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Selective Involvement of the Amygdala in Systemic Lupus Erythematosus
BACKGROUND: Antibodies specifically affect the amygdala in a mouse model of systemic lupus erythematosus (SLE). The aim of our study was to investigate whether there is also specific involvement of the amygdala in human SLE. METHODS AND FINDINGS: We analyzed a group of 37 patients with neuropsychiat...
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1702559/ https://www.ncbi.nlm.nih.gov/pubmed/17177602 http://dx.doi.org/10.1371/journal.pmed.0030499 |
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author | Emmer, Bart J van der Grond, Jeroen Steup-Beekman, Gerda M Huizinga, Tom W. J van Buchem, Mark A |
author_facet | Emmer, Bart J van der Grond, Jeroen Steup-Beekman, Gerda M Huizinga, Tom W. J van Buchem, Mark A |
author_sort | Emmer, Bart J |
collection | PubMed |
description | BACKGROUND: Antibodies specifically affect the amygdala in a mouse model of systemic lupus erythematosus (SLE). The aim of our study was to investigate whether there is also specific involvement of the amygdala in human SLE. METHODS AND FINDINGS: We analyzed a group of 37 patients with neuropsychiatric SLE (NP-SLE), 21 patients with SLE, and a group of 12 healthy control participants with diffusion weighted imaging (DWI). In addition, in a subset of eight patients, plasma was available to determine their anti-NMDAR antibody status. From the structural magnetic resonance imaging data, the amygdala and the hippocampus were segmented, as well as the white and gray matter, and the apparent diffusion coefficient (ADC) was retrieved. ADC values between controls, patients with SLE, and patients with NP-SLE were tested using analysis of variance with post-hoc Bonferroni correction. No differences were found in the gray or white matter segments. The average ADC in the amygdala of patients with NP-SLE and SLE (940 × 10(−6) mm(2)/s; p = 0.006 and 949 × 10(−6) mm(2)/s; p = 0.019, respectively) was lower than in healthy control participants (1152 × 10(−6) mm(2)/s). Mann-Whitney analysis revealed that the average ADC in the amygdala of patients with anti-NMDAR antibodies (n = 4; 802 × 10(−6) mm(2)/s) was lower (p = 0.029) than the average ADC of patients without anti-NMDAR antibodies (n = 4; 979 × 10(−6) mm(2)/s) and also lower (p = 0.001) than in healthy control participants. CONCLUSIONS: This is the first study to our knowledge to observe damage in the amygdala in patients with SLE. Patients with SLE with anti-NMDAR antibodies had more severe damage in the amygdala compared to SLE patients without anti-NMDAR antibodies. |
format | Text |
id | pubmed-1702559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-17025592007-03-24 Selective Involvement of the Amygdala in Systemic Lupus Erythematosus Emmer, Bart J van der Grond, Jeroen Steup-Beekman, Gerda M Huizinga, Tom W. J van Buchem, Mark A PLoS Med Research Article BACKGROUND: Antibodies specifically affect the amygdala in a mouse model of systemic lupus erythematosus (SLE). The aim of our study was to investigate whether there is also specific involvement of the amygdala in human SLE. METHODS AND FINDINGS: We analyzed a group of 37 patients with neuropsychiatric SLE (NP-SLE), 21 patients with SLE, and a group of 12 healthy control participants with diffusion weighted imaging (DWI). In addition, in a subset of eight patients, plasma was available to determine their anti-NMDAR antibody status. From the structural magnetic resonance imaging data, the amygdala and the hippocampus were segmented, as well as the white and gray matter, and the apparent diffusion coefficient (ADC) was retrieved. ADC values between controls, patients with SLE, and patients with NP-SLE were tested using analysis of variance with post-hoc Bonferroni correction. No differences were found in the gray or white matter segments. The average ADC in the amygdala of patients with NP-SLE and SLE (940 × 10(−6) mm(2)/s; p = 0.006 and 949 × 10(−6) mm(2)/s; p = 0.019, respectively) was lower than in healthy control participants (1152 × 10(−6) mm(2)/s). Mann-Whitney analysis revealed that the average ADC in the amygdala of patients with anti-NMDAR antibodies (n = 4; 802 × 10(−6) mm(2)/s) was lower (p = 0.029) than the average ADC of patients without anti-NMDAR antibodies (n = 4; 979 × 10(−6) mm(2)/s) and also lower (p = 0.001) than in healthy control participants. CONCLUSIONS: This is the first study to our knowledge to observe damage in the amygdala in patients with SLE. Patients with SLE with anti-NMDAR antibodies had more severe damage in the amygdala compared to SLE patients without anti-NMDAR antibodies. Public Library of Science 2006-12 2006-12-19 /pmc/articles/PMC1702559/ /pubmed/17177602 http://dx.doi.org/10.1371/journal.pmed.0030499 Text en © 2006 Emmer et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Emmer, Bart J van der Grond, Jeroen Steup-Beekman, Gerda M Huizinga, Tom W. J van Buchem, Mark A Selective Involvement of the Amygdala in Systemic Lupus Erythematosus |
title | Selective Involvement of the Amygdala in Systemic Lupus Erythematosus |
title_full | Selective Involvement of the Amygdala in Systemic Lupus Erythematosus |
title_fullStr | Selective Involvement of the Amygdala in Systemic Lupus Erythematosus |
title_full_unstemmed | Selective Involvement of the Amygdala in Systemic Lupus Erythematosus |
title_short | Selective Involvement of the Amygdala in Systemic Lupus Erythematosus |
title_sort | selective involvement of the amygdala in systemic lupus erythematosus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1702559/ https://www.ncbi.nlm.nih.gov/pubmed/17177602 http://dx.doi.org/10.1371/journal.pmed.0030499 |
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