Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Background: Sitagliptin is known as an antidiabetic agent inhibiting the dipeptidyl peptidase-4. Although sitagliptin may influence weight, controversial results have been reported, and there is no general agreement on this issue. Therefore, this study assessed the effect of sitagliptin as monotherapy and add-on therapy to metformin on weight reduction in overweight or obese cases with type 2 diabetes.

Methods: We reviewed the following databases to identify all relevant papers published until 1st April 2021: Web of Science, MEDLINE, Embase, Scopus, Cochrane Central Register of Controlled Trials Cochrane Library, and Google Scholar. The research included all clinical trials investigating the effect of sitagliptin in obese or overweight adult patients with type 2 diabetes without any language restriction.

Results: In total, eighteen randomized controlled trials with 2009 participants were included in our meta-analysis. Results showed supplementation of sitagliptin has led to weight loss for sitagliptin treated (MD  -0.99; 95% CI; (-1.87, -0.12); p=0.026)) and sitagliptin+metformin treated groups (MD  -1.09; 95% CI; (-1.69, -0.49); p<0.001)). Also, the intervention has influenced body mass index in sitagliptin treated (MD  -0.23; 95% CI; (-0.45, 0.02); p=0.033)) and sitagliptin+metformin treated groups (MD -0.52; 95% CI; (-0.96, 0.08); p=0.020)) comparing to placebo.

Conclusion: Our results demonstrated that sitagliptin administration with or without metformin might reduce the body weight and body mass index if these drugs are taken for more than 6 months.

Download full-text PDF

Source
http://dx.doi.org/10.1055/a-1555-2797DOI Listing

Publication Analysis

Top Keywords

sitagliptin monotherapy
8
monotherapy add-on
8
metformin weight
8
weight loss
8
overweight obese
8
patients type
8
type diabetes
8
controlled trials
8
sitagliptin
6
effects sitagliptin
4

Similar Publications

Dipeptidyl peptidase 4 inhibitors (DPP-4 inhibitors) are used as second-line drugs in the treatment of type 2 diabetes mellitus (T2DM) patients. They act by preventing the breakdown of incretin hormones, which enhance insulin secretion and reduce glucagon secretion. Vildagliptin and sitagliptin are more commonly used DPP-4 inhibitors.

View Article and Find Full Text PDF

Polycystic ovary syndrome (PCOS) is one of the most common endocrine disorders in women of reproductive age, characterized by insulin resistance, chronic inflammation, and hormonal imbalances. Metformin is widely used in the treatment of this syndrome; however, existing evidence suggests that its effectiveness alone in improving PCOS-related parameters is limited. In recent years, reports have indicated that sitagliptin may improve ovarian cycles and ovulation in women with PCOS.

View Article and Find Full Text PDF

Background: Type 1 diabetes is characterised by the immune-mediated destruction of pancreatic beta cells. We aimed to determine the effectiveness of immunotherapies for preserving residual beta cell function in newly diagnosed (stage 3) type 1 diabetes.

Methods: Searches were carried out in MEDLINE, Embase, Cochrane CENTRAL and trial registries until 31st Jul 2024.

View Article and Find Full Text PDF

Context: There is an unmet need for type 2 diabetes (T2D) treatments in addition to metformin and insulin for adolescents. This is due to the challenges of monotherapy in youth with T2D and need for treatment escalation to maintain glycemic control in youth generally more so than in young adults.

Objective: We assessed the efficacy and safety of sodium-glucose co-transporter-2 (SGLT2) or dipeptidyl peptidase-4 (DPP-4) inhibitor monotherapies in adolescents and young adults with T2D not on active therapy.

View Article and Find Full Text PDF

Aims: Dapagliflozin and sitagliptin exhibit variable efficacy in managing type 2 diabetes mellitus (T2DM), with outcomes influenced by factors like body mass index (BMI). However, biochemical determinants of treatment response remain poorly defined. This study aimed to determine whether baseline alanine aminotransferase (ALT) levels can independently predict differential responses to these drugs.

View Article and Find Full Text PDF