Evidence map›Paper›PMID 41695614›Full record

ArticleMolecular neurodegeneration advances2026

Pretangle tau pathology accrual in the default mode network during the progression of Alzheimer's disease.

Betul Kara, Ian M Kelly, John S Beck, Nathan Kuhn, Elliott J Mufson, Irving E Vega, Nicholas M Kanaan, Scott E Counts

Abstract read
In one paragraph

Article in Molecular neurodegeneration advances, 2026. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Betul KaraDepartment of Translational Neuroscience, Michigan State University, 400 Monroe Ave NW, Grand Rapids, MI 49503 USA.
Ian M KellyDepartment of Translational Neuroscience, Michigan State University, 400 Monroe Ave NW, Grand Rapids, MI 49503 USA.
John S BeckDepartment of Translational Neuroscience, Michigan State University, 400 Monroe Ave NW, Grand Rapids, MI 49503 USA.
Nathan KuhnDepartment of Translational Neuroscience, Michigan State University, 400 Monroe Ave NW, Grand Rapids, MI 49503 USA.
Elliott J MufsonDepartment of Translational Neuroscience, Barrow Neurological Institute, Phoenix, AZ 85013 USA.
Irving E VegaDepartment of Translational Neuroscience, Michigan State University, 400 Monroe Ave NW, Grand Rapids, MI 49503 USA.
Nicholas M KanaanDepartment of Translational Neuroscience, Michigan State University, 400 Monroe Ave NW, Grand Rapids, MI 49503 USA.
Scott E CountsDepartment of Translational Neuroscience, Michigan State University, 400 Monroe Ave NW, Grand Rapids, MI 49503 USA.

Funding

Rush Alzheimer's Disease Research CenterP30AG072975 · NIA · RUSH UNIVERSITY MEDICAL CENTER · PI Lisa L Barnes, Julie A. Schneider · 2021 to 2026
$24.7M
NIA NIH HHS P30 AG072975
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a secondary tauopathy characterized by the accumulation of aggregated amyloid-beta (Aβ) peptides as extracellular neuritic and diffuse plaques, alongside hyperphosphorylated tau aggregates forming intracellular neurofibrillary tangles (NFTs). Although NFT pathology is strongly linked to neurodegeneration and cognitive decline in AD, growing evidence suggests that soluble "pretangle" aggregates of tau, formed prior to NFT development, are the primary neurotoxic species driving disease progression and cognitive impairment. We quantified pretangle tau moieties in postmortem tissues of the default mode network (DMN), a resting state connectome that mediates episodic memory and falters early in AD, to determine the association between DMN tau pathology and antemortem cognitive status. To accomplish this, we assayed postmortem fixed and frozen tissue from frontal cortex (FC), posterior cingulate cortex (PCC), and precuneus (PreC) DMN hubs obtained from participants of the Rush Religious Orders Study (RROS). Immunohistochemical and biochemical quantification was performed using site-specific tau antibodies recognizing pathological pretangle epitopes pS422 (phosphorylation at tau residue serine 422), TOC1 (tau oligomers), and TNT2 (N-terminal tau misfolding), as well as the mid-stage NFT marker TauC3 (C-terminal tau truncation). Pretangle tau profiles included neuropil threads and neuronal inclusions as early as Braak stage III, with significant increases from Braak stage IV to V across the DMN hubs. There was a step-wise increase in the pretangle markers in subjects who died with no cognitive impairment (NCI) to mild cognitive impairment (MCI) to AD. The increase in pretangle tau pathology accrual correlated with poorer antemortem neuropsychological tests, including episodic memory, semantic memory, and a global cognitive Supplementary Information: The online version contains supplementary material available at 10.1186/s44477-026-00019-y.

Indexed as

Alzheimer's diseaseCognitionDefault mode networkOligomerPretangleTau

Identifiers

PMID41695614
PMCPMC12901210

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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.