Abdi Dezfouli Ramin, Zargar Balajam Narges, Shirazi Sara, Heshmat Ramin, Shafiee Gita
Chronic Diseases Research Center, Endocrinology and Metabolism Population Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
Trials. 2024 Dec 23;25(1):848. doi: 10.1186/s13063-024-08700-x.
Diabetes is a significant risk factor for sarcopenia, a muscle dystrophy affecting older individuals. Sarcopenia management typically involves resistance exercise and oral supplements. Given the limitations of resistance training for many elderly individuals, oral supplements play a crucial role in treatment. This study is a protocol for evaluating the efficacy of the Sarcomeal® supplement, a mixture of whey protein, creatine, branch-chained amino acids (BCAAs), glutamine, and hydroxyl-methyl-butyrate (HMB) in diabetic people who also have sarcopenia. METHODS AND ANALYSIS: This study is a randomized clinical trial, in which sixty diabetic sarcopenia patients who meet the inclusion criteria will be randomly assigned to the control or the intervention group with a 1:1 allocation. The intervention group will receive one Sarcomeal® supplement sachet plus 1000 IU of vitamin D daily and both groups will be recommended to consume protein-rich food, be educated about the disease, and perform light exercises for 12 weeks. Anthropometric measurements, body composition analysis, muscle strength assessments, and blood tests will be conducted at the trial's start and end.
It is hypothesized that the Sarcomeal® supplement plus vitamin D may be beneficial for the management of diabetic sarcopenia by reducing inflammation, oxidative stress, and glucose metabolism. The outcome of this trial will provide a basis for prescribing sarcomeal to patients with diabetic sarcopenia.
This protocol is registered at the Iranian Registry of Clinical Trials (IRCT20230831059311N1) and also is approved by the ethics committee of Tehran University of Medical Sciences (September 2023, IR.TUMS.EMRI.REC.1402.071).
Iranian Registry of Clinical Trials (ID: IRCT20230831059311N1).
糖尿病是肌少症的一个重要风险因素,肌少症是一种影响老年人的肌肉萎缩症。肌少症的管理通常包括抗阻运动和口服补充剂。鉴于许多老年人进行抗阻训练存在局限性,口服补充剂在治疗中起着关键作用。本研究是一项评估Sarcomeal®补充剂疗效的方案,该补充剂是一种由乳清蛋白、肌酸、支链氨基酸(BCAAs)、谷氨酰胺和羟基甲基丁酸(HMB)组成的混合物,用于患有肌少症的糖尿病患者。
本研究是一项随机临床试验,将60名符合纳入标准的糖尿病肌少症患者以1:1的比例随机分配至对照组或干预组。干预组将每天服用一袋Sarcomeal®补充剂加1000国际单位的维生素D,两组均被建议食用富含蛋白质的食物,接受疾病教育,并进行12周的轻度运动。在试验开始和结束时进行人体测量、身体成分分析、肌肉力量评估和血液检测。
据推测,Sarcomeal®补充剂加维生素D可能通过减轻炎症、氧化应激和改善葡萄糖代谢,对糖尿病肌少症的管理有益。本试验的结果将为给糖尿病肌少症患者开Sarcomeal补充剂提供依据。
本方案已在伊朗临床试验注册中心(IRCT20230831059311N1)注册,并获得德黑兰医科大学伦理委员会批准(2023年9月,IR.TUMS.EMRI.REC.1402.071)。
伊朗临床试验注册中心(编号:IRCT20230831059311N1)。