Demoly Pascal, Liu Andrew H, Rodriguez Del Rio Pablo, Pedersen Soren, Casale Thomas B, Price David
Division of Allergy, Department of Pulmonology, Hôpital Arnaud de Villeneuve, Montpellier, France.
IDESP Inserm, University, Hospital of Montpellier, Montpellier, France.
J Asthma Allergy. 2022 Aug 16;15:1069-1080. doi: 10.2147/JAA.S362588. eCollection 2022.
Asthma afflicts an estimated 339 million people globally and is associated with ill health, disability, and early death. Strong risk factors for developing asthma are genetic predisposition and environmental exposure to inhaled substances that may provoke allergic reactions. Asthma guidelines recommend identifying causal or trigger allergens with specific IgE (sIgE) testing after a diagnosis of asthma has been made. Allergy testing with sIgE targets subpopulations of patients considered at high risk, such as those with frequent exacerbations, emergency visits or hospitalizations, or uncontrolled symptoms. Specific recommendations apply to preschool children, school-age children, patients with persistent or difficult-to-control asthma, patients needing oral corticosteroids or high-dose inhaled steroids, patients seeking understanding and guidance about their disease, and candidates for advanced therapies (biologics, allergen immunotherapy). Allergen skin testing is common in specialized settings but less available in primary care. Blood tests for total and sIgE are accessible and yield quantifiable results for tested allergens, useful for detecting sensitization. Results are interpreted in the context of the patient's clinical presentation, age, and relevant allergen exposures. Incorporating sIgE testing into asthma management adds objective information to identify specific allergies and can guide personalized treatment plans, which reinforce patient-doctor communication. Test results can also be used to predict exacerbations and response to therapies. Additional diagnostic information can be gleaned from (i) eosinophil count ≥300 μL, which significantly increases the odds of having exacerbations, and emerging eosinophil biomarkers (eg, eosinophil-derived neurotoxin), which can be measured in plasma or serum samples, and (ii) fractional exhaled nitric oxide (FeNO), with values ≥25 ppb regarded as the cutoff for diagnosis, evaluating inhaled corticosteroid response, and of probable response to anti-IgE, anti-IL4 and anti-IL5 receptor biologics. Referral to asthma/allergy specialists is warranted when the initial diagnosis is uncertain, and when asthma symptoms, impairment, or exacerbations are repeated or severe.
全球估计有3.39亿人患有哮喘,哮喘与健康不佳、残疾和过早死亡相关。哮喘发病的强烈风险因素是遗传易感性和环境中接触可能引发过敏反应的吸入性物质。哮喘指南建议在确诊哮喘后,通过特异性IgE(sIgE)检测来识别病因性或触发型过敏原。使用sIgE进行过敏检测针对的是被认为高风险的患者亚群,例如那些频繁发作、急诊就诊或住院,或症状控制不佳的患者。具体建议适用于学龄前儿童、学龄儿童、持续性或难以控制的哮喘患者、需要口服糖皮质激素或高剂量吸入性糖皮质激素的患者、寻求对其疾病的理解和指导的患者,以及高级治疗(生物制剂、变应原免疫疗法)的候选者。变应原皮肤试验在专科环境中很常见,但在初级保健中较难获得。总IgE和sIgE的血液检测容易进行,并且能为检测的过敏原产生可量化的结果,有助于检测致敏情况。结果需结合患者的临床表现、年龄和相关变应原暴露情况进行解读。将sIgE检测纳入哮喘管理可增加识别特定过敏的客观信息,并能指导个性化治疗方案,加强医患沟通。检测结果还可用于预测发作和对治疗的反应。其他诊断信息可从以下方面获得:(i)嗜酸性粒细胞计数≥300/μL,这会显著增加发作几率,以及新兴的嗜酸性粒细胞生物标志物(如嗜酸性粒细胞衍生神经毒素),可在血浆或血清样本中测量;(ii)呼出一氧化氮分数(FeNO),值≥25 ppb被视为诊断、评估吸入性糖皮质激素反应以及对抗IgE、抗IL4和抗IL5受体生物制剂可能反应的临界值。当初始诊断不确定,以及哮喘症状、功能损害或发作反复或严重时,应转诊至哮喘/过敏专科医生处。