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Multi-organ investigation in 16 CADASIL families from central Italy sharing the same R1006C mutation.

Authors :
Ragno M
Pianese L
Cacchiò G
Manca A
Scarcella M
Silvestri S
Di Marzio F
Caiazzo AR
Silvaggio F
Tasca G
Mirabella M
Trojano L
Source :
Neuroscience letters [Neurosci Lett] 2012 Jan 06; Vol. 506 (1), pp. 116-20. Date of Electronic Publication: 2011 Nov 02.
Publication Year :
2012

Abstract

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) may involve many target organs with relevant variability among affected individuals. We performed a multi-organ assessment tapping nervous system, skeletal muscle and cardiovascular system in thirty-nine individuals belonging to 16 families from Central Italy sharing the same R1006C CADASIL mutation. Stroke prevalence was larger in female patients (66.7%) than in males (23.8%); high levels of CKemia were quite frequent (21.6%) and were related to a myopathy without mitochondrial alterations; several individuals had atrial septal aneurysm (10.3%). No specific relationships between common cardiovascular risk factors and clinical manifestations were found. The present systematic study thus identified several gender-related, myopathic and cardiovascular peculiarities of R1006C mutation. This kind of comprehensive approach is necessary to define clinical course, prognosis and treatment options for a multi-organ disease such as CADASIL.<br /> (Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1872-7972
Volume :
506
Issue :
1
Database :
MEDLINE
Journal :
Neuroscience letters
Publication Type :
Academic Journal
Accession number :
22079340
Full Text :
https://doi.org/10.1016/j.neulet.2011.10.062