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首页> 外文期刊>Clinical and experimental allergy : >Depressive symptom‐associated IL IL ‐1β and TNF TNF ‐α release correlates with impaired bronchodilator response and neutrophilic airway inflammation in asthma
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Depressive symptom‐associated IL IL ‐1β and TNF TNF ‐α release correlates with impaired bronchodilator response and neutrophilic airway inflammation in asthma

机译:抑郁的症状相关的IL-1β和TNF TNF-α释放与哮喘中受损的支气管扩张剂反应和中性气动气道炎症相关联

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Summary Background Depressive symptoms worsen asthma outcomes; however, the mechanism remains largely unexplored. Objective This study aimed to determine whether depressive symptom‐associated immune inflammation correlates with impaired bronchodilator response ( BDR ) and airway inflammatory phenotypes. Methods Eligible adults with asthma (n?=?198) underwent clinical assessment, sputum induction and blood sampling. Depressive symptoms were defined by scores on the depression subscale of the Hospital Anxiety and Depression Scale ( HADS ‐D). Pre‐ and post‐bronchodilator spirometry was performed for BDR . Airway inflammatory phenotypes were defined by sputum cell counts. CRP , IL ‐1β, IL ‐5, IL ‐6, IL ‐8, TNF ‐α, IFN ‐γ, CCL 17 and CCL 22 in serum and sputum were detected. Results Compared with the non‐depressive group (n?=?174), the depressive group (n?=?24) exhibited impaired BDR ( P? = ? 0.032) and increased sputum neutrophils ( P? = ? 0.023), which correlated with the HADS ‐D scores ( P? = ? 0.027 and P? = ? 0.029). Levels of IL ‐1β, TNF ‐α and IFN ‐γ in the serum and those of IL ‐1β and IFN ‐γ in the sputum were elevated in the depressive group compared to those in the non‐depressive group (all P? ? 0.05). Multiple regression models indicated that TNF ‐α in the sputum and IL ‐1β, IL ‐6 and IFN ‐γ in both the serum and sputum were inversely associated with BDR ; TNF ‐α in the sputum and IL ‐1β in both the serum and sputum were positively correlated with sputum neutrophils. Mediation analyses revealed that IL ‐1β and TNF ‐α in the sputum and IL ‐1β in both the serum and sputum mediate the correlations of the HADS ‐D scores with BDR and sputum neutrophils, respectively. Conclusions and Clinical Relevance Asthma patients with depressive symptoms present worse asthma control, which is most likely explained by impaired BDR and neutrophilic airway inflammation. IL ‐1β and TNF ‐α, which are two key pro‐inflammatory cytokines that mediate the correlation of depressive symptoms with impaired BDR and neutrophilic airway inflammation, may serve as targeted biomarkers in the neuropsychological phenotype of asthma; however, this result needs to be further validated.
机译:摘要背景抑郁症状恶化了哮喘结果;但是,该机制仍然很大程度上是未开发的。目的本研究旨在确定抑郁症状相关的免疫炎症是否与受损的支气管扩张剂反应(BDR)和气道炎症表型相关联。方法符合条件的成人哮喘(n?= 198)临床评估,痰诱导和血液取样。抑郁症状由医院焦虑和抑郁尺度的抑郁症次数(HADS -D)的分数定义。对BDR进行支气管胆管肺炎血管测定法。通过痰细胞计数定义了气道炎症表型。检测CRP,IL-1β,IL-5,IL -6,IL-8,TNF-α,IFN-γ,CCL 17和CCL 22在血清和痰中。结果与非抑郁组(N?= 174)相比,抑郁组(n?=Δ24)表现出受损的BDR(P?= 0.032)和增加的痰中性粒细胞(P?= 0.023),其相关随着患有的分数(p?= 0.027和p?= 0.029)。与非抑制基团中的那些相比,在抑郁基团中升高了血清中的IL-1β,TNF-α和IFN-γ和痰中的IL-1β和IFN-γ的水平(所有p≤1。 ?0.05)。多元回归模型表明,在血清和痰中的痰和IL-1β,IL -6和IFN-γ中的TNF-α与BDR相反;在血清和痰中的痰中和IL-1β中的TNF-α与痰中子粒细胞呈正相关。中介分析显示,血清和痰中的痰和IL-1β中的IL-1β和TNF-α分别介导HASS-D分别与BDR和痰中性粒细胞的相关性。结论和临床关联哮喘抑郁症状的哮喘患者呈现较差的哮喘控制,最有可能通过受损的BDR和中性粒细胞炎症解释。 IL-1β和TNF-α,这是两个关键促炎细胞因子,介导BDR和中性粒细胞炎症受损的抑郁症状的相关性,可作为哮喘神经心理表型的靶向生物标志物;但是,此结果需要进一步验证。

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