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首页> 外文期刊>Journal of Cachexia, Sarcopenia and Muscle >Erratum to: Recent developments in the treatment of cachexia: highlights from the 6th Cachexia Conference
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Erratum to: Recent developments in the treatment of cachexia: highlights from the 6th Cachexia Conference

机译:勘误:恶病质治疗的最新进展:第六届恶病质会议的要点

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Erratum to: J Cachexia Sarcopenia Muscle;DOI 10.1007/s13539-012-0061-y;The report of the highlights from the 6th Cachexia Conference was unfortunately published without the abstract and keywords; these are supplied here.;Abstract Both cachexia and sarcopenia are associated with muscle wasting, although cachexia may also involve other tissues. Muscle wasting is encountered in the advanced stages of many chronic illnesses. Several ongoing pre-clinical and clinical studies are expected to ameliorate this clinical problem. This article highlights the pre-clinical and clinical studies in the field of wasting disorders that were presented at the 6th Cachexia Conference in Milan, Italy, in December 2011. Effective treatments are urgently needed in order to improve the patients’ survival and quality of life. We describe ongoing research into muscle proteolytic pathways and the principal actors in skeletal muscle wasting. Novel therapeutic approaches include interleukin-6 such as receptor antibody tocilizumab, interleukin-1 receptor antagonist such as IP 1510 or selective androgen receptor modulators such as enobosarm and LGD-4033. Other candidates embraced the anabolic/catabolic transforming agent MT-102, naturally occurring peptide hormones such as ghrelin and synthetic orally active ghrelin receptor agonist anamorelin or the erythropoietin analogues ARA284 and ARA286.;Keywords Cachexia · Wasting · Sarcopenia · Therapy;This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
机译:勘误至:J恶病质肌肉症; DOI 10.1007 / s13539-012-0061-y;不幸的是,第六届恶病质会议上的要点报告没有摘要和关键词。摘要恶病质和肌肉减少症均与肌肉消瘦有关,尽管恶病质也可能涉及其他组织。在许多慢性疾病的晚期阶段,都会发生肌肉消瘦。有望进行一些正在进行的临床前和临床研究,以改善这一临床问题。本文重点介绍了2011年12月在意大利米兰举行的第六届Cachexia会议上介绍的饮食失调领域的临床前和临床研究。迫切需要有效的治疗方法,以改善患者的生存和生活质量。我们描述了正在进行的对肌肉蛋白水解途径和骨骼肌消瘦的主要参与者的研究。新的治疗方法包括白细胞介素6(例如受体抗体tocilizumab),白细胞介素1受体拮抗剂(例如IP 1510)或选择性雄激素受体调节剂(例如enobosarm和LGD-4033)。其他候选药物包括合成代谢/分解代谢转化剂MT-102,天然存在的肽激素(如生长素释放肽和合成的口服活性生长素释放肽受体激动剂anamorelin或促红细胞生成素类似物ARA284和ARA286)。根据知识共享署名非商业使用许可的条款,该许可允许在任何媒介中进行任何非商业使用,分发和复制,但要注明原始作者和出处。

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