Literature DB >> 29249364

Resting state fMRI studies in SPG4-linked hereditary spastic paraplegia.

Xinxin Liao1, Mufang Huang1, Wu Xing2, Xinwei Wu1, Weihua Liao2, Xiaoyi Wang2, Beisha Tang3, Lu Shen4.   

Abstract

OBJECTIVE: The study aimed to investigate the functional alterations of spontaneous brain activity in patients with spastic paraplegia type 4 (SPG4), and the relationship with the severity of spasticity.
METHODS: Twelve patients with SPG4 and ten healthy controls underwent resting-state functional magnetic resonance imaging (rs-fMRI). Amplitude of low-frequency fluctuation (ALFF) and regional homogeneity (ReHo) were used to characterize regional neural function, and functional connectivity (FC) was used to evaluate the functional integration of the brain network.
RESULTS: Compared to healthy controls, patients with SPG4 exhibited significantly decreased ReHo values in the medial superior frontal gyrus. ALFF values were lower in left insula and higher in right precentral and superior frontal gyrus of the patient group. Increased ALFF values in the right precentral gyrus negatively correlated with Spastic Paraplegia Rating Scale (SPRS) scores in the patients. The connectivity study showed that the SPG4 patients had one increased FC between the left middle frontal gyrus to the left middle orbitofrontal gyrus, and pairs of decreased FC.
CONCLUSIONS: Our findings confirm that the baseline regional neural activity and interregional connectivity are altered in many brain regions in patients with SPG4, and certain changes are correlated with disease severity, providing potential diagnostic markers for SPG4.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  ALFF; ReHo; Resting-state; Spastic paraplegia type 4 (SPG4); fMRI

Mesh:

Year:  2017        PMID: 29249364     DOI: 10.1016/j.jns.2017.10.048

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  4 in total

1.  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

Review 2.  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

3.  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

4.  Cortical Damage Associated With Cognitive and Motor Impairment in Hereditary Spastic Paraplegia: Evidence of a Novel SPAST Mutation.

Authors:  Jian-Zhong Lin; Hong-Hua Zheng; Qi-Lin Ma; Chen Wang; Li-Ping Fan; Han-Ming Wu; Dan-Ni Wang; Jia-Xing Zhang; Yi-Hong Zhan
Journal:  Front Neurol       Date:  2020-05-27       Impact factor: 4.003

  4 in total

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