Primary Care Education Consortium, Charlotte, NC, USA.
Janssen Scientific Affairs LLC, Titusville, NJ, USA.
Curr Med Res Opin. 2019 Sep;35(9):1607-1614. doi: 10.1080/03007995.2019.1605160. Epub 2019 May 3.
To evaluate the impact of a 0.2% reduction in glycated hemoglobin (HbA1c) on treatment intensification, poor HbA1c control and HbA1c goal attainment in patients with type 2 diabetes mellitus (T2DM) initiated on a sodium glucose co-transporter 2 (SGLT2) inhibitor (SGLT2i). IQVIATM Health Plan Claims Data - US and IQVIATM Ambulatory EMR Data - US databases (29 October 2012-31 March 2016) were used to identify adults with T2DM initiated on an SGLT2i (index date) who had HbA1c measurements pre- and post-index, and ≥6 months of eligibility pre-index (baseline). HbA1c change was defined as the difference between the first post-index and the last pre-index measurements. Cox regression models were used to assess treatment intensification, poor HbA1c control (i.e. HbA1c > 9%, among patients <9% at baseline) and goal attainment (HbA1c < 7%, <8%; among patients with HbA1c above goal at baseline) adjusting for HbA1c change and baseline characteristics. Patients were observed up to one year after the first HbA1c measurement or end of eligibility. Hazard ratios (HRs) and 95% confidence intervals (CIs) were reported. A total of 938 patients (mean age 54.9, 42.5% female, mean HbA1c 8.5%) were selected. Following SGLT2i initiation, each 0.2% reduction in HbA1c levels was associated with a decreased risk of treatment intensification (HR [95% CI] = 0.90 [0.86-0.92]), a decreased likelihood of reaching HbA1c > 9% (HR [95% CI] = 0.85 [0.79-0.88]) and higher likelihoods of achieving a treatment goal of HbA1c < 7% (HR [95% CI] = 1.17 [1.12-1.21]) and HbA1c < 8% (HR [95% CI] = 1.08 [1.04-1.10]). In T2DM patients, each HbA1c reduction of 0.2% following the initiation of an SGLT2i was associated with a significant positive impact on treatment intensification and HbA1c goal attainment.
评估糖化血红蛋白(HbA1c)降低 0.2%对 2 型糖尿病(T2DM)患者强化治疗、HbA1c 控制不佳和 HbA1c 达标率的影响,这些患者起始接受钠-葡萄糖协同转运蛋白 2(SGLT2)抑制剂(SGLT2i)治疗。使用 IQVIA 健康计划理赔数据-美国和 IQVIA 门诊电子病历数据-美国数据库(2012 年 10 月 29 日至 2016 年 3 月 31 日),确定起始 SGLT2i(索引日期)的 T2DM 成年患者,这些患者具有索引前和索引后的 HbA1c 测量值,并且在索引前有≥6 个月的入组资格(基线)。HbA1c 变化定义为首次索引后和最后一次索引前测量值之间的差异。使用 Cox 回归模型评估强化治疗、HbA1c 控制不佳(即,基线时 HbA1c<9%的患者,HbA1c>9%)和目标达标(HbA1c<7%,<8%;基线时 HbA1c 高于目标值的患者),调整 HbA1c 变化和基线特征。患者在第一次 HbA1c 测量值或入组资格结束后,最多随访一年。报告风险比(HRs)和 95%置信区间(CIs)。共选择了 938 名患者(平均年龄 54.9 岁,42.5%为女性,平均 HbA1c 为 8.5%)。在起始 SGLT2i 治疗后,HbA1c 水平每降低 0.2%,强化治疗的风险降低(HR [95%CI] = 0.90 [0.86-0.92]),HbA1c>9%的可能性降低(HR [95%CI] = 0.85 [0.79-0.88]),HbA1c<7%的治疗目标达标率(HR [95%CI] = 1.17 [1.12-1.21])和 HbA1c<8%(HR [95%CI] = 1.08 [1.04-1.10])的可能性增加。在 T2DM 患者中,起始 SGLT2i 治疗后 HbA1c 每降低 0.2%,对强化治疗和 HbA1c 目标达标率均有显著的积极影响。