Evidence map›Paper›PMID 30225830›Full record

ArticleBrain structure & function2018

Whole mouse brain structural connectomics using magnetic resonance histology.

Nian Wang, Robert J Anderson, Alexandra Badea, Gary Cofer, Russell Dibb, Yi Qi, G Allan Johnson

Abstract read
In one paragraph

Article in Brain structure & function, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing 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

51 citing papers in PubMed.

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  18. Merged magnetic resonance and light sheet microscopy of the whole mouse brain.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
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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

7 authors.

Nian WangCenter for In Vivo Microscopy, Department of Radiology, Duke University Medical Center, Durham, NC, USA.ORCID http://orcid.org/0000-0001-6547-8580
Robert J AndersonCenter for In Vivo Microscopy, Department of Radiology, Duke University Medical Center, Durham, NC, USA.
Alexandra BadeaCenter for In Vivo Microscopy, Department of Radiology, Duke University Medical Center, Durham, NC, USA.
Gary CoferCenter 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.
G Allan JohnsonCenter for In Vivo Microscopy, Department of Radiology, Duke University Medical Center, Durham, NC, USA. gjohnson@duke.edu.

Funding

INTEGRATED CENTER FOR IN VIVO MICROSCOPYP41EB015897 · NIBIB · DUKE UNIVERSITY · PI JOHNSON, GEORGE ALLAN · 2012 to 2017
$7.4M
Waxholm Space for Rodent NeuroinformaticsR01NS096720 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI GEE, JAMES C · 2016 to 2019
$2.4M
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
Agilent Direct Drive 9.4T MRS/MRI ConsoleS10OD010683 · OD · DUKE UNIVERSITY · PI JOHNSON, GEORGE ALLAN · 2012 to 2012
$597k
National Institute of Health 1S10OD010683-01NIA NIH HHS AG041211NIA NIH HHS K01 AG041211NIA NIH HHS R56 AG057895NIBIB NIH HHS P41 EB015897NIH HHS 1R01NS096720-01A1NIH HHS S10 OD010683NINDS NIH HHS R01 NS096720
6 · The paper itself

Abstract

Diffusion tensor histology holds great promise for quantitative characterization of structural connectivity in mouse models of neurological and psychiatric conditions. There has been extensive study in both the clinical and preclinical domains on the complex tradeoffs between the spatial resolution, the number of samples in diffusion q-space, scan time, and the reliability of the resultant data. We describe here a method for accelerating the acquisition of diffusion MRI data to support quantitative connectivity measurements in the whole mouse brain using compressed sensing (CS). The use of CS allows substantial increase in spatial resolution and/or reduction in scan time. Compared to the fully sampled results at the same scan time, the subtle anatomical details of the brain, such as cortical layers, dentate gyrus, and cerebellum, were better visualized using CS due to the higher spatial resolution. Compared to the fully sampled results at the same spatial resolution, the scalar diffusion metrics, including fractional anisotropy (FA) and mean diffusivity (MD), showed consistently low error across the whole brain (< 6.0%) even with 8.0 times acceleration. The node properties of connectivity (strength, cluster coefficient, eigenvector centrality, and local efficiency) demonstrated correlation of better than 95.0% between accelerated and fully sampled connectomes. The acceleration will enable routine application of this technology to a wide range of mouse models of neurologic diseases.

Indexed as

AnimalsBrainConnectomeDiffusion Magnetic Resonance ImagingDiffusion Tensor ImagingMaleMice, Inbred C57BLWhite MatterCompressed sensing (CS)ConnectomeDiffusion magnetic resonance imaging (dMRI)Graph theoretical analysisMagnetic resonance histology (MRH)Tractography

Identifiers

PMID30225830
PMCPMC7053251

What OpenQuestion holds

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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.