# Heterogeneous effect of saxagliptin on glucose fluctuation and β-cell function in T1DM: a multicentre, randomised trial

**Authors:** Yun Shi, Min Shen, Yong Gu, Yang Chen, Kuanfeng Xu, Ji Hu, Chen Fang, Heming Guo, Ning Xu, Guofeng Wang, Weiping Lu, Sha Tao, Songqing Zhao, Chengxia Fang, Jianhua Ma, Rengna Yan, Rui Sun, Li Qian, Chenguang Wu, Hui Jiang, Tao Yang

PMC · DOI: 10.1038/s41387-026-00411-3 · Nutrition & Diabetes · 2026-03-02

## TL;DR

This study tested if saxagliptin could help manage blood sugar fluctuations and preserve beta-cell function in type 1 diabetes patients.

## Contribution

The study is the first to show saxagliptin may preserve beta-cell function in T1DM, with genetic variants influencing treatment response.

## Key findings

- Saxagliptin did not reduce glucose fluctuations in T1DM patients.
- Saxagliptin was associated with higher C-peptide levels, suggesting possible preservation of beta-cell function.
- Certain genetic variants in incretin-related genes influenced treatment outcomes like HbA1c and C-peptide levels.

## Abstract

We aimed to explore whether saxagliptin, a dipeptidyl peptidase-IV inhibitor, could ameliorate glucose fluctuations and maintain β-cell function in T1DM.

A multicentre, open-label, randomised trial was performed, including 184 T1DM patients from six medical centres. These patients received insulin with or without saxagliptin at 5 mg per day for 24 weeks. The primary endpoint was the change from the baseline value of the MAGE, as measured by a CGMS after 24 weeks. The secondary endpoints included the change from baseline value of islet function during the 3-hour BMTT, HbA1c, and insulin dosage. The exploratory analysis was the influence of SNPs in the incretin-related genes on saxagliptin treatment outcomes. No differences were observed between the two groups in MAGE after treatment for 24 weeks. The change of C-peptidemax levels from baseline to 24 weeks in SAXA group (insulin plus saxagliptin) was higher than in CONT group (insulin only) [p = 0.040]. No difference were observed between the groups in HbA1c, insulin dosage after 24 weeks. In SAXA group, rs10305439, rs10305441 of GLP1R and rs6233 of PCSK1/3 were associated with HbA1c response (p = 0.026, 0.019, and 0.048 respectively); the G allele of rs2143734 of GLP1R were associated with lower change of fasting C-peptide from baseline (p = 0.029)

The saxagliptin did not ameliorate glucose fluctuations; however, it appeared to maintain β-cell function to some extent, and SNPs in the incretin-related gene may indicate responsiveness to DPP-IV inhibitors in T1DM.

ClinicalTrials. Gov number, NCT 02307695

## Linked entities

- **Genes:** GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740]
- **Chemicals:** saxagliptin (PubChem CID 11243969)
- **Diseases:** T1DM (MONDO:0005147)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, DPP4 (dipeptidyl peptidase 4) [NCBI Gene 1803] {aka ADABP, ADCP2, CD26, DPPIV, TP103}
- **Chemicals:** C-peptide (MESH:D002096), glucose (MESH:D005947), saxagliptin (MESH:C502994), C-peptidemax (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs2143734, rs10305439, rs10305441, rs6233

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12987927