Effectiveness and Safety of Sodium-Glucose Cotransporter 2 Inhibitors Added to Dual or Triple Treatment in Patients with Type 2 Diabetes Mellitus

被引:0
|
作者
Hong, Yesol [1 ]
Jeon, Yoomin [2 ,4 ]
Choi, Yoona [2 ,4 ]
Chung, Tae Kyu [2 ,4 ]
Lee, Howard [1 ,3 ,4 ]
机构
[1] Seoul Natl Univ, Grad Sch Convergence Sci & Technol, Dept Mol Med & Biopharmaceut Sci, Seoul 03080, South Korea
[2] Seoul Natl Univ, Grad Sch Convergence Sci & Technol, Dept Appl Bioengn, Seoul, South Korea
[3] Seoul Natl Univ, Coll Med & Hosp, Dept Clin Pharmacol & Therapeut, Seoul, South Korea
[4] Ctr Convergence Approaches Drug Dev, Seoul, South Korea
关键词
Diabetes mellitus; type; 2; Blood glucose; Observational study; Sodium-glucose transporter 2 inhibitors; Hypoglycemic agents; DOUBLE-BLIND; RISK-FACTOR; ADD-ON; METFORMIN; CANAGLIFLOZIN; EFFICACY; THERAPY; PLACEBO; EMPAGLIFLOZIN; GUIDELINES;
D O I
10.1007/s13300-023-01518-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction We evaluated the effectiveness and safety of sodium-glucose cotransporter 2 inhibitor (SGLT2i) add-on treatment in patients with type 2 diabetes mellitus (T2DM) in the real-world setting.Methods This single-center retrospective study used the clinical database of Seoul National University Hospital in South Korea. Patients who received metformin monotherapy or combination therapy with >= 1 other oral hypoglycemic medication and had a baseline glycosylated hemoglobin (HbA1c) between 7.0% and 10.5% were included. Propensity score matching was applied between patients treated with and without SGLT2 inhibitors (SGLT2i and non-SGLT2i groups, respectively). Changes in HbA1c from baseline to week 26 were compared between the SGLT2i and non-SGLT2i groups, and risk of adverse events (AE) were also assessed.Results A total of 1106 patients were included. At week 26, HbA1c was significantly more reduced by 0.35 percentage points in the SGLT2i group than in the non-SGLT2i group (95% CI 0.30-0.41, P < 0.001). Likewise, the proportion of patients achieving HbA1c < 7% was also significantly higher (51.9% vs. 37.6%, P < 0.05) in the SGLT2i group than in the non-SGLT2i group. The risk of adverse events in the SGLT2i group was mostly comparable with those in the non-SGLT2i group except for diseases of the liver, pain, hypertensive diseases, and metabolic disorders, which showed significantly higher odds in the SGLT2i group.Conclusions SGLT2i add-on treatment is an effective and safe therapeutic option for patients with T2DM in the real-world practice setting.
引用
收藏
页码:487 / 496
页数:10
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