治疗雷特综合征的特罗非肽简介:设计、开发和潜在治疗位置。

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2024-11-06 eCollection Date: 2024-01-01 DOI:10.2147/DDDT.S383133
Laura Camillo, Marco Pozzi, Pia Bernardo, Simone Pisano, Maria Nobile
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引用次数: 0

摘要

特罗非肽是针对雷特综合征患者提出的第一种药物治疗方法。它是甘氨酸-脯氨酸-谷氨酸的一种长半衰期衍生物,通常是胰岛素样生长因子 1 降解时排出的三肽。由于其结构中含有谷氨酸和甘氨酸,特罗菲奈特被认为可通过调节 NMDA 受体发挥作用,从而使神经元的活动和存活恢复正常。在一系列短期和长期试验中,特罗菲奈肽显示出良好的疗效,可改善临床总体印象改善量表和雷特综合征行为问卷的评分,但只对某些分量表(即一般情绪分量表和重复性面部运动分量表)有特定效果。对其他分量表或癫痫、心脏和骨骼相关症状没有影响。特罗芬肽的主要不良反应包括腹泻、呕吐和随之而来的体重下降,其严重程度足以导致停药。由于每天需要服用大量的特罗芬肽,这些不良反应几乎无法避免。其他固有的使用限制可能还包括药物供应时间有限(根据体重,一瓶药物只能使用三天),以及每瓶药物的成本相对较高。特罗非奈肽没有直接的竞争对手:目前,治疗雷特综合征的单一症状,如癫痫发作或攻击行为的药物,是为没有雷特综合征的患者开发的。这导致疗效不理想,不良反应风险增加。特罗非肽在治疗中的地位还有待根据临床试验的结果、其实际可用性以及干预的机会窗口来确定。此外,如果在大脑发育阶段及早使用特罗菲奈特,可能会起到治疗作用,而如果给年轻成年人使用,则可能只是对症治疗,目前还没有这方面的数据。在竞争疗法进入市场后,特罗芬肽在治疗中的地位需要重新评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Profile of Trofinetide in the Treatment of Rett Syndrome: Design, Development and Potential Place in Therapy.

Trofinetide is a first-in-class pharmacological treatment proposed for patients with Rett Syndrome. It is a long half-life derivative of glycine-proline-glutamate, the tripeptide normally excided from Insulin-like Growth Factor 1 upon degradation. Due to containing glutamate and glycine in its structure, trofinetide is thought to act through NMDA receptor modulation, thus providing a normalization of neuronal activity and survival. Trofinetide was tested in a series of short and long-term trials, showing good efficacy at improving scores on the Clinical Global Impression-Improvement scale and Rett Syndrome Behavior Questionnaire, with specific effect only on some subscales, ie General Mood subscale and Repetitive Face Movement subscale. No effects were documented on other subscales or on epilepsy, heart and bone -related symptoms. The main adverse effects of trofinetide, severe enough to determine discontinuation, include diarrhea, vomiting, and consequent weight loss. These may be scarcely avoidable, given the need to assume a very large amount of trofinetide per day. Other inherent limitations of use possibly regard the limited duration of drug supplies, as one bottle may last three days only, depending on weight, and the relatively high cost per bottle. Trofinetide has no direct competitors: single symptoms of the Rett Syndrome, for instance, seizures or aggressive behaviors, are currently treated with drugs that have been developed for patients without the Rett Syndrome. This leads to suboptimal efficacy and increased risk of adverse effects. The place in therapy of trofinetide is yet to be determined, based on the results of clinical trials, on its practical usability, and on the windows of opportunity for intervention. Moreover, trofinetide may be curative if given early enough during brain development, or merely symptomatic if given to young adults, and no data exist on this aspect. The place in therapy of trofinetide will require reassessment after competing treatments enter the market.

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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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