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Airway biomarkers of the oxidant burden in asthma and chronic obstructive pulmonary disease: Current and future perspectives

机译:哮喘和慢性阻塞性肺疾病中氧化剂负担的气道生物标志物:当前和未来观点

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摘要

The pathogenesis of asthma and chronic obstructive pulmonary disease (COPD) has been claimed to be attributable to increased systemic and local oxidative stress. Detection of the oxidant burden and evaluation of their progression and phenotypes by oxidant biomarkers have proved challenging and difficult. A large number of asthmatics are cigarette smokers and smoke itself contains oxidants complicating further the use of oxidant biomarkers. One of the most widely used oxidant markers in asthma is exhaled nitric oxide (NO), which plays an important role in the pathogenesis of asthma and disease monitoring. Another oxidant marker that has been widely investigated in COPD is 8-isoprostane, but it is probably not capable of differentiating asthma from COPD, or even sensitive in the early assessment of these diseases. None of the current biomarkers have been shown to be better than exhaled NO in asthma. There is a need to identify new biomarkers for obstructive airway diseases, especially their differential diagnosis. A comprehensive evaluation of oxidant markers and their combinations will be presented in this review. In brief, it seems that additional analyses utilizing powerful tools such as genomics, metabolomics, lipidomics, and proteomics will be required to improve the specificity and sensitivity of the next generation of biomarkers.
机译:哮喘和慢性阻塞性肺疾病(COPD)的发病机理据称可归因于全身和局部氧化应激的增加。已经证明通过氧化剂生物标记物检测氧化剂负荷并评估其进程和表型是具有挑战性和困难的。大量哮喘病患者是吸烟者,烟雾本身含有氧化剂,使氧化剂生物标记物的使用进一步复杂化。哮喘中最广泛使用的氧化剂之一是呼出气一氧化氮(NO),它在哮喘的发病机理和疾病监测中起着重要的作用。在COPD中已广泛研究的另一种氧化剂标志物是8-异前列腺素,但它可能无法区分哮喘和COPD,甚至在早期评估这些疾病时也不敏感。在哮喘中,目前没有任何生物标志物比呼出NO更好。有必要确定阻塞性气道疾病的新生物标志物,尤其是其鉴别诊断。本文将对氧化剂标志物及其组合进行全面评估。简而言之,似乎将需要利用基因组学,代谢组学,脂质组学和蛋白质组学等强大工具进行额外分析,以提高下一代生物标志物的特异性和敏感性。

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