Literature DB >> 35593959

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

Mirco Cosottini1, Graziella Donatelli2,3, Ivana Ricca4, Francesca Bianchi5, Daniela Frosini6, Vincenzo Montano5, Gianmichele Migaleddu7, Eleonora Del Prete5, Alessandra Tessa4, Paolo Cecchi7,8, Claudio D'Amelio1, Gabriele Siciliano5, Michelangelo Mancuso5, Filippo Maria Santorelli4.   

Abstract

OBJECTIVES: Hereditary spastic paraplegia (HSP) is a group of genetic neurodegenerative diseases characterised by upper motor neuron (UMN) impairment of the lower limbs. The differential diagnosis with primary lateral sclerosis (PLS) and amyotrophic lateral sclerosis (ALS) can be challenging. As microglial iron accumulation was reported in the primary motor cortex (PMC) of ALS cases, here we assessed the radiological appearance of the PMC in a cohort of HSP patients using iron-sensitive MR imaging and compared the PMC findings among HSP, PLS, and ALS patients.
METHODS: We included 3-T MRI scans of 23 HSP patients, 7 PLS patients with lower limb onset, 8 ALS patients with lower limb and prevalent UMN onset (UMN-ALS), and 84 ALS patients with any other clinical picture. The PMC was visually rated on 3D T2*-weighted images as having normal signal intensity, mild hypointensity, or marked hypointensity, and differences in the frequency distribution of signal intensity among the diseases were investigated.
RESULTS: The marked hypointensity in the PMC was visible in 3/22 HSP patients (14%), 7/7 PLS patients (100%), 6/8 UMN-ALS patients (75%), and 35/84 ALS patients (42%). The frequency distribution of normal signal intensity, mild hypointensity, and marked hypointensity in HSP patients was different than that in PLS, UMN-ALS, and ALS patients (p < 0.01 in all cases).
CONCLUSIONS: Iron-sensitive imaging of the PMC could provide useful information in the diagnostic work - up of adult patients with a lower limb onset UMN syndrome, as the cortical hypointensity often seen in PLS and ALS cases is apparently rare in HSP patients. KEY POINTS: • The T2* signal intensity of the primary motor cortex was investigated in patients with HSP, PLS with lower limb onset, and ALS with lower limb and prevalent UMN onset (UMN-ALS) using a clinical 3-T MRI sequence. • Most HSP patients had normal signal intensity in the primary motor cortex (86%); on the contrary, all the PLS and the majority of UMN-ALS patients (75%) had marked cortical hypointensity. • The T2*-weighted imaging of the primary motor cortex could provide useful information in the differential diagnosis of sporadic adult-onset UMN syndromes.
© 2022. The Author(s), under exclusive licence to European Society of Radiology.

Entities:  

Keywords:  Amyotrophic lateral sclerosis; Hereditary spastic paraplegia; Magnetic resonance imaging; Primary lateral sclerosis; Primary motor cortex

Year:  2022        PMID: 35593959     DOI: 10.1007/s00330-022-08865-6

Source DB:  PubMed          Journal:  Eur Radiol        ISSN: 0938-7994            Impact factor:   7.034


  58 in total

Review 1.  The neuropathology of hereditary spastic paraparesis.

Authors:  R P Bruyn
Journal:  Clin Neurol Neurosurg       Date:  1992       Impact factor: 1.876

2.  Hereditary (familial) spastic paraplegia; further clinical and pathologic observations.

Authors:  G A SCHWARZ; C N LIU
Journal:  AMA Arch Neurol Psychiatry       Date:  1956-02

Review 3.  Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms.

Authors:  Sara Salinas; Christos Proukakis; Andrew Crosby; Thomas T Warner
Journal:  Lancet Neurol       Date:  2008-12       Impact factor: 44.182

Review 4.  Hereditary Spastic Paraplegia: Clinical and Genetic Hallmarks.

Authors:  Paulo Victor Sgobbi de Souza; Wladimir Bocca Vieira de Rezende Pinto; Gabriel Novaes de Rezende Batistella; Thiago Bortholin; Acary Souza Bulle Oliveira
Journal:  Cerebellum       Date:  2017-04       Impact factor: 3.847

5.  Strümpell's familial spastic paraplegia: genetics and neuropathology.

Authors:  W M Behan; M Maia
Journal:  J Neurol Neurosurg Psychiatry       Date:  1974-01       Impact factor: 10.154

Review 6.  Hereditary spastic paraplegia.

Authors:  Sireesha Murala; Elanagan Nagarajan; Pradeep C Bollu
Journal:  Neurol Sci       Date:  2021-01-13       Impact factor: 3.307

7.  Autosomal recessive spastic paraplegia with hypoplastic corpus callosum, multisystem degeneration and ubiquitinated eosinophilic granules.

Authors:  K Wakabayashi; H Kobayashi; S Kawasaki; H Kondo; H Takahashi
Journal:  Acta Neuropathol       Date:  2001-01       Impact factor: 17.088

Review 8.  Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches.

Authors:  Samuel Shribman; Evan Reid; Andrew H Crosby; Henry Houlden; Thomas T Warner
Journal:  Lancet Neurol       Date:  2019-07-31       Impact factor: 44.182

Review 9.  Challenges and Controversies in the Genetic Diagnosis of Hereditary Spastic Paraplegia.

Authors:  Lydia Saputra; Kishore Raj Kumar
Journal:  Curr Neurol Neurosci Rep       Date:  2021-02-28       Impact factor: 5.081

10.  The extent of axonal loss in the long tracts in hereditary spastic paraplegia.

Authors:  G C Deluca; G C Ebers; M M Esiri
Journal:  Neuropathol Appl Neurobiol       Date:  2004-12       Impact factor: 8.090

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