Assessing the Efficacy and Safety of Combined DPP-4 Inhibitor and Insulin Treatment in Patients with Type 2 Diabetes: a Meta-analysis
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The use of DPP-4 inhibitors in combination with insulin has been proposed as an alternative therapeutic option for poorly controlled type 2 diabetes (T2D) patients. We thus performed a meta-analysis of randomized controlled trials (RCTs) to assess the efficacy and safety of this combination therapy in adult T2D patients. Seven eligible studies involving 3,384 participants were included for the study. The resulting data revealed that the combination therapy of DPP-4 inhibitor and insulin is associated with a modest reduction in HbA1c (-0.52%; 95% CI -0.59 to -0.44), a decrease in 2h-PPG (-1.81 mmol/l; -2.23 to -1.38), and an increase in the proportion of patients reaching the target HbA1c of ≤ 7% (RR 2.24; 95% CI 1.80 to 2.77) without increasing the risk of hypoglycemia (RR 1.04; 0.83 to 1.31) or body weight (-0.11 kg; -0.56 to 0.33), as compared with other anti-diabetic treatments. These results support that this combination therapy could serve as a potential therapeutic strategy that offers an alternative option for patients inadequately controlled on other anti-diabetic agents in clinical practice.
Mohammadzadeh M, Athari S, Ghiasi F, Keyhanmanesh R, Ghaffari-Nasab A, Roshangar L Appl Biochem Biotechnol. 2024; 196(10):7074-7088.
PMID: 38478319 DOI: 10.1007/s12010-024-04870-1.
Shibuki K, Shimada S, Aoyama T J Diabetes Res. 2020; 2020:6321826.
PMID: 33224988 PMC: 7673952. DOI: 10.1155/2020/6321826.
Yang J, Tian Q, Tang Y, Shah A, Zhang R, Chen G Diabetes Ther. 2020; 11(10):2371-2382.
PMID: 32876863 PMC: 7509019. DOI: 10.1007/s13300-020-00914-x.
Wang N, Yang T, Li J, Zhang X Diabetes Metab Syndr Obes. 2019; 12:1513-1526.
PMID: 31692532 PMC: 6710543. DOI: 10.2147/DMSO.S202024.
BE-SMART (Basal Early Strategies to Maximize HbA1c Reduction with Oral Therapy): Expert Opinion.
Bajaj S, Das A, Kalra S, Sahay R, Saboo B, Das S Diabetes Ther. 2019; 10(4):1189-1204.
PMID: 31102253 PMC: 6612329. DOI: 10.1007/s13300-019-0629-z.