Medical Research Institute of New Zealand, Wellington, New Zealand; Victoria University of Wellington, Wellington, New Zealand.
Medical Research Institute of New Zealand, Wellington, New Zealand.
J Allergy Clin Immunol Pract. 2018 Nov-Dec;6(6):1982-1988.e1. doi: 10.1016/j.jaip.2018.03.004. Epub 2018 Mar 30.
Type 2 biomarkers that predict both likelihood of future severe exacerbations and response to mAb therapy in asthma would be useful clinically in identifying patients both at greater risk of hospitalization and most likely to benefit from mAb therapy.
To describe the association between type 2 biomarkers, blood eosinophils, fractional exhaled nitric oxide (Feno), serum periostin, and serum IgE, and time to severe exacerbation in a broad asthma population.
Participants from 2 adult asthma cohorts with baseline measurements of blood eosinophils, Feno, serum periostin, and serum IgE were reviewed after at least 12 months to obtain an exacerbation history, corroborated with general practitioner and hospital medical records. The association between baseline type 2 biomarkers and time to exacerbation was described by Cox proportional hazard ratios (HRs) using multivariate models.
A total of 212 participants were followed for a median (range) 3.8 (1.1-5.3) years; 67 of 212 (32%) had at least 1 severe exacerbation. The HRs (95% CI) of baseline type 2 biomarkers and time to exacerbation were as follows: blood eosinophils per 0.1 × 10/L increase, 0.89 (0.76-1.05), P = .17; log Feno per 0.693 increase, 0.65 (0.52-0.81), P < .001; log serum periostin per 0.693 increase, 0.62 (0.35-1.09), P = .10; log serum IgE per 0.693 increase, 0.89 (0.80-1.00), P = .05.
The positive association between type 2 biomarkers and risk of severe exacerbations in populations with severe refractory asthma does not extend to mild and moderate asthma. Non-type 2 asthma may represent a phenotype associated with an increased risk of severe exacerbations in a broad asthma population.
能够预测未来严重加重风险和单克隆抗体治疗反应的 2 型生物标志物在临床上识别住院风险较高和最有可能从单克隆抗体治疗中获益的患者方面将非常有用。
描述 2 型生物标志物(嗜酸性粒细胞、呼出气一氧化氮分数、血清骨桥蛋白和血清 IgE)与广泛哮喘人群严重加重时间之间的关系。
回顾了至少有 12 个月随访期的 2 个成人哮喘队列的研究参与者,以获取加重史,这些信息与全科医生和医院病历相吻合。使用多变量模型,通过 Cox 比例风险比(HR)描述基线 2 型生物标志物与加重时间之间的关系。
共有 212 名参与者中位(范围)随访 3.8(1.1-5.3)年;212 名参与者中有 67 名(32%)至少发生 1 次严重加重。基线 2 型生物标志物与加重时间的 HR(95%CI)如下:每增加 0.1×10/L 嗜酸性粒细胞计数,0.89(0.76-1.05),P=0.17;每增加 0.693 个单位的 log Feno,0.65(0.52-0.81),P<0.001;每增加 0.693 个单位的 log 血清骨桥蛋白,0.62(0.35-1.09),P=0.10;每增加 0.693 个单位的 log 血清 IgE,0.89(0.80-1.00),P=0.05。
在严重难治性哮喘人群中,2 型生物标志物与严重加重风险之间的正相关关系并不适用于轻度和中度哮喘。非 2 型哮喘可能代表一种表型,与广泛哮喘人群中严重加重风险增加相关。