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Lookup NU author(s): Dr Salman Razvi
This is the authors' accepted manuscript of an article that has been published in its final definitive form by Wiley-Blackwell Publishing Ltd., 2023.
For re-use rights please refer to the publisher's terms and conditions.
Objective: Glucagon-like peptide-1 receptor agonist (GLP-1 RA) therapy in patients with type 2 diabetes and obesity leads to a significant reduction in serum thyrotropin (TSH) levels but it is unclear whether this is related to weight loss and improvement in sensitivity to thyroid hormones (TH). Methods: We prospectively analysed clinical and biochemical data in patients with type 2 diabetes and obesity who were commenced on the GLP-1 RA exenatide and followed them for 12 months. We assessed the relationship between changes in body weight and serum TSH and resistance to TH indices. Results: In 112 patients (mean age 53.5years, 43.8% female, mean body mass index 39.8kg/m2), 12 months of exenatide treatment was associated with a mean (95%CI) percent body weight loss of 6.5% (5.0% to 8.1%) and change in serum TSH of -0.25mU/L (-0.43 to -0.06). There was a significant negative and non-linear relationship between change in serum TSH and percent body weight loss: -0.25mU/L with 5%, -0.4mU/L with 10%, and -0.5mU/L with 15%, respectively, whereas a rise in serum TSH of 0.5mU/L was associated with 5% weight gain. There were no changes observed in serum FT4 levels with weight loss but a significant reduction in resistance to TH indices was noted. Conclusions: Exenatide therapy reduces serum TSH levels and improves central sensitivity to TH action over 12 months via its effect on weight loss. The effectiveness of weight loss strategies, rather than TH replacement, should be investigated in individuals with obesity and mildly raised serum TSH levels.
Author(s): Tee SuAnn, Tsatlidis V, Razvi S
Publication type: Article
Publication status: Published
Journal: Clinical Endocrinology
Year: 2023
Volume: 99
Issue: 4
Pages: 401-408
Print publication date: 01/10/2023
Online publication date: 26/02/2023
Acceptance date: 24/02/2023
Date deposited: 24/02/2023
ISSN (print): 0300-0664
ISSN (electronic): 1365-2265
Publisher: Wiley-Blackwell Publishing Ltd.
URL: https://doi.org/10.1111/cen.14901
DOI: 10.1111/cen.14901
ePrints DOI: 10.57711/x8nr-h689
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