A Multicenter, Open-Label, Single-Arm Trial of the Efficacy and Safety of Empagliflozin Treatment for Refractory Diabetes Mellitus with Insulin Resistance (EMPIRE-01)

被引:3
|
作者
Hirota, Yushi [1 ]
Kakei, Yasumasa [2 ]
Imai, Junta [3 ]
Katagiri, Hideki [3 ]
Ebihara, Ken [4 ]
Wada, Jun [5 ]
Suzuki, Junichi [6 ]
Urakami, Tatsuhiko [6 ]
Omori, Takashi [7 ]
Ogawa, Wataru [1 ]
机构
[1] Kobe Univ, Grad Sch Med, Dept Internal Med, Div Diabet & Endocrinol, 7-5-1 Kusunoki Cho,Chuo Ku, Kobe 6500017, Japan
[2] Kobe Univ Hosp, Clin & Translat Res Ctr, Kobe, Japan
[3] Tohoku Univ, Grad Sch Med, Dept Metab & Diabet, Sendai, Miyagi, Japan
[4] Jichi Med Univ, Dept Internal Med, Div Endocrinol & Metab, Tochigi, Japan
[5] Okayama Univ, Fac Med Dent & Pharmaceut Sci, Dept Nephrol Rheumatol Endocrinol & Metab, Okayama, Japan
[6] Nihon Univ, Sch Med, Dept Pediat & Child Hlth, Tokyo, Japan
[7] Kyoto Univ, Grad Sch Med, Dept Clin Biostat, Kyoto, Japan
关键词
Empagliflozin; Genetic insulin resistance syndrome; Lipoatrophic diabetes; SGLT2; inhibitor; Type A insulin resistance syndrome; Type B insulin resistance syndrome; COTRANSPORTER; 2; INHIBITOR; LIPODYSTROPHY SYNDROMES; DOUBLE-BLIND; ADD-ON; KETOACIDOSIS; METFORMIN; DISEASES; THERAPY; 24-WEEK;
D O I
10.1007/s13300-023-01526-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionInsulin resistance syndrome and lipoatrophic diabetes are characterized by severe insulin resistance and are often refractory to treatment. Trials assessing the efficacy of antidiabetes drugs for these rare conditions have been limited, however. Sodium-glucose cotransporter 2 (SGLT2) inhibitors, which lower glycemia independently of insulin action, have shown efficacy for type 2 diabetes with insulin resistance. We here investigated the efficacy and safety of the SGLT2 inhibitor empagliflozin for treatment of insulin resistance syndrome and lipoatrophic diabetes.MethodsThe trial was conducted at five academic centers in Japan and included seven patients with insulin resistance syndrome and one patient with lipoatrophic diabetes. Participants received 10 mg of empagliflozin daily. If the hemoglobin A1c (HbA1c) level was >= 7.0% (52 mmol/mol) after 12 weeks, the dose was adjusted to 25 mg. The study duration was 24 weeks, and the primary outcome was the change in HbA1c level by the end of the treatment period. Safety evaluations were performed for all participants.ResultsBy the end of the 24-week treatment period, the mean HbA1c level for all eight patients had decreased by 0.99 percentage points (10.8 mmol/mol) (95% confidence interval [CI], 0.59 to 1.38 percentage points, 6.6 to 14.9 mmol/mol) and the mean fasting plasma glucose concentration had declined by 63.9 mg/dL (3.55 mmol/L) (95% CI 25.5 to 102.3 mg/dL, 1.42 to 5.68 mmol/L). Continuous glucose monitoring revealed a reduction in mean glucose levels from 164.3 +/- 76.1 to 137.6 +/- 46.6 mg/dL (9.13 +/- 4.23 to 7.65 +/- 2.59 mmol/L) as well as an increase in the time in range (70-180 mg/dL) from 58.9 +/- 36.1% to 70.8 +/- 18.3%. Seventeen mild adverse events were recorded in five individuals throughout the study period. No severe events were reported. The mean body mass showed a slight decrease and the mean serum ketone body concentration showed a slight increase during treatment.ConclusionOur results demonstrate that empagliflozin shows a certain level of efficacy and safety for treatment of insulin resistance syndrome and lipoatrophic diabetes.Trial RegistrationjRCTs2051190029 and NCT04018365.
引用
收藏
页码:533 / 545
页数:13
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