哮喘异质性与血液中炎性模式的研究

2009/07/30

    目前对与炎症模式相关的哮喘异质性的研究逐渐变热。为了评估疾病的表型特点,尤其是临床表现。R Nadif等研究者从法国“遗传和环境相关哮喘”(EGEA)流行病研究中选取了381名有哮喘典型症状的患者,得到其血液中炎症模式。四种血液炎性模式的定义是根据嗜酸细胞(EOS)和中性粒细胞(NEU)计数截点来决定的。血样中250 EOS/mm3定义为EOShi,5000 NEU/mm3定义为NEUhi。临床症状表现为典型哮喘和慢性阻塞性肺疾病(COPD)样症状,并将病情量化评分。
    结果发现,56.2%哮喘患者的血样表现为EOSlo 型(即<250 EOS/mm3)。血样表现为EOShi型的哮喘患者其IgE较高、FEV1较低,且比血样EOSlo型的患者哮喘更易发病。EOSlo型的患者其中性粒细胞炎症程度NEUhi与皮肤点刺实验阳性反应相关性不大(OR 0.44, 95% CI 0.20 to 0.96)。血样EOShi型的哮喘患者,在不考虑年龄、性别、吸烟史和吸及糖皮质激素治疗史的情况下,中性粒细胞的炎性反应不能解释哮喘的发病和严重程度及分级,但却与夜间哮喘症状的发作明显相关(OR 5.21, 95% CI 1.44 to 18.8)。非吸烟的哮喘人群中,有慢性阻塞性肺疾病(COPD)样症状,尤其是有顽固性咳痰的患者,其血样中中性粒细胞炎性表现更明显,而与嗜酸粒细胞升高关系不明显(OR 2.35, 95% CI 1.08 to 5.10)。
    由此研究得出:哮喘的症状与血液嗜酸细胞和中性粒细胞升高有关。同时考虑嗜酸细胞和中性粒细胞两种炎性反应,可能有助于对哮喘的深入研究。
 
(于娜  沈阳中国医科大学附属第一医院呼吸内科 110001 摘译)
(Thorax 2009;64:374-380)
 

Heterogeneity of asthma according to blood inflammatory patterns

R Nadif1, V Siroux2, M-P Oryszczyn1, C Ravault1, C Pison1, I Pin3, F Kauffmann1 on behalf of the Epidemiological study on the Genetics and Environment of Asthma (EGEA)  

Rationale: There is increasing interest regarding asthma heterogeneity in relation to inflammatory patterns.  
Objectives: To assess phenotypic characteristics, in particular clinical presentation of the disease, in 381 well-characterised adults with asthma from the French Epidemiological study on the Genetics and Environment of Asthma (EGEA) according to their blood inflammatory pattern.  
Methods: Four blood inflammatory patterns were defined according to eosinophil (EOS) and neutrophil (NEU) count cut-off points. Samples with 250 EOS/mm3 were classified as EOShi and those with 5000 NEU/mm3 as NEUhi. Clinical characteristics include typical asthma and chronic obstructive pulmonary disease (COPD)-like symptoms, as well as composite quantitative scores addressing the activity of the disease.  
Results: A substantial number of those with asthma (56.2%) had the EOSlo pattern (<250 EOS/mm3). Patients with asthma who had the EOShi pattern had higher immunoglobulin E (IgE), a lower forced expiratory volume in 1 s (FEV1) and presented a more active asthma than those with the EOSlo pattern. Among those with the EOSlo pattern, neutrophil inflammation (NEUhi) was related to a less frequent positive skin prick test response (OR 0.44, 95% CI 0.20 to 0.96). Among those with the EOShi pattern, neutrophil inflammation did not explain current asthma or asthma activity, and was significantly related to nocturnal symptoms (OR 5.21, 95% CI 1.44 to 18.8) independently of age, sex, smoking and inhaled corticosteroid treatment. In non-smokers with asthma, COPD-like symptoms, in particular chronic phlegm, were more frequent in those with neutrophil inflammation, independent of eosinophil inflammation.  
Conclusions: Besides eosinophilia, neutrophil inflammation assessed in the blood is related to specific characteristics of asthma. Considering simultaneously neutrophilic and eosinophilic inflammation may contribute to help to disentangle this complex disease.
 


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