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The role of MAPT gene in Chinese dementia patients: a P301L pedigree study and brief literature review
BACKGROUND AND PURPOSE: Frontotemporal dementia (FTD) is the second most common presenile dementia characterized by behavioral changes and language impairment. The diagnosis of FTD relies heavily on neuroimaging, and sometimes on genetic screening. However, the genetic components in Chinese FTD pati...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018486/ https://www.ncbi.nlm.nih.gov/pubmed/29950844 http://dx.doi.org/10.2147/NDT.S155521 |
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author | He, Shuang Chen, Shuai Xia, Ming-Rong Sun, Zhi-Kun Huang, Yue Zhang, Jie-Wen |
author_facet | He, Shuang Chen, Shuai Xia, Ming-Rong Sun, Zhi-Kun Huang, Yue Zhang, Jie-Wen |
author_sort | He, Shuang |
collection | PubMed |
description | BACKGROUND AND PURPOSE: Frontotemporal dementia (FTD) is the second most common presenile dementia characterized by behavioral changes and language impairment. The diagnosis of FTD relies heavily on neuroimaging, and sometimes on genetic screening. However, the genetic components in Chinese FTD patients remain largely unknown. Only a few FTD cases with established mutations have been reported in China. This study reported the detailed clinical and neuroimaging features in a Chinese behavioral variant FTD family. The role of MAPT gene mutation in Chinese dementia patients was also reviewed. METHODS: By detailed inquiry of all affected individuals in the family, this study summarized the main clinical features of the disease. Four candidate genes (MAPT, PSEN1, PSEN2, and APP) were screened by direct sequencing. Structural magnetic resonance imaging (MRI), functional imaging of cerebral blood flow with arterial spin-labeled MRI (ASL-MRI), and cerebral metabolism with fluorodeoxyglucose positron emission tomography (FDG-PET) were collected in the proband and healthy mutation carriers. RESULTS: By direct sequencing of candidate genes (MAPT, PSEN1, PSEN2, and APP), this study identified the P301L mutation in the MAPT gene in the proband and three unaffected family members. The phenotype of the affected cases was consistent within the pedigree. In this genetically proven behavioral variant FTD (bvFTD) patient, the maps of hypoperfusion on ASL-MRI look fairly similar to the hypometabolism on FDG-PET. The clinical feature for this bvFTD was in line with the hypoperfusion or hypometabolism pattern on functional neuroimagings. The phenotype of P301L in east Asia seems similar to western countries. CONCLUSION: For the inherited FTD patients, ASL-MRI and genetic identification were strongly recommended for the final diagnosis. In case of being underestimated, the role of MAPT gene mutation in Chinese FTD patients warrants further investigation. |
format | Online Article Text |
id | pubmed-6018486 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60184862018-06-27 The role of MAPT gene in Chinese dementia patients: a P301L pedigree study and brief literature review He, Shuang Chen, Shuai Xia, Ming-Rong Sun, Zhi-Kun Huang, Yue Zhang, Jie-Wen Neuropsychiatr Dis Treat Original Research BACKGROUND AND PURPOSE: Frontotemporal dementia (FTD) is the second most common presenile dementia characterized by behavioral changes and language impairment. The diagnosis of FTD relies heavily on neuroimaging, and sometimes on genetic screening. However, the genetic components in Chinese FTD patients remain largely unknown. Only a few FTD cases with established mutations have been reported in China. This study reported the detailed clinical and neuroimaging features in a Chinese behavioral variant FTD family. The role of MAPT gene mutation in Chinese dementia patients was also reviewed. METHODS: By detailed inquiry of all affected individuals in the family, this study summarized the main clinical features of the disease. Four candidate genes (MAPT, PSEN1, PSEN2, and APP) were screened by direct sequencing. Structural magnetic resonance imaging (MRI), functional imaging of cerebral blood flow with arterial spin-labeled MRI (ASL-MRI), and cerebral metabolism with fluorodeoxyglucose positron emission tomography (FDG-PET) were collected in the proband and healthy mutation carriers. RESULTS: By direct sequencing of candidate genes (MAPT, PSEN1, PSEN2, and APP), this study identified the P301L mutation in the MAPT gene in the proband and three unaffected family members. The phenotype of the affected cases was consistent within the pedigree. In this genetically proven behavioral variant FTD (bvFTD) patient, the maps of hypoperfusion on ASL-MRI look fairly similar to the hypometabolism on FDG-PET. The clinical feature for this bvFTD was in line with the hypoperfusion or hypometabolism pattern on functional neuroimagings. The phenotype of P301L in east Asia seems similar to western countries. CONCLUSION: For the inherited FTD patients, ASL-MRI and genetic identification were strongly recommended for the final diagnosis. In case of being underestimated, the role of MAPT gene mutation in Chinese FTD patients warrants further investigation. Dove Medical Press 2018-06-18 /pmc/articles/PMC6018486/ /pubmed/29950844 http://dx.doi.org/10.2147/NDT.S155521 Text en © 2018 He et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research He, Shuang Chen, Shuai Xia, Ming-Rong Sun, Zhi-Kun Huang, Yue Zhang, Jie-Wen The role of MAPT gene in Chinese dementia patients: a P301L pedigree study and brief literature review |
title | The role of MAPT gene in Chinese dementia patients: a P301L pedigree study and brief literature review |
title_full | The role of MAPT gene in Chinese dementia patients: a P301L pedigree study and brief literature review |
title_fullStr | The role of MAPT gene in Chinese dementia patients: a P301L pedigree study and brief literature review |
title_full_unstemmed | The role of MAPT gene in Chinese dementia patients: a P301L pedigree study and brief literature review |
title_short | The role of MAPT gene in Chinese dementia patients: a P301L pedigree study and brief literature review |
title_sort | role of mapt gene in chinese dementia patients: a p301l pedigree study and brief literature review |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018486/ https://www.ncbi.nlm.nih.gov/pubmed/29950844 http://dx.doi.org/10.2147/NDT.S155521 |
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