Diabetes Care Center, Jinnouchi Hospital, 6-2-3 Kuhonji, Chuo-ku, Kumamoto, 862-0976, Japan.
Division of Cardiovascular Medicine, Diabetes Care Center, Jinnouchi Hospital, Kumamoto, Japan.
Clin Drug Investig. 2018 Jan;38(1):19-27. doi: 10.1007/s40261-017-0580-6.
Obesity is globally recognized as an important clinical problem and sodium-glucose co-transporter 2 (SGLT2) inhibitors are considered a suitable therapy for obese patients with type 2 diabetes mellitus (T2DM). We examined the clinical factors associated with initial decrease in body-fat percentage (Fat %) induced by SGLT2 inhibitors in patients with T2DM.
We retrospectively enrolled patients newly treated with SGLT2 inhibitors in addition to ongoing medications at Jinnouchi Hospital between April 2014 and December 2015. We examined the SGLT2 inhibitor-induced change in body composition by using a bioelectrical impedance analyzer (InBody770) before SGLT2 inhibitor administration and after 4 weeks' treatment.
A total of 175 patients with T2DM were enrolled and we analyzed 148 patients. Add-on SGLT2 inhibitor treatment significantly reduced body weight (- 1.04 ± 1.18 kg, p < 0.01), total fat quantity (- 0.62 ± 1.19 kg, p < 0.01), and Fat % (- 0.4 ± 1.4%, p < 0.01). Pretreatment levels of glycated hemoglobin (HbA1c) [odds ratio (OR), 1.61; 95% confidence interval (CI), 1.15-2.25, p < 0.01] and smoking (OR, 2.65; 95% CI, 1.14-6.15, p = 0.02) were significantly associated factors for greater fat-reduction defined as more than 0.4% (median) decrease in Fat % in multivariate logistic regression analysis. In receiver operator characteristic analysis, the cut-off value of pretreatment levels of HbA1c for a greater Fat % decrease was 7.7% (sensitivity 53% and specificity 69%, p < 0.01).
Additional treatment with SGLT2 inhibitors effectively decreased Fat % in T2DM patients with high HbA1c levels before SGLT2 inhibitor administration. Our results suggest a greater initial response in Fat % reduction to SGLT2 inhibitor therapy in diabetic patients with pretreatment HbA1c levels ≥ 7.7%.
肥胖症在全球范围内被认为是一个重要的临床问题,钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂被认为是肥胖 2 型糖尿病(T2DM)患者的合适治疗方法。我们研究了与 SGLT2 抑制剂治疗 T2DM 患者初始体脂肪百分比(Fat%)下降相关的临床因素。
我们回顾性地招募了 2014 年 4 月至 2015 年 12 月在仁久井医院接受 SGLT2 抑制剂联合现有药物治疗的新患者。在开始 SGLT2 抑制剂治疗前和治疗 4 周后,我们使用生物电阻抗分析仪(InBody770)检查 SGLT2 抑制剂诱导的身体成分变化。
共纳入 175 例 T2DM 患者,我们分析了 148 例患者。SGLT2 抑制剂的附加治疗显著降低了体重(-1.04±1.18kg,p<0.01)、总脂肪量(-0.62±1.19kg,p<0.01)和 Fat%(-0.4±1.4%,p<0.01)。糖化血红蛋白(HbA1c)[比值比(OR),1.61;95%置信区间(CI),1.15-2.25,p<0.01]和吸烟[OR,2.65;95%CI,1.14-6.15,p=0.02]的治疗前水平是 Fat%减少更多(定义为 Fat%下降超过中位数 0.4%)的显著相关因素。在多元逻辑回归分析中,HbA1c 的治疗前水平的截断值为 7.7%,用于更大的 Fat%降低(敏感性为 53%,特异性为 69%,p<0.01)。
在开始 SGLT2 抑制剂治疗前,SGLT2 抑制剂的附加治疗可有效降低 T2DM 患者的 Fat%。我们的结果表明,在 SGLT2 抑制剂治疗前 HbA1c 水平≥7.7%的糖尿病患者中,SGLT2 抑制剂治疗的初始 Fat%降低反应更大。