Evidence map›Paper›PMID 40619807›Full record

ArticleBalkan medical journal2025

Tau Pathology in the Medial Temporal Lobe and Neocortex: Implications for Cognitive Unimpaired in Cognitively Unimpaired Older Adults.

İdris Demirsoy

Abstract read
In one paragraph

Article in Balkan medical journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

1 author.

İdris DemirsoyDepartment of Neurology, University of California, California, USA.ORCID 0000-0002-3321-4748

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The accumulation of proteins such as amyloid-beta and tau, which disrupt normal cellular processes, characterizes Alzheimer's disease (AD). Cognitive decline is strongly linked to tau pathology, which initially manifests in the medial temporal lobe (MTL). Aims: To investigated the association between cognitive performance and regional tau accumulation, as measured by positron emission tomography (PET) imaging, in cognitively normal older adults. Understanding this relationship is critical for early intervention before noticeable cognitive decline emerges. Study Design: Retrospective study. Methods: Tau PET scans were conducted on 440 participants enrolled in the anti-amyloid treatment in asymptomatic Alzheimer's (A4) study. The participants, aged 65-85, were cognitively unimpaired and had complete demographic and genetic profiles. Tau levels in the MTL and temporal neocortex (NEO) was quantified using composite metrics. Cognitive function was evaluated using the preclinical Alzheimer's cognitive composite (PACC) and its individual components. Multiple linear regression models were applied to determine the associations between tau burden and cognitive outcomes, including interaction terms to evaluate the moderating roles of sex and apolipoprotein E (APOE)-ε4 genotype. Results: The average participant age was 71.8 years (standard deviation = 4.84), with females comprising 58% of the sample. Greater tau accumulation in both tauMTL and tauNEO regions was significantly associated with lower cognitive scores. Specifically, reduced PACC scores ( Conclusion: Elevated tau deposition in the MTL and NEO is associated with diminished cognitive function, particularly in memory and processing speed domains. Notably, tau accumulation in the MTL showed a strong association with poorer outcomes on memory-related cognitive measures. The limited influence of sex and APOE-ε4 genotype highlights tau pathology as a key contributor to early cognitive decline in preclinical AD.

Indexed as

CognitionNeocortextau ProteinsTemporal LobeAgedAged, 80 and overAlzheimer DiseaseFemaleHumansMaleNeuropsychological TestsPositron-Emission TomographyRetrospective Studiestau Proteins

Identifiers

PMID40619807
PMCPMC12240214

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Registered trials

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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.