Airway wall thickening and emphysema show independent familial aggregation in chronic obstructive pulmonary disease.

RATIONALE: It is unclear whether airway wall thickening and emphysema make independent contributions to airflow limitation in chronic obstructive pulmonary disease (COPD) and whether these phenotypes cluster within families. OBJECTIVE: To determine whether airway wall thickening and emphysema: (i) make independent contributions to the severity of COPD and (ii) show independent aggregation in families of individuals with COPD. METHODS: Index cases with COPD and their smoking siblings underwent spirometry and were offered high resolution computed tomography (HRCT) scans of the thorax to assess the severity of airway wall thickening and emphysema. RESULTS: 3096 individuals were recruited to the study of whom 1159 (519 probands and 640 siblings) had technically adequate HRCT scans without significant non-COPD-related thoracic disease. Airway wall thickness correlated with pack-years smoked (p</=0.001) and symptoms of chronic bronchitis (p<0.001). FEV1 (expressed as % predicted) was independently associated with airway wall thickness at a lumen perimeter of 10mm (p=0.0001) and 20 mm (p=0.0013) and emphysema at -950 HU (p<0.0001). There was independent familial aggregation of both the emphysema (adjusted OR 2.1, C.I. 1.1 to 4.0, p</=0.02) and airway disease phenotypes (p<0.0001) of COPD. CONCLUSIONS: Airway wall thickening and emphysema make independent contributions to airflow obstruction in COPD. These phenotypes show independent aggregation within families of individuals with COPD suggesting that different genetic factors influence these disease processes.