Division of Diabetes, University of Texas Health Science Center, San Antonio, Texas.
J Clin Endocrinol Metab. 2020 Oct 1;105(10). doi: 10.1210/clinem/dgaa494.
To examine the effect of combination therapy with canagliflozin plus liraglutide versus each agent alone on beta cell function in type 2 diabetes mellitus (T2DM) patients.
A total of 45 poorly controlled (HbA1c = 7%-11%) T2DM patients received an oral glucose tolerance test (OGTT) before and after 16 weeks of treatment with: (i) liraglutide (LIRA); (ii) canagliflozin (CANA); (iii) liraglutide plus canagliflozin (CANA/LIRA).
Both liraglutide and canagliflozin significantly lowered HbA1c with no significant additive effect of the combination on HbA1c (0.89%, 1.43%, and 1.67% respectively). Insulin secretion during the OGTT, measured with (∆C-Pep/∆G)0-120, increased in the 3 groups (from 0.30 ± 0.06 to 0.48 ± 0.10; 0.29 ± 0.05 to 0.98 ± 0.23; and 0.24 ± 0.06 to 1.09 ± 0.12 in subjects receiving CANA, LIRA and CANA/LIRA respectively; P = 0.02 for CANA vs LIRA, P < 0.0001, CANA/LIRA vs CANA), and the increase in insulin secretion was associated with an increase in beta cell glucose sensitivity (29 ± 5 to 55 ± 11; 33 ± 6 to 101 ± 16; and 28 ± 6 to 112 ± 12, respectively; P = 0.01 for CANA vs LIRA, P < 0.0001, CANA/LIRA vs CANA). No significant difference in the increase in insulin secretion or beta cell glucose sensitivity was observed between subjects in LIRA or CANA/LIRA groups. The decrease in HbA1c strongly and inversely correlated with the increase in beta cell glucose sensitivity (r = 0.71, P < 0.001). In multivariate regression model, improved beta cell glucose sensitivity was the strongest predictor of HbA1c decrease with each therapy.
Improved beta cell glucose sensitivity with canagliflozin monotherapy and liraglutide monotherapy or in combination is major factor responsible for the HbA1c decrease. Canagliflozin failed to produce an additive effect to improve beta cell glucose sensitivity above that observed with liraglutide.
研究卡格列净联合利拉鲁肽与各单药治疗相比对 2 型糖尿病(T2DM)患者β细胞功能的影响。
共 45 例血糖控制不佳(HbA1c = 7%-11%)的 T2DM 患者分别接受了以下治疗 16 周前后的口服葡萄糖耐量试验(OGTT):(i)利拉鲁肽(LIRA);(ii)卡格列净(CANA);(iii)利拉鲁肽加卡格列净(CANA/LIRA)。
利拉鲁肽和卡格列净均显著降低 HbA1c,联合用药对 HbA1c 无显著附加作用(分别为 0.89%、1.43%和 1.67%)。OGTT 期间胰岛素分泌增加,以(∆C-Pep/∆G)0-120 表示,3 组均增加(分别从 0.30 ± 0.06 增加至 0.48 ± 0.10;0.29 ± 0.05 增加至 0.98 ± 0.23;0.24 ± 0.06 增加至 1.09 ± 0.12,接受 CANA、LIRA 和 CANA/LIRA 的受试者;P = 0.02,CANA 与 LIRA 相比,P < 0.0001,CANA/LIRA 与 CANA 相比),胰岛素分泌的增加与β细胞葡萄糖敏感性的增加相关(分别为 29 ± 5 增加至 55 ± 11;33 ± 6 增加至 101 ± 16;28 ± 6 增加至 112 ± 12;P = 0.01,CANA 与 LIRA 相比,P < 0.0001,CANA/LIRA 与 CANA 相比)。LIRA 或 CANA/LIRA 组受试者的胰岛素分泌或β细胞葡萄糖敏感性增加无显著差异。HbA1c 的降低与β细胞葡萄糖敏感性的增加呈强烈负相关(r = 0.71,P < 0.001)。多元回归模型显示,β细胞葡萄糖敏感性的改善是每种治疗方法降低 HbA1c 的最强预测因素。
卡格列净单药治疗、利拉鲁肽单药治疗或联合治疗均可改善β细胞葡萄糖敏感性,是 HbA1c 降低的主要原因。卡格列净未能产生优于利拉鲁肽的额外作用来改善β细胞葡萄糖敏感性。