Department of Medicine, Geisel School of Medicine at Dartmouth, Hanover, NH; Department of Respiratory Services, Valley Regional Hospital, Claremont, NH.
Department of Respiratory Medicine, University of Exeter Medical School, College of Medicine and Health, University of Exeter, Exeter, England.
Chest. 2021 Aug;160(2):491-498. doi: 10.1016/j.chest.2021.03.049. Epub 2021 Apr 1.
Biomarkers in COPD may be clinical (prior exacerbation history), physiologic (FEV), or blood based (eosinophil count or fibrinogen level). Recent interest in using biomarkers to predict response to therapy in clinical practice has emerged. The benefits of inhaled therapy depend on the correct use of the inhaler, including an appropriate inspiratory flow. Of the available delivery systems, dry powder inhalers are unique because they have an internal resistance, are breath actuated, and are flow dependent. Ideally, the user inhales "forcefully" to generate turbulent energy (determined by an individual's inspiratory flow and the resistance of the device) within the device that disaggregates the powder so that the individual inhales the medication particles into the lower respiratory tract. Because of specific features of dry powder inhalers and the required optimal inspiratory flow, an unmet need exists to identify individuals who are likely or unlikely to benefit from dry powder medications. Peak inspiratory flow, defined as the maximum airflow generated during inhalation against the simulated resistance of a dry powder inhaler, is a physiologic measure that has biological plausibility, has good test characteristics (repeatability and reliability), and is generalizable. Current evidence supports peak inspiratory flow as a predictive therapeutic biomarker to optimize therapy in both outpatients with COPD as well as those hospitalized for an exacerbation before discharge. This approach is consistent with the precepts of precision medicine, which considers differences in a person's biological features, exposure, and lifestyle to prevent and treat disease.
COPD 的生物标志物可能是临床的(先前的加重病史)、生理学的(FEV)或基于血液的(嗜酸性粒细胞计数或纤维蛋白原水平)。最近,人们对使用生物标志物来预测临床实践中治疗反应的兴趣已经出现。吸入治疗的益处取决于吸入器的正确使用,包括适当的吸气流量。在可用的输送系统中,干粉吸入器是独特的,因为它们具有内部阻力,是呼吸驱动的,并且依赖于流量。理想情况下,使用者会“用力”吸气,在设备内产生湍流能量(由个人的吸气流量和设备的阻力决定),使粉末解聚,从而使个人将药物颗粒吸入下呼吸道。由于干粉吸入器的特定特征和所需的最佳吸气流量,存在一个未满足的需求,即确定哪些人可能或不可能从干粉药物中受益。吸气峰流速定义为在吸入过程中针对干粉吸入器的模拟阻力产生的最大气流,是一种具有生物学合理性、良好测试特性(可重复性和可靠性)且具有通用性的生理测量方法。目前的证据支持吸气峰流速作为一种预测治疗性生物标志物,以优化 COPD 门诊患者以及因加重而住院的患者在出院前的治疗。这种方法符合精准医学的原则,该原则考虑了一个人在生物学特征、暴露和生活方式方面的差异,以预防和治疗疾病。