Department of Health Sciences, University "Magna Græcia" of Catanzaro, Catanzaro, Italy.
Complex Operative Structure Endocrinology-Diabetology, Hospital Pugliese-Ciaccio, Catanzaro, Italy.
J Diabetes Res. 2019 Nov 4;2019:3971060. doi: 10.1155/2019/3971060. eCollection 2019.
SGLT-2 (sodium-glucose cotransporter-2) inhibitors are a novel class of oral hypoglycemic agents for the management of type 2 diabetes mellitus (T2DM). Herein, we aimed to assess the long-term effectiveness and safety of SGLT-2 inhibitors in a Southern Italy population of subjects affected by T2DM.
408 diabetic patients treated with one of the three SGLT-2 inhibitors currently available in Italy (dapagliflozin, empagliflozin, and canagliflozin), either alone or in combination with other antidiabetic drugs, were retrospectively assessed at baseline, during, and after 18 months of continuous therapy.
Treatment with SGLT-2 inhibitors resulted in a median decrease in HbA1c of 0.9%, with a percentage of decrement of 12 in relation to the baseline value, followed by a significant reduction ( < 0.001) in fasting plasma glucose. Variations in HbA1c occurred independently of the baseline clinical or biochemical characteristics. In addition, treatment with SGLT-2 inhibitors reduced body weight ( < 0.008) and decreased diastolic blood pressure ( = 0.004). With regard to safety outcomes, 66 patients out of 91 stopped SGLT-2 inhibitors during follow-up because of chronic or recurring genital infections, while the rest experienced other adverse events, such as urinary tract infections, polyuria, nausea, hypotension, dizziness, acute coronary event, worsening of glycemic control status, and rapid deterioration of renal function.
In our patients' population, the glycometabolic effects of SGLT-2 inhibitors were durable and comparable to those observed in multicenter randomized controlled trials. This notwithstanding safety concerns must be raised regarding the frequent occurrence of genitourinary infections and the risk of a rapid decline of renal function in patients with evidence of volume depletion and/or receiving other medications which can adversely affect kidney function.
SGLT-2(钠-葡萄糖协同转运蛋白-2)抑制剂是一种新型的口服降糖药物,用于治疗 2 型糖尿病(T2DM)。在此,我们旨在评估 SGLT-2 抑制剂在意大利南部地区 T2DM 患者中的长期疗效和安全性。
回顾性评估了 408 例接受目前在意大利上市的三种 SGLT-2 抑制剂(达格列净、恩格列净和卡格列净)中的一种治疗的糖尿病患者,这些患者单独或与其他降糖药物联合使用,评估了他们在基线、治疗 18 个月期间和治疗结束后的情况。
SGLT-2 抑制剂治疗使 HbA1c 中位数降低 0.9%,与基线值相比下降了 12%,随后空腹血糖显著降低(<0.001)。HbA1c 的变化与基线临床或生化特征无关。此外,SGLT-2 抑制剂治疗降低了体重(<0.008)和舒张压(=0.004)。安全性方面,91 例患者中有 66 例在随访期间因慢性或复发性生殖器感染而停用 SGLT-2 抑制剂,其余患者出现了其他不良反应,如尿路感染、多尿、恶心、低血压、头晕、急性冠状动脉事件、血糖控制状态恶化和肾功能迅速恶化。
在我们的患者人群中,SGLT-2 抑制剂的血糖代谢效果持久,与多中心随机对照试验观察到的结果相当。尽管如此,我们必须对频繁发生的泌尿生殖系统感染以及容量不足的患者肾功能迅速下降的风险提出安全方面的担忧,和/或正在接受可能对肾功能产生不利影响的其他药物治疗的患者。