New surfactant protein C gene mutations associated with diffuse lung disease

Loïc Guillot (1) , Ralph Epaud (2) , Guillaume Thouvenin (1) , Laurence Jonard (2) , Amira Mohsni (2) , Remy Couderc (2) , François Counil (3) , Jacques de Blic (4) , Rola Abou Taam (4) , Muriel Le Bourgeois (4) , Philippe Reix (5) , Florence Flamein (1) , Annick Clément (2) , Delphine Feldmann (2)

1 UMRS893 - Centre de Recherche Saint-Antoine
2 CHU Trousseau [APHP]
3 Hôpital Arnaud de Villeneuve [CHRU Montpellier]
4 Service de Pneumologie Allergologie [CHU Necker]
5 Service de Pédiatrie, Pneumologie, Allergologie et Mucoviscidose

Mutations in the surfactant protein C gene () have been recently associated with the development of diffuse lung disease, particularly sporadic and familial interstitial lung disease (ILD). We have investigated the prevalence and the spectrum of mutations in a large cohort of infants and children with diffuse lung disease and suspected with surfactant dysfunction. One hundred twenty-one children were first screened for the common mutation, p.Ile73Thr (I73T). Ten unrelated patients were shown to carry this mutation. The I73T mutation was inherited in 6 cases, and appeared in 4. The 111 patients without the I73T mutation were screened for the entire coding sequence of . Of these, eight (seven unrelated) subjects were shown to carry a novel mutant allele of . All these seven new mutations are located in the BRICHOS domain except the p.Val39Ala (V39A) mutation, which is in the surfactant protein C (SP-C) mature peptide. Our results confirm that mutations are a frequent cause of diffuse lung disease, and that I73T is the most frequent mutation associated with diffuse lung disease.

Mots clés: Molecular genetics; Diffuse parenchymal lung disease

Loïc Guillot, Ralph Epaud, Guillaume Thouvenin, Laurence Jonard, Amira Mohsni, et al.. New surfactant protein C gene mutations associated with diffuse lung disease. Journal of Medical Genetics, 2009, 46 (7), pp.490. ⟨10.1136/jmg.2009.066829⟩. ⟨hal-00552694⟩