Evidence map›Paper›PMID 38400760›Full record

ArticleAnnals of neurology2024

Increased Cortical Thickness in Alzheimer's Disease.

Tony X Phan, Sheena Baratono, William Drew, Aaron M Tetreault, Michael D Fox, R Ryan Darby, Alzheimer's Disease Neuroimaging Initiative, Alzheimer's Disease Metabolomics Consortium

Open access · hybridAbstract read
In one paragraph

Article in Annals of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 3% of its field
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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

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  10. Spectral normative modeling of brain structure.medRxiv : the preprint server for health sciences · 2025
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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

8 authors at 3 institutions in 1 country.

Tony X PhanDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TN.ORCID 0000-0003-4594-7284
Sheena BaratonoCenter for Brain Circuit Therapeutics, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
William DrewCenter for Brain Circuit Therapeutics, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.ORCID 0000-0002-9178-8731
Aaron M TetreaultDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TN.
Michael D Fox *Center for Brain Circuit Therapeutics, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.ORCID 0000-0001-8848-6399
R Ryan Darby *Department of Neurology, Vanderbilt University Medical Center, Nashville, TN.ORCID 0000-0003-0326-1268
Alzheimer's Disease Neuroimaging Initiative
Alzheimer's Disease Metabolomics Consortium
Brigham and Women's Hospital · USVanderbilt University Medical Center · USAlzheimer’s Disease Neuroimaging Initiative · US

Funding

Transdiagnostic memory, mood and motor circuits in Alzheimer's and neurodegenerative diseaseR56AG069086 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI FOX, MICHAEL D · 2021 to 2021
$873k
Cognitive and Neural Mechanisms of Antisocial Behavior in Frontotemporal DementiaK23AG070320 · NIA · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DARBY, RICHARD RYAN · 2021 to 2025
$857k
Alzheimer's AssociationNIA NIH HHS K23 AG070320NIA NIH HHS R56 AG069086NIH HHS 1K23AG070320-01A1NIH HHS R56AG069086
6 · The paper itself

Abstract

objectivePatients with Alzheimer's disease (AD) have diffuse brain atrophy, but some regions, such as the anterior cingulate cortex (ACC), are spared and may even show increase in size compared to controls. The extent, clinical significance, and mechanisms associated with increased cortical thickness in AD remain unknown. Recent work suggested neural facilitation of regions anticorrelated to atrophied regions in frontotemporal dementia. Here, we aim to determine whether increased thickness occurs in sporadic AD, whether it relates to clinical symptoms, and whether it occur in brain regions functionally connected to-but anticorrelated with-locations of atrophy.

methodsCross-sectional clinical, neuropsychological, and neuroimaging data from the Alzheimer's Disease Neuroimaging Initiative were analyzed to investigate cortical thickness in AD subjects versus controls. Atrophy network mapping was used to identify brain regions functionally connected to locations of increased thickness and atrophy.

resultsAD patients showed increased thickness in the ACC in a region-of-interest analysis and the visual cortex in an exploratory analysis. Increased thickness in the left ACC was associated with preserved cognitive function, while increased thickness in the left visual cortex was associated with hallucinations. Finally, we found that locations of increased thickness were functionally connected to, but anticorrelated with, locations of brain atrophy (r = -0.81, p < 0.05).

interpretationOur results suggest that increased cortical thickness in Alzheimer's disease is relevant to AD symptoms and preferentially occur in brain regions functionally connected to, but anticorrelated with, areas of brain atrophy. Implications for models of compensatory neuroplasticity in response to neurodegeneration are discussed. ANN NEUROL 2024;95:929-940.

Indexed as

Alzheimer DiseaseAtrophyMagnetic Resonance ImagingAgedAged, 80 and overBrain Cortical ThicknessCerebral CortexCross-Sectional StudiesFemaleGyrus CinguliHumansMaleMiddle Aged

Identifiers

PMID38400760
PMCPMC11060923
OpenAlexW4392120347

What OpenQuestion holds

Textmetadata
LicenceTDM
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.