Department of Clinical Epidemiology, Institute of Clinical Medicine, Aarhus University Hospital, Aarhus, Denmark.
Novo Nordisk Scandinavia AB, Ørestad, Copenhagen, Denmark.
Diabetes Care. 2017 Jun;40(6):800-807. doi: 10.2337/dc16-2271. Epub 2017 Apr 12.
We investigated the association of early achieved HbA level and magnitude of HbA reduction with subsequent risk of cardiovascular events or death in patients with type 2 diabetes who initiate metformin.
This was a population-based cohort study including all metformin initiators with HbA tests in Northern Denmark, 2000-2012. Six months after metformin initiation, we classified patients by HbA achieved (<6.5% or higher) and by magnitude of HbA change from the pretreatment baseline. We used Cox regression to examine subsequent rates of acute myocardial infarction, stroke, or death, controlling for baseline HbA and other confounding factors.
We included 24,752 metformin initiators (median age 62.5 years, 55% males) with a median follow-up of 2.6 years. The risk of a combined outcome event gradually increased with rising levels of HbA achieved compared with a target HbA of <6.5%: adjusted hazard ratio (HR) 1.18 (95% CI 1.07-1.30) for 6.5-6.99%, HR 1.23 (1.09-1.40) for 7.0-7.49%, HR 1.34 (1.14-1.57) for 7.5-7.99%, and HR 1.59 (1.37-1.84) for ≥8%. Results were consistent for individual outcome events and robust by age-group and other patient characteristics. A large absolute HbA reduction from baseline also predicted outcome: adjusted HR 0.80 (0.65-0.97) for Δ = -4, HR 0.98 (0.80-1.20) for Δ = -3, HR 0.92 (0.78-1.08) for Δ = -2, and HR 0.99 (0.89-1.10) for Δ = -1 compared with no HbA change (Δ = 0).
A large initial HbA reduction and achievement of low HbA levels within 6 months after metformin initiation are associated with a lower risk of cardiovascular events and death in patients with type 2 diabetes.
我们研究了在开始使用二甲双胍的 2 型糖尿病患者中,早期达到的 HbA 水平和 HbA 降低幅度与心血管事件或死亡的后续风险之间的关系。
这是一项基于人群的队列研究,纳入了 2000 年至 2012 年在丹麦北部接受 HbA 检测的所有二甲双胍起始治疗者。在开始使用二甲双胍治疗后 6 个月,我们根据 HbA 水平(<6.5%或更高)和治疗前基线时 HbA 变化幅度对患者进行分类。我们使用 Cox 回归来检查急性心肌梗死、中风或死亡的后续发生率,同时控制基线 HbA 和其他混杂因素。
我们纳入了 24752 名开始使用二甲双胍的患者(中位年龄 62.5 岁,55%为男性),中位随访时间为 2.6 年。与目标 HbA<6.5%相比,随着达到的 HbA 水平逐渐升高,复合结局事件的风险逐渐增加:调整后的危险比(HR)为 1.18(95%CI 1.07-1.30),6.5-6.99%;HR 为 1.23(1.09-1.40),7.0-7.49%;HR 为 1.34(1.14-1.57),7.5-7.99%;HR 为 1.59(1.37-1.84),≥8%。各单项结局事件的结果一致,且在年龄组和其他患者特征方面稳健。基线时 HbA 较大幅度降低也预示着结局:与 HbA 无变化(Δ=0)相比,Δ=-4 时 HR 为 0.80(0.65-0.97),Δ=-3 时 HR 为 0.98(0.80-1.20),Δ=-2 时 HR 为 0.92(0.78-1.08),Δ=-1 时 HR 为 0.99(0.89-1.10)。
在开始使用二甲双胍后 6 个月内,HbA 初始较大幅度降低并达到低 HbA 水平与 2 型糖尿病患者的心血管事件和死亡风险降低相关。