# Switch from premixed insulin analogue to degludec-liraglutide combination: a CGM study

**Authors:** Nika Aleksandra Kravos Tramšek, Andrijana Koceva, Mitja Krajnc

PMC · DOI: 10.3389/fendo.2025.1715800 · Frontiers in Endocrinology · 2025-11-05

## TL;DR

Switching from premixed insulin to a combination of degludec and liraglutide improved blood sugar control and reduced insulin use in people with type 2 diabetes.

## Contribution

Demonstrates the efficacy of iDegLira over premixed insulin in improving glycemic control and reducing hypoglycemia risk.

## Key findings

- Improved HbA1c and time in range with iDegLira compared to premixed insulin.
- Significant reduction in total daily insulin dose and modest weight loss observed.
- No increased risk of hypoglycemia with the new treatment combination.

## Abstract

Basal insulin with glucagon-like peptide-1 receptor agonist could be preferred over premixed insulin for intensification in type 2 diabetes due to better glycemic control, lower hypoglycemia risk, and favorable effects on body weight. Comparative data on premixed insulin and the combination of degludec and liraglutide (iDegLira) are limited.

We conducted a 24-week single-arm prospective study to evaluate the impact of iDegLira compared to premixed insulin on the regulation of diabetes and glucovariability using continuous glucose monitoring (CGM), HbA1c, and anthropometric measurements. A total of 37 participants with type 2 diabetes (20 male and 17 female, aged 70.2 ± 10.0 years with BMI 31.0 (28.0-34.0) kg/m2 and duration of diabetes for 15.2 ± 7.7 years) were switched from premixed insulin treatment to iDegLira. The primary outcome was the change in HbA1c. Secondary outcomes included change in time in range (TIR) from baseline to 6 months, change in time below range (TBR), change in nocturnal hypoglycemia, glucovariability, insulin dose and body weight.

We observed improved glycemic control on iDegLira with improvement of average fasting glucose (6.92 ± 1.64 vs. 8.25 ± 2.2 mmol/l; p<0.031), HbA1c (7.10 ± 0.7% vs. 7.39 ± 0.7% p=0.045) and TIR (71.2 ± 17.2% vs. 64.3 ± 18.0; p=0.027). These results were accompanied by a nearly halved total daily insulin dose (-21 units/day, p<0.001) and a modest reduction of body weight.

iDegLira improved glycemic control, resulting in a lower HbA1c and higher TIR, alongside beneficial effects on body weight and total daily insulin doses. While numerical reductions in hypoglycemia did not reach statistical significance, treatment was not associated with an increased risk of hypoglycemia. iDegLira can be an efficient and safe treatment option, providing simplified treatment with improved glycemic control.

## Linked entities

- **Chemicals:** degludec (PubChem CID 118984462), liraglutide (PubChem CID 16134956)
- **Diseases:** type 2 diabetes (MONDO:0005148), hypoglycemia (MONDO:0004946)

## Full-text entities

- **Genes:** GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** reduction of body weight (MESH:D001835), type 2 diabetes (MESH:D003924), hypoglycemia (MESH:D007003), diabetes (MESH:D003920)
- **Chemicals:** glucose (MESH:D005947), degludec (MESH:C571886), iDegLira (MESH:C000613158)

## Full text

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## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12626799/full.md

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Source: https://tomesphere.com/paper/PMC12626799