Increased mucins pinned to worsening cystic fibrosis symptoms

Tuesday, June 3, 2014 - 06:00 in Health & Medicine

The first quantitative evidence that mucins – the protein framework of mucus – are significantly increased in cystic fibrosis patients, and play a major role in failing lung function, has been presented by researchers. The research shows that a three-fold increase of mucins dramatically increases the water-draining power of the mucus layer. This hinders mucus clearance in the CF lung, resulting in infection, inflammation, and ultimately lung failure.

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