Evidence map›Paper›PMID 41256114›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Arachnoid Granulation Morphologies Associate with β-Amyloid and Tau Pathology in Older Adults.

Rashi I Mehta, Tianhao Wang, Aubrey Lewis, Claire E Walker, Caroline Gebczak, Lisa L Barnes, David A Bennett, Rupal I Mehta

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 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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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

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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

8 authors.

Rashi I Mehta
Tianhao Wang
Aubrey Lewis
Claire E Walker
Caroline Gebczak
Lisa L Barnes
David A Bennett
Rupal I Mehta

Funding

Arachnoid Granulation Senescence in Aging, CAA and Alzheimer's DiseaseR21AG079221 · NIA · RUSH UNIVERSITY MEDICAL CENTER · PI MEHTA, RUPAL I. · 2022 to 2022
$435k
NIA NIH HHS R21 AG079221
6 · The paper itself

Abstract

introductionArachnoid granulations (AG) enlarge with age, yet limited studies evaluate AG in neurodegeneration. Here, we investigate associations of AG morphology with Alzheimer's disease (AD) pathology.

methodsMacroscopic AG properties were systematically evaluated along dorsal postmortem brain specimens from older adults (n=882). Regression models were used to analyze their associations with AD neuropathologic indices, controlling for demographic factors.

resultsParticipants died at mean age of 90.62 (SD=6.98) years. β-amyloid (Odds ratio/OR, 0.79 [95% CI, 0.66-0.95]) and neurofibrillary tangles (OR, 0.84 [95% CI, 0.71-0.98]) inversely associated with global AG count. Similarly, β-amyloid (OR, 0.78 [95% CI, 0.65-0.92]) and B (Braak) score (OR, 0.80 [95% CI, 0.66-0.96]) inversely associated with global AG patch count. DISCUSSION: β-amyloid and tau pathology are associated with AG morphologies. Future studies should explore the mechanisms underlying these associations across disease stage and demographic factors.

Identifiers

PMID41256114
PMCPMC12622154

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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.