Insulin Glargine is more suitable than Exenatide to prevent muscle loss in non-obese type 2 diabetic patients with NAFLD
Abstract Aim: The aim of this study was to investigate 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) was obtained with the cross-sectional Dixonfat magnetic resonance images at the fourth lumber veterbra. Results: There were no significant differences in age, BMI, gender, and PMA in Insulin Glargine and Exenatide group at baseline. After treatment, PMA tended to increase by 13.13 (-215.52, 280.80) mm2 in Insulin Glargine group and decrease by 149.09 (322.90,-56.39) mm2 in Exenatide group (both p >0.05). Subgroup analysis showed a 560.64 (77.88, 1043.40) (mm2) increase of PMA in Insulin group relative to Exenatide group in patients with BMI < 28kg/m2 (p = 0.031), after adjusting for gender, age and research center. Interaction analysis showed an interaction between BMI and treatment (p = 0.009). However, no interaction was observed among subgroups with a BMI ≥ 28kg/m2 or with different genders and ages. Conclusion: Compared to the Exenatide, Insulin Glargine can relativity increase PMA in T2DM patients with BMI< 28 kg/m2 and NAFLD.
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Erschienen in
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Insulin Glargine is more suitable than Exenatide to prevent muscle loss in non-obese type 2 diabetic patients with NAFLD ; day:31 ; month:07 ; year:2023
Experimental and clinical endocrinology & diabetes ; (31.07.2023)
- Beteiligte Personen und Organisationen
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liu, lin
gao, jian
wang, ruwen
yan, jinghua
zhang, jingtian
lin, huandong
rao, shengxiang
yao, xiuzhong
wu, weiyun
hua, bian
zhang, zhitian
Liu, Jiaojiao
guo, shanshan
gao, xin
yan, hongmei
- DOI
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10.1055/a-2145-1004
- URN
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urn:nbn:de:101:1-2023091411023616867056
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:57 MESZ
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Beteiligte
- liu, lin
- gao, jian
- wang, ruwen
- yan, jinghua
- zhang, jingtian
- lin, huandong
- rao, shengxiang
- yao, xiuzhong
- wu, weiyun
- hua, bian
- zhang, zhitian
- Liu, Jiaojiao
- guo, shanshan
- gao, xin
- yan, hongmei