Literature DB >> 22696581

White and grey matter abnormalities in patients with SPG11 mutations.

Marcondes C França1, Clarissa L Yasuda, Fabrício R S Pereira, Anelyssa D'Abreu, Camila M Lopes-Ramos, Madalena V Rosa, Fernando Cendes, Iscia Lopes-Cendes.   

Abstract

BACKGROUND: Mutations in SPG11 are the most frequent known cause of autosomal recessive hereditary spastic paraplegia. Corpus callosum thinning is a hallmark of the condition but little is known about damage to other structures in the CNS.
OBJECTIVE: To evaluate in vivo cerebral damage in patients with SPG11 mutations.
METHODS: 5 patients and 15 age and sex matched healthy controls underwent high resolution diffusion tensor imaging (32 directions) and a T1 volumetric (1 mm slices) acquisition protocol in a 3 T scanner (Philips Achieva). These sequences were then analysed through voxel based morphometry (VBM) and tract based spatial statistics (TBSS).
RESULTS: Mean age of the patients was 23.6±4.5 years (range 14-45) and mean duration of disease was 12 years (range 5-15). All patients presented with progressive spastic paraplegia and three were already wheelchair bound when first evaluated. Mutations found were: c.529_533delATATT, c.704_705delAT, c.733_734delAT, c.118C>T and c.7256A>G. VBM identified significant grey matter atrophy in both the thalamus and lentiform nuclei. TBSS analyses revealed reduced fractional anisotropy involving symmetrically subcortical white matter of the temporal and frontal lobes, the cingulated gyrus, cuneus, striatum, corpus callosum and brainstem.
CONCLUSIONS: Widespread white matter damage in patients with SPG11 mutations has been demonstrated. Grey matter atrophy was prominent in both the thalamus and basal ganglia but not in the cerebral cortex. These findings suggest that neuronal damage/dysfunction is more widespread than previously recognised in this condition.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22696581     DOI: 10.1136/jnnp-2011-300129

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  18 in total

Review 1.  Genotype-phenotype associations in hereditary spastic paraplegia: a systematic review and meta-analysis on 13,570 patients.

Authors:  Maryam Erfanian Omidvar; Shahram Torkamandi; Somaye Rezaei; Behnam Alipoor; Mir Davood Omrani; Hossein Darvish; Hamid Ghaedi
Journal:  J Neurol       Date:  2019-11-19       Impact factor: 4.849

2.  Brain white matter involvement in hereditary spastic paraplegias: analysis with multiple diffusion tensor indices.

Authors:  G Aghakhanyan; A Martinuzzi; F Frijia; M Vavla; H Hlavata; A Baratto; N Martino; G Paparella; D Montanaro
Journal:  AJNR Am J Neuroradiol       Date:  2014-04-30       Impact factor: 3.825

3.  Thalamic atrophy in patients with pure hereditary spastic paraplegia type 4.

Authors:  Francisco Grandas; Manuel Desco; Francisco J Navas-Sánchez; Alberto Fernández-Pena; Daniel Martín de Blas; Yasser Alemán-Gómez; Luís Marcos-Vidal; Juan A Guzmán-de-Villoria; Pilar Fernández-García; Julia Romero; Irene Catalina; Laura Lillo; José L Muñoz-Blanco; Andrés Ordoñez-Ugalde; Beatriz Quintáns; Julio Pardo; María-Jesús Sobrido; Susanna Carmona
Journal:  J Neurol       Date:  2021-01-28       Impact factor: 4.849

4.  Systematic Analysis of Brain MRI Findings in Adaptor Protein Complex 4-Associated Hereditary Spastic Paraplegia.

Authors:  Darius Ebrahimi-Fakhari; Julian E Alecu; Marvin Ziegler; Gregory Geisel; Catherine Jordan; Angelica D'Amore; Rebecca C Yeh; Shyam K Akula; Afshin Saffari; Sanjay P Prabhu; Mustafa Sahin; Edward Yang
Journal:  Neurology       Date:  2021-09-20       Impact factor: 9.910

5.  Microstructural integrity of cerebral fiber tracts in hereditary spastic paraparesis with SPG11 mutation.

Authors:  M-K Pan; S-C Huang; Y-C Lo; Chih-Chao Yang; T-W Cheng; Chi-Cheng Yang; M-S Hua; M-J Lee; W-Y I Tseng
Journal:  AJNR Am J Neuroradiol       Date:  2012-12-06       Impact factor: 3.825

6.  Tensor-based morphometry using scalar and directional information of diffusion tensor MRI data (DTBM): Application to hereditary spastic paraplegia.

Authors:  Neda Sadeghi; Filippo Arrigoni; Maria Grazia D'Angelo; Cibu Thomas; M Okan Irfanoglu; Elizabeth B Hutchinson; Amritha Nayak; Pooja Modi; Maria Teresa Bassi; Carlo Pierpaoli
Journal:  Hum Brain Mapp       Date:  2018-09-25       Impact factor: 5.038

7.  Multimodal MRI-based study in patients with SPG4 mutations.

Authors:  Thiago J R Rezende; Milena de Albuquerque; Gustavo M Lamas; Alberto R M Martinez; Brunno M Campos; Raphael F Casseb; Cynthia B Silva; Lucas M T Branco; Anelyssa D'Abreu; Iscia Lopes-Cendes; Fernando Cendes; Marcondes C França
Journal:  PLoS One       Date:  2015-02-06       Impact factor: 3.240

8.  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

9.  Clinical and genetic study of hereditary spastic paraplegia in Canada.

Authors:  Nicolas Chrestian; Nicolas Dupré; Ziv Gan-Or; Anna Szuto; Shiyi Chen; Anil Venkitachalam; Jean-Denis Brisson; Jodi Warman-Chardon; Sohnee Ahmed; Setareh Ashtiani; Heather MacDonald; Noreen Mohsin; Karim Mourabit-Amari; Pierre Provencher; Kym M Boycott; Dimitri J Stavropoulos; Patrick A Dion; Peter N Ray; Oksana Suchowersky; Guy A Rouleau; Grace Yoon
Journal:  Neurol Genet       Date:  2016-12-05

Review 10.  Cognitive dysfunction in hereditary spastic paraplegias and other motor neuron disorders.

Authors:  Ingrid Faber; Lucas Melo T Branco; Marcondes Cavalvante França Júnior
Journal:  Dement Neuropsychol       Date:  2016 Oct-Dec
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.