Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations
Article first published online: 31 JAN 2011
© 2011 John Wiley & Sons A/S
Volume 81, Issue 2, pages 150–157, February 2012
How to Cite
Arnoldi, A., Crimella, C., Tenderini, E., Martinuzzi, A., D'Angelo, M., Musumeci, O., Toscano, A., Scarlato, M., Fantin, M., Bresolin, N. and Bassi, M. (2012), Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations. Clinical Genetics, 81: 150–157. doi: 10.1111/j.1399-0004.2011.01624.x
- Issue published online: 12 JAN 2012
- Article first published online: 31 JAN 2011
- Accepted manuscript online: 10 JAN 2011 06:51AM EST
- Received 24 September 2010, revised and accepted for publication 22 December 2010
- cholesterol metabolism;
- complex HSP phenotype;
Arnoldi A, Crimella C, Tenderini E, Martinuzzi A, D’Angelo MG, Musumeci O, Toscano A, Scarlato M, Fantin M, Bresolin N, Bassi MT. Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations.
Spastic paraplegia type 5 (SPG5) is caused by mutations in CYP7B1, a gene encoding the cytochrome P-450 oxysterol 7-α-hydroxylase, CYP7B1, an enzyme implicated in the cholesterol metabolism. Mutations in CYP7B1 were found in both pure and complicated forms of the disease with a mutation frequency of 7.7% in pure recessive cases. The mutation frequency in complex forms, approximately 6.6%, is more controversial and needs to be refined. We studied in more detail the SPG5-related spectrum of complex phenotypes by screening CYPB1 for mutations in a large cohort of 105 Italian hereditary spastic paraplegias (HSPs) index patients including 50 patients with a complicated HSP (cHSP) phenotype overlapping the SPG11- and the SPG15-related forms except for the lack of thin corpus callosum and 55 pure patients. Five CYP7B1 mutations, three of which are novel, were identified in four patients, two with a complex form of the disease and two with a pure phenotype. The CYP7B1 mutation frequencies obtained in both complicated and pure familial cases are comparable to the known ones. These results obtained extend the range of SPG5-related phenotypes and reveal variability in clinical presentation, disease course and functional profile in the SPG5-related patients while providing with some clues for molecular diagnosis in cHSP.