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The diagnostic value of midbrain hyperechogenicity in ALS is limited for discriminating key ALS differential diagnoses

BACKGROUND: Hyperechogenicity of the substantia nigra was recently reported in patients with sporadic ALS with a frequency similar to PD. Data on the diagnostic utility compared to key differential diagnoses of ALS do not exist yet. METHODS: We prospectively enrolled 43 patients with ALS, 29 with my...

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Autores principales: Hermann, Andreas, Reuner, Ulrike, Schaefer, Jochen, Fathinia, Panteha, Leimert, Tordis, Kassubek, Jan, Leimert, Mario, Ludolph, Albert C, Storch, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379542/
https://www.ncbi.nlm.nih.gov/pubmed/25879789
http://dx.doi.org/10.1186/s12883-015-0280-x
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author Hermann, Andreas
Reuner, Ulrike
Schaefer, Jochen
Fathinia, Panteha
Leimert, Tordis
Kassubek, Jan
Leimert, Mario
Ludolph, Albert C
Storch, Alexander
author_facet Hermann, Andreas
Reuner, Ulrike
Schaefer, Jochen
Fathinia, Panteha
Leimert, Tordis
Kassubek, Jan
Leimert, Mario
Ludolph, Albert C
Storch, Alexander
author_sort Hermann, Andreas
collection PubMed
description BACKGROUND: Hyperechogenicity of the substantia nigra was recently reported in patients with sporadic ALS with a frequency similar to PD. Data on the diagnostic utility compared to key differential diagnoses of ALS do not exist yet. METHODS: We prospectively enrolled 43 patients with ALS, 29 with myasthenia gravis, 25 patients with inflammatory neuropathy, and 13 with cervical canal stenosis. All patients were examined by a blinded investigator using transcranial B-mode sonography planimetrically measuring hyperechogenic areas of the midbrain representing the substantia nigra. RESULTS: Mean midbrain hyperechogenic area was increased in ALS compared to non-ALS differentials. ROC analysis revealed only small area under the curve for detecting ALS (AUC: 0.669 [95%CI: 0.56-0.78]; p = 0.006). Highest Youden index was observed for area size of <0.14 cm(2) (Youden index: 0.28). Using this cut-off score and that generated from normative data of healthy controls, area size measurements provided a sensitivity of only 46-58% and specificity of 69-83% for detecting ALS. No correlations of hyperechogenic area sizes in ALS patients were found to age, gender, ALS subtype (bulbar versus spinal form), disease duration or ALS-FRS-R score. CONCLUSIONS: Midbrain hyperechogenicity is reproducibly found in ALS patients, but its diagnostic value for discriminating ALS from its key differentials is limited.
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spelling pubmed-43795422015-04-01 The diagnostic value of midbrain hyperechogenicity in ALS is limited for discriminating key ALS differential diagnoses Hermann, Andreas Reuner, Ulrike Schaefer, Jochen Fathinia, Panteha Leimert, Tordis Kassubek, Jan Leimert, Mario Ludolph, Albert C Storch, Alexander BMC Neurol Research Article BACKGROUND: Hyperechogenicity of the substantia nigra was recently reported in patients with sporadic ALS with a frequency similar to PD. Data on the diagnostic utility compared to key differential diagnoses of ALS do not exist yet. METHODS: We prospectively enrolled 43 patients with ALS, 29 with myasthenia gravis, 25 patients with inflammatory neuropathy, and 13 with cervical canal stenosis. All patients were examined by a blinded investigator using transcranial B-mode sonography planimetrically measuring hyperechogenic areas of the midbrain representing the substantia nigra. RESULTS: Mean midbrain hyperechogenic area was increased in ALS compared to non-ALS differentials. ROC analysis revealed only small area under the curve for detecting ALS (AUC: 0.669 [95%CI: 0.56-0.78]; p = 0.006). Highest Youden index was observed for area size of <0.14 cm(2) (Youden index: 0.28). Using this cut-off score and that generated from normative data of healthy controls, area size measurements provided a sensitivity of only 46-58% and specificity of 69-83% for detecting ALS. No correlations of hyperechogenic area sizes in ALS patients were found to age, gender, ALS subtype (bulbar versus spinal form), disease duration or ALS-FRS-R score. CONCLUSIONS: Midbrain hyperechogenicity is reproducibly found in ALS patients, but its diagnostic value for discriminating ALS from its key differentials is limited. BioMed Central 2015-03-14 /pmc/articles/PMC4379542/ /pubmed/25879789 http://dx.doi.org/10.1186/s12883-015-0280-x Text en © Hermann et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Hermann, Andreas
Reuner, Ulrike
Schaefer, Jochen
Fathinia, Panteha
Leimert, Tordis
Kassubek, Jan
Leimert, Mario
Ludolph, Albert C
Storch, Alexander
The diagnostic value of midbrain hyperechogenicity in ALS is limited for discriminating key ALS differential diagnoses
title The diagnostic value of midbrain hyperechogenicity in ALS is limited for discriminating key ALS differential diagnoses
title_full The diagnostic value of midbrain hyperechogenicity in ALS is limited for discriminating key ALS differential diagnoses
title_fullStr The diagnostic value of midbrain hyperechogenicity in ALS is limited for discriminating key ALS differential diagnoses
title_full_unstemmed The diagnostic value of midbrain hyperechogenicity in ALS is limited for discriminating key ALS differential diagnoses
title_short The diagnostic value of midbrain hyperechogenicity in ALS is limited for discriminating key ALS differential diagnoses
title_sort diagnostic value of midbrain hyperechogenicity in als is limited for discriminating key als differential diagnoses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379542/
https://www.ncbi.nlm.nih.gov/pubmed/25879789
http://dx.doi.org/10.1186/s12883-015-0280-x
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