口服西马鲁肽诱导2型糖尿病患者体脂量减少而不影响肌肉量

Syutaro Uchiyama, Yukiyoshi Sada, Syohei Mihara, Yosuke Sasaki, Masakatsu Sone, Yasushi Tanaka
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引用次数: 1

摘要

背景:体内脂肪过多可能是胰岛素抵抗和糖尿病的主要原因。但是通过限制能量来减轻体重可以同时减少脂肪和肌肉。骨骼肌是调节葡萄糖代谢的重要器官,骨骼肌的减少会使葡萄糖代谢恶化。因此,2型糖尿病患者以减脂为主而不显著减少肌肉为佳。此前有报道称,糖尿病患者注射的降糖药胰高血糖素样肽-1受体激动剂(GLP-1RAs)利拉鲁肽和半马鲁肽能减少脂肪,但对肌肉的影响较小。最近,口服西马鲁肽被开发出来,据报道可以减轻体重,但对肌肉的影响尚未得到充分评估。方法:这是一项非介入性回顾性纵向研究。我们评估了25名日本2型糖尿病患者口服西马鲁肽治疗24周后对体脂和肌肉质量的影响。在基线、12周和24周进行实验室检查和生物电阻抗分析(BIA)体成分测试,并评估对血糖控制和体成分的影响。结果:血红蛋白A1c在12周时显著降低,在24周时进一步改善(基线时8.7±0.87%;12周7.6±1.00%;24周7.0±0.80%;平均值±标准误差(SE))。体脂显著降低(28.3±1.52 kg);12周26.8±1.59 kg;24周25.5±1.57 kg;平均±SE),全身瘦质量无显著变化(基线时为48.1±1.92 kg;12周47.7±1.93 kg;24周47.6±1.89 kg;平均值±SE)。此外,阑尾骨骼肌指数(SMI)定义为阑尾骨骼肌质量(ASM)/高度平方(单位;Kg /m2)也没有变化。结论:在日本2型糖尿病患者中,口服西马鲁肽治疗24周后,血糖控制得到改善,体脂减少,但肌肉量没有减少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Oral Semaglutide Induces Loss of Body Fat Mass Without Affecting Muscle Mass in Patients With Type 2 Diabetes.

Oral Semaglutide Induces Loss of Body Fat Mass Without Affecting Muscle Mass in Patients With Type 2 Diabetes.

Oral Semaglutide Induces Loss of Body Fat Mass Without Affecting Muscle Mass in Patients With Type 2 Diabetes.

Background: Excessive body fat may be a major cause of insulin resistance and diabetes. But body weight reduction by energy restriction may simultaneously reduce both fat and muscle. Skeletal muscle is an important organ for glucose metabolism regulation, and loss of muscle may deteriorate glucose metabolism. Therefore, it is preferable to predominantly reduce fat without significant loss of muscle with weight loss in patients with type 2 diabetes. Previously, the anti-diabetic agent glucagon-like peptide-1 receptor agonists (GLP-1RAs) liraglutide and semaglutide given by injection were reported to decrease fat with less effect on muscle in diabetic patients. Recently oral semaglutide was developed and was reported to decrease body weight, but the effect on muscle has not been fully evaluated.

Methods: This was a non-interventional retrospective longitudinal study. We evaluated the effect of 24-week treatment with oral semaglutide on body fat and muscle mass in 25 Japanese patients with type 2 diabetes. Laboratory examination and body composition test by bioelectrical impedance analysis (BIA) were performed at baseline, 12 weeks, and 24 weeks, and the effects on glycemic control and body composition were assessed.

Results: Hemoglobin A1c significantly decreased at 12 weeks and further ameliorated at 24 weeks (8.7±0.87% at baseline; 7.6±1.00% at 12 weeks; 7.0±0.80% at 24 weeks; mean ± standard error (SE)). While body fat significantly decreased (28.3 ± 1.52 kg at baseline; 26.8 ± 1.59 kg at 12 weeks; 25.5 ± 1.57 kg at 24 weeks; mean ± SE), whole-body lean mass was not significantly changed (48.1 ± 1.92 kg at baseline; 47.7 ± 1.93 kg at 12 weeks; 47.6 ± 1.89 kg at 24 weeks; mean ± SE). Furthermore, the appendicular skeletal muscle index (SMI) defined as appendicular skeletal muscle mass (ASM)/height squared (units; kg/m2) was also unchanged.

Conclusion: The 24-week treatment with oral semaglutide ameliorated glycemic control with reduction of body fat but not muscle mass in Japanese patients with type 2 diabetes.

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