哮喘 COPD 重叠综合征

Ziaul Huq
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引用次数: 0

摘要

哮喘-慢性阻塞性肺疾病(COPD)重叠综合征(ACOS)是描述同时具有哮喘和慢性阻塞性肺疾病特征的患者的术语,最早由哮喘全球倡议(GINA)和慢性阻塞性肺疾病全球倡议(GOLD)的联合部分于2014年提出,2017年GINA将其修订为ACO(哮喘-慢性阻塞性肺疾病重叠)。从流行病学角度看,2% 的普通人群、29.6% 的哮喘患者和 26.5% 的 COPD 患者患有 ACO。与单纯哮喘或慢性阻塞性肺病患者相比,ACO 患者的症状负担更重、病情加重更频繁、生活质量更差、肺功能下降更快、医疗资源使用更多,但 ACO 的全球诊断标准尚无定论。ACOS 的临床定义和分类差异很大,这影响了我们对该疾病的患病率、诊断和治疗的理解。在临床实践中,大多数情况下哮喘与慢性阻塞性肺病(COPD)的诊断和鉴别相对简单;但也有一些患者同时表现出两种疾病的特征。慢性阻塞性肺疾病在全球老年人(40 岁及以上)中发病率很高,与吸烟和接触环境中的烟草烟雾或烟尘有关。慢性阻塞性肺病的典型特征是持续的气流阻塞和气道慢性炎症。哮喘也会出现气道炎症,但这两种呼吸系统疾病的炎症细胞类型却截然不同。活组织检查显示,慢性阻塞性肺病的炎症主要表现为 CD8+ T 淋巴细胞、中性粒细胞和巨噬细胞的增加,但在病情恶化时也可观察到痰中嗜酸性粒细胞的增加。相比之下,哮喘的炎症通常表现为 CD4+ T 淋巴细胞和嗜酸性粒细胞的增加。哮喘也是一种慢性阻塞性肺病,但在轻度和中度严重哮喘中,气流阻塞对吸入皮质类固醇和支气管扩张剂的治疗有反应,因此不是持续性的,而且是可逆的。ACO 患者通常具有与慢性阻塞性肺病相同的哮喘和慢性阻塞性肺病症状,包括咳嗽、咳痰、气短和喘息。然而,与仅患有哮喘或慢性阻塞性肺病的患者相比,ACO 患者的病情恶化率要高出 4 至 5 倍。此外,研究还发现,ACO 患者到急诊科就诊和入院的次数更多。 体格检查结果包括喘息和过度充气征象,与慢性阻塞性肺病的检查结果相同。然而,检查结果可能是正常的,中间会有周期性加重。需要进行更多的研究,以更好地描述患者的特征,并获得 ACOS 的标准化定义,该定义应基于最能预测个体患者治疗反应的标志物:134
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Asthma COPD Overlap Syndrome
Asthma-chronic obstructive pulmonary disease (COPD) overlap syndrome (ACOS) is a term to describe patients with both features of asthma and COPD, firstly proposed by a joint section of the Global Initiative for Asthma (GINA) and the Global Initiative for Chronic Obstructive Pulmonary Disease (GOLD) in 2014, and revised to ACO (Asthma COPD Overlap) in GINA 2017. ACO is epidemiologically considered in 2% of the general population, 29.6% of asthmatic patients and 26.5% of COPD patients. Patients with ACO have a greater burden of symptoms, frequent exacerbations, poor quality of life, a more rapid decline in lung function and greater use of healthcare resources compared to patients with asthma or COPD alone, but global diagnostic criteria for ACO are inconclusive. Clinical definitions and classifications for ACOS vary widely, which impacts our understanding of prevalence, diagnosis and treatment of the condition. The diagnosis and differentiation of asthma from chronic obstructive pulmonary disease (COPD) in clinical practice is relatively straightforward in the majority of cases; however, some patients exhibit characteristics of both diseases. Where uncertainty exists regarding the correct diagnosis of asthma, COPD or both, this may represent a phenotype known as asthma-COPD overlap syndrome (ACOS) COPD is highly prevalent in the global population of older adults (40 years of age and older) and has been associated with smoking and exposure to environmental tobacco smoke or fumes. COPD is typically characterized by persistent airflow obstruction and chronic inflammation of the airways. Airway inflammation is also seen in asthma; however, there are distinct differences in the type of inflammatory cells seen in these two respiratory diseases. Biopsies reveal that inflammation in COPD is characterized predominantly by increases in CD8+ T-lymphocytes, neutrophils, and macrophages , although increases in eosinophils have been observed in sputum at the time of exacerbation . In contrast, inflammation in asthma is commonly characterized by increases in CD4+ T-lymphocytes and eosinophils. Asthma is also a chronic obstructive lung disease, but in mild and moderately severe asthma, airflow obstruction responds to treatment with inhaled corticosteroids and bronchodilators and is therefore not persistent and is reversible.  Patients with ACO usually have the same asthma and COPD symptoms, including cough, sputum production, shortness of breath, and wheezing. However, exacerbation rates were 4 to 5 times higher in ACO patients compared with those with asthma or COPD alone. Also, it was found that patients with ACO have more emergency department visits and hospital admission.  The physical examination findings include wheezing and hyperinflation signs, the same as in chronic obstructive lung disease findings. However, findings can be normal, with periodic exacerbations in between.More research is needed to better characterize patients and to obtain a standardized definition of ACOS that is based on markers that best predict treatment response in individual patients. Bangladesh J Medicine 2024; Vol. 35, No. 2, Supplementation: 134
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