Evidence map›Paper›PMID 40330657›Full record

ArticleProceedings. IEEE International Symposium on Biomedical Imaging2024

ADAPTIVE JOINT DATA SELECTION FOR SPARSITY BASED ARTERIAL SPIN LABELING MRI DENOISING.

Hangfan Liu, Bo Li, Yiran Li, John A Detre, Ze Wang

Abstract read
In one paragraph

Article in Proceedings. IEEE International Symposium on Biomedical Imaging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

5 authors.

Hangfan LiuUniversity of Maryland School of Medicine, Baltimore, MD 21202 USA.
Bo LiUniversity of Maryland School of Medicine, Baltimore, MD 21202 USA.
Yiran LiUniversity of Maryland School of Medicine, Baltimore, MD 21202 USA.
John A DetrePerelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104 USA.
Ze WangUniversity of Maryland School of Medicine, Baltimore, MD 21202 USA.

Funding

QAQC Johns Hopkins Institute for Clinical and Translational ResearchUL1TR003098 · NCATS · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2019 to 2023
$57.7M
High Spatial and Temporal Resolution MRI Mapping of Oxygen Consumption in HumansP41EB029460 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI Ravinder Reddy · 2021 to 2026
$7.6M
Academic Industrial Partnership on Advanced Perfusion MRIR01EB031080 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI Yulin V Chang, JOHN A DETRE · 2022 to 2026
$2.7M
Diversity Supplement to Brain entropy mapping in Alzheimer's DiseaseR01AG070227 · NIA · UNIVERSITY OF MARYLAND BALTIMORE · PI WANG, ZE · 2021 to 2024
$2.5M
Deep-Learning Enhanced ASL MRI For Early AD AssessmentR01AG081693 · NIA · UNIVERSITY OF MARYLAND BALTIMORE · PI Ze Wang · 2024 to 2026
$2.3M
Assessing ASL CBF as a biomarker for early Alzheimer's disease detection and disease progressionR01AG060054 · NIA · UNIVERSITY OF MARYLAND BALTIMORE · PI WANG, ZE · 2019 to 2021
$1.7M
Automated Quality Evaluation and Harmonization for Multisite ASL MRI DataR21AG080518 · NIA · UNIVERSITY OF PENNSYLVANIA · PI DOLUI, SUDIPTO, WANG, ZE · 2023 to 2024
$453k
NCATS NIH HHS UL1 TR003098NIA NIH HHS R01 AG060054NIA NIH HHS R01 AG070227NIA NIH HHS R01 AG081693NIA NIH HHS R21 AG080518NIBIB NIH HHS P41 EB029460NIBIB NIH HHS R01 EB031080
6 · The paper itself

Abstract

Arterial spin-labeled (ASL) perfusion MRI remains the only non-invasive, radiation-free method for quantifying regional tissue perfusion. ASL MRI computes perfusion signals from the difference of the spin-labeled images and spin-untagged control images. Limited by the T1 decay of the labeled arterial blood, ASL MRI signal is subject to a low signal-to-noise ratio. This issue is particularly vexing due to the absence of ground truth and the difficulty in preserving image textures amidst substantial noise reduction efforts. One major avenue for tackling this challenge involves leveraging the sparsity of image signals, a technique widely employed in unsupervised image denoising. Compared to global models operating at the slice level, enhanced local sparse models not only improve the separation of signal from noise but also preserves local structures more effectively. This paper introduces a joint data selection strategy tailored for ASL denoising, which capitalizes on the strong correlation between paired label and control (L/C) images to identify and assemble highly correlated content, forming potentially sparse matrices. The application of sparsity regularization to these matrices is inherently more adaptive to local structures. Crucially, the proposed method does not rely on any ground-truth training data. In real-world testing with an ASL MRI dataset, the proposed approach remarkably enhances the quality of ASL perfusion maps, utilizing only a single pair of L/C images, and outperforms the conventional pipeline that necessitates multiple L/C pairs.

Indexed as

Arterial spin labeling (ASL) perfusiondenoisingMRIsparse representation

Identifiers

PMID40330657
PMCPMC12053564

What OpenQuestion holds

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Registered trials

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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.