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Diminished white matter integrity in patients with systemic lupus erythematosus

PURPOSE: Systemic lupus erythematosus (SLE) is an autoimmune connective tissue disease that can affect the central nervous system. Neuropsychiatric symptoms are found in 25–70% of patients. Using diffusion tensor imaging (DTI) various studies have reported changes in white matter integrity in SLE pa...

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Autores principales: Schmidt-Wilcke, Tobias, Cagnoli, Patricia, Wang, Page, Schultz, Thomas, Lotz, Anne, Mccune, William J., Sundgren, Pia C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141982/
https://www.ncbi.nlm.nih.gov/pubmed/25161895
http://dx.doi.org/10.1016/j.nicl.2014.07.001
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author Schmidt-Wilcke, Tobias
Cagnoli, Patricia
Wang, Page
Schultz, Thomas
Lotz, Anne
Mccune, William J.
Sundgren, Pia C.
author_facet Schmidt-Wilcke, Tobias
Cagnoli, Patricia
Wang, Page
Schultz, Thomas
Lotz, Anne
Mccune, William J.
Sundgren, Pia C.
author_sort Schmidt-Wilcke, Tobias
collection PubMed
description PURPOSE: Systemic lupus erythematosus (SLE) is an autoimmune connective tissue disease that can affect the central nervous system. Neuropsychiatric symptoms are found in 25–70% of patients. Using diffusion tensor imaging (DTI) various studies have reported changes in white matter integrity in SLE patients with neuropsychiatric symptoms (NPSLE patients). The purpose of this study was to investigate, if regional changes in white matter integrity can also be detected in SLE patients without neuropsychiatric symptoms (non-NPSLE patients). METHODS: Applying DTI and tract based spatial statistics (TBSS) we investigated 19 NPSLE patients, 19 non-NPSLE and 18 healthy controls. Groups were matched for age and sex. Image pre-processing was performed using FSL, following the TBSS pipeline (eddy current correction, estimation of fractional anisotropy (FA), normalization, skeletonization of the group mean FA image). A general linear model with threshold-free cluster enhancement was used to assess significant differences between the three groups. RESULTS: Statistical analyses revealed several regions of decreased prefrontal white matter integrity (decreased FA) in both groups of SLE patients. The changes found in the non-NPSLE patients (as compared to healthy controls) overlapped with those in the NPSLE patients, but were not as pronounced. CONCLUSIONS: Our data suggest that changes in regional white matter integrity, in terms of a decrease in FA, are present not only in NPSLE patients, but also in non-NPSLE patients, though to a lesser degree. We also demonstrate that the way statistical maps are corrected for multiple comparisons has a profound influence on whether alterations in white matter integrity in non-NPSLE patients are deemed significant.
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spelling pubmed-41419822014-08-26 Diminished white matter integrity in patients with systemic lupus erythematosus Schmidt-Wilcke, Tobias Cagnoli, Patricia Wang, Page Schultz, Thomas Lotz, Anne Mccune, William J. Sundgren, Pia C. Neuroimage Clin Article PURPOSE: Systemic lupus erythematosus (SLE) is an autoimmune connective tissue disease that can affect the central nervous system. Neuropsychiatric symptoms are found in 25–70% of patients. Using diffusion tensor imaging (DTI) various studies have reported changes in white matter integrity in SLE patients with neuropsychiatric symptoms (NPSLE patients). The purpose of this study was to investigate, if regional changes in white matter integrity can also be detected in SLE patients without neuropsychiatric symptoms (non-NPSLE patients). METHODS: Applying DTI and tract based spatial statistics (TBSS) we investigated 19 NPSLE patients, 19 non-NPSLE and 18 healthy controls. Groups were matched for age and sex. Image pre-processing was performed using FSL, following the TBSS pipeline (eddy current correction, estimation of fractional anisotropy (FA), normalization, skeletonization of the group mean FA image). A general linear model with threshold-free cluster enhancement was used to assess significant differences between the three groups. RESULTS: Statistical analyses revealed several regions of decreased prefrontal white matter integrity (decreased FA) in both groups of SLE patients. The changes found in the non-NPSLE patients (as compared to healthy controls) overlapped with those in the NPSLE patients, but were not as pronounced. CONCLUSIONS: Our data suggest that changes in regional white matter integrity, in terms of a decrease in FA, are present not only in NPSLE patients, but also in non-NPSLE patients, though to a lesser degree. We also demonstrate that the way statistical maps are corrected for multiple comparisons has a profound influence on whether alterations in white matter integrity in non-NPSLE patients are deemed significant. Elsevier 2014-07-10 /pmc/articles/PMC4141982/ /pubmed/25161895 http://dx.doi.org/10.1016/j.nicl.2014.07.001 Text en © 2014 The Authors. Published by Elsevier Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Schmidt-Wilcke, Tobias
Cagnoli, Patricia
Wang, Page
Schultz, Thomas
Lotz, Anne
Mccune, William J.
Sundgren, Pia C.
Diminished white matter integrity in patients with systemic lupus erythematosus
title Diminished white matter integrity in patients with systemic lupus erythematosus
title_full Diminished white matter integrity in patients with systemic lupus erythematosus
title_fullStr Diminished white matter integrity in patients with systemic lupus erythematosus
title_full_unstemmed Diminished white matter integrity in patients with systemic lupus erythematosus
title_short Diminished white matter integrity in patients with systemic lupus erythematosus
title_sort diminished white matter integrity in patients with systemic lupus erythematosus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141982/
https://www.ncbi.nlm.nih.gov/pubmed/25161895
http://dx.doi.org/10.1016/j.nicl.2014.07.001
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