4.6 Article

Aetiology of bronchiectasis in Guangzhou, southern China

期刊

RESPIROLOGY
卷 20, 期 5, 页码 739-748

出版社

WILEY
DOI: 10.1111/resp.12528

关键词

aetiology; bronchiectasis; clinical characteristic; diagnostic test; idiopathic

资金

  1. Changjiang Scholars and Innovative Research Team in University [ITR0961]
  2. National Key Technology R&D Program of the 12th National Five-year Development Plan [2012BAI05B01]
  3. National Key Scientific & Technology Support Program: Collaborative Innovation of Clinical Research for Chronic Obstructive Pulmonary Disease and Lung Cancer [2013BAI09B09]
  4. National Natural Science Foundation [81400010]
  5. Scientific Research Projects for Medical Doctors and Researchers from Overseas, Guangzhou Medical University [2014C21]

向作者/读者索取更多资源

Background and objectiveAetiologies of bronchiectasis in mainland China and their comparisons with those in western countries are unknown. We aimed to investigate bronchiectasis aetiologies in Guangzhou, southern China, and to determine ethnic or geographic differences with reports from western countries. MethodsConsecutive patients with steady-state bronchiectasis were randomly recruited. Past history was meticulously extracted. Patients underwent physical examination, saccharine test, humoral immunity assays, gastroesophageal reflux scoring and sputum culture. Fiberoptic bronchoscopy, total immunoglobin E (IgE) and Aspergillus fumigatus-specific IgE measurement, 24-h gastroesophageal pH monitoring and miscellaneous screening tests were performed, if indicated. This entailed comparisons on aetiologies with literature reports. ResultsWe enrolled 148 patients (44.613.8 years, 92 females), most of whom had mild to moderate bronchiectasis. Idiopathic (46.0%), post-infectious (27.0%) and immunodeficiency (8.8%) were the most common aetiologies. Miscellaneous aetiologies consisted of asthma (5.4%), gastroesophageal reflux (4.1%), aspergillosis (2.7%), congenital lung malformation (2.0%), Kartagener syndrome (1.4%), rheumatoid arthritis (1.4%), chronic obstructive pulmonary disease (0.7%), Young's syndrome (0.7%), yellow nail's syndrome (0.7%), eosinophilic bronchiolitis (0.7%) and foreign bodies (0.7%). No notable differences in clinical characteristics between idiopathic and known aetiologies were found. Ethnic or geographic variations of aetiologies were overall unremarkable. ConclusionsIdiopathic, post-infectious and immunodeficiency constitute major bronchiectasis aetiologies in Guangzhou. Clinical characteristics of patients between known aetiologies and idiopathic bronchiectasis were similar. Ethnicity and geography only account for limited differences in aetiologic spectra. These findings will offer rationales for early diagnosis and management of bronchiectasis in future studies and clinical practice in China. This is the first report on bronchiectasis aetiologies in mainland China. Idiopathic, post-infectious and immunodeficiency were the most common aetiologies. No significant differences were found in ethnicity or geography. Our findings will shed light on early diagnosis and management of bronchiectasis in future studies and clinical practice in China.

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