Department of General Medicine, Fremantle Hospital and Health Service, Palmyra DC, Western Australia, Australia.
Medical School, University of Western Australia, Perth, Western Australia, Australia.
BMJ Open Diabetes Res Care. 2023 Jul;11(4). doi: 10.1136/bmjdrc-2023-003501.
The aim of this study was to compare mortality in community-based Australians with type 1 diabetes (T1D), without diabetes, or with type 2 diabetes (T2D).
The longitudinal observational Fremantle Diabetes Study Phase I (FDS1) T1D cohort, matched people without diabetes from the FDS1 catchment area, and matched FDS1 participants with T2D were followed up from entry (1993-1996) to death/end-2017. Mortality rates (MRs) and mortality rate ratios (MRRs) were calculated. Cox regression models identified independent determinants of death.
Of 121 participants with T1D and 484 age/sex/postcode-matched people without diabetes (pooled mean±SD age 43.1±15.3 years, 59.2% men), 55 (45.5%, MR 25.7 (95% CI 19.4 to 33.5)/1000 person-years) and 88 (18.2%, MR 8.5 (95% CI 6.8 to 10.4)/1000 person-years), respectively, died during 12 541 person-years of follow-up (MRR 3.04 (95% CI 2.13 to 4.31), p<0.001). Among participants with T1D, diagnosis at age 18-27 years and baseline HbA, urinary albumin:creatinine ratio, and retinopathy were independent predictors of death (p≤0.011). Twenty-five FDS1 participants died from cardiovascular disease (MR 11.7 (95% CI 7.6 to 17.3)/1000 person-years) vs 28 residents without diabetes (MR 2.7 (95% CI 1.8 to 3.9)/1000 person-years; MRR (95% CI) 4.34 (2.43, 7.73) (p<0.001). There were 93 FDS1 participants with T1D who were age/sex matched with an FDS1 participant with T2D and 53 (57.0%) and 37 (39.8%), respectively, died (p=0.027). In pooled Cox regression analysis, T1D was not a determinant of mortality (HR 1.18 (95% CI 0.71 to 1.97), p=0.523).
T1D substantially increases the risk of death, especially when diagnosed in late adolescence/young adulthood. Diabetes type does not influence mortality after adjustment for key confounding variables.
本研究旨在比较社区中患有 1 型糖尿病(T1D)、无糖尿病或 2 型糖尿病(T2D)的澳大利亚人的死亡率。
这项纵向观察性弗里曼特尔糖尿病研究第一阶段(FDS1)T1D 队列研究,将 FDS1 研究区域内无糖尿病的患者进行匹配,将 FDS1 参与者中患有 T2D 的患者进行匹配,并从入组(1993-1996 年)开始进行随访,直至死亡/2017 年底。计算死亡率(MRs)和死亡率比值(MRRs)。Cox 回归模型确定了死亡的独立决定因素。
在 121 名 T1D 患者和 484 名年龄/性别/邮政编码匹配的无糖尿病患者(平均年龄±标准差为 43.1±15.3 岁,59.2%为男性)中,分别有 55 名(45.5%,MR 25.7(95%CI 19.4 至 33.5)/1000 人年)和 88 名(18.2%,MR 8.5(95%CI 6.8 至 10.4)/1000 人年)死亡,随访期间共随访了 12541 人年(MRR 3.04(95%CI 2.13 至 4.31),p<0.001)。在 T1D 患者中,18-27 岁时的诊断以及基线时的 HbA、尿白蛋白/肌酐比值和视网膜病变是死亡的独立预测因素(p≤0.011)。在 FDS1 患者中,有 25 名死于心血管疾病(MR 11.7(95%CI 7.6 至 17.3)/1000 人年),而在无糖尿病的 28 名居民中(MR 2.7(95%CI 1.8 至 3.9)/1000 人年;MRR(95%CI)为 4.34(2.43,7.73)(p<0.001)。在 FDS1 中有 93 名 T1D 患者与 FDS1 中患有 T2D 的患者进行了年龄/性别匹配,其中 53 名(57.0%)和 37 名(39.8%)分别死亡(p=0.027)。在合并 Cox 回归分析中,T1D 不是死亡率的决定因素(HR 1.18(95%CI 0.71 至 1.97),p=0.523)。
T1D 显著增加了死亡的风险,尤其是在青少年晚期/成年早期诊断时。在调整了关键混杂因素后,糖尿病类型并不影响死亡率。