TY  - CONF
AU  - Pasternak, Maurice
AU  - Mirza, Saira S
AU  - Paterson, Andrew D
AU  - Tartaglia, Carmela
AU  - Mitchell, Sara
AU  - Black, Sandra E
AU  - Freedman, Morris
AU  - Tang-Wai, David F
AU  - Rogaeva, Ekaterina
AU  - Cash, David M
AU  - Bocchetta, Martina
AU  - van Swieten, John
AU  - Laforce, Robert
AU  - Tagliavini, Fabrizio
AU  - Borroni, Barbara
AU  - Galimberti, Daniela
AU  - Rowe, James B
AU  - Graff, Caroline
AU  - Finger, Elizabeth
AU  - Sorbi, Sandro
AU  - de Mendonça, Alexandre
AU  - Butler, Christopher
AU  - Gerhard, Alexander
AU  - Sánchez-Valle, Raquel
AU  - Moreno, Fermin
AU  - Synofzik, Matthis
AU  - Vandenberghe, Rik
AU  - Ducharme, Simon
AU  - Levin, Johannes
AU  - Otto, Markus
AU  - Santana, Isabel
AU  - Rohrer, Jonathan D
AU  - Masellis, Mario
TI  - TMEM106B modulates disease severity in genetic frontotemporal dementia phenoconverters
JO  - Alzheimer's and dementia
VL  - 21 Suppl 2
IS  - Suppl 2
SN  - 1552-5260
M1  - DZNE-2025-01478
SP  - e103532
PY  - 2025
AB  - A common variant within TMEM106B is associated with risk for Frontotemporal Lobar Degeneration-Tar DNA binding Protein-43 (FTLD-TDP). A recent study has shown that the minor allele G of TMEM106B-rs1990622 confers protection against FTLD-TDP in symptomatic mutation carriers through reductions in NfL serum levels, brain atrophy, and cognitive decline. It is unknown whether this protective effect is present in phenoconverters of the disease.We included 518 participants from the GENetic Frontotemporal dementia Initiative (GENFI), which recruits genetic FTD cases and their family members, both carriers and non-carriers of FTD mutations. Of these, 21 were phenoconverters, 209 were non-carrier controls, 70 were presymptomatic and 45 symptomatic C9orf72 carriers, 92 presymptomatic and 29 symptomatic GRN carriers, and 39 presymptomatic and 13 symptomatic MAPT carriers. Effects of interaction between TMEM106B-rs1990622 and phenoconverter status were examined using mixed effects models, with a random effects structure featuring subjects nested within families and fixed effects for age at baseline and sex. Serum neurofilament light chain (NfL) was measured using the Simoa platform. Cognitive assessment included the Mini-Mental State Examination (MMSE), tests of attention, processing speed, executive function, and language, as well as the Cambridge Behavioural Inventory (CBI), with mixed effects also including years of education as a covariate. Brain volumetry was assessed using T1-weighted MRI and these mixed effect models also included additional covariates of total intracranial volume and scanner site.In phenoconverters, each copy of the protective allele G was associated with a significant reduction in the rate of serum NfL accumulation (-5.33 pg/mL/year; p = 7.79 × 10-9). Structural imaging analyses revealed decreased rates of atrophy in fronto-orbital regions and the insular cortex among protective allele carriers. Cognitive trajectories showed significantly slower decline across multiple domains including general cognition (MMSE; p = 0.003), attention and processing speed (p = 2.2 × 10-4), executive function (p = 2.6 × 10-7), language (p = 2.9 × 10-3), and behavioural symptoms as measured by CBI (p = 9.5 × 10-3).The TMEM106B-rs1990622 protective variant significantly modulates disease progression in genetic FTD phenoconverters across multiple markers, suggesting its potential as a therapeutic target.
T2  - Alzheimer’s Association International Conference
CY  - 27 Jul 2025 - 31 Jul 2025, Toronto (Canada)
Y2  - 27 Jul 2025 - 31 Jul 2025
M2  - Toronto, Canada
KW  - Humans
KW  - Male
KW  - Female
KW  - Nerve Tissue Proteins: genetics
KW  - Middle Aged
KW  - Biomarkers: blood
KW  - Membrane Proteins: genetics
KW  - Frontotemporal Dementia: genetics
KW  - Frontotemporal Dementia: pathology
KW  - Aged
KW  - C9orf72 Protein: genetics
KW  - Brain: pathology
KW  - Brain: diagnostic imaging
KW  - tau Proteins: genetics
KW  - Progranulins: genetics
KW  - Neurofilament Proteins: blood
KW  - Mutation: genetics
KW  - Magnetic Resonance Imaging
KW  - Atrophy
KW  - Nerve Tissue Proteins (NLM Chemicals)
KW  - Biomarkers (NLM Chemicals)
KW  - TMEM106B protein, human (NLM Chemicals)
KW  - Membrane Proteins (NLM Chemicals)
KW  - C9orf72 Protein (NLM Chemicals)
KW  - tau Proteins (NLM Chemicals)
KW  - Progranulins (NLM Chemicals)
KW  - Neurofilament Proteins (NLM Chemicals)
KW  - C9orf72 protein, human (NLM Chemicals)
KW  - MAPT protein, human (NLM Chemicals)
KW  - neurofilament protein L (NLM Chemicals)
LB  - PUB:(DE-HGF)1 ; PUB:(DE-HGF)16
C6  - pmid:41449512
C2  - pmc:PMC12741048
DO  - DOI:10.1002/alz70856_103532
UR  - https://pub.dzne.de/record/283071
ER  -