Literature DB >> 28448978

Quantitative Evaluation of Brain Stem Atrophy Using Magnetic Resonance Imaging in Adult Patients with Alexander Disease.

Tomokatsu Yoshida1, Rei Yasuda, Ikuko Mizuta, Masanori Nakagawa, Toshiki Mizuno.   

Abstract

Brain MRI in adult patients with Alexander disease (AxD) mainly shows atrophy in the medulla oblongata. However, currently there is no quantitative standard for assessing this atrophy. In this study, we quantitatively evaluated the brain stem of AxD patients with glial fibrillary acidic protein (GFAP) mutation using conventional MRI to evaluate its usefulness as an aid to diagnosing AxD in daily clinical practice. Nineteen AxD patients with GFAP mutation were compared with 14 patients negative for GFAP mutation in whom AxD was suspected due to "atrophy of the medulla oblongata." In the GFAP mutation-positive group, the sagittal diameter of the medulla oblongata, the ratio of the diameter of the medulla oblongata to that of the midbrain (MO/MB), and the ratio of the sagittal diameter of the medulla oblongata to that of the pons (MO/Po) were significantly smaller compared to those of the GFAP mutation-negative group (p < 0.01). The sensitivity and specificity of each parameter were 87.5 and 92.3%, 91.7 and 81.3%, and 88.2 and 100% with a sagittal diameter of the medulla oblongata <9.0 mm, MO/MB <0.60, and sagittal MO/Po <0.46, respectively. These parameters can provide very useful information to differentially diagnose AxD from other disorders associated with brain stem atrophy in adult patients.
© 2017 S. Karger AG, Basel.

Entities:  

Keywords:  Alexander disease; Atrophy; Magnetic resonance imaging; Medulla oblongata

Mesh:

Year:  2017        PMID: 28448978     DOI: 10.1159/000475661

Source DB:  PubMed          Journal:  Eur Neurol        ISSN: 0014-3022            Impact factor:   1.710


  4 in total

1.  A novel in-frame GFAP p.E138_L148del mutation in Type II Alexander disease with atypical phenotypes.

Authors:  You-Ri Kang; So-Hyun Lee; Ni-Hsuan Lin; Seung-Jin Lee; Ai-Wen Yang; Gopalakrishnan Chandrasekaran; Kyung Wook Kang; Mi Sun Jin; Myeong-Kyu Kim; Ming-Der Perng; Seok-Yong Choi; Tai-Seung Nam
Journal:  Eur J Hum Genet       Date:  2022-03-04       Impact factor: 5.351

2.  A novel de novo mutation in the PURA gene associated with a new clinical finding: large brainstem.

Authors:  María Elena Rodríguez-García; Francisco Javier Cotrina-Vinagre; Elena Arranz-Canales; Ana Martínez de Aragón; Laura Hernández-Sánchez; Fátima Rodríguez-Fornés; Patricia Carnicero-Rodríguez; Montserrat Morales-Conejo; Elena Martín-Hernández; Francisco Martínez-Azorín
Journal:  J Genet       Date:  2020       Impact factor: 1.166

3.  Towards genomic database of Alexander disease to identify variations modifying disease phenotype.

Authors:  Rei Yasuda; Masakazu Nakano; Tomokatsu Yoshida; Ryuichi Sato; Hiroko Adachi; Yuichi Tokuda; Ikuko Mizuta; Kozo Saito; Jun Matsuura; Masanori Nakagawa; Kei Tashiro; Toshiki Mizuno
Journal:  Sci Rep       Date:  2019-10-14       Impact factor: 4.379

Review 4.  Identification of a novel de novo pathogenic variant in GFAP in an Iranian family with Alexander disease by whole-exome sequencing.

Authors:  Katayoun Heshmatzad; Niloofar Naderi; Tannaz Masoumi; Hamidreza Pouraliakbar; Samira Kalayinia
Journal:  Eur J Med Res       Date:  2022-09-10       Impact factor: 4.981

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.