Overall Efficacy and Safety of Sodium-Glucose Cotransporter 2 Inhibitor Luseogliflozin Versus Dipeptidyl-Peptidase 4 Inhibitors: Multicenter, Open-Label, Randomized-Controlled Trial (J-SELECT study)

被引:4
作者
Sugawara, Masahiro [1 ]
Fukuda, Masahiro [2 ]
Sakuma, Ichiro [3 ]
Wakasa, Yutaka [4 ]
Funayama, Hideaki [5 ]
Kondo, Akira [6 ]
Itabashi, Naoki [7 ]
Maruyama, Yasuyuki [8 ]
Kamiyama, Takashi [9 ]
Utsunomiya, Yasunori [10 ]
Yamauchi, Akira
Yoshii, Hidenori
Yamada, Hirokazu
Mochizuki, Koichi
机构
[1] Sugawara Clin, 3-9-16 Syakujii Machi, Nerima, Tokyo 1770041, Japan
[2] Fukuda Clin, 1-6-1 Miyahara, Osaka, Osaka 5320003, Japan
[3] Caress Sapporo Hokko Mem Clin, Kita-17,Higashi-8,1-15, Sapporo, Hokkaido 0650027, Japan
[4] Wakasa Med Clin, 3-16-25 Sainen, Kanazawa, Ishikawa 9200024, Japan
[5] Funayama Med Clin, 1-13-14 Tomioka, Koto, Tokyo 1350047, Japan
[6] Kondo Hosp, 1-6-25 Nishi Shinhama Cho, Tokushima 7708008, Japan
[7] Itabashi Clin, 815-1 Higashi Ushigaya, Koga, Ibaraki 3060232, Japan
[8] Iwatsuki Minami Hosp, 2256 Kuroya Iwatsuki, Saitama 3390033, Japan
[9] Kamiyama Clin, 5-21-18 Takanodai, Nerima, Tokyo 1770033, Japan
[10] Hoya Hosp, 4-50-15 Minami Oizumi, Nerima, Tokyo 1780064, Japan
关键词
Composite endpoint; Dipeptidyl-peptidase; 4; inhibitor; Estimated glomerular filtration rate; Glycated hemoglobin; Luseogliflozin; Overall efficacy; Pulse rate; Sodium-glucose cotransporter 2 inhibitor; Systolic blood pressure; Weight; HEART-RATE; DIABETES-MELLITUS; GLYCEMIC CONTROL; BLOOD-PRESSURE; DOUBLE-BLIND; ADD-ON; TYPE-2; METFORMIN; SITAGLIPTIN; THERAPY;
D O I
10.1007/s13300-023-01438-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionEvidence of a direct comparison between dipeptidyl-peptidase 4 inhibitors (DPP-4is) and sodium-glucose cotransporter 2 inhibitors (SGLT2is) remains lacking, and no clear treatment strategy or rationale has been established using these drugs. This study aimed to compare the overall efficacy and safety of DPP-4is and the SGLT2i luseogliflozin in patients with type 2 diabetes mellitus (T2DM).MethodsPatients with T2DM who had not used antidiabetic agents or who had used antidiabetic agents other than SGLT2is and DPP-4is were enrolled in the study after written informed consent had been obtained. The enrolled patients were subsequently randomly assigned to either the luseogliflozin or DPP-4i group and followed up for 52 weeks. The primary (composite) endpoint was the proportion of patients who showed improvement in & GE; 3 endpoints among the following five endpoints from baseline to week 52: glycated hemoglobin (HbA1c), weight, estimated glomerular filtration rate (eGFR), systolic blood pressure, and pulse rate.ResultsA total of 623 patients were enrolled in the study and subsequently randomized to either the luseogliflozin or DPP-4i groups. The proportion of patients who showed improvement in & GE; 3 endpoints at week 52 was significantly higher in the luseogliflozin group (58.9%) than in the DPP-4i group (35.0%) (p < 0.001). When stratified by body mass index (BMI) (< 25 or & GE; 25 kg/m(2)) or age (< 65 or & GE; 65 years), regardless of BMI or age, the proportion of patients who achieved the composite endpoint was significantly higher in the luseogliflozin group than in the DPP-4i group. Hepatic function and high-density lipoprotein-cholesterol were also significantly improved in the luseogliflozin group compared with the DPP-4i group. The frequency of non-serious/serious adverse events did not differ between the groups.ConclusionThis study showed the overall efficacy of luseogliflozin compared with DPP-4is over the mid/long term, regardless of BMI or age. The results suggest the importance of assessing multiple aspects regarding the effects of diabetes management.
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收藏
页码:1517 / 1535
页数:19
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