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DOI: 10.1055/a-2145-1004
Insulin Glargine is More Suitable Than Exenatide in Preventing Muscle Loss in Non-Obese Type 2 Diabetic Patients with NAFLD
Funding Information Medical Guidance Project of Shanghai Science and Technology Commission — 19401931100 to Wang XY; Science and Technology Commission of Shanghai Municipality — http://dx.doi. org/10.13039/501100003399; 21ZR1413200 to HM Yan; Scientific Research and Development Foundation of Zhongshan Hospital, Fudan University — 2019ZSFZ10 to HD LIN
Abstract
Aim This study investigated the effects of insulin glargine and exenatide on the muscle mass of patients with newly diagnosed type 2 diabetes (T2DM) and nonalcoholic fatty liver disease (NAFLD).
Methods We performed a post-hoc analysis of our previously study, a 24-week randomized controlled multicenter clinical trial (ClinicalTrials.gov, NCT02303730). Seventy-six patients were randomly assigned 1:1 to receive insulin glargine or exenatide treatment. The changes in psoas muscle area (PMA) (mm2) were obtained with the cross-sectional Dixonfat magnetic resonance images at the fourth lumber vertebra.
Results There were no significant differences in age, BMI, gender, and PMA in insulin glargine and exenatide groups at baseline. After treatment, PMA tended to increase by 13.13 (–215.52, 280.80) mm2 in the insulin glargine group and decrease by 149.09 (322.90–56.39) mm2 in the exenatide group (both p>0.05). Subgroup analysis showed a 560.64 (77.88, 1043.40) (mm2) increase of PMA in the insulin group relative to the Exenatide group in patients with BMI<28 kg/m2 (p0.031) after adjusting for gender, age, and research center. Interaction analysis showed an interaction between BMI and treatment (p0.009). However, no interaction was observed among subgroups with a BMI≥28 kg/m2 or with different genders and ages.
Conclusion Compared to exenatide, insulin glargine can relativity increase PMA in patients with T2DM having BMI<28 kg/m2 and NAFLD.
Key words
body composition - basal insulin - exenatide - fatty liver disease - type 2 diabetes - clinical trial* These authors contributed equally: Lin Liu, Ruwen Wang, Jian Gao
Publication History
Received: 08 December 2022
Received: 27 June 2023
Accepted: 28 June 2023
Accepted Manuscript online:
31 July 2023
Article published online:
04 October 2023
© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).
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References
- 1 Li Y, Teng D, Shi X. et al. Prevalence of diabetes recorded in mainland China using 2018 diagnostic criteria from the American Diabetes Association: National cross sectional study. BMJ (Clinical research ed) 2020; 369: m997
- 2 Salomon JA, Wang H, Freeman MK. et al. Healthy life expectancy for 187 countries, 1990-2010: A systematic analysis for the Global Burden Disease Study 2010. Lancet 2012; 380: 2144-2162
- 3 Dunning T, Sinclair A, Colagiuri S. New IDF Guideline for managing type 2 diabetes in older people. Diabetes Res Clin Pract 2014; 103: 538-540
- 4 Cho NH, Shaw JE, Karuranga S. et al. IDF Diabetes Atlas: Global estimates of diabetes prevalence for 2017 and projections for 2045. Diabetes Res Clin Pract 2018; 138: 271-281
- 5 Izzo A, Massimino E, Riccardi G. et al. A narrative review on sarcopenia in type 2 diabetes mellitus: Prevalence and associated factors. Nutrients 2021; 13
- 6 Cruz-Jentoft AJ, Bahat G, Bauer J. et al. Sarcopenia: Revised European consensus on definition and diagnosis. Age and Ageing 2019; 48: 16-31
- 7 Delbono O, Rodrigues ACZ, Bonilla HJ. et al. The emerging role of the sympathetic nervous system in skeletal muscle motor innervation and sarcopenia. Ageing Res Rev 2021; 67: 101305
- 8 Shafiee G, Keshtkar A, Soltani A. et al. Prevalence of sarcopenia in the world: A systematic review and meta- analysis of general population studies. J Diabetes Metab Disord 2017; 16: 21
- 9 Papadopoulou SK. Sarcopenia: A contemporary health problem among older adult populations. Nutrients 2020; 12
- 10 Ida S, Nakai M, Ito S. et al. Association between sarcopenia and mild cognitive impairment using the Japanese version of the SARC-F in elderly patients with diabetes. J Am Med Dir Assoc 2017; 18: 809.e809-809.e813
- 11 Cruz-Jentoft AJ, Landi F, Schneider SM. et al. Prevalence of and interventions for sarcopenia in ageing adults: A systematic review. Report of the International Sarcopenia Initiative (EWGSOP and IWGS). Age Ageing 2014; 43: 748-759
- 12 Wang T, Feng X, Zhou J. et al. Type 2 diabetes mellitus is associated with increased risks of sarcopenia and pre-sarcopenia in Chinese elderly. Sci Rep 2016; 6: 38937
- 13 Cobo A, Vázquez LA, Reviriego J. et al. Impact of frailty in older patients with diabetes mellitus: An overview. Endocrinologia y nutricion: Organo de la Sociedad Espanola de Endocrinologia y Nutricion 2016; 63: 291-303
- 14 Anagnostis P, Gkekas NK, Achilla C. et al. Type 2 diabetes mellitus is associated with increased risk of sarcopenia: A systematic review and meta-analysis. Calcif Tissue Int 2020; 107: 453-463
- 15 Saatmann N, Zaharia OP, Loenneke JP. et al. Effects of blood flow restriction exercise and possible applications in type 2 diabetes. Trends Endocrinol Metab 2021; 32: 106-117
- 16 Billot M, Calvani R, Urtamo A. et al. Preserving mobility in older adults with physical frailty and sarcopenia: opportunities, Challenges, and recommendations for physical activity interventions. Clin Interv Aging 2020; 15: 1675-1690
- 17 Zhang X, Zhao Y, Chen S. et al. Anti-diabetic drugs and sarcopenia: emerging links, mechanistic insights, and clinical implications. J Cachexia Sarcopenia Muscle 2021; 12: 1368-1379
- 18 Wu CN, Tien KJ. The impact of antidiabetic agents on sarcopenia in type 2 diabetes: A literature review. J Diabetes Res 2020; 2020: 9368583
- 19 Bouchi R, Fukuda T, Takeuchi T. et al. Insulin treatment attenuates decline of muscle mass in Japanese patients with type 2 diabetes. Calcif Tissue Int 2017; 101: 1-8
- 20 Prídavková D, Samoš M, Kazimierová I. et al. Insulin pump therapy - influence on body fat redistribution, skeletal muscle mass and ghrelin, leptin changes in T1D patients. Obes Facts 2018; 11: 454-464
- 21 Perna S, Guido D, Bologna C. et al. Liraglutide and obesity in elderly: efficacy in fat loss and safety in order to prevent sarcopenia. A perspective case series study. Aging Clin Exp Res 2016; 28: 1251-1257
- 22 Ida S, Kaneko R, Imataka K. et al. Effects of antidiabetic drugs on muscle mass in type 2 diabetes mellitus. Curr Diabetes Rev 2021; 17: 293-303
- 23 McCrimmon RJ, Catarig AM, Frias JP. et al. Effects of once-weekly semaglutide vs once-daily canagliflozin on body composition in type 2 diabetes: A substudy of the SUSTAIN 8 randomised controlled clinical trial. Diabetologia 2020; 63: 473-485
- 24 Liu L, Yan H, Xia M. et al. Efficacy of exenatide and insulin glargine on nonalcoholic fatty liver disease in patients with type 2 diabetes. Diabetes Metab Res Rev 2020; 36: e3292
- 25 Zeng MD, Fan JG, Lu LG. et al. Guidelines for the diagnosis and treatment of nonalcoholic fatty liver diseases. J Dig Dis 2008; 9: 108-112
- 26 Meek SE, Persson M, Ford GC. et al. Differential regulation of amino acid exchange and protein dynamics across splanchnic and skeletal muscle beds by insulin in healthy human subjects. Diabetes 1998; 47: 1824-1835
- 27 O'Neill BT, Lee KY, Klaus K. et al. Insulin and IGF-1 receptors regulate FoxO-mediated signaling in muscle proteostasis. J Clin Invest 2016; 126: 3433-3446
- 28 Dutour A, Abdesselam I, Ancel P. et al. Exenatide decreases liver fat content and epicardial adipose tissue in patients with obesity and type 2 diabetes: A prospective randomized clinical trial using magnetic resonance imaging and spectroscopy. Diabetes Obes Metab 2016; 18: 882-891
- 29 Hong Y, Lee JH, Jeong KW. et al. Amelioration of muscle wasting by glucagon-like peptide-1 receptor agonist in muscle atrophy. J Cachexia Sarcopenia Muscle 2019; 10: 903-918