Evidence map›Paper›PMID 38260648›Full record

ArticlemedRxiv : the preprint server for health sciences2024

Psychotic symptoms are associated with elevated tau PET signal in the amygdala independent of Alzheimer's disease clinical severity and amyloid burden.

Aubrey S Johnson, Galen Ziaggi, Anna C Smith, Hannah Houlihan, Lauren B Heuer, Diana S Guzmán, Amarachukwu Okafor, Edward D Huey, Daniel Talmasov, Frank Provenzano and 3 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 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, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Aubrey S JohnsonTaub Institute for Research on Alzheimer's disease and the Aging Brain, Gertrude H. Sergievsky Center, Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032.ORCID 0000-0002-0111-4128
Galen ZiaggiTaub Institute for Research on Alzheimer's disease and the Aging Brain, Gertrude H. Sergievsky Center, Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032.
Anna C SmithTaub Institute for Research on Alzheimer's disease and the Aging Brain, Gertrude H. Sergievsky Center, Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032.
Hannah HoulihanTaub Institute for Research on Alzheimer's disease and the Aging Brain, Gertrude H. Sergievsky Center, Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032.
Lauren B HeuerTaub Institute for Research on Alzheimer's disease and the Aging Brain, Gertrude H. Sergievsky Center, Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032.
Diana S GuzmánTaub Institute for Research on Alzheimer's disease and the Aging Brain, Gertrude H. Sergievsky Center, Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032.
Amarachukwu OkaforTaub Institute for Research on Alzheimer's disease and the Aging Brain, Gertrude H. Sergievsky Center, Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032.
Edward D HueyDepartment of Psychiatry and Human Behavior, Alpert Medical School of Brown University, Providence, RI 02906.
Daniel TalmasovDepartments of Neurology and Psychiatry, Columbia University Irving Medical Center, New York, NY 10032.ORCID 0000-0002-4179-1713
Frank ProvenzanoTaub Institute for Research on Alzheimer's disease and the Aging Brain, Gertrude H. Sergievsky Center, Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032.
William C KreislTaub Institute for Research on Alzheimer's disease and the Aging Brain, Gertrude H. Sergievsky Center, Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032.
Patrick J LaoTaub Institute for Research on Alzheimer's disease and the Aging Brain, Gertrude H. Sergievsky Center, Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032.
Alzheimer’s Disease Neuroimaging Initiative
Columbia University Irving Medical Center · USBrown University · US

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
Research Education CoreP30AG066462 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PHILIP L DE JAGER · 2020 to 2026
$30.1M
Research Training in Late-Life NeuroPsychiatric DisordersT32MH020004 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Patrick J Brown · 1998 to 2026
$6.1M
Genetic basis of neuropsychiatric symptoms in Alzheimer's diseaseU01AG079850 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Gary Wayne Beecham, Edward D Huey · 2023 to 2026
$3.0M
Neuroanatomical associations with the factor structure underlying neuropsychiatric symptoms in Alzheimer's diseaseR01AG062268 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HUEY, EDWARD D · 2018 to 2022
$2.5M
Using RDoC Negative and Positive Valence Paradigms to Investigate the Mechanisms of Neuropsychiatric Symptoms (NPS) in Alzheimer's Disease and Related DementiasR01MH120794 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HUEY, EDWARD D · 2019 to 2023
$2.1M
Understanding the mechanisms linking small vessel cerebrovascular disease and Alzheimer's disease pathophysiology with neurodegeneration and cognition during midlifeR00AG065506 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LAO, PATRICK JORDAN · 2023 to 2025
$742k
NIA NIH HHS P30 AG066462NIA NIH HHS R00 AG065506NIA NIH HHS R01 AG062268NIA NIH HHS U01 AG024904NIA NIH HHS U01 AG079850NIMH NIH HHS R01 MH120794NIMH NIH HHS T32 MH020004
6 · The paper itself

Abstract

Background: Psychosis in Alzheimer's disease (AD) is associated with worse outcomes, yet no established biomarkers exist for early diagnosis and intervention. We compared tau PET burden across older individuals with and without psychotic symptoms. Methods: [ Results: Tau was greater in individuals with psychotic symptoms in the amygdala in region-of-interest analyses, and in amygdala, thalamus, putamen, right hippocampus, right entorhinal cortex, and right frontal cortex in voxel-based analyses. When considering different onset and type of psychotic symptoms, tau binding was greatest in those with concurrent delusions. Conclusion: Elevated tau in limbic regions may be relevant for psychotic symptoms in aging and AD.

Identifiers

PMID38260648
PMCPMC10802760
OpenAlexW4390837309

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.