Infections, autoimmunity and immunodeficiencies are the leading etiologies of non-cystic fibrosis bronchiectasis in adults from the southwest of Colombia.

Andrés F Zea-Vera, Carlos Andrés Rodríguez, Sebastián Giraldo, Mario Alejandro Chacón, Luis Fernando Guerrero, Ricardo Mosquera, Raúl Andrés Vallejo, Fabio Samir Vargas, María Andrea García, María A Rengifo, Anilza Bonelo, Maximiliano Parra
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Abstract

Introduction: Non-cystic fibrosis bronchiectasis is a complex medical condition with multiple etiologies, characterized by chronic productive cough and radiologic evidence of airway lumen dilation and wall thickening. Associated exacerbations and declining lung function contribute to increasing disability and mortality. There are no data about the prevalence of non-cystic fibrosis bronchiectasis etiologies in the Colombian population.

Objective: To investigate non-cystic fibrosis bronchiectasis etiology and clinical characteristics in adults evaluated in the southwest of Colombia.

Materials and methods: We conducted a cross-sectional, non-interventional study. Subjects diagnosed with non-cystic fibrosis bronchiectasis were referred to by their healthcare providers and then enrolled between October 2018 and April 2021. Medical records and radiological studies were evaluated. Participants underwent laboratory tests, including complete blood count, serum immunoglobulin levels, and, in some cases, additional tests.

Results: We included 161 subjects. The average age was 50 years old, and 59% were females. Bronchiectasis etiology was identified in 84.6% of the cases. Postinfectious (34.6%) and immune disorders (25.3%), represented by autoimmunity (13.6%) and immunodeficiency (11.7%), were the leading causes. Gender differences were noted in autoimmune (females: 18.8% versus males: 6.1%, p = 0.021) and immunodeficiency-related bronchiectasis (males: 21.2% versus females 5.2%, p = 0.002). Immunodeficiencies-associated bronchiectases were more frequent in subjects under 50 years of age, while chronic obstructive pulmonary disease-associated bronchiectases were common in subjects over 50 years of age.

Discussion: The etiologies of non-cystic fibrosis bronchiectasis in Colombia are diverse, exhibiting notable differences from other global regions. Serum immunoglobulin levels and clinical immunologist consultation should be prioritized in diagnosing patients with unclear bronchiectasis etiology, particularly those with recurrent sinopulmonary infections.

感染、自身免疫和免疫缺陷是哥伦比亚西南部成人非囊性纤维化支气管扩张的主要病因。
简介:非囊性纤维化支气管扩张症是一种复杂的医学病症,有多种病因,以慢性多产性咳嗽和气道管腔扩张和管壁增厚的影像学证据为特征。相关的恶化和肺功能下降导致残疾和死亡率增加。没有关于哥伦比亚人群中非囊性纤维化支气管扩张病因患病率的数据。目的:探讨哥伦比亚西南部成人非囊性纤维化支气管扩张的病因和临床特点。材料和方法:我们进行了一项横断面、非介入性研究。诊断为非囊性纤维化支气管扩张的受试者由其医疗保健提供者推荐,然后在2018年10月至2021年4月期间入组。对医疗记录和放射学研究进行了评估。参与者进行了实验室检查,包括全血细胞计数、血清免疫球蛋白水平,在某些情况下还进行了额外的检查。结果:我们纳入了161名受试者。平均年龄为50岁,59%为女性。支气管扩张的病因占84.6%。感染后(34.6%)和以自身免疫(13.6%)和免疫缺陷(11.7%)为代表的免疫紊乱(25.3%)是主要原因。自身免疫(女性:18.8%,男性:6.1%,p = 0.021)和免疫缺陷相关的支气管扩张(男性:21.2%,女性:5.2%,p = 0.002)存在性别差异。免疫缺陷相关的支气管扩张在50岁以下的受试者中更为常见,而慢性阻塞性肺疾病相关的支气管扩张在50岁以上的受试者中更为常见。讨论:哥伦比亚非囊性纤维化支气管扩张的病因多样,与全球其他地区有显著差异。血清免疫球蛋白水平和临床免疫学咨询在诊断病因不明的患者时应优先考虑,特别是那些复发性肺感染的患者。
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