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Transcranial sonography in carriers of Gaucher disease
Background: Glucocerebrosidase (GBA) mutation is the most common genetic risk factor in Parkinson’s disease (PD). Transcranial sonography (TCS) shows increased substantia nigra (SN) echogenicity in both idiopathic and genetic forms of PD. The goal of this study was to compare maximal area of SN hype...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420695/ https://www.ncbi.nlm.nih.gov/pubmed/30886682 |
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author | Omrani, Fatemeh Ansari-Damavandi, Shahla Zamani, Babak Omrani, Zahra Mohammadzade, Nahid Rohani, Sadra Rohani, Mohammad |
author_facet | Omrani, Fatemeh Ansari-Damavandi, Shahla Zamani, Babak Omrani, Zahra Mohammadzade, Nahid Rohani, Sadra Rohani, Mohammad |
author_sort | Omrani, Fatemeh |
collection | PubMed |
description | Background: Glucocerebrosidase (GBA) mutation is the most common genetic risk factor in Parkinson’s disease (PD). Transcranial sonography (TCS) shows increased substantia nigra (SN) echogenicity in both idiopathic and genetic forms of PD. The goal of this study was to compare maximal area of SN hyperechogenicity (aSNmax) and diameter of third ventricle (DTV) between GBA mutation carriers and healthy controls. Methods: Twenty-six carriers of GBA mutation and twenty-six healthy controls underwent TCS. The aSNmax and the DTV were measured. Mini-mental status examination (MMSE) and demographic data of the subjects were recorded, too. Results: Mean aSNmax in GBA mutation carriers was significantly higher (0.31 ± 0.06 cm(2)) than controls (0.16 ± 0.04 cm(2)). Moreover, DTV was significantly higher in GBA mutation carriers group (3.98 ± 0.90 vs 3.29 ± 0.56 cm). Conclusion: Increased SN echogenicity and increased third ventricle diameter in GBA mutation carriers may be caused by alterations in iron metabolism with reference to their genetic status. |
format | Online Article Text |
id | pubmed-6420695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Tehran University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-64206952019-03-18 Transcranial sonography in carriers of Gaucher disease Omrani, Fatemeh Ansari-Damavandi, Shahla Zamani, Babak Omrani, Zahra Mohammadzade, Nahid Rohani, Sadra Rohani, Mohammad Iran J Neurol Short Communication Background: Glucocerebrosidase (GBA) mutation is the most common genetic risk factor in Parkinson’s disease (PD). Transcranial sonography (TCS) shows increased substantia nigra (SN) echogenicity in both idiopathic and genetic forms of PD. The goal of this study was to compare maximal area of SN hyperechogenicity (aSNmax) and diameter of third ventricle (DTV) between GBA mutation carriers and healthy controls. Methods: Twenty-six carriers of GBA mutation and twenty-six healthy controls underwent TCS. The aSNmax and the DTV were measured. Mini-mental status examination (MMSE) and demographic data of the subjects were recorded, too. Results: Mean aSNmax in GBA mutation carriers was significantly higher (0.31 ± 0.06 cm(2)) than controls (0.16 ± 0.04 cm(2)). Moreover, DTV was significantly higher in GBA mutation carriers group (3.98 ± 0.90 vs 3.29 ± 0.56 cm). Conclusion: Increased SN echogenicity and increased third ventricle diameter in GBA mutation carriers may be caused by alterations in iron metabolism with reference to their genetic status. Tehran University of Medical Sciences 2018-07-06 /pmc/articles/PMC6420695/ /pubmed/30886682 Text en Copyright © 2015 Iranian Neurological Association, and Tehran University of Medical Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Omrani, Fatemeh Ansari-Damavandi, Shahla Zamani, Babak Omrani, Zahra Mohammadzade, Nahid Rohani, Sadra Rohani, Mohammad Transcranial sonography in carriers of Gaucher disease |
title | Transcranial sonography in carriers of Gaucher disease |
title_full | Transcranial sonography in carriers of Gaucher disease |
title_fullStr | Transcranial sonography in carriers of Gaucher disease |
title_full_unstemmed | Transcranial sonography in carriers of Gaucher disease |
title_short | Transcranial sonography in carriers of Gaucher disease |
title_sort | transcranial sonography in carriers of gaucher disease |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420695/ https://www.ncbi.nlm.nih.gov/pubmed/30886682 |
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