Evidence map›Paper›PMID 30940494›Full record

ArticleMagnetic resonance imaging2019

Multivariate MR biomarkers better predict cognitive dysfunction in mouse models of Alzheimer's disease.

Alexandra Badea, Natalie A Delpratt, R J Anderson, Russell Dibb, Yi Qi, Hongjiang Wei, Chunlei Liu, William C Wetsel, Brian B Avants, Carol Colton

Open access · greenAbstract read
In one paragraph

Article in Magnetic resonance imaging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  10. Likelihood ratio statistics for gene set enrichment in Alzheimer's disease pathways.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2021
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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

10 authors at 5 institutions in 2 countries.

Alexandra BadeaCenter for In Vivo Microscopy, Department of Radiology, Duke University Medical Center, Durham, NC, USA; Department of Neurology, Duke University Medical Center, Durham, NC, USA; Brain Imaging and Analysis Center, Duke University, Durham, NC, USA. Electronic address: alexandra.badea@duke.edu.
Natalie A DelprattCenter for In Vivo Microscopy, Department of Radiology, Duke University Medical Center, Durham, NC, USA.
R J AndersonCenter for In Vivo Microscopy, Department of Radiology, Duke University Medical Center, Durham, NC, USA.
Russell DibbCenter for In Vivo Microscopy, Department of Radiology, Duke University Medical Center, Durham, NC, USA.
Yi QiCenter for In Vivo Microscopy, Department of Radiology, Duke University Medical Center, Durham, NC, USA.
Hongjiang WeiInstitute for Medical Imaging Technology, School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China. Electronic address: hongjiang.wei@sjtu.edu.cn.
Chunlei LiuDepartment of Electrical Engineering and Computer Science, University of California, Berkeley, CA, USA.
William C WetselDepartment of Psychiatry and Behavioral Sciences, Cell Biology, Neurobiology, Duke University Medical Center, Durham, NC, USA.
Brian B AvantsDepartment of Radiology and Medical Imaging, University of Virginia, Charlottesville, VA, USA.
Carol ColtonDepartment of Neurology, Duke University Medical Center, Durham, NC, USA.
Duke Medical Center · USDuke University · USShanghai Jiao Tong University · CNUniversity of California, Berkeley · USUniversity of Virginia · US

Funding

INTEGRATED CENTER FOR IN VIVO MICROSCOPYP41EB015897 · NIBIB · DUKE UNIVERSITY · PI JOHNSON, GEORGE ALLAN · 2012 to 2017
$7.4M
Sex and APOE genotype interact to alter immune regulated metabolism in ADRF1AG057895 · NIA · DUKE UNIVERSITY · PI BADEA, ALEXANDRA, COLTON, CAROL ANNE · 2019 to 2019
$5.8M
Brain networks in mouse models of agingR01AG066184 · NIA · DUKE UNIVERSITY · PI BADEA, ALEXANDRA · 2019 to 2023
$3.8M
Immune-based nutrient deprivation and neurodegenerative diseaseR01AG045422 · NIA · DUKE UNIVERSITY · PI COLTON, CAROL ANNE · 2013 to 2017
$2.3M
Sex and APOE genotype interact to alter immune regulated metabolism in ADR56AG057895 · NIA · DUKE UNIVERSITY · PI BADEA, ALEXANDRA, COLTON, CAROL ANNE · 2017 to 2017
$1.1M
Quantitative MR Microscopy of Phenotypic Biomarkers in Alzheimer's DiseaseK01AG041211 · NIA · DUKE UNIVERSITY · PI BADEA, ALEXANDRA · 2014 to 2018
$642k
Immune regulated amino acid pathways in Alzheimer's DiseaseR56AG051765 · NIA · DUKE UNIVERSITY · PI COLTON, CAROL ANNE · 2016 to 2016
$623k
NIA NIH HHS K01 AG041211NIA NIH HHS R01 AG045422NIA NIH HHS R01 AG066184NIA NIH HHS R56 AG051765NIA NIH HHS R56 AG057895NIA NIH HHS RF1 AG057895NIBIB NIH HHS P41 EB015897
6 · The paper itself

Abstract

To understand multifactorial conditions such as Alzheimer's disease (AD) we need brain signatures that predict the impact of multiple pathologies and their interactions. To help uncover the relationships between pathology affected brain circuits and cognitive markers we have used mouse models that represent, at least in part, the complex interactions altered in AD, while being raised in uniform environments and with known genotype alterations. In particular, we aimed to understand the relationship between vulnerable brain circuits and memory deficits measured in the Morris water maze, and we tested several predictive modeling approaches. We used in vivo manganese enhanced MRI traditional voxel based analyses to reveal regional differences in volume (morphometry), signal intensity (activity), and magnetic susceptibility (iron deposition, demyelination). These regions included hippocampus, olfactory areas, entorhinal cortex and cerebellum, as well as the frontal association area. The properties of these regions, extracted from each of the imaging markers, were used to predict spatial memory. We next used eigenanatomy, which reduces dimensionality to produce sets of regions that explain the variance in the data. For each imaging marker, eigenanatomy revealed networks underpinning a range of cognitive functions including memory, motor function, and associative learning, allowing the detection of associations between context, location, and responses. Finally, the integration of multivariate markers in a supervised sparse canonical correlation approach outperformed single predictor models and had significant correlates to spatial memory. Among a priori selected regions, expected to play a role in memory dysfunction, the fornix also provided good predictors, raising the possibility of investigating how disease propagation within brain networks leads to cognitive deterioration. Our cross-sectional results support that modeling approaches integrating multivariate imaging markers provide sensitive predictors of AD-like behaviors. Such strategies for mapping brain circuits responsible for behaviors may help in the future predict disease progression, or response to interventions.

Indexed as

Disease Models, AnimalMagnetic Resonance ImagingAlzheimer DiseaseAnimalsBehavior, AnimalBiomarkersBrainBrain MappingCognitionCognitive DysfunctionContrast MediaCross-Sectional StudiesDisease ProgressionFornix, BrainGenotypeHippocampusBiomarkersContrast MediaAlzheimer's diseaseBehaviorBiomarkersMagnetic resonance imagingMemoryMouse modelsMultivariate analysisPredictive modeling

Identifiers

PMID30940494
PMCPMC6859063
OpenAlexW2907163680

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.