葡萄球菌肠毒素特异性IgE致敏:老年哮喘固定气流阻塞的潜在预测因子。

IF 4.1 2区 医学 Q2 ALLERGY
Ha-Kyeong Won, Woo-Jung Song, Sung do Moon, Kyoung-Hee Sohn, Ju-Young Kim, Byung-Keun Kim, Heung-Woo Park, Claus Bachert, Sang Heon Cho
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引用次数: 2

摘要

目的:金黄色葡萄球菌肠毒素特异性免疫球蛋白E (SE-sIgE)致敏倾向于随着年龄的增长而增加,并且已知与老年人的哮喘和严重程度相关。然而,SE-sIgE对老年人的长期影响尚不清楚。本研究旨在探讨老年哮喘患者SE-sIgE与固定气流阻塞(FAO)之间的关系。方法:对223例老年哮喘患者和89例对照组进行分析。评估患者的人口统计学、慢性鼻窦炎(CRS)病史、哮喘持续时间、急性发作频率和肺功能,然后进行2年的前瞻性随访。在基线时测定血清总IgE和SE-sIgE水平。气流阻塞定义为基线时1秒用力呼气量(FEV1)/用力肺活量(FVC)比值< 0.7,2年随访时FEV1/FVC比值< 0.7。结果:在基线时,气流阻塞的患病率为29.1%。与无气流阻塞的患者相比,有气流阻塞的患者明显更多为男性、有吸烟史、合并CRS、SE-sIgE水平较高。多因素logistic回归分析显示,气流阻塞与当前吸烟和基线时SE-sIgE致敏性显著相关。经过2年的随访,基线SE-sIgE致敏性始终与FAO相关。同时,每年加重次数与SE-sIgE水平显著相关。结论:老年哮喘患者随访2年后,基线SE-sIgE致敏与哮喘加重次数和FAO显著相关。这些发现为进一步研究SE-sIgE致敏对气道重塑的直接和介导作用提供了依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Staphylococcal Enterotoxin-Specific IgE Sensitization: A Potential Predictor of Fixed Airflow Obstruction in Elderly Asthma.

Staphylococcal Enterotoxin-Specific IgE Sensitization: A Potential Predictor of Fixed Airflow Obstruction in Elderly Asthma.

Staphylococcal Enterotoxin-Specific IgE Sensitization: A Potential Predictor of Fixed Airflow Obstruction in Elderly Asthma.

Staphylococcal Enterotoxin-Specific IgE Sensitization: A Potential Predictor of Fixed Airflow Obstruction in Elderly Asthma.

Purpose: Staphylococcus aureus enterotoxin-specific immunoglobulin E (SE-sIgE) sensitization tends to increase with age and is known to be associated with asthma and severity in older adults. However, the long-term impact of SE-sIgE in the elderly remains unknown. This study aimed to examine the relationships between SE-sIgE and fixed airflow obstruction (FAO) in a cohort of elderly asthmatics.

Methods: A total of 223 elderly asthmatics and 89 controls were analyzed. Patients were assessed for demographics, history of chronic rhinosinusitis (CRS), asthma duration, acute exacerbation frequency, and lung function at baseline and then were prospectively followed up for 2 years. Serum total IgE and SE-sIgE levels were measured at baseline. Airflow obstruction was defined as forced expiratory volume in 1 second (FEV1)/forced vital capacity (FVC) ratio < 0.7 at baseline and FAO was defined as FEV1/FVC ratio < 0.7 over the 2-year follow-up.

Results: At baseline, the prevalence of airflow obstruction was 29.1%. Patients with airflow obstruction were significantly more likely to be male, and have a positive smoking history, comorbid CRS, and higher levels of SE-sIgE than those without airflow obstruction. Multivariate logistic regression analysis showed that airflow obstruction was significantly associated with current smoking and SE-sIgE sensitization at baseline. After the 2-year follow-up, baseline SE-sIgE sensitization was consistently related to FAO. Meanwhile, the number of exacerbations per year was significantly correlated with SE-sIgE levels.

Conclusions: Baseline SE-sIgE sensitization was significantly associated with the number of asthma exacerbations and FAO after the 2-year follow-up in elderly asthmatics. These findings warrant further investigation of the direct and mediating roles of SE-sIgE sensitization on airway remodeling.

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来源期刊
CiteScore
6.10
自引率
6.80%
发文量
53
审稿时长
>12 weeks
期刊介绍: The journal features cutting-edge original research, brief communications, and state-of-the-art reviews in the specialties of allergy, asthma, and immunology, including clinical and experimental studies and instructive case reports. Contemporary reviews summarize information on topics for researchers and physicians in the fields of allergy and immunology. As of January 2017, AAIR do not accept case reports. However, if it is a clinically important case, authors can submit it in the form of letter to the Editor. Editorials and letters to the Editor explore controversial issues and encourage further discussion among physicians dealing with allergy, immunology, pediatric respirology, and related medical fields. AAIR also features topics in practice and management and recent advances in equipment and techniques for clinicians concerned with clinical manifestations of allergies and pediatric respiratory diseases.
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