P63 Assessment Of Regional Variability In Matrix Metalloproteinase Concentrations By Ct Informed Bronchoalveolar Lavage In Patients With Copd

Abstract

Background Matrix metalloproteinases (MMPs) are a family of proteolytic enzymes involved in the normal physiological turnover of the pulmonary extracellular matrix. They have been implicated in animal models of emphysema. However, there have been conflicting results in human studies, largely due to the anatomical regional variability and heterogeneity of COPD not being taken into account. This study aims to understand the role of MMPs in COPD by using CT analysis to guide regional bronchoalveolar lavage (BAL) and employing multiplex profiling of this fluid. Methods Twelve mild-to-moderate COPD patients (FEV1/FVC ratio 50%) underwent high resolution spiral chest CT. This was reported by a thoracic radiologist and lobes with most and least evidence of disease (emphysema or bronchial wall thickening) were identified. During bronchoscopy 100 ml of saline was instilled into each of these lobes and the BAL was collected. This fluid was filtered and then concentrated 2-fold by lyophilisation. MMP-1, -2, -3, -7, -8 and -9 were measured using a multiplex ELISA. Sample protein concentration was determined using a Bradford assay. MMP concentration was corrected for BAL protein concentration. Results MMPs and protein were successfully detected in BAL. Median values for MMP-1, -2, -3, -7, -8 and -9 were all increased in the diseased lobe compared to the relatively preserved lobe. This was significant for MMP-2 and -3 and trended towards significance for MMP-1 and -7 (Table 1). Conclusion These results suggest that certain MMPs are present in greater quantities in areas of the lungs most affected by COPD, adding to the evidence that they may be involved in the pathogenesis of the disease. This study also demonstrates the regional anatomical variability of COPD in respect to imaging abnormalities and the underlying disease processes. Regional sampling needs to be considered in future studies to enable full understanding of the heterogeneous pathological mechanisms involved in COPD.