Evidence map›Paper›PMID 41820226›Full record

ArticleMagnetic resonance in medicine2026

Double Asymmetric Spin Echo EPI (dASE-EPI) Enables fMRI of the Entire Rat Brain at 9.4 T.

Kyle A Johnson, Hanbing Lu, Jason W Sidabras

Abstract read
In one paragraph

Article in Magnetic resonance in medicine, 2026. 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
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0citing papers in PubMed
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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

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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

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

3 authors.

Kyle A JohnsonDepartment of Biophysics, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.ORCID 0009-0003-5227-090X
Hanbing LuNeuroimaging Research Branch, National Institute on Drug Abuse, National Institutes of Health, Baltimore, Maryland, USA.ORCID 0000-0003-0469-4321
Jason W SidabrasDepartment of Biophysics, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.ORCID 0000-0002-4537-7501

Funding

NIH HHS 5R01GM149568-03
6 · The paper itself

Abstract

purposeDevelopment and evaluation of a double asymmetric spin echo planar imaging (dASE-EPI) sequence to balance sensitivity to blood oxygenation level-dependent (BOLD) contrast with mitigation of susceptibility-induced intravoxel spin dephasing in ultra high-field rodent brain imaging.

methodsA dASE-EPI pulse sequence was implemented and resting-state BOLD fMRI was acquired in the rat brain. Data acquired with dASE-EPI were compared to conventional gradient-recalled EPI. Functional connectivity analyses were performed to assess detection of established networks and to evaluate signal recovery in regions affected by susceptibility (e.g., amygdala, hypothalamic nuclei).

resultsdASE-EPI was found to provide BOLD sensitivity that was non-inferior to conventional GRE-EPI while substantially reducing susceptibility-related signal loss. Established functional networks including the bilateral insular, bilateral sensory, and default mode network were reliably detected with dASE-EPI. Functional connectivity of the amygdala, which was obscured in GRE-EPI, was recoverable with the proposed sequence.

conclusionThe proposed dASE-EPI pulse sequence is a viable solution when studying brain regions which suffer from severe susceptibility artifacts.

Indexed as

BrainBrain MappingEcho-Planar ImagingImage Processing, Computer-AssistedMagnetic Resonance ImagingAlgorithmsAnimalsMaleRatsRats, Sprague-DawleyamygdalaBOLDfunctional connectivitysusceptibility

Identifiers

PMID41820226
PMCPMC13156424

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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.