乙酰左旋肉碱和烟酰胺预防1型糖尿病。支持治疗的文献综述。病例报告,五年治疗评价

Ivan Fern, Ez, M. Tonietti, M. C. Camberos, I. Bergadá, A. Schenone, M. Szlago, M. Tellechea, Gustavo Fretchtel, L. Trifone, J. Cresto
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引用次数: 2

摘要

在第一部分,本文综述了1型糖尿病的公认知识,其生理病理,细胞因子的重要性和诱导凋亡和坏死在其演变过程中。在这项工作中,我们更详细地描述了乙酰左旋肉碱和烟酰胺对这种细胞破坏机制的抑制作用。我们还解释了他们的协会的互补作用,这给治疗提供了支持。在第二部分中,我们介绍了8名儿童在5年内口服50 mg/Kg乙酰左旋肉碱加25 mg/Kg烟酰胺治疗的完整演变。我们发表了这些儿童在治疗后的前2年的进化(JPEM 26:347, 2013)。患儿自身抗体阳性,与1型糖尿病患者有血缘关系。静脉葡萄糖耐量试验(IVGTT)显示第一阶段胰岛素释放量为48 μU,进入方案,并用于儿童进化。8名儿童中有7名停止了治疗,因为他们的代谢参数正常化,没有人患上糖尿病。所有儿童对IVGTT的胰岛素反应均增加(1.44 ~ 5.69倍)。在治疗过程中,这8个孩子中有7个将阳性自身抗体变为阴性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acetyl-L-Carnitine and Nicotinamide for Prevention of Type 1 Diabetes. I-Literature Review which Gave Support to the Treatment. II-Case Report, Evaluation of Five Years Treatment
In the first part, this article review the accepted knowledge of type 1 diabetes, its physiopathology, the importance of cytokines and the induction of apoptosis and necrosis during its evolution. Throughout this work we describe in more detail the inhibition of this mechanism of cell destruction by acetyl-L-carnitine and nicotinamide. We also explain the complementary action of their association which gave support to the treatment. In the second part, we present the complete evolution of 8 children treated with the oral medication of 50 mg/Kg of acetyl-L-carnitine plus 25 mg/Kg of nicotinamide during 5 years. We published the first 2 years of evolution under treatment in these children (JPEM 26: 347, 2013). The children had positive auto-antibodies and were consanguineous of type 1 diabetic patients. The intravenous glucose tolerance test (IVGTT) showed a first phase of insulin release minor of 48 μU to enter in the protocol, and the same test was used for children evolution. Seven out eight children stopped the treatment because they normalized the metabolic parameters and no one became diabetic. All children increased the insulin response to IVGTT (between 1.44 to 5.69 times). Along the treatment, seven of these eight children turned their positive auto-antibodies into negatives.
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