Division of Diabetes, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Division of Diabetes, University of Texas Health Science Center at San Antonio, San Antonio, TX
Diabetes Care. 2020 Jun;43(6):1234-1241. doi: 10.2337/dc18-2460. Epub 2020 Mar 27.
To examine the effect of combination therapy with canagliflozin plus liraglutide on HbA, endogenous glucose production (EGP), and body weight versus each therapy alone.
Forty-five patients with poorly controlled (HbA 7-11%) type 2 diabetes mellitus (T2DM) on metformin with or without sulfonylurea received a 9-h measurement of EGP with [3-H]glucose infusion, after which they were randomized to receive ) liraglutide 1.2 mg/day (LIRA), ) canagliflozin 100 mg/day (CANA), or ) liraglutide 1.2 mg plus canagliflozin 100 mg (CANA/LIRA) for 16 weeks. At 16 weeks, the EGP measurement was repeated.
The mean decrease from baseline to 16 weeks in HbA was -1.67 ± 0.29% ( = 0.0001), -0.89 ± 0.24% ( = 0.002), and -1.44 ± 0.39% ( = 0.004) in patients receiving CANA/LIRA, CANA, and LIRA, respectively. The decrease in body weight was -6.0 ± 0.8 kg ( < 0.0001), -3.5 ± 0.5 kg ( < 0.0001), and -1.9 ± 0.8 kg ( = 0.03), respectively. CANA monotherapy caused a 9% increase in basal rate of EGP ( < 0.05), which was accompanied by a 50% increase ( < 0.05) in plasma glucagon-to-insulin ratio. LIRA monotherapy reduced plasma glucagon concentration and inhibited EGP. In CANA/LIRA-treated patients, EGP increased by 15% ( < 0.05), even though the plasma insulin response was maintained at baseline and the CANA-induced rise in plasma glucagon concentration was blocked.
These results demonstrate that liraglutide failed to block the increase in EGP caused by canagliflozin despite blocking the rise in plasma glucagon and preventing the decrease in plasma insulin concentration caused by canagliflozin. The failure of liraglutide to prevent the increase in EGP caused by canagliflozin explains the lack of additive effect of these two agents on HbA.
研究卡格列净联合利拉鲁肽治疗与单一疗法相比对糖化血红蛋白(HbA)、内源性葡萄糖生成(EGP)和体重的影响。
45 例血糖控制不佳(HbA7-11%)的 2 型糖尿病(T2DM)患者在服用二甲双胍加或不加磺酰脲类药物的基础上接受了 9 小时的[3-H]葡萄糖输注 EGP 测量,之后他们被随机分配接受)利拉鲁肽 1.2mg/天(LIRA),)卡格列净 100mg/天(CANA),或)利拉鲁肽 1.2mg 加卡格列净 100mg(CANA/LIRA)治疗 16 周。在 16 周时,重复 EGP 测量。
从基线到 16 周,接受 CANA/LIRA、CANA 和 LIRA 治疗的患者的 HbA 分别下降-1.67 ± 0.29%(=0.0001)、-0.89 ± 0.24%(=0.002)和-1.44 ± 0.39%(=0.004)。体重下降分别为-6.0 ± 0.8kg(<0.0001)、-3.5 ± 0.5kg(<0.0001)和-1.9 ± 0.8kg(=0.03)。CANA 单药治疗可使 EGP 基础率增加 9%(<0.05),同时使血浆胰高血糖素与胰岛素比值增加 50%(<0.05)。LIRA 单药治疗可降低血浆胰高血糖素浓度并抑制 EGP。在接受 CANA/LIRA 治疗的患者中,尽管维持了基线时的胰岛素反应,并阻断了 CANA 引起的血浆胰高血糖素浓度升高,但 EGP 增加了 15%(<0.05)。
这些结果表明,尽管利拉鲁肽可阻断卡格列净引起的血浆胰高血糖素升高并防止卡格列净引起的血浆胰岛素浓度降低,但它未能阻断卡格列净引起的 EGP 升高。利拉鲁肽未能防止卡格列净引起的 EGP 升高,这解释了这两种药物联合使用对 HbA 没有相加作用的原因。