Evidence map›Paper›PMID 40240239›Full record

ArticleJournal of cystic fibrosis : official journal of the European Cystic Fibrosis Society2025

Cystic Fibrosis-related neurodegenerative disease associated with tauopathy and cognitive decline in aged CF mice.

Danica F Patton-Parfyonov, Xinming Wang, Sarah Barker, Deborah A Corey, Edwin Vázquez-Rosa, Nichele Abeyesundere, Whitney M Ward, Rebecca Darrah, Jung-A A Woo, David E Kang and 2 more

Abstract read
In one paragraph

Article in Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Danica F Patton-ParfyonovDepartment of Genetics and Genome Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
Xinming WangDepartment of Pathology, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
Sarah BarkerBrain Health Medicines Center, Harrington Discovery Institute, University Hospitals, Cleveland Medical Center, Cleveland, OH 44106, USA; Geriatric Psychiatry, GRECC, Louis Stokes VA Medical Center, Cleveland, OH 44106, USA; Institute for Transformative Molecular Medicine, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA; Department of Pathology, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA; Department of Psychiatry, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
Deborah A CoreyDepartment of Genetics and Genome Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
Edwin Vázquez-RosaBrain Health Medicines Center, Harrington Discovery Institute, University Hospitals, Cleveland Medical Center, Cleveland, OH 44106, USA; Geriatric Psychiatry, GRECC, Louis Stokes VA Medical Center, Cleveland, OH 44106, USA; Institute for Transformative Molecular Medicine, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA; Department of Pathology, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA; Department of Psychiatry, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
Nichele AbeyesundereDepartment of Genetics and Genome Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
Whitney M WardDepartment of Psychiatry, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
Rebecca DarrahDepartment of Genetics and Genome Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
Jung-A A WooDepartment of Pathology, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
David E KangDepartment of Pathology, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
Andrew A PieperBrain Health Medicines Center, Harrington Discovery Institute, University Hospitals, Cleveland Medical Center, Cleveland, OH 44106, USA; Geriatric Psychiatry, GRECC, Louis Stokes VA Medical Center, Cleveland, OH 44106, USA; Institute for Transformative Molecular Medicine, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA; Department of Pathology, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA; Department of Neurosciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA; Department of Psychiatry, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
Thomas J KelleyDepartment of Genetics and Genome Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA. Electronic address: Thomas.kelley@case.edu.

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007250 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI HUANG, ALEX YEE-CHEN · 1985 to 2023
$33.4M
Chemical, Structural and Cell-Signaling Interrogation of 15-Prostanglandin Dehydrogenase in Tissue Repair and RegenerationRM1GM142002 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI MARKOWITZ, SANFORD D., PIEPER, ANDREW A · 2021 to 2025
$6.9M
Medical Scientist Training Program at Case Western Reserve UniversityT32GM152319 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI Heather Broihier, Alex Yee-Chen Huang · 2024 to 2026
$5.1M
Alzheimer's MultiOme Data Repurposing: Artificial Intelligence, Network Medicine, and Therapeutics DiscoveryU01AG073323 · NIA · CLEVELAND CLINIC LERNER COM-CWRU · PI BEKRIS, LYNN, CHENG, FEIXIONG · 2021 to 2025
$4.0M
Neuroprotective actions of cystathionine g-lyase through gasotransmitter hydrogen sulfide signalingR01AG071512 · NIA · JOHNS HOPKINS UNIVERSITY · PI Bindu Paul · 2022 to 2026
$3.4M
Altered Circadian Rhythm Regulation in Cystic FibrosisR01HL156928 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI DARRAH, REBECCA J, KELLEY, THOMAS J · 2022 to 2025
$2.5M
Deubiquitinase USP19 in TDP-43 pathogenesis.RF1NS122218 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI KANG, DAVID E, WOO, JUNGA "ALEXA" · 2022 to 2022
$1.8M
Deubiquitinase USP19 in TDP-43 pathogenesis.R01NS122218 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI David E Kang, JungA Alexa Woo · 2025 to 2026
$1.2M
The Alzheimer's Disease Translational Data Science Training ProgramT32AG071474 · NIA · CASE WESTERN RESERVE UNIVERSITY · PI BUSH, WILLIAM S · 2021 to 2025
$1.1M
BLRD VA I01 BX005976NHLBI NIH HHS R01 HL156928NIA NIH HHS R01 AG071512NIA NIH HHS T32 AG071474NIA NIH HHS U01 AG073323NIGMS NIH HHS RM1 GM142002NIGMS NIH HHS T32 GM007250NIGMS NIH HHS T32 GM152319NINDS NIH HHS R01 NS122218NINDS NIH HHS RF1 NS122218
6 · The paper itself

Abstract

backgroundHighly effective modulator therapies (HEMT) are increasing the lifespan for many people with cystic fibrosis (pwCF), making it necessary to identify and understand CF specific age-related consequences. In this study, we examine the impact of aging on cognitive function and age-related brain pathology in a CF mouse model focusing on phospho-Tau (pTau) pathology.

methodsCognitive function was measured by novel object recognition and spontaneous alternation behavior tests. Hippocampal neuronal function was assessed by measuring long-term potentiation (LTP) electrophysiology, the synaptic correlate of learning and memory. Tau pathology was assessed by immunohistochemical analyses and western blot assessment of pTau levels in CF mouse brain, as well as human nasal epithelial cells isolated from pwCF.

resultsCognitive function declined progressively with age in Cftr (G542X/G542X) (G542X) mice, a model of CF, compared to wild-type (WT) littermate controls. LTP was also deficient in older G542X mice. Increased pTau was observed by staining and western blot analysis in the hippocampus of aged CF mice. Secondary impacts of tauopathy, including increased microglial uptake of cholesterol and reduced neuronal density were also observed. Lastly, human nasal epithelial cells from pwCF were found to display elevated pTau levels compared to non-CF controls.

conclusionsAging CF mice develop tauopathy, cognitive decline, LTP impairment, microglial activation, and neurodegeneration that is not experienced by age-matched WT littermates, a condition herein termed cystic fibrosis-related neurodegeneration (CFND). These findings suggest that pwCF may be at risk for tauopathy-related neurodegeneration and cognitive impairment with aging.

Indexed as

AgingCognitive DysfunctionCystic FibrosisNeurodegenerative DiseasesTauopathiesAnimalsDisease Models, AnimalHippocampusHumansLong-Term PotentiationMicetau Proteinstau ProteinsCognitionCystic fibrosisDementiaTauopathy

Identifiers

PMID40240239
PMCPMC12403229

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.