Natural disease history and characterisation of SUMF1 molecular defects in ten unrelated patients with multiple sulfatase deficiency

Frédérique Sabourdy (1, 2) , Lionel Mourey (3) , Emmanuelle Le Trionnaire (1) , Nathalie Bednarek (4) , Catherine Caillaud (5) , Yves Chaix (6) , Marie-Ange Delrue (7) , Anne Dusser (8) , Roseline Froissart (9) , Roselyne Garnotel , Nathalie Guffon , André Megarbane (10) , Hélène Ogier de Baulny (11) , Jean-Michel Pédespan (12) , Samia Pichard (11) , Vassili Valayannopoulos (5) , Alain Verloes (11) , Thierry Levade (2)

1 Institut Fédératif de Biologie (IFB)
2 CRCT - Centre de Recherches en Cancérologie de Toulouse
3 IPBS - Institut de pharmacologie et de biologie structurale
4 Hôpital universitaire Robert Debré [Reims]
5 Hôpital Necker - Enfants Malades [AP-HP]
6 ICHN - Imagerie cérébrale et handicaps neurologiques
7 U1211 INSERM/MRGM - Laboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux)
8 Hôpital Bicêtre [AP-HP, Le Kremlin-Bicêtre]
9 HCL - Hospices Civils de Lyon
10 USJ - Université Saint-Joseph de Beyrouth
11 Hôpital Robert Debré
12 Université de Bordeaux Ségalen [Bordeaux 2]

Background: Multiple sulfatase deficiency is a rare inherited metabolic disorder caused by mutations in the SUMF1 gene. The disease remains poorly known, often leading to a late diagnosis. This study aimed to provide improved knowledge of the disease, through complete clinical, biochemical, and molecular descriptions of a cohort of unrelated patients. The main objective was to identify prognostic markers, both phenotypic and genotypic, to accelerate the diagnosis and improve patient care. Methods: The phenotypes of ten unrelated patients were fully documented at the clinical and biochemical levels. The long-term follow-up of each patient allowed correlations of the phenotypes to the disease outcomes. Each patient’s molecular defects were also identified. Site-directed mutagenesis was used to individually express the mutants and assess their stability. Characterisation of the protein mutants was completed by in silico analyses based on sequence comparisons and structural models. Results: The most severe cases were characterised by the presence of non-neurological symptoms as well as the occurrence of psychomotor regression before 2 years of age. Nine novel SUMF1 mutations were identified. Clinically severe forms were often associated with SUMF1 mutations that strongly affected the protein stability and/or catalytic function as predicted from in silico and western blot analyses. Conclusions: This detailed clinical description and follow-up of a cohort of patients, together with the molecular characterisation of their underlying defects, contribute to improved knowledge of multiple sulfatase deficiency. Predictors of a bad prognosis were the presence of several non-neurological symptoms and the onset of psychomotor regression before 2 years of age. No strict correlation existed between in vitro residual sulfatase activity and disease severity. Genotype–phenotype correlations related to previously reported mutants were strengthened. These and previous observations allow not only improved prediction of the disease outcome but also provision of appropriate care for patients, in the expectation of specific treatment developmen

Domaines: Génomique, Transcriptomique et Protéomique [q-bio.GN]; Médecine humaine et pathologie

Frédérique Sabourdy, Lionel Mourey, Emmanuelle Le Trionnaire, Nathalie Bednarek, Catherine Caillaud, et al.. Natural disease history and characterisation of SUMF1 molecular defects in ten unrelated patients with multiple sulfatase deficiency. Orphanet Journal of Rare Diseases, 2015, 10, pp.31. ⟨10.1186/s13023-015-0244-7⟩. ⟨hal-03002953⟩