Cargando…
Early-stage differentiation between Alzheimer’s disease and frontotemporal lobe degeneration: Clinical, neuropsychology, and neuroimaging features
BACKGROUND: Alzheimer’s disease (AD) and frontotemporal lobar degeneration (FTLD) are the two most common forms of neurodegenerative dementia. Although both of them have well-established diagnostic criteria, achieving early diagnosis remains challenging. Here, we aimed to make the differential diagn...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9659748/ https://www.ncbi.nlm.nih.gov/pubmed/36389060 http://dx.doi.org/10.3389/fnagi.2022.981451 |
_version_ | 1784830265944702976 |
---|---|
author | Li, Pan Quan, Wei Wang, Zengguang Liu, Ying Cai, Hao Chen, Yuan Wang, Yan Zhang, Miao Tian, Zhiyan Zhang, Huihong Zhou, Yuying |
author_facet | Li, Pan Quan, Wei Wang, Zengguang Liu, Ying Cai, Hao Chen, Yuan Wang, Yan Zhang, Miao Tian, Zhiyan Zhang, Huihong Zhou, Yuying |
author_sort | Li, Pan |
collection | PubMed |
description | BACKGROUND: Alzheimer’s disease (AD) and frontotemporal lobar degeneration (FTLD) are the two most common forms of neurodegenerative dementia. Although both of them have well-established diagnostic criteria, achieving early diagnosis remains challenging. Here, we aimed to make the differential diagnosis of AD and FTLD from clinical, neuropsychological, and neuroimaging features. MATERIALS AND METHODS: In this retrospective study, we selected 95 patients with PET-CT defined AD and 106 patients with PET-CT/biomarker-defined FTLD. We performed structured chart examination to collect clinical data and ascertain clinical features. A series of neuropsychological scales were used to assess the neuropsychological characteristics of patients. Automatic tissue segmentation of brain by Dr. Brain tool was used to collect multi-parameter volumetric measurements from different brain areas. All patients’ structural neuroimage data were analyzed to obtain brain structure and white matter hyperintensities (WMH) quantitative data. RESULTS: The prevalence of vascular disease associated factors was higher in AD patients than that in FTLD group. 56.84% of patients with AD carried at least one APOE ε4 allele, which is much high than that in FTLD patients. The first symptoms of AD patients were mostly cognitive impairment rather than behavioral abnormalities. In contrast, behavioral abnormalities were the prominent early manifestations of FTLD, and few patients may be accompanied by memory impairment and motor symptoms. In direct comparison, patients with AD had slightly more posterior lesions and less frontal atrophy, whereas patients with FTLD had more frontotemporal atrophy and less posterior lesions. The WMH burden of AD was significantly higher, especially in cortical areas, while the WMH burden of FTLD was higher in periventricular areas. CONCLUSION: These results indicate that dynamic evaluation of cognitive function, behavioral and psychological symptoms, and multimodal neuroimaging are helpful for the early diagnosis and differentiation between AD and FTLD. |
format | Online Article Text |
id | pubmed-9659748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96597482022-11-15 Early-stage differentiation between Alzheimer’s disease and frontotemporal lobe degeneration: Clinical, neuropsychology, and neuroimaging features Li, Pan Quan, Wei Wang, Zengguang Liu, Ying Cai, Hao Chen, Yuan Wang, Yan Zhang, Miao Tian, Zhiyan Zhang, Huihong Zhou, Yuying Front Aging Neurosci Aging Neuroscience BACKGROUND: Alzheimer’s disease (AD) and frontotemporal lobar degeneration (FTLD) are the two most common forms of neurodegenerative dementia. Although both of them have well-established diagnostic criteria, achieving early diagnosis remains challenging. Here, we aimed to make the differential diagnosis of AD and FTLD from clinical, neuropsychological, and neuroimaging features. MATERIALS AND METHODS: In this retrospective study, we selected 95 patients with PET-CT defined AD and 106 patients with PET-CT/biomarker-defined FTLD. We performed structured chart examination to collect clinical data and ascertain clinical features. A series of neuropsychological scales were used to assess the neuropsychological characteristics of patients. Automatic tissue segmentation of brain by Dr. Brain tool was used to collect multi-parameter volumetric measurements from different brain areas. All patients’ structural neuroimage data were analyzed to obtain brain structure and white matter hyperintensities (WMH) quantitative data. RESULTS: The prevalence of vascular disease associated factors was higher in AD patients than that in FTLD group. 56.84% of patients with AD carried at least one APOE ε4 allele, which is much high than that in FTLD patients. The first symptoms of AD patients were mostly cognitive impairment rather than behavioral abnormalities. In contrast, behavioral abnormalities were the prominent early manifestations of FTLD, and few patients may be accompanied by memory impairment and motor symptoms. In direct comparison, patients with AD had slightly more posterior lesions and less frontal atrophy, whereas patients with FTLD had more frontotemporal atrophy and less posterior lesions. The WMH burden of AD was significantly higher, especially in cortical areas, while the WMH burden of FTLD was higher in periventricular areas. CONCLUSION: These results indicate that dynamic evaluation of cognitive function, behavioral and psychological symptoms, and multimodal neuroimaging are helpful for the early diagnosis and differentiation between AD and FTLD. Frontiers Media S.A. 2022-10-31 /pmc/articles/PMC9659748/ /pubmed/36389060 http://dx.doi.org/10.3389/fnagi.2022.981451 Text en Copyright © 2022 Li, Quan, Wang, Liu, Cai, Chen, Wang, Zhang, Tian, Zhang and Zhou. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Aging Neuroscience Li, Pan Quan, Wei Wang, Zengguang Liu, Ying Cai, Hao Chen, Yuan Wang, Yan Zhang, Miao Tian, Zhiyan Zhang, Huihong Zhou, Yuying Early-stage differentiation between Alzheimer’s disease and frontotemporal lobe degeneration: Clinical, neuropsychology, and neuroimaging features |
title | Early-stage differentiation between Alzheimer’s disease and frontotemporal lobe degeneration: Clinical, neuropsychology, and neuroimaging features |
title_full | Early-stage differentiation between Alzheimer’s disease and frontotemporal lobe degeneration: Clinical, neuropsychology, and neuroimaging features |
title_fullStr | Early-stage differentiation between Alzheimer’s disease and frontotemporal lobe degeneration: Clinical, neuropsychology, and neuroimaging features |
title_full_unstemmed | Early-stage differentiation between Alzheimer’s disease and frontotemporal lobe degeneration: Clinical, neuropsychology, and neuroimaging features |
title_short | Early-stage differentiation between Alzheimer’s disease and frontotemporal lobe degeneration: Clinical, neuropsychology, and neuroimaging features |
title_sort | early-stage differentiation between alzheimer’s disease and frontotemporal lobe degeneration: clinical, neuropsychology, and neuroimaging features |
topic | Aging Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9659748/ https://www.ncbi.nlm.nih.gov/pubmed/36389060 http://dx.doi.org/10.3389/fnagi.2022.981451 |
work_keys_str_mv | AT lipan earlystagedifferentiationbetweenalzheimersdiseaseandfrontotemporallobedegenerationclinicalneuropsychologyandneuroimagingfeatures AT quanwei earlystagedifferentiationbetweenalzheimersdiseaseandfrontotemporallobedegenerationclinicalneuropsychologyandneuroimagingfeatures AT wangzengguang earlystagedifferentiationbetweenalzheimersdiseaseandfrontotemporallobedegenerationclinicalneuropsychologyandneuroimagingfeatures AT liuying earlystagedifferentiationbetweenalzheimersdiseaseandfrontotemporallobedegenerationclinicalneuropsychologyandneuroimagingfeatures AT caihao earlystagedifferentiationbetweenalzheimersdiseaseandfrontotemporallobedegenerationclinicalneuropsychologyandneuroimagingfeatures AT chenyuan earlystagedifferentiationbetweenalzheimersdiseaseandfrontotemporallobedegenerationclinicalneuropsychologyandneuroimagingfeatures AT wangyan earlystagedifferentiationbetweenalzheimersdiseaseandfrontotemporallobedegenerationclinicalneuropsychologyandneuroimagingfeatures AT zhangmiao earlystagedifferentiationbetweenalzheimersdiseaseandfrontotemporallobedegenerationclinicalneuropsychologyandneuroimagingfeatures AT tianzhiyan earlystagedifferentiationbetweenalzheimersdiseaseandfrontotemporallobedegenerationclinicalneuropsychologyandneuroimagingfeatures AT zhanghuihong earlystagedifferentiationbetweenalzheimersdiseaseandfrontotemporallobedegenerationclinicalneuropsychologyandneuroimagingfeatures AT zhouyuying earlystagedifferentiationbetweenalzheimersdiseaseandfrontotemporallobedegenerationclinicalneuropsychologyandneuroimagingfeatures |