Institute of Epidemiology and Medical Biometry, ZIBMT, University of Ulm, Ulm, Germany; German Center for Diabetes Research (DZD), München-Neuherberg, Germany.
German Center for Diabetes Research (DZD), München-Neuherberg, Germany; Department of Internal Medicine 1, University of Lübeck, Germany.
Diabetes Res Clin Pract. 2018 Dec;146:162-171. doi: 10.1016/j.diabres.2018.10.011. Epub 2018 Oct 24.
Failure to intensify treatment of patients with type 2 diabetes (T2D) in a timely manner is a common challenge. If newer oral anti-diabetic drugs (NOADs) such as dipeptidyl peptidase-4 inhibitors (DPP-4i) and sodium/glucose cotransporter 2 inhibitors (SGLT-2i) do not achieve metabolic control, injectable therapy like insulin or glucagon-like Peptide 1 (GLP-1) receptor agonists are required. We investigated the time in poor glycaemic control (PC, HbA1c > 7%, >7.5%, >8%) in adults with T2D treated with DPP-4i/SGLT-2i until treatment intensification with insulin/GLP-1 or until the most recent documented visit.
T2D ≥ 18 years were identified from the diabetes patient follow-up registry (DPV), which captures data from diabetes specialist care. Patients with ≥2 documented visits with DPP-4i/SGLT-2i treatment and with the most recent treatment year ≥2015 were included.
The study population consisted of 4576 patients treated with DPP-4i/SGLT-2i. A subgroup of 1416 patients were intensified with an injectable therapy. Mean time in PC until intensification with insulin/GLP-1 was 16.7 months (HbA1c > 7%), 15.7 and 15.1 months (HbA1c > 7.5%, HbA1c > 8%) in this subgroup, respectively. Mean time in PC until most recent visit was 12.6, 9.9 and 8.4 months in the subgroup of patients without treatment intensification.
Even with NOADs, a substantial proportion of T2D do not achieve good metabolic control. These findings may be due to individualized target setting for HbA1c, or reluctance of patients and physicians towards injectable therapy. Effective diabetes management strategies are necessary to reduce the risk of adverse outcomes and to increase quality of life in T2D.
未能及时加强 2 型糖尿病(T2D)患者的治疗是一个常见的挑战。如果新型口服抗糖尿病药物(NOAD)如二肽基肽酶-4 抑制剂(DPP-4i)和钠/葡萄糖协同转运蛋白 2 抑制剂(SGLT-2i)不能达到代谢控制,就需要使用胰岛素或胰高血糖素样肽 1(GLP-1)受体激动剂等注射疗法。我们研究了接受 DPP-4i/SGLT-2i 治疗的 T2D 成人在血糖控制不佳(PC,HbA1c>7%、>7.5%、>8%)期间的时间,直到开始胰岛素/GLP-1 强化治疗或直至最近一次有记录的就诊。
从糖尿病患者随访登记处(DPV)中确定了年龄≥18 岁的 T2D 患者,该登记处记录了糖尿病专科护理的数据。纳入了至少有 2 次记录的 DPP-4i/SGLT-2i 治疗且最近治疗年份≥2015 年的患者。
研究人群包括 4576 名接受 DPP-4i/SGLT-2i 治疗的患者。1416 名患者亚组接受了注射治疗强化。在该亚组中,开始胰岛素/GLP-1 强化治疗前,HbA1c>7%、HbA1c>7.5%和 HbA1c>8%的患者 PC 时间的平均值分别为 16.7 个月、15.7 个月和 15.1 个月。在未进行治疗强化的患者亚组中,PC 时间的平均值分别为 12.6、9.9 和 8.4 个月。
即使使用了 NOAD,仍有相当一部分 T2D 患者未达到良好的代谢控制。这些发现可能是由于对 HbA1c 设定了个体化目标,或者是患者和医生对注射疗法的抵触。需要有效的糖尿病管理策略来降低不良结局的风险,提高 T2D 患者的生活质量。