Glucagon-like peptide 1 receptor agonist (GLP-1 RA): long-term effect on kidney function in patients with type 2 diabetes.
J Diabetes Complications · 2015
Last updated 2026-05-28In a one-year study of 30 people with type 2 diabetes, those treated with the GLP-1 drug liraglutide saw their kidney function (measured as GFR) drop by 11 mL/min/1.73 m², similar to a short-term effect. Their urine albumin excretion rate (a kidney-related measure) also decreased by 27%, and their 24-hour blood pressure dropped by 8.2 mmHg. No changes were seen in the 7 untreated participants.
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| Journal | J Diabetes Complications, 2015 |
|---|---|
| Citations | 54 |
| Relative citation ratio | 1.95 |
| NIH percentile | 73 |
| Molecules | — |
| Conditions studied | Type 2 Diabetes, Chronic Kidney Disease |
Abstract
AIMS: In a short-term study including 31 patients with type 2 diabetes, glucagon-like peptide 1 receptor agonist (GLP-1 RA) treatment was associated with a significant reversible decline in GFR. Twenty-three patients re-initiated GLP-1 RA treatment after the primary study, and the aim was to investigate the long-term effect on kidney function.
METHODS: We included 30 patients in a one-year extension study, all initially treated with liraglutide for seven weeks. During follow-up 23 were treated with liraglutide and seven untreated. Primary outcome was change in GFR ((51)Cr-EDTA plasma clearance).
RESULTS: Patients were 61.5 (10.0) years and HbA(1c) 60.1 (13.8) mmol/mol. Baseline GFR was 100.6 (24.9) mL/min/1.73 m(2) and was reduced by 11 (95% CI: 6.6-15.7, p < 0.001) mL/min/1.73 m(2), independent of change in 24-h systolic blood pressure (SBP), weight, UAER or HbA(1c) (p≥0.33). Geometric mean (IQR) of UAER was 25.5 (9.9-50.9) mg/d and was reduced by 27 (95% CI: 5-44; p = 0.020)%, and 24-h SBP was reduced by 8.2 (p = 0.048) mmHg. No changes occurred in untreated patients.
CONCLUSIONS: Long-term treatment with liraglutide was associated with a reduction in measured GFR similar to the effect during short-term treatment, suggesting a metabolic or haemodynamic reversible effect and not structural changes. Moreover, UAER and 24-h SBP were reduced.
TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT01499108.
Verbatim abstract via PubMed 25935863 ↗