001     283025
005     20251222101655.0
024 7 _ |a 10.1002/alz.70695
|2 doi
024 7 _ |a pmid:41057914
|2 pmid
024 7 _ |a pmc:PMC12504049
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024 7 _ |a 1552-5260
|2 ISSN
024 7 _ |a 1552-5279
|2 ISSN
037 _ _ |a DZNE-2025-01437
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Soltaninejad, Mahdie
|b 0
245 _ _ |a White matter hyperintensities precede other biomarkers in GRN frontotemporal dementia.
260 _ _ |a Hoboken, NJ
|c 2025
|b Wiley
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
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336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
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336 7 _ |a Journal Article
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520 _ _ |a Increased white matter hyperintensities (WMHs) have been reported in genetic frontotemporal dementia (FTD) in small studies, but the sequence of WMH abnormalities relative to other biomarkers is unclear.Using a large dataset (n = 763 GENFI2 participants), we measured WMHs and examined them across genetic FTD variants and stages. Cortical and subcortical volumes were parcellated, and serum neurofilament light chain (NfL) levels were measured. Biomarker progression was assessed with discriminative event-based and regression modeling.Symptomatic GRN carriers showed elevated WMHs, primarily in the frontal lobe, while no significant increase was observed in symptomatic C9orf72 or MAPT carriers. WMH abnormalities preceded NfL elevation, ventricular enlargement, and cortical atrophy. Longitudinally, baseline WMHs predicted subcortical changes, while subcortical volumes did not predict WMH changes, suggesting WMHs may precede neurodegeneration.WMHs are elevated in a subset of GRN-associated FTD. When present, they appear early and should be considered in disease progression models.Elevated WMH volumes are found predominantly in symptomatic GRN. WMH accumulation is mostly observed in the frontal lobe. WMH abnormalities appear early in GRN-associated FTD, before NfL, atrophy, and ventriculomegaly. Longitudinally, WMH volumes can predict subcortical changes, but not vice versa. WMHs are key early markers in GRN-associated FTD and should be included in progression models.
536 _ _ |a 353 - Clinical and Health Care Research (POF4-353)
|0 G:(DE-HGF)POF4-353
|c POF4-353
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: pub.dzne.de
650 _ 7 |a C9orf72
|2 Other
650 _ 7 |a FTD
|2 Other
650 _ 7 |a GRN
|2 Other
650 _ 7 |a MAPT
|2 Other
650 _ 7 |a biomarker sequence
|2 Other
650 _ 7 |a dementia
|2 Other
650 _ 7 |a disease progression
|2 Other
650 _ 7 |a early marker
|2 Other
650 _ 7 |a event‐based modeling
|2 Other
650 _ 7 |a magnetic resonance imaging
|2 Other
650 _ 7 |a neurodegeneration
|2 Other
650 _ 7 |a neurofilament light chain
|2 Other
650 _ 7 |a neuroimaging
|2 Other
650 _ 7 |a progranulin
|2 Other
650 _ 7 |a white matter
|2 Other
650 _ 7 |a Biomarkers
|2 NLM Chemicals
650 _ 7 |a Progranulins
|2 NLM Chemicals
650 _ 7 |a GRN protein, human
|2 NLM Chemicals
650 _ 7 |a C9orf72 Protein
|2 NLM Chemicals
650 _ 7 |a Neurofilament Proteins
|2 NLM Chemicals
650 _ 7 |a neurofilament protein L
|2 NLM Chemicals
650 _ 7 |a tau Proteins
|2 NLM Chemicals
650 _ 7 |a C9orf72 protein, human
|2 NLM Chemicals
650 _ 7 |a MAPT protein, human
|2 NLM Chemicals
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Frontotemporal Dementia: genetics
|2 MeSH
650 _ 2 |a Frontotemporal Dementia: pathology
|2 MeSH
650 _ 2 |a Frontotemporal Dementia: diagnostic imaging
|2 MeSH
650 _ 2 |a White Matter: pathology
|2 MeSH
650 _ 2 |a White Matter: diagnostic imaging
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Female
|2 MeSH
650 _ 2 |a Biomarkers: blood
|2 MeSH
650 _ 2 |a Progranulins: genetics
|2 MeSH
650 _ 2 |a Middle Aged
|2 MeSH
650 _ 2 |a Magnetic Resonance Imaging
|2 MeSH
650 _ 2 |a C9orf72 Protein: genetics
|2 MeSH
650 _ 2 |a Neurofilament Proteins: blood
|2 MeSH
650 _ 2 |a Aged
|2 MeSH
650 _ 2 |a Disease Progression
|2 MeSH
650 _ 2 |a tau Proteins: genetics
|2 MeSH
650 _ 2 |a Atrophy
|2 MeSH
700 1 _ |a Dadar, Mahsa
|b 1
700 1 _ |a Collins, D Louis
|b 2
700 1 _ |a Rajabli, Reza
|b 3
700 1 _ |a Venkatraghavan, Vikram
|b 4
700 1 _ |a Bouzigues, Arabella
|b 5
700 1 _ |a Russell, Lucy L
|b 6
700 1 _ |a Foster, Phoebe H
|b 7
700 1 _ |a Ferry-Bolder, Eve
|b 8
700 1 _ |a van Swieten, John C
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700 1 _ |a Jiskoot, Lize C
|b 10
700 1 _ |a Seelaar, Harro
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700 1 _ |a Sanchez-Valle, Raquel
|b 12
700 1 _ |a Laforce, Robert
|b 13
700 1 _ |a Graff, Caroline
|b 14
700 1 _ |a Galimberti, Daniela
|b 15
700 1 _ |a Vandenberghe, Rik
|b 16
700 1 _ |a de Mendonça, Alexandre
|b 17
700 1 _ |a Tiraboschi, Pietro
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700 1 _ |a Santana, Isabel
|b 19
700 1 _ |a Gerhard, Alexander
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700 1 _ |a Levin, Johannes
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|u dzne
700 1 _ |a Nacmias, Benedetta
|b 22
700 1 _ |a Otto, Markus
|b 23
700 1 _ |a Bertoux, Maxime
|b 24
700 1 _ |a Lebouvier, Thibaud
|b 25
700 1 _ |a Butler, Chris R
|b 26
700 1 _ |a Ber, Isabelle Le
|b 27
700 1 _ |a Finger, Elizabeth
|b 28
700 1 _ |a Tartaglia, Maria Carmela
|b 29
700 1 _ |a Masellis, Mario
|b 30
700 1 _ |a Rowe, James B
|b 31
700 1 _ |a Synofzik, Matthis
|0 P:(DE-2719)2811275
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700 1 _ |a Moreno, Fermin
|b 33
700 1 _ |a Borroni, Barbara
|b 34
700 1 _ |a Rohrer, Jonathan D
|b 35
700 1 _ |a Iturria-Medina, Yasser
|b 36
700 1 _ |a Ducharme, Simon
|b 37
700 1 _ |a Consortium, GENFI
|b 38
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773 _ _ |a 10.1002/alz.70695
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910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
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Marc 21