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Current status and future directions for diagnostic markers of drug-induced vascular injury

机译:药物性血管损伤的诊断标志物的现状和未来方向

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摘要

Recently, there has been an increased incidence of vascular toxicity in pre-clinical toxicology studies. This is of concern because of the uncertain relevance and extrapolation of this finding to humans. In dogs, profound heart rate (HR) and mean arterial pressure (MAP) changes were considered surrogate markers for drug-induced vascular injury until the early 1990s when endothelin receptor antagonists (ETRA) did not significantly alter HR or MAP but induced identical lesions in the coronary arteries of dogs. Thus significant alterations in HR and MAP were found not to be a prerequisite for this lesion. Clinically, the potential for vascular injury coupled with the lack of an unequivocal non-invasive diagnostic marker is an issue of concern to pharmaceutical companies and the regulatory authorities. Therefore, qualification and validation of biomarkers as diagnostic tools for drug-induced vascular injury would add great value to risk management and expedite the drug development process. This review focuses on the status, progress and future trends in vascular biology aimed at identification and development of diagnostic markers that are specific, sensitive and possess potential utility in both a pre-clinical and clinical setting.
机译:最近,在临床前毒理学研究中血管毒性的发生率增加了。这是令人关注的,因为该发现与人类之间的不确定性和外推性。在犬中,深刻的心率(HR)和平均动脉压(MAP)的变化被认为是药物引起的血管损伤的替代标志物,直到1990年代初内皮素受体拮抗剂(ETRA)并未显着改变HR或MAP而是在相同的条件下诱发相同的病变狗的冠状动脉。因此,发现HR和MAP的明显改变不是该病变的先决条件。在临床上,潜在的血管损伤加上缺乏明确的非侵入性诊断标记是制药公司和监管机构关注的问题。因此,对生物标志物作为药物诱导的血管损伤的诊断工具进行鉴定和验证将为风险管理增加价值,并加快药物开发过程。这篇综述着重于血管生物学的现状,进展和未来趋势,旨在鉴定和开发特异,敏感并在临床前和临床环境中均具有潜在效用的诊断标志物。

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  • 来源
    《Cancer Biomarkers》 |2005年第1期|15-28|共14页
  • 作者单位

    Global Safety Assessment, AstraZeneca Pharmaceuticals, Alderely Park, UK;

    Global Safety Assessment, AstraZeneca Pharmaceuticals, Alderely Park, UK;

    Global Safety Assessment, AstraZeneca Pharmaceuticals, Alderely Park, UK;

    Global Safety Assessment, AstraZeneca Pharmaceuticals, Alderely Park, UK;

    Toxicology Program, Department of Environmental Health Sciences, The University of Michigan, Ann Arbor, MI, USA;

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