Sjogren-Larsson syndrome brain volumetric reductions demonstrated with an automated software

Author:

Castro José Thiago de Souza de1ORCID,Saab Camilo Lotfi1ORCID,Souto Mariam Patrícia Auada2ORCID,Ortolam Juliane Giselle1ORCID,Steiner Carlos Eduardo3ORCID,Rezende Thiago Junqueira Ribeiro de4ORCID,Reis Fabiano1ORCID

Affiliation:

1. Universidade Estadual de Campinas, Faculdade de Ciências Médicas, Departamento de Anestesiologia, Oncologia e Radiologia, Campinas SP, Brazil.

2. Universidade Estadual de Campinas, Faculdade de Ciências Médicas, Departamento de Clínica Médica, Campinas SP, Brazil.

3. Universidade Estadual de Campinas, Faculdade de Ciências Médicas, Departamento de Medicina Translacional , Campinas SP, Brazil.

4. Universidade Estadual de Campinas, Faculdade de Ciências Médicas, Departamento de Neurologia, Campinas SP, Brazil.

Abstract

Abstract Background Sjogren-Larsson syndrome (SLS) is a neurocutaneous disease with an autosomal recessive inheritance, caused by mutations in the gene that encodes fatty aldehyde dehydrogenase (ALDH3A2), clinically characterized by ichthyosis, spastic diplegia, and cognitive impairment. Brain imaging plays an essential role in the diagnosis, demonstrating a nonspecific leukoencephalopathy. Data regarding brain atrophy and grey matter involvement is scarce and discordant. Objective We performed a volumetric analysis of the brain of two siblings with SLS with the aim of detecting deep grey matter nuclei, cerebellar grey matter, and brainstem volume reduction in these patients. Methods Volume data obtained from the brain magnetic resonance imaging (MRI) of the two patients using an automated segmentation software (Freesurfer) was compared with the volumes of a healthy control group. Results Statistically significant volume reduction was found in the cerebellum cortex, the brainstem, the thalamus, and the pallidum nuclei. Conclusion Volume reduction in grey matter leads to the hypothesis that SLS is not a pure leukoencephalopathy. Grey matter structures affected in the present study suggest a dysfunction more prominent in the thalamic motor pathways.

Publisher

Georg Thieme Verlag KG

Subject

Neurology,Neurology (clinical)

Reference30 articles.

1. Sjögren-Larsson syndrome in Brazil is caused by a common c.1108-1G–>C splice-site mutation in the ALDH3A2 gene;M P Auada;Br J Dermatol,2006

2. Sjogren-Larsson Syndrome: Mechanisms and Management;P S Bindu;Appl Clin Genet,2020

3. MR of the brain in Sjögren-Larsson syndrome;F Van Mieghem;AJNR Am J Neuroradiol,1997

4. MR imaging and proton MR spectroscopic studies in Sjögren-Larsson syndrome: characterization of the leukoencephalopathy;M A Willemsen;AJNR Am J Neuroradiol,2004

5. Cortical surface-based analysis. I. Segmentation and surface reconstruction;A M Dale;Neuroimage,1999

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