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Basal and stimulated calcitonin levels in patients with type 2 diabetes did not change during 1 year of Liraglutide treatment.

Metabolism · 2016

Last updated 2026-05-28

In a study of 26 people with type 2 diabetes taking the GLP-1 drug liraglutide for one year, blood tests showed that their baseline and stimulated calcitonin levels stayed within normal ranges throughout the treatment. Small temporary increases in stimulated calcitonin were seen at 1–3 months, but these levels later returned to baseline by 6–12 months.

AI summary of the abstract below.

JournalMetabolism, 2016
Citations8
Relative citation ratio0.29
NIH percentile18
Molecules liraglutide
Conditions studied Type 2 Diabetes

Abstract

BACKGROUND AND AIMS: The administration of Liraglutide, a long-acting GLP-1 receptor (GLP-1R) agonist, is associated with C-cell adenomas and carcinomas in rats. In humans, GLP-1R is highly expressed in C-cells hyperplasia (CCH) and in medullary thyroid cancer (MTC), though no changes in basal serum calcitonin (bCT) levels were recorded in type 2 diabetic (T2DM) patients treated with Liraglutide. To diagnose the possible development of CCH during Liraglutide treatment, we evaluated CT levels stimulated by calcium test (sCT). MATERIALS AND METHODS: bCT and sCT and metabolic and anthropometric parameters were evaluated in 26 T2DM patients at baseline and at 1, 3, 6 and 12 months of treatment. RESULTS: In all patients, bCT remained within the normal range during the entire study period. In females and males, the higher sCT values were reached after 3 months and 1 month, respectively, with a progressive reduction at 6-12 months. The greater decrease of HbA1c values was reached at 3 months, while body weight and waist circumference decreased over the first 4 weeks of therapy. Lipase levels significantly increased, with a peak value at 1 month. CONCLUSION: The chronic administration of Liraglutide did not lead to statistically significant variations in both bCT and sCT. Stimulated CT levels increased, though always below the normal range, during the first 1-3 months of treatment, and progressively decreased to baseline levels. This finding is consistent with the effects recorded at the glycometabolic level, and suggests the possible induction of a drug tolerance involving also the C cells and thus preventing CCH.

Verbatim abstract via PubMed 26683791 ↗

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