Evidence map›Paper›PMID 41468379›Full record

ArticlePloS one2025

Polygenic associations with clinical and neuropathological trait heterogeneity across TDP-43 proteinopathies.

Barbara E Spencer, David J Irwin, Vivianna M Van Deerlin, EunRan Suh, Edward B Lee, Lauren Elman, Colin C Quinn, Defne Amado, Michael Baer, Murray Grossman and 2 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Barbara E SpencerDepartment of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.ORCID https://orcid.org/0000-0002-1685-2967
David J IrwinDepartment of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Vivianna M Van DeerlinDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
EunRan SuhDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Edward B LeeDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Lauren ElmanDepartment of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Colin C QuinnDepartment of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Defne AmadoDepartment of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.ORCID https://orcid.org/0000-0001-6202-3900
Michael BaerDepartment of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Murray GrossmanDepartment of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
David A WolkDepartment of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Corey T McMillanDepartment of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.ORCID https://orcid.org/0000-0002-7581-6405

Funding

Research Education ComponentP30AG072979 · NIA · UNIVERSITY OF PENNSYLVANIA · PI DAVID A WOLK · 2021 to 2026
$24.8M
Understanding Environmental Contributions to Heterogeneity in bvFTD.P01AG066597 · NIA · UNIVERSITY OF PENNSYLVANIA · PI David John Irwin · 2020 to 2026
$18.8M
Microscopic and Large-Scale Networks of Molecular Pathology in Frontotemporal Lobar DegenerationR01NS109260 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI IRWIN, DAVID JOHN · 2019 to 2023
$3.8M
Genetic Contributions to Phenotypic Heterogeneity in the ALS-FTD SpectrumRF1NS145263 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI MCMILLAN, COREY T · 2025 to 2025
$3.2M
Shared and disparate genomic features of TDP-43 proteinopathiesF32AG079618 · NIA · UNIVERSITY OF PENNSYLVANIA · PI SPENCER, BARBARA ELIZABETH · 2022 to 2024
$218k
NIA NIH HHS F32 AG079618NIA NIH HHS P01 AG066597NIA NIH HHS P30 AG072979NINDS NIH HHS R01 NS109260NINDS NIH HHS RF1 NS145263
6 · The paper itself

Abstract

TDP-43 proteinopathies, including amyotrophic lateral sclerosis (ALS), frontotemporal lobar degeneration with TDP-43 (FTLD-TDP), and limbic-predominant age-related TDP-43 encephalopathy, encompass a spectrum of clinical and neuropathological traits. Despite mounting evidence for shared genetic risk across TDP-43 proteinopathies, the modifiers of individual-level traits are unknown. We aimed to identify polygenic contributions to trait heterogeneity across TDP-43 proteinopathies. We used weighted correlation analysis of GWAS summary statistics for ALS, FTLD-TDP, and hippocampal sclerosis of aging (HS-Aging) to identify data-driven clusters of highly correlated single nucleotide polymorphisms (SNPs). We performed gene ontology enrichment analysis for each identified cluster. We derived cluster-specific polygenic scores and evaluated their association with clinical and neuropathological traits in an independently evaluated sample of individuals who met neuropathological and/or genetic criteria for FTLD-TDP or ALS (n = 260). We identified 5 distinct data-driven clusters, including 3 GWAS phenotype-specific clusters (FTLD-TDP, ALS, HS-Aging) and 2 clusters representing the overlap between a pair of GWAS phenotypes (ALS-FTLD and FTLD-HS). Pathway analysis revealed biologically meaningful associations including distinct GWAS phenotype-specific processes within clusters. Cluster-specific ALS and FTLD-TDP polygenic risk each associated with individual-level clinical traits, even within the context of autosomal dominant mutation carriers, where higher ALS polygenic risk associated with neuromuscular impairment and higher FTLD-TDP polygenic risk associated with cognitive-behavioral impairment. Moreover, higher FTLD-TDP polygenic risk associated with higher TDP-43 burden within characteristic FTLD-TDP brain regions. We suggest that there are polygenic modifiers of clinical and neuropathological traits across TDP-43 proteinopathies that may contribute to individual-level differences, including likelihood for developing FTLD or ALS.

Indexed as

Amyotrophic Lateral SclerosisDNA-Binding ProteinsMultifactorial InheritanceTDP-43 ProteinopathiesAgedFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleMiddle AgedPhenotypePolymorphism, Single NucleotideDNA-Binding ProteinsTARDBP protein, human

Identifiers

PMID41468379
PMCPMC12752993

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.