# Pioglitazone as Add-On to Metformin and Dapagliflozin Yields Significant Enhancements in Glycemic Control in Poorly Controlled Type 2 Diabetes: A Meta-Analysis of Randomized Controlled Trials

**Authors:** Sara Sabbagh, Ahmed Hegazy, Ahmed Adel, Abdullah Ali, Mohamed Alquddosy, Sara Khalid, Abdallah M Ibrahim, Ahmed Mohamed, Abdelrahman Mostafa, Ahmed Hassan, Ola Mohamed, Rawan Mesbah, Osama Osman, Mohamed Hamouda Elkasaby

PMC · DOI: 10.7759/cureus.92794 · Cureus · 2025-09-20

## TL;DR

Adding pioglitazone to metformin and dapagliflozin improves blood sugar control in type 2 diabetes patients who aren't responding well to the dual therapy.

## Contribution

This meta-analysis demonstrates that pioglitazone enhances glycemic control and metabolic parameters when added to metformin and dapagliflozin in poorly controlled T2DM.

## Key findings

- Pioglitazone 15 mg significantly reduced HbA1c and fasting plasma glucose in T2DM patients.
- The 30 mg dose of pioglitazone improved insulin resistance and lipid parameters but increased body weight.
- No significant increase in serious adverse events or hypoglycemia was observed with pioglitazone.

## Abstract

This systematic review and meta-analysis aimed to evaluate the efficacy and safety of pioglitazone as an add-on therapy to dual treatment with metformin and dapagliflozin in adults with type 2 diabetes mellitus (T2DM) inadequately controlled on this regimen. We conducted a systematic review and meta-analysis of randomized controlled trials (RCTs) comparing pioglitazone (15 or 30 mg) versus placebo as an add-on to metformin (1,000 mg/day) and dapagliflozin (10 mg/day). Four databases (PubMed, Scopus, Cochrane CENTRAL, and Web of Science) were searched through December 2024. Primary outcomes included changes in hemoglobin A1c (HbA1c), the proportion of patients achieving a therapeutic glycemic response, and fasting plasma glucose (FPG). Secondary outcomes were insulin resistance, β-cell function, lipid parameters, body weight, blood pressure, and adverse events. Mean difference (MD) and standard deviation (SD) were used to describe the continuous variables. For categorical variables, we used the risk ratio (RR) and 95% confidence interval (CI). We included three RCTs, comprising a total of 856 patients: 363 received pioglitazone 15 mg, 124 received the 30 mg dose, and 369 received a placebo. Pioglitazone 15 mg significantly reduced HbA1c (MD = -0.42 percentage point, 95% CI = -0.51 to -0.33; p < 0.00001) and FPG (MD = -12.41 mg/dL). The 30 mg dose yielded greater reductions in HbA1c (MD = -0.84 percentage point) and FPG (MD = -21.49 mg/dL). It also improved homeostatic model assessment of insulin resistance, high-density lipoprotein cholesterol, and triglycerides, but increased body weight. No significant differences in serious adverse events or hypoglycemia were observed. Most outcomes had moderate to high certainty. Adding pioglitazone to metformin and dapagliflozin significantly enhances glycemic control and improves metabolic parameters with an acceptable safety profile, supporting its role as an effective triple oral therapy in T2DM.

## Linked entities

- **Chemicals:** pioglitazone (PubChem CID 4829), metformin (PubChem CID 4091), dapagliflozin (PubChem CID 9887712)
- **Diseases:** type 2 diabetes mellitus (MONDO:0005148), T2DM (MONDO:0005148)

## Full-text entities

- **Diseases:** hypoglycemia (MESH:D007003), T2DM (MESH:D003924), insulin resistance (MESH:D007333)
- **Chemicals:** Metformin (MESH:D008687), Dapagliflozin (MESH:C529054), glucose (MESH:D005947), lipid (MESH:D008055), triglycerides (MESH:D014280), Pioglitazone (MESH:D000077205)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12536928/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12536928/full.md

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Source: https://tomesphere.com/paper/PMC12536928