Abstract

Type 1 diabetes mellitus (T1DM) with obesity is increasingly common, prompting effective clinical interventions to induce weight loss in this population. We present 3 patients with T1DM and obesity prescribed a glucagon-like peptide 1 receptor agonist (GLP-1RA) and pramlintide. Case 1: A 32-year-old male with obstructive sleep apnea (OSA) who lost −20.9 kg (−16.1% of total body weight [TBW]) over 10 months on semaglutide and pramlintide. Case 2: A 68-year-old female with diabetic retinopathy, coronary artery disease, hypertension, hypothyroidism, and depression/anxiety initially treated with topiramate, losing −8.4 kg, but experiencing weight plateau. After adding dulaglutide and pramlintide, she lost an additional −12.8 kg (−14.0% TBW) over 7 months, with total weight loss of −21.2 kg (−23.1% TBW). Case 3: A 49-year-old female with hypertension, hypothyroidism, and depression who lost −14.6 kg (−17.9% TBW) over 6 months on semaglutide and pramlintide. No significant side effects were experienced. All patients reported decreased insulin requirements on pramlintide, and hemoglobin A1c levels remained constant or decreased throughout the treatment period. Pramlintide and GLP-1RA resulted in excellent weight loss in our patients with obesity and T1DM. This combination may have a synergistic effect on the gut-brain axis. More research is required to substantiate these findings.

Details

Title
Combined GLP-1 Receptor Agonist and Amylin Analogue Pharmacotherapy to Treat Obesity Comorbid With Type 1 Diabetes
Author
Wong, Gunther 1 ; Garner, Erica M 1 ; Srivastava, Gitanjali 1   VIAFID ORCID Logo 

 Department of Medicine, Division of Diabetes, Endocrinology & Metabolism, Vanderbilt University School of Medicine , Nashville, TN 37232 , USA 
Publication year
2023
Publication date
Mar 2023
Publisher
Oxford University Press
e-ISSN
27551520
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3191359451
Copyright
© The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.