治疗肾上腺功能不全的新型药物:临床前和早期临床试验结果。

IF 4.9 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Andrew Peel, R Louise Rushworth, David J Torpy
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引用次数: 0

摘要

简介肾上腺功能不全目前影响着 300 多万人口,其发病率和死亡率高于普通人群。目前的糖皮质激素替代疗法因缺乏可靠的生物标志物指导用药、患者间代谢差异和治疗窗口狭窄而受到限制。发病率和死亡率的增加可能与糖皮质激素暴露不足或过度以及皮质醇昼夜节律受损有关。需要新的药物来模拟生理性皮质醇分泌和个体化糖皮质激素剂量:糖皮质激素治疗的历史、目前的局限性和新型慢性治疗糖皮质激素给药机制。文献检索包括对 Pubmed 和 Embase 的检索,使用的术语有:肾上腺功能不全、Chronocort、Plenadren、持续皮下氢化可的松输注(CHSI)、糖皮质激素受体调节剂:糖皮质激素慢性疗法对于优化糖皮质激素暴露和减少并发症是必要的。目前的口服时间疗法可改善剂量功能,但只能以特定的增量进行调节,且无法适应皮质醇的昼夜节律变化。目前的数据显示生活质量有所改善,但发病率或死亡率却没有改善。CHSI在个体化糖皮质激素剂量方面具有巨大潜力,但需要一个合适的糖皮质激素充足性生物标志物才能实施。未来研究的途径包括确定糖皮质激素充足性生物标志物、开发间质或全身皮质醇监测或开发糖皮质激素受体调节剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel agents to treat adrenal insufficiency: findings of preclinical and early clinical trials.

Introduction: Adrenal insufficiency currently affects over 300/million population, with higher morbidity and mortality compared to the general population. Current glucocorticoid replacement therapy is limited by a lack of reliable biomarkers to guide dosing, inter-patient variation in metabolism and narrow therapeutic window. Increased morbidity and mortality may relate to unappreciated under- or over-exposure to glucocorticoids and impaired cortisol circadian rhythm. New agents are required to emulate physiological cortisol secretion and individualize glucocorticoid dosing.

Areas covered: History of glucocorticoid therapy, current limitations, and novel chronotherapeutic glucocorticoid delivery mechanisms. Literature search incorporated searches of PubMed and Embase utilizing terms such as adrenal insufficiency, Chronocort, Plenadren, continuous subcutaneous hydrocortisone infusion (CHSI), and glucocorticoid receptor modulator.

Expert opinion: Glucocorticoid chronotherapy is necessary to optimize glucocorticoid exposure and minimize complications. Current oral chronotherapeutics provide improved dosing functionality, but are modifiable only in specific increments and cannot accommodate ultradian cortisol variation. Current data show improvement in quality of life but not morbidity or mortality outcomes. CHSI has significant potential for individualized glucocorticoid dosing, but would require a suitable biomarker of glucocorticoid adequacy to be implementable. Avenues for future research include determining a glucocorticoid sufficiency biomarker, development of interstitial or systemic cortisol monitoring, or development of glucocorticoid receptor modulators.

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来源期刊
CiteScore
10.00
自引率
0.00%
发文量
71
审稿时长
6-12 weeks
期刊介绍: Expert Opinion on Investigational Drugs (ISSN 1354-3784 [print], 1744-7658 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles and original papers on drugs in preclinical and early stage clinical development, providing expert opinion on the scope for future development. The Editors welcome: Reviews covering preclinical through to Phase II data on drugs or drug classes for specific indications, and their potential impact on future treatment strategies Drug Evaluations reviewing the clinical and pharmacological data on a particular drug Original Research papers reporting the results of clinical investigations on agents that are in Phase I and II clinical trials The audience consists of scientists, managers and decision-makers in the pharmaceutical industry, and others closely involved in R&D.
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