Journal Article DZNE-2025-00563

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Sex differences in clinical phenotypes of behavioral variant frontotemporal dementia.

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2025
Wiley Hoboken, NJ

Alzheimer's and dementia 21(4), e14608 () [10.1002/alz.14608]

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Abstract: Higher male prevalence in sporadic behavioral variant frontotemporal dementia (bvFTD) has been reported. We hypothesized differences in phenotypes between genetic and sporadic bvFTD females resulting in underdiagnosis of sporadic bvFTD females.We included genetic and sporadic bvFTD patients from two multicenter cohorts. We compared behavioral and cognitive symptoms, and gray matter volumes, between genetic and sporadic cases in each sex.Females with sporadic bvFTD showed worse compulsive behavior (p = 0.026) and language impairments (p = 0.024) compared to females with genetic bvFTD (n = 152). Genetic bvFTD females had smaller gray matter volumes than sporadic bvFTD females, particularly in the parietal lobe.Females with sporadic bvFTD exhibit a distinct clinical phenotype compared to females with genetic bvFTD. This difference may explain the discrepancy in prevalence between genetic and sporadic cases, as some females without genetic mutations may be misdiagnosed due to atypical bvFTD symptom presentation.Sex ratio is equal in genetic behavioral variant of frontotemporal dementia (bvFTD), whereas more males are present in sporadic bvFTD. Distinct neuropsychiatric phenotypes exist between sporadic and genetic bvFTD in females. Phenotype might explain the sex ratio difference between sporadic and genetic cases.

Keyword(s): Humans (MeSH) ; Frontotemporal Dementia: genetics (MeSH) ; Frontotemporal Dementia: pathology (MeSH) ; Frontotemporal Dementia: diagnostic imaging (MeSH) ; Female (MeSH) ; Male (MeSH) ; Phenotype (MeSH) ; Middle Aged (MeSH) ; Aged (MeSH) ; Magnetic Resonance Imaging (MeSH) ; Gray Matter: pathology (MeSH) ; Gray Matter: diagnostic imaging (MeSH) ; Sex Characteristics (MeSH) ; Neuropsychological Tests (MeSH) ; Cohort Studies (MeSH) ; Sex Factors (MeSH) ; Brain: pathology (MeSH) ; Brain: diagnostic imaging (MeSH) ; behavioral variant frontotemporal dementia ; clinical diagnosis ; diversity ; sex difference

Classification:

Contributing Institute(s):
  1. Clinical Neurodegeneration (AG Levin)
  2. Clinical Research (Munich) (Clinical Research (Munich))
  3. Parkinson Genetics (AG Gasser)
Research Program(s):
  1. 353 - Clinical and Health Care Research (POF4-353) (POF4-353)

Appears in the scientific report 2025
Database coverage:
Medline ; Creative Commons Attribution CC BY 4.0 ; OpenAccess ; Clarivate Analytics Master Journal List ; Current Contents - Clinical Medicine ; DEAL Wiley ; Essential Science Indicators ; IF >= 10 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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Institute Collections > M DZNE > M DZNE-Clinical Research (Munich)
Document types > Articles > Journal Article
Institute Collections > TÜ DZNE > TÜ DZNE-AG Gasser
Institute Collections > M DZNE > M DZNE-AG Levin
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 Record created 2025-04-28, last modified 2025-05-04