Literature DB >> 25611737

Hereditary Spastic Paraplegia: Beyond Clinical Phenotypes toward a Unified Pattern of Central Nervous System Damage.

Federica Agosta1, Marina Scarlato1, Edoardo G Spinelli1, Elisa Canu1, Sara Benedetti1, Maria Teresa Bassi1, Carlo Casali1, Maria Sessa1, Massimiliano Copetti1, Elisabetta Pagani1, Giancarlo Comi1, Maurizio Ferrari1, Andrea Falini1, Massimo Filippi1.   

Abstract

PURPOSE: To investigate whether specific patterns of brain gray matter (GM) regional volumes and white matter (WM) microstructural abnormalities and spinal cord atrophy occur in patients with pure and complicated hereditary spastic paraplegias (HSPs). Relationships between clinical and cognitive features of patients with HSP who had brain and cervical cord damage were also investigated.
MATERIALS AND METHODS: This study was approved by the local ethical committees on human studies, and written informed consent from all subjects was obtained prior to enrollment. Forty-four patients with HSP (20 genetically defined cases and 24 without genetic diagnosis) and 19 healthy control subjects underwent clinical, neuropsychological, and advanced magnetic resonance (MR) imaging evaluations. Patterns of GM atrophy and WM microstructural damage obtained by using structural and diffusion-tensor MR imaging were compared between groups. Cervical cord atrophy was also assessed by using an active surface method. Correlations between clinical, cognitive, and diffusion-tensor MR imaging measures were evaluated.
RESULTS: Clinical data showed that spastic paraplegia is accompanied by a number of other features, including sensory disturbances, and verbal and spatial memory deficits, not only in complicated HSP but also in pure HSP. MR imaging demonstrated a similar involvement of motor, association, and cerebellar WM pathways (P < .05, family-wise error corrected for multiple comparisons) and cervical cord (P < .001) in patients with HSP relative to healthy control subjects, regardless of their clinical picture. The severity of WM damage correlated with the degree of spasticity (P < .05, family-wise error corrected) and cognitive impairment (r values, -0.39 to 0.51; P values, .001-.05) in both pure and complicated HSP.
CONCLUSION: The detection of a distributed pattern of central nervous system damage in patients with pure and complicated HSP suggests that the "primary" corticospinal tract involvement known to occur in these patients may be associated with a neurodegenerative process, which spreads out to extramotor regions, likely via anatomic connections. This observation is in line with emerging pieces of evidence that, independent of the clinical phenotype, there is a common neurodegenerative cascade shared by different neurologic disorders.

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Year:  2015        PMID: 25611737     DOI: 10.1148/radiol.14141715

Source DB:  PubMed          Journal:  Radiology        ISSN: 0033-8419            Impact factor:   11.105


  13 in total

1.  Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21.

Authors:  Marina Scarlato; Andrea Citterio; Alessandra Barbieri; Claudia Godi; Elena Panzeri; Maria Teresa Bassi
Journal:  J Neurol       Date:  2017-07-27       Impact factor: 4.849

2.  White Matter Alterations in Spastic Paraplegia Type 5: A Multiparametric Structural MRI Study and Correlations with Biochemical Measurements.

Authors:  Y Liu; Z Ye; J Hu; Z Xiao; F Zhang; X Yang; W Chen; Y Fu; D Cao
Journal:  AJNR Am J Neuroradiol       Date:  2021-11-18       Impact factor: 3.825

3.  Iron-sensitive MR imaging of the primary motor cortex to differentiate hereditary spastic paraplegia from other motor neuron diseases.

Authors:  Mirco Cosottini; Graziella Donatelli; Ivana Ricca; Francesca Bianchi; Daniela Frosini; Vincenzo Montano; Gianmichele Migaleddu; Eleonora Del Prete; Alessandra Tessa; Paolo Cecchi; Claudio D'Amelio; Gabriele Siciliano; Michelangelo Mancuso; Filippo Maria Santorelli
Journal:  Eur Radiol       Date:  2022-05-20       Impact factor: 7.034

Review 4.  Patient-Derived Stem Cell Models in SPAST HSP: Disease Modelling and Drug Discovery.

Authors:  Gautam Wali; Carolyn M Sue; Alan Mackay-Sim
Journal:  Brain Sci       Date:  2018-07-31

Review 5.  Neuroimaging in Hereditary Spastic Paraplegias: Current Use and Future Perspectives.

Authors:  Felipe Franco da Graça; Thiago Junqueira Ribeiro de Rezende; Luiz Felipe Rocha Vasconcellos; José Luiz Pedroso; Orlando Graziani P Barsottini; Marcondes C França
Journal:  Front Neurol       Date:  2019-01-16       Impact factor: 4.003

6.  Mutations in the SPAST gene causing hereditary spastic paraplegia are related to global topological alterations in brain functional networks.

Authors:  Rosaria Rucco; Marianna Liparoti; Francesca Jacini; Fabio Baselice; Antonella Antenora; Giuseppe De Michele; Chiara Criscuolo; Antonio Vettoliere; Laura Mandolesi; Giuseppe Sorrentino; Pierpaolo Sorrentino
Journal:  Neurol Sci       Date:  2019-02-08       Impact factor: 3.307

7.  Hereditary spastic paraplegia: An "ears of the lynx" magnetic resonance imaging sign in a patient with recessive genetic type 11.

Authors:  Emiliano Ruiz Romagnoli; Manuel Perez Akly; Luis A Miquelini; Jorge A Funes; Cristina H Besada
Journal:  Neuroradiol J       Date:  2020-09-04

8.  Spinal Cord Gray and White Matter Damage in Different Hereditary Spastic Paraplegia Subtypes.

Authors:  K R Servelhere; R F Casseb; F D de Lima; T J R Rezende; L P Ramalho; M C França
Journal:  AJNR Am J Neuroradiol       Date:  2021-01-21       Impact factor: 3.825

9.  Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study.

Authors:  Andrea Martinuzzi; Domenico Montanaro; Marinela Vavla; Gabriella Paparella; Paolo Bonanni; Olimpia Musumeci; Erika Brighina; Hana Hlavata; Giuseppe Rossi; Gayane Aghakhanyan; Nicola Martino; Alessandra Baratto; Maria Grazia D'Angelo; Francesca Peruch; Marianna Fantin; Alessia Arnoldi; Andrea Citterio; Chiara Vantaggiato; Vincenzo Rizzo; Antonio Toscano; Nereo Bresolin; Maria Teresa Bassi
Journal:  PLoS One       Date:  2016-04-14       Impact factor: 3.240

10.  Mechanism of impaired microtubule-dependent peroxisome trafficking and oxidative stress in SPAST-mutated cells from patients with Hereditary Spastic Paraplegia.

Authors:  Gautam Wali; Ratneswary Sutharsan; Yongjun Fan; Romal Stewart; Johana Tello Velasquez; Carolyn M Sue; Denis I Crane; Alan Mackay-Sim
Journal:  Sci Rep       Date:  2016-05-27       Impact factor: 4.379

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