Confirmation of oxidative stress and fatty acid disturbances in two further Papillon–Lefèvre syndrome families with identification of a new mutation

Authors


  • Conflicts of interest

      Conflicts of interest
    • The authors declare that there are no conflicts of interest in this study.

    Funding sources

      Funding sources
    • No external funding, apart from the support of the authors' institution, was available for this study.

Abstract

Background

We have previously reported oxidative and fatty acids disturbances in one Papillon–Lefèvre syndrome (PLS) family. This Mendelian condition characterized by palmar plantar keratosis and severe aggressive periodontitis, is caused by mutations in the cathepsin C (CTSC) gene. In this study, we have analysed two further unrelated PLS families to confirm this association.

Methods

Mutations were identified by direct sequencing of CTSC. Biochemical analyses were performed in probands and their relatives in order to determine plasma levels of vitamin E, CoQ10, lipid hydroperoxides (HP) and fatty acid patterns.

Results

Pathogenic CTSC mutations were identified in both families including a new mutation (c504C>G). Both probands showed low levels of vitamin E and CoQ10, and high levels of lipid HP, and also very low levels of docohexaenoic acid.

Conclusions

The previously reported oxidative and fatty acids disturbances were confirmed as a feature of this condition in two further families. There are low levels of antioxidant markers and high levels of oxidative markers, in addition of low levels of some anti-inflammatory fatty acids in persons suffering PLS and some of their relatives.

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