Evidence map›Paper›PMID 38895308›Full record

ArticlebioRxiv : the preprint server for biology2024

Medial amygdalar tau is associated with anxiety symptoms in preclinical Alzheimer's disease.

Joyce S Li, Samantha M Tun, Bronte Ficek-Tani, Wanwan Xu, Selena Wang, Corey L Horien, Takuya Toyonaga, Shreya S Nuli, Caroline J Zeiss, Albert R Powers and 3 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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

5 · Who and what money

Authors and funding

13 authors.

Joyce S LiDepartment of Neurology, Yale School of Medicine, New Haven, CT.
Samantha M TunDepartment of Neurology, Yale School of Medicine, New Haven, CT.
Bronte Ficek-TaniUniversity of Washington School of Medicine, Seattle, WA.
Wanwan XuDepartment of Biostatistics, Yale School of Medicine, New Haven, CT.
Selena WangDepartment of Biostatistics, Yale School of Medicine, New Haven, CT.
Corey L HorienYale School of Medicine, New Haven, CT.
Takuya ToyonagaDepartment of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT.
Shreya S NuliYale University, New Haven, CT.
Caroline J ZeissDepartment of Comparative Medicine, Yale School of Medicine, New Haven, CT.
Albert R PowersDepartment of Psychiatry, Yale School of Medicine, New Haven, CT.
Yize ZhaoDepartment of Biostatistics, Yale School of Medicine, New Haven, CT.
Elizabeth C MorminoDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA.
Carolyn A FredericksDepartment of Neurology, Yale School of Medicine, New Haven, CT.ORCID 0000-0002-7051-6382

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007205 · NIGMS · YALE UNIVERSITY · PI KAZMIERCZAK, BARBARA I · 1985 to 2019
$42.9M
Yale Alzheimer Disease Research CenterP30AG066508 · NIA · YALE UNIVERSITY · PI STEPHEN M STRITTMATTER, CHRISTOPHER H VAN DYCK · 2020 to 2026
$30.2M
PREMAP - Predictors and Risk Evaluation for Menopause-Associated PsychosisR01MH131768 · NIMH · YALE UNIVERSITY · PI Albert R Powers · 2023 to 2026
$3.6M
Neural Mechanisms of Voluntary Control Over HallucinationsR01MH129721 · NIMH · YALE UNIVERSITY · PI POWERS, ALBERT R · 2022 to 2024
$2.5M
Thalamic Contributions to Functional Network Abnormalities in Alzheimer's DiseaseK23AG059919 · NIA · YALE UNIVERSITY · PI FREDERICKS, CAROLYN ANNE · 2019 to 2023
$1.0M
A Hearing Test for Hallucinations: Toward Development of Computational Markers for Early DiagnosisK23MH115252 · NIMH · YALE UNIVERSITY · PI POWERS, ALBERT R · 2018 to 2022
$983k
Toward a Computationally-Informed, Personalized Treatment for HallucinationsR21MH122940 · NIMH · YALE UNIVERSITY · PI POWERS, ALBERT R · 2020 to 2021
$404k
NIA NIH HHS K23 AG059919NIA NIH HHS P30 AG066508NIGMS NIH HHS T32 GM007205NIMH NIH HHS K23 MH115252NIMH NIH HHS R01 MH129721NIMH NIH HHS R01 MH131768NIMH NIH HHS R21 MH122940Wellcome Trust
6 · The paper itself

Abstract

backgroundWhile the amygdala receives early tau deposition in Alzheimer's disease (AD) and is involved in social and emotional processing, the relationship between amygdalar tau and early neuropsychiatric symptoms in AD is unknown. We sought to determine whether focal tau binding in the amygdala and abnormal amygdalar connectivity were detectable in a preclinical AD cohort and identify relationships between these and self-reported mood symptoms.

methodsWe examined n=598 individuals (n=347 amyloid-positive (58% female), n=251 amyloid-negative (62% female); subset into tau PET and fMRI cohorts) from the A4 Study. In our tau PET cohort, we used amygdalar segmentations to examine representative nuclei from three functional divisions of the amygdala. We analyzed between-group differences in division-specific tau binding in the amygdala in preclinical AD. We conducted seed-based functional connectivity analyses from each division in the fMRI cohort. Finally, we conducted exploratory post-hoc correlation analyses between neuroimaging biomarkers of interest and anxiety and depression scores.

resultsAmyloid-positive individuals demonstrated increased tau binding in medial and lateral amygdala (

conclusionsOur findings suggest that preclinical tau deposition in the amygdala may result in meaningful changes in functional connectivity which may predispose patients to mood symptoms.

Indexed as

amygdalaanxietydefault mode networkfunctional networkspreclinical Alzheimer’s diseasetau

Identifiers

PMID38895308
PMCPMC11185761

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.