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Glucagon-like-1 receptor agonists and sodium/glucose cotransporter-2 inhibitors combination—are we exploiting their full potential in a real life setting? (CROSBI ID 289828)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Cigrovski Berković, Maja ; Bilić-Ćurčić, Ines ; Bozek, Tomislav ; Herman Mahecic, Davorka ; Klobučar Majanovic, Sanja ; Canecki-Varžić, Silvija ; Andrić, Jelena ; Marušić, Srećko ; Mrzljak, Anna Glucagon-like-1 receptor agonists and sodium/glucose cotransporter-2 inhibitors combination—are we exploiting their full potential in a real life setting? // World journal of diabetes, 11 (2020), 11; 540-552. doi: 10.4239/wjd.v11.i11.540

Podaci o odgovornosti

Cigrovski Berković, Maja ; Bilić-Ćurčić, Ines ; Bozek, Tomislav ; Herman Mahecic, Davorka ; Klobučar Majanovic, Sanja ; Canecki-Varžić, Silvija ; Andrić, Jelena ; Marušić, Srećko ; Mrzljak, Anna

engleski

Glucagon-like-1 receptor agonists and sodium/glucose cotransporter-2 inhibitors combination—are we exploiting their full potential in a real life setting?

BACKGROUND The sodium/glucose cotransporter-2 inhibitors (SGLT-2i) and glucagon-like-1 receptor agonists (GLP-1RA) are antidiabetic agents effective both in hemoglobin A1c (HbA1c) reduction (with a low risk of hypoglycemia) and cardiovascular event prevention. In patients with type 2 diabetes, the add-on value of combination therapy of GLP- 1RA and an SGLT-2i seems promising. AIM To investigate whether the efficacy of GLP-1RA and SGLT-2i combination observed in randomized controlled trials translates into therapeutic benefits in the Croatian population during routine clinical practice and follow-up. METHODS We included 200 type 2 diabetes patients with poor glycemic control and analyzed the effects of treatment intensification with (1) GLP- 1RA on top of SGLT- 2i, (2) SGLT-2i on top of GLP- 1RA compared to (3) simultaneous addition of both agents. The primary study endpoint was the proportion of participants with HbA1c < 7.0% and/or 5% bodyweight reduction. Secondary outcomes included changes in fasting plasma glucose (FPG), prandial plasma glucose, low- density lipoprotein cholesterol, estimated glomerular filtration rate (eGFR), and cardiovascular (CV) incidents assessment over a follow-up period of 12 mo. RESULTS The majority of patients were over 65- years-old, had diabetes duration for more than 10 years. The initial body mass index was 39.41 ± 5.49 kg/m2 and HbA1c 8.32 ± 1.26%. Around half of the patients in all three groups achieved target HbA1c below 7%. A more pronounced decrease in the HbA1c seen with simultaneous SGLT-2i and GLP-1RA therapy was a result of higher baseline HbA1c and not the effect of initiating combination therapy. The number of patients achieving FPG below 7.0 mmol/L was significantly higher in the SGLT-2i group (P = 0.021), and 5% weight loss was dominantly achieved in the simultaneous therapy group (P = 0.044). A composite outcome (reduction of HbA1c below 7% (53 mmol/mol) with 5% weight loss) was achieved in 32.3% of total patients included in the study. Only 18.2% of patients attained composite outcome defined as HbA1c below 7% (53 mmol/mol) with 5% weight loss and low- density lipoprotein cholesterol < 2.5 mmol/L. There were no significant differences between treatment groups. No differences were observed regarding CV incidents or eGFR according to treatment group over a follow-up period. CONCLUSION Combination therapy with GLP-1RA and SGLT-2i is effective in terms of metabolic control, although it remains to be determined whether simultaneous or sequential intensification is better.

sodium/glucose cotransporter-2 inhibitors ; glucagon-like-1 receptor agonists ; type 2 diabetes mellitus ; body weight ; glycemic control ; cardiovascular complications

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Podaci o izdanju

11 (11)

2020.

540-552

objavljeno

1948-9358

10.4239/wjd.v11.i11.540

Povezanost rada

Kliničke medicinske znanosti

Poveznice