Evidence map›Paper›PMID 41659563›Full record

ArticlebioRxiv : the preprint server for biology2026

Spatial transcriptomics reveals brain-wide circadian disruption in an Alzheimer's disease model.

Alon Gelber, Haylie Romero, Dominic Burrows, Daniel S Whittaker, Daniel Carlin, Eran A Mukamel, Paula Desplats

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Alon GelberDepartment of Bioengineering, University of California San Diego; La Jolla, United States.ORCID 0000-0002-3776-6400
Haylie RomeroDepartment of Neuroscience, University of California San Diego; La Jolla, United States.
Dominic BurrowsDepartment of Cognitive Science, University of California San Diego; La Jolla, United States.ORCID 0000-0002-5728-1574
Daniel S WhittakerDepartment of Neuroscience, University of California San Diego; La Jolla, United States.ORCID 0000-0002-4293-5192
Daniel CarlinDepartment of Neuroscience, University of California San Diego; La Jolla, United States.
Eran A MukamelDepartment of Cognitive Science, University of California San Diego; La Jolla, United States.ORCID 0000-0003-3203-9535
Paula DesplatsDepartment of Neuroscience, University of California San Diego; La Jolla, United States.ORCID 0000-0002-4758-4280

Funding

Cell-type-specific neural circuit connectomes in the mouse models of aging and Alzheimer's diseaseU01AG076791 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI Kim Green, ERAN A MUKAMEL · 2022 to 2026
$13.6M
Circadian dysfunction and Epigenetic alterations in the pathogenesis of Alzheimer's DiseaseRF1AG061831 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DESPLATS, PAULA ALEJANDRA, WELSH, DAVID K · 2019 to 2020
$3.6M
NIA NIH HHS RF1 AG061831NIA NIH HHS U01 AG076791
6 · The paper itself

Abstract

Diurnal rhythms in brain transcription align neural, immune, and metabolic processes with the light-dark cycle and are profoundly disrupted in Alzheimer's disease (AD). However, the regional organization of diurnal transcription in the healthy and diseased brain remains poorly defined. Using large-scale spatial transcriptomics, we mapped 24-hour rhythmic transcription across cortical and subcortical regions of the mouse brain. We identified marked regional differences in rhythmicity, including distinct oscillatory signatures across cortical areas and along the rostro-caudal axis. In the APP23 mouse model of AD, pathology-vulnerable brain regions exhibited early, region-specific disruption of diurnal transcription prior to substantial amyloid plaque deposition. These findings reveal a spatially organized architecture of brain diurnal rhythms and identify early rhythmic dysregulation as a feature of Alzheimer's disease pathogenesis.

Identifiers

PMID41659563
PMCPMC12874051

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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.