# Can DPP-4 Inhibitors Improve Glycemic Control and Preserve Beta-Cell Function in Type 1 Diabetes Mellitus? A Systematic Review

**Authors:** Henrique Villa Chagas, Lucas Fornari Laurindo, Victória Dogani Rodrigues, Jesselina Francisco dos Santos Haber, Eduardo Federighi Baisi Chagas, Sandra Maria Barbalho

PMC · DOI: 10.3390/diseases14010028 · 2026-01-09

## TL;DR

This review examines whether DPP-4 inhibitors can help manage blood sugar and protect beta-cell function in people with type 1 diabetes.

## Contribution

The study systematically evaluates the inconsistent effects of DPP-4 inhibitors in type 1 diabetes, highlighting the need for standardized research.

## Key findings

- HbA1c levels showed mixed results across studies, with some showing significant reductions.
- Time in glycemic target range improved in one study but not consistently elsewhere.
- C-peptide levels varied, suggesting possible but inconsistent beta-cell preservation.

## Abstract

Background/Objectives: The objective was to analyze the effects of Dipeptidyl Peptidase-4 (DPP-4) inhibitors on glycemic control, insulin dose, and preservation of β-pancreatic function (C-peptide) in patients with type 1 diabetes mellitus (T1DM). Methods: A systematic review was performed following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, with a search in the PubMed database. Five randomized clinical trials evaluating the use of different DPP-4 inhibitors in patients with T1DM were selected, measuring parameters including glycated hemoglobin (HbA1c), C-peptide, time in glycemic target/range (TIR), and daily insulin dose. Results: HbA1c showed significant reduction in some studies and no significant alterations in others. TIR increased in one study (~77.87% → ~84.40%). C-peptide showed variable effects across studies. The insulin dose did not show a substantial reduction. Conclusions: DPP-4 inhibitors demonstrated modest benefits for glycemic control and preservation of β-cell function in T1DM, but these effects were inconsistent due to methodological heterogeneity. Standardized studies are needed to define beneficial subgroups and long-term efficacy.

## Linked entities

- **Diseases:** type 1 diabetes mellitus (MONDO:0005147), T1DM (MONDO:0005147)

## Full-text entities

- **Diseases:** T1DM (MESH:D003922)
- **Chemicals:** insulin (MESH:D007328), C-peptide (MESH:D002096)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12840483/full.md

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Source: https://tomesphere.com/paper/PMC12840483