Racha Abi Melhem, Marc Assaad, Khalil El Gharib, Hussein Rabah, Ali Kassem, Jordyn Salak, Saif Abu-Baker, Ahmad Itani
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The distinction of EA is very important in the light of emergent type 2 inflammation targeted therapies.</p><p><strong>Methods: </strong>We performed a 1-year (2018) retrospective cohort analysis of the Nationwide Inpatient Database (NIS). We included all adult patients presenting with severe asthma. Patients were stratified into two groups: eosinophilic severe asthma and non-eosinophilic severe asthma. The primary outcomes measures were the prevalence of chronic steroid use, status asthmaticus, family history of asthma, food, drug and environmental allergies, presence of nasal polyps, allergic rhinitis, allergic dermatitis, need for mechanical ventilation, need for oxygen supplementation, gastroesophageal reflux disease, in-hospital mortality, and length of stay. We performed descriptive statistics. Continuous parametric variables were reported using a mean and standard deviation. Continuous nonparametric variables were reported using a median and interquartile range. To compare the characteristics of the two groups, we used the independent <i>t</i>-test for continuous parametric variables and the Mann-Whitney U test for continuous nonparametric variables. The Chi-square test was used to assess differences in categorical variables.</p><p><strong>Results: </strong>A total of 2,646 patients were included, out of which 882 belonged to the eosinophilic group and 1,764 were in the non-eosinophilic group. Comparing EA versus NEA, we have found that eosinophilic group was characterized by higher percentage of steroid use (18.3% vs. 9.5%, P < 0.001). This group also had higher rates of status asthmaticus and positive family history (P = 0.009 and 0.004, respectively). The presence of allergies, allergic rhinitis, nasal polyps, and allergic dermatitis was higher among patients with eosinophilia. The need for mechanical ventilation and supplemental oxygen was also higher among this group (P < 0.001 for both); however, there was no significant difference in mortality rate (P = 0.347) and the length of hospital stay was similar in both groups (P < 0.001).</p><p><strong>Conclusion: </strong>We showed herein that the eosinophilic subtype of asthma differs widely from the non-eosinophilic phenotype. Clinically, patients with eosinophilia might exhibit different symptomatology, more atopy, and concomitant comorbidities. However, this group might have better response to steroid therapy and might benefit from the new emergent T2 immune targeted therapy. The identification of EA is crucial for better disease control.</p>","PeriodicalId":94329,"journal":{"name":"Journal of clinical medicine research","volume":"16 4","pages":"133-137"},"PeriodicalIF":1.6000,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11073386/pdf/","citationCount":"0","resultStr":"{\"title\":\"The Determinants of Eosinophilia in Patients With Severe Asthma.\",\"authors\":\"Racha Abi Melhem, Marc Assaad, Khalil El Gharib, Hussein Rabah, Ali Kassem, Jordyn Salak, Saif Abu-Baker, Ahmad Itani\",\"doi\":\"10.14740/jocmr5162\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Asthma is defined by the Global Initiative for Asthma (GINA) as a heterogeneous disease characterized by chronic airway inflammation. The pathogenesis of the disease is better understood with the comprehension of immunological pathways. These pathways differ by the type of recruited cells and released interleukin (IL). Thus, asthma can be classified into subtypes based on the underlying immune mechanism: eosinophilic asthma (EA) and non-eosinophilic asthma (NEA). Patients with EA tend to respond better to inhaled corticosteroid as compared to those with NEA. The distinction of EA is very important in the light of emergent type 2 inflammation targeted therapies.</p><p><strong>Methods: </strong>We performed a 1-year (2018) retrospective cohort analysis of the Nationwide Inpatient Database (NIS). We included all adult patients presenting with severe asthma. Patients were stratified into two groups: eosinophilic severe asthma and non-eosinophilic severe asthma. The primary outcomes measures were the prevalence of chronic steroid use, status asthmaticus, family history of asthma, food, drug and environmental allergies, presence of nasal polyps, allergic rhinitis, allergic dermatitis, need for mechanical ventilation, need for oxygen supplementation, gastroesophageal reflux disease, in-hospital mortality, and length of stay. We performed descriptive statistics. Continuous parametric variables were reported using a mean and standard deviation. Continuous nonparametric variables were reported using a median and interquartile range. To compare the characteristics of the two groups, we used the independent <i>t</i>-test for continuous parametric variables and the Mann-Whitney U test for continuous nonparametric variables. 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引用次数: 0
摘要
背景:哮喘全球倡议(GINA)将哮喘定义为一种以慢性气道炎症为特征的异质性疾病。随着对免疫学途径的了解,人们对这种疾病的发病机理有了更好的认识。这些途径因招募细胞的类型和释放的白细胞介素(IL)而异。因此,哮喘可根据潜在的免疫机制分为亚型:嗜酸性粒细胞性哮喘(EA)和非嗜酸性粒细胞性哮喘(NEA)。与非嗜酸性粒细胞性哮喘患者相比,嗜酸性粒细胞性哮喘患者对吸入皮质类固醇的反应往往更好。鉴于2型炎症靶向疗法的出现,区分EA非常重要:我们对全国住院患者数据库(NIS)进行了为期 1 年(2018 年)的回顾性队列分析。我们纳入了所有患有严重哮喘的成年患者。患者被分为两组:嗜酸粒细胞性重症哮喘和非嗜酸粒细胞性重症哮喘。主要结果指标包括长期使用类固醇、哮喘状态、哮喘家族史、食物、药物和环境过敏、鼻息肉、过敏性鼻炎、过敏性皮炎、机械通气需求、氧气补充需求、胃食管反流病、院内死亡率和住院时间。我们进行了描述性统计。连续参数变量使用平均值和标准差进行报告。非参数连续变量采用中位数和四分位距进行报告。为了比较两组患者的特征,我们对连续参数变量采用独立 t 检验,对连续非参数变量采用 Mann-Whitney U 检验。在评估分类变量的差异时,我们使用了卡方检验(Chi-square test):共纳入 2,646 例患者,其中 882 例属于嗜酸性粒细胞组,1,764 例属于非嗜酸性粒细胞组。对比 EA 和 NEA,我们发现嗜酸性粒细胞组使用类固醇的比例更高(18.3% 对 9.5%,P < 0.001)。嗜酸性粒细胞组患哮喘和阳性家族史的比例也更高(P = 0.009 和 0.004)。嗜酸性粒细胞增多症患者出现过敏、过敏性鼻炎、鼻息肉和过敏性皮炎的比例较高。嗜酸性粒细胞增多症患者对机械通气和补充氧气的需求也较高(P < 0.001),但死亡率无显著差异(P = 0.347),两组患者的住院时间相似(P < 0.001):结论:我们的研究表明,嗜酸性粒细胞亚型哮喘与非嗜酸性粒细胞表型哮喘有很大不同。在临床上,嗜酸性粒细胞增多的患者可能会表现出不同的症状、更多的过敏症和并发症。不过,这类患者对类固醇治疗的反应可能更好,并可能从新出现的 T2 免疫靶向治疗中获益。识别 EA 对于更好地控制疾病至关重要。
The Determinants of Eosinophilia in Patients With Severe Asthma.
Background: Asthma is defined by the Global Initiative for Asthma (GINA) as a heterogeneous disease characterized by chronic airway inflammation. The pathogenesis of the disease is better understood with the comprehension of immunological pathways. These pathways differ by the type of recruited cells and released interleukin (IL). Thus, asthma can be classified into subtypes based on the underlying immune mechanism: eosinophilic asthma (EA) and non-eosinophilic asthma (NEA). Patients with EA tend to respond better to inhaled corticosteroid as compared to those with NEA. The distinction of EA is very important in the light of emergent type 2 inflammation targeted therapies.
Methods: We performed a 1-year (2018) retrospective cohort analysis of the Nationwide Inpatient Database (NIS). We included all adult patients presenting with severe asthma. Patients were stratified into two groups: eosinophilic severe asthma and non-eosinophilic severe asthma. The primary outcomes measures were the prevalence of chronic steroid use, status asthmaticus, family history of asthma, food, drug and environmental allergies, presence of nasal polyps, allergic rhinitis, allergic dermatitis, need for mechanical ventilation, need for oxygen supplementation, gastroesophageal reflux disease, in-hospital mortality, and length of stay. We performed descriptive statistics. Continuous parametric variables were reported using a mean and standard deviation. Continuous nonparametric variables were reported using a median and interquartile range. To compare the characteristics of the two groups, we used the independent t-test for continuous parametric variables and the Mann-Whitney U test for continuous nonparametric variables. The Chi-square test was used to assess differences in categorical variables.
Results: A total of 2,646 patients were included, out of which 882 belonged to the eosinophilic group and 1,764 were in the non-eosinophilic group. Comparing EA versus NEA, we have found that eosinophilic group was characterized by higher percentage of steroid use (18.3% vs. 9.5%, P < 0.001). This group also had higher rates of status asthmaticus and positive family history (P = 0.009 and 0.004, respectively). The presence of allergies, allergic rhinitis, nasal polyps, and allergic dermatitis was higher among patients with eosinophilia. The need for mechanical ventilation and supplemental oxygen was also higher among this group (P < 0.001 for both); however, there was no significant difference in mortality rate (P = 0.347) and the length of hospital stay was similar in both groups (P < 0.001).
Conclusion: We showed herein that the eosinophilic subtype of asthma differs widely from the non-eosinophilic phenotype. Clinically, patients with eosinophilia might exhibit different symptomatology, more atopy, and concomitant comorbidities. However, this group might have better response to steroid therapy and might benefit from the new emergent T2 immune targeted therapy. The identification of EA is crucial for better disease control.