Division of Graduate Entry Medicine, School of Medicine, University of Nottingham, Nottingham, UK.
Nephrol Dial Transplant. 2020 Mar 1;35(3):471-477. doi: 10.1093/ndt/gfy258.
Albuminuria is a recognized diagnostic and prognostic marker of chronic kidney disease and cardiovascular (CV) risk but the well-known relationship between increments in urinary albumin:creatinine ratio (UACR) and CV outcomes and mortality has not been fully explored in insulin-treated patients with type 2 diabetes (T2D) in routine clinical care.
We investigated data for insulin users with T2D from UK general practices between 2007 and 2014. The UACR at the time of insulin initiation was measured and categorized as <10, 10- 29, 30-300 and >300 mg/g. Patients were followed up for 5 years or the earliest occurrence of all-cause mortality, non-fatal myocardial infarction or stroke. Cox proportional hazards models were fitted to estimate the risk of a composite of these events.
A total of 12 725 patients with T2D (mean age 58.6 ± 13.8 years, mean haemoglobin A1c 8.7 ± 1.8%) initiating insulin therapy between 2007 and 2014 met the inclusion criteria. Compared with patients whose ACR levels at insulin initiation were <10 mg/g, the adjusted risk of the 3-point composite endpoint was 9, 30 and 98% higher in those with ACR levels between 10-29, 30-300 and >300 mg/g, respectively, after a follow-up period of 5 years. The ACR category on its own did not predict risk of all-cause mortality.
This study shows that in patients with T2D on insulin therapy, increased urinary ACR is independently associated with an increased risk of major adverse CV events and all-cause mortality.
白蛋白尿是慢性肾脏病和心血管(CV)风险的公认诊断和预后标志物,但在常规临床护理中,接受胰岛素治疗的 2 型糖尿病(T2D)患者中,尿白蛋白与肌酐比值(UACR)的增加与 CV 结局和死亡率之间的这种众所周知的关系尚未得到充分探讨。
我们研究了 2007 年至 2014 年期间英国普通诊所中使用胰岛素的 T2D 患者的数据。在开始使用胰岛素时测量 UACR,并分为<10、10-29、30-300 和>300mg/g。患者随访 5 年或直至全因死亡率、非致死性心肌梗死或中风的最早发生。使用 Cox 比例风险模型来估计这些事件复合的风险。
共有 12725 例 2007 年至 2014 年间开始胰岛素治疗的 T2D 患者(平均年龄 58.6±13.8 岁,平均糖化血红蛋白 8.7±1.8%)符合纳入标准。与 UACR 水平在胰岛素起始时<10mg/g 的患者相比,UACR 水平在 10-29、30-300 和>300mg/g 之间的患者调整后的复合终点风险分别高 9、30 和 98%,随访 5 年后。单独的 UACR 类别并不能预测全因死亡率的风险。
这项研究表明,在接受胰岛素治疗的 T2D 患者中,增加的 UACR 与主要不良 CV 事件和全因死亡率的风险增加独立相关。