Clinical associations of CSF TMEM106B in familial and sporadic frontotemporal lobar degeneration

CSF TMEM106B concentrations are influenced by the TMEM106B rs1990622 genotype, and correlate with disease severity and brain volume in both genetic and sporadic FTLD. Lower levels of CSF TMEM106B correlate with more severe disease and brain atrophy. Disease severity is more strongly associated with CSF NfL, while brain volumes are more strongly associated with CSF TMEM106B. CSF TMEM106B may have value as a biomarker of neurodegeneration in FTLD.

Authors

Institutions

Publication Details

Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70856_103985
Primary Topic
Lysosomal Storage Disorders Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Clinical associations of CSF TMEM106B in familial and sporadic frontotemporal lobar degeneration

Lawren VandeVrede, Mark Sanderson‐Cimino, Hilary W. Heuer, Adam M. Staffaroni et al.
Alzheimer s & Dementia
Lysosomal Storage Disorders Research
article

Clinical associations of CSF TMEM106B in familial and sporadic frontotemporal lobar degeneration

Lawren VandeVrede, Mark Sanderson‐Cimino, Hilary W. Heuer, Adam M. Staffaroni, Peter Alexander Ljubenkov, Joseph Loureiro, Casey Cook, Yann Cobigo, Julio C. Rojas, Binita Rajbanshi, Argentina Lario Lago, Julia D Webb, Eden V. Barragan, Molly Olzinski, Brad F Boeve, Jingyao Li, Howard J. Rosen, Rosa Rademakers, Eliana Marisa Ramos, Adam L. Boxer, Leonard Petrucelli, Rowan Saloner, Katie Worringer
article en

Abstract

CSF TMEM106B concentrations are influenced by the TMEM106B rs1990622 genotype, and correlate with disease severity and brain volume in both genetic and sporadic FTLD. Lower levels of CSF TMEM106B correlate with more severe disease and brain atrophy. Disease severity is more strongly associated with CSF NfL, while brain volumes are more strongly associated with CSF TMEM106B. CSF TMEM106B may have value as a biomarker of neurodegeneration in FTLD.

Alzheimer s & DementiaVol. 21(S2)
University of Antwerp (BE), University of California, Los Angeles (US), University of California, San Francisco (US), WinnMed (US), University Memory and Aging Center (US), Novartis (United States) (US), Mayo Clinic in Arizona (US), VIB-UAntwerp Center for Molecular Neurology (BE), Mayo Clinic in Florida (US)
Openalex Percentile: Top 33%
Lysosomal Storage Disorders Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Clinical associations of CSF TMEM106B in familial and sporadic frontotemporal lobar degeneration — Lawren VandeVrede, Mark Sanderson‐Cimino, et al. · Alzheimer s & Dementia (2025) | TGRS Research Map | TGRS