Department of Endocrinology, Beijing Jishuitan Hospital, Beijing, People's Republic of China.
Department of Clinical Diabetes and Epidemiology, Baker Heart and Diabetes Institute, Level 4, 99 Commercial Road, Melbourne, VIC, 3004, Australia.
Diabetologia. 2018 May;61(5):1055-1063. doi: 10.1007/s00125-018-4544-z. Epub 2018 Feb 22.
AIMS/HYPOTHESIS: Current evidence suggests that type 2 diabetes may have a greater impact on those with earlier diagnosis (longer duration of disease), but data are limited. We examined the effect of age at diagnosis of type 2 diabetes on the risk of all-cause and cause-specific mortality over 15 years.
The data of 743,709 Australians with type 2 diabetes who were registered on the National Diabetes Services Scheme (NDSS) between 1997 and 2011 were examined. Mortality data were derived by linking the NDSS to the National Death Index. All-cause mortality and mortality due to cardiovascular disease (CVD), cancer and all other causes were identified. Poisson regression was used to model mortality rates by sex, current age, age at diagnosis, diabetes duration and calendar time.
The median age at registration on the NDSS was 60.2 years (interquartile range [IQR] 50.9-69.5) and the median follow-up was 7.2 years (IQR 3.4-11.3). The median age at diagnosis was 58.6 years (IQR 49.4-67.9). A total of 115,363 deaths occurred during 7.20 million person-years of follow-up. During the first 1.8 years after diabetes diagnosis, rates of all-cause and cancer mortality declined and CVD mortality was constant. All mortality rates increased exponentially with age. An earlier diagnosis of type 2 diabetes (longer duration of disease) was associated with a higher risk of all-cause mortality, primarily driven by CVD mortality. A 10 year earlier diagnosis (equivalent to 10 years' longer duration of diabetes) was associated with a 1.2-1.3 times increased risk of all-cause mortality and about 1.6 times increased risk of CVD mortality. The effects were similar in men and women. For mortality due to cancer (all cancers and colorectal and lung cancers), we found that earlier diagnosis of type 2 diabetes was associated with lower mortality compared with diagnosis at an older age.
CONCLUSIONS/INTERPRETATION: Our findings suggest that younger-onset type 2 diabetes increases mortality risk, and that this is mainly through earlier CVD mortality. Efforts to delay the onset of type 2 diabetes might, therefore, reduce mortality.
目的/假设:目前的证据表明,2 型糖尿病可能对那些更早被诊断(疾病持续时间更长)的患者影响更大,但数据有限。我们研究了 2 型糖尿病患者的诊断年龄对 15 年内全因和死因特异性死亡率的影响。
我们对 1997 年至 2011 年间在国家糖尿病服务计划(NDSS)注册的 743709 名澳大利亚 2 型糖尿病患者的数据进行了检查。通过将 NDSS 与国家死亡指数相链接来获取死亡率数据。确定了全因死亡率以及心血管疾病(CVD)、癌症和所有其他原因导致的死亡率。使用泊松回归模型按性别、当前年龄、诊断年龄、糖尿病病程和日历时间来对死亡率进行建模。
NDSS 注册的中位数年龄为 60.2 岁(四分位间距 [IQR] 50.9-69.5),中位随访时间为 7.2 年(IQR 3.4-11.3)。诊断时的中位数年龄为 58.6 岁(IQR 49.4-67.9)。在 720 万人年的随访期间,共有 115363 人死亡。在糖尿病诊断后的头 1.8 年内,全因和癌症死亡率下降,而 CVD 死亡率保持不变。所有死亡率均随年龄呈指数增长。2 型糖尿病的较早诊断(疾病持续时间较长)与全因死亡率的风险增加相关,主要与 CVD 死亡率增加有关。早诊断 10 年(相当于糖尿病病程延长 10 年)与全因死亡率增加 1.2-1.3 倍以及 CVD 死亡率增加约 1.6 倍相关。这些影响在男性和女性中相似。对于癌症(所有癌症和结直肠癌、肺癌)导致的死亡率,我们发现 2 型糖尿病的早期诊断与较晚年龄诊断相比,死亡率较低。
结论/解释:我们的研究结果表明,2 型糖尿病的发病年龄较小会增加死亡率风险,这主要是由于早期 CVD 死亡率的增加。因此,努力延迟 2 型糖尿病的发病可能会降低死亡率。