You are here

Article Text

Article menu

This article has a correction. Please see:

Download PDFPDF
Mutation report
New surfactant protein C gene mutations associated with diffuse lung disease
  1. L Guillot1,2,
  2. R Epaud1,2,3,
  3. G Thouvenin1,2,
  4. L Jonard4,
  5. A Mohsni4,
  6. R Couderc4,
  7. F Counil5,
  8. J de Blic6,
  9. R A Taam6,
  10. M Le Bourgeois6,
  11. P Reix7,
  12. F Flamein1,2,
  13. A Clement1,2,3,
  14. D Feldmann4
  1. 1
    INSERM UMR_S U938, Paris, France
  2. 2
    UPMC Univ Paris, France
  3. 3
    AP-HP, Hôpital Armand Trousseau, Pediatric Pulmonary Department, Paris, France
  4. 4
    AP-HP, Hôpital Armand Trousseau, Biochemistry Department, Paris, France
  5. 5
    Hôpital Arnaud de Villeneuve, Centre Hospitalier Universitaire de Montpellier, Montpellier, France
  6. 6
    Université Paris Descartes, AP-HP, Hôpital Necker Enfants Malades, Pediatric Pneumology-allergology Department, Paris, France
  7. 7
    Groupement Hospitalier Est, Pediatric Pneumology-Allergology Department, Lyon, France
  1. Dr D Feldmann, Hôpital Armand Trousseau, Laboratoire de Biochimie, 26, Avenue du Dr Arnold Netter, 75571 Paris cedex 12, France; delphine.feldmann{at}trs.aphp.fr

Abstract

Background: Mutations in the surfactant protein C gene (SFTPC) have been recently associated with the development of diffuse lung disease, particularly sporadic and familial interstitial lung disease (ILD).

Objective: We have investigated the prevalence and the spectrum of SFTPC mutations in a large cohort of infants and children with diffuse lung disease and suspected with surfactant dysfunction.

Method and results: 121 children were first screened for the common SFTPC mutation, p.Ile73Thr (I73T). Ten unrelated patients were shown to carry this mutation. The I73T mutation was inherited in six cases, and appeared de novo in four. The 111 patients without the I73T mutation were screened for the entire coding sequence of SFTPC. Of these, eight (seven unrelated) subjects were shown to carry a novel mutant allele of SFTPC. 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.

Conclusions: Our results confirm that SFTPC mutations are a frequent cause of diffuse lung disease, and that I73T is the most frequent SFTPC mutation associated with diffuse lung disease.

https://doi.org/10.1136/jmg.2009.066829

Statistics from Altmetric.com

    Request Permissions

    If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

    View Full Text

    Footnotes

    • LG and RE contributed equally to this work

    • Funding: This work was supported by the Département de la Recherche Clinique et du Développement (PHRC 2007, “Surfactant disorders associated with chronic lung disease in children”).

    • Competing interests: None declared.

    • Patient consent: Obtained.

    Linked Articles

    • Correction
      Correction
      BMJ Publishing Group Ltd
      Journal of Medical Genetics 2010; 47 485-485 Published Online First: 30 Jun 2010. doi: 10.1136/jmg.2009.066829corr1