Uchiyama Syutaro, Sada Yukiyoshi, Mihara Syohei, Sasaki Yosuke, Sone Masakatsu, Tanaka Yasushi
Diabetes Center, Yokohama General Hospital, 2201-5 Kurogane-cho, Aoba-ku, Yokohama, Kanagawa 225-0025, Japan.
Division of Metabolism and Endocrinology, St. Marianna University School of Medicine, 2-16-1, Sugao, Miyamae-ku, Kawasaki, Kanagawa 216-8511, Japan.
J Clin Med Res. 2023 Jul;15(7):377-383. doi: 10.14740/jocmr4987. Epub 2023 Jul 31.
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.
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.
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/m) was also unchanged.
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.
体内脂肪过多可能是胰岛素抵抗和糖尿病的主要原因。但通过能量限制减轻体重可能会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,肌肉流失可能会使葡萄糖代谢恶化。因此,对于2型糖尿病患者,在减轻体重时最好主要减少脂肪而不造成明显的肌肉流失。此前,有报道称注射用抗糖尿病药物胰高血糖素样肽-1受体激动剂(GLP-1RAs)利拉鲁肽和司美格鲁肽可减少糖尿病患者的脂肪,对肌肉的影响较小。最近,口服司美格鲁肽被研发出来,据报道可减轻体重,但对肌肉的影响尚未得到充分评估。
这是一项非干预性回顾性纵向研究。我们评估了25例日本2型糖尿病患者接受口服司美格鲁肽治疗24周对体脂和肌肉量的影响。在基线、12周和24周时进行实验室检查和通过生物电阻抗分析(BIA)进行身体成分测试,并评估对血糖控制和身体成分的影响。
糖化血红蛋白在12周时显著下降,并在24周时进一步改善(基线时为8.7±0.87%;12周时为7.6±1.00%;24周时为7.0±0.80%;均值±标准误(SE))。虽然体脂显著减少(基线时为28.3±1.52kg;12周时为26.8±1.59kg;24周时为25.5±1.57kg;均值±SE),但全身瘦体重没有显著变化(基线时为48.1±1.92kg;12周时为47.7±1.93kg;24周时为47.6±1.89kg;均值±SE)。此外,定义为四肢骨骼肌质量(ASM)/身高平方(单位:kg/m²)的四肢骨骼肌指数(SMI)也没有变化。
在日本2型糖尿病患者中,口服司美格鲁肽治疗24周可改善血糖控制,同时减少体脂但不减少肌肉量。