG at 100-125 mg/dl did not have the predictive power for later increases in CVD or diabetes mortality.
本文旨在评估台湾不同空腹血糖(FBG)水平下的死亡风险,尤其关注空腹血糖受损(IFG)的糖尿病前期患者。
对政府雇员和学校教师进行了平均11年的随访。通过Cox回归分析,计算了36386名年龄在40 - 69岁之间受试者的死亡风险。
FBG≥110mg/dl与全因、心血管疾病(CVD)和糖尿病死亡风险增加相关。当IFG定义为110 - 125mg/dl时,与CVD和/或糖尿病死亡显著增加相关。在对已知的CVD风险因素进行调整后,这些死亡风险仍然升高。IFG组与FBG≥126mg/dl组共享的风险因素特征比与FBG<110mg/dl组更多。当IFG定义为100 - 125mg/dl时,受试者数量增加了两倍,但由于纳入了100 - 109mg/dl组,死亡风险大幅降低。最低FBG组,即50 - 75mg/dl,全因死亡风险显著增加两倍。
全因死亡率与FBG之间总体呈J形关系。当IFG定义为110 - 125mg/dl时,是一个独立的风险因素,应作为一种疾病积极治疗,因为其随后的CVD和糖尿病死亡风险显著增加。新定义的100 - 125mg/dl的IFG对随后CVD或糖尿病死亡率的增加没有预测能力。