Evidence map›Paper›PMID 37812536›Full record

ArticleIEEE journal of biomedical and health informatics2023

Deeply Accelerated Arterial Spin Labeling Perfusion MRI for Measuring Cerebral Blood Flow and Arterial Transit Time.

Yiran Li, Ze Wang

Abstract read
In one paragraph

Article in IEEE journal of biomedical and health informatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Advances in artificial intelligence for neuroimaging.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2026
    Review
  2. Article
  3. 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

2 authors.

Yiran Li
Ze Wang

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
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
Assessing chronic pain using brain entropy mappingR21AG082345 · NIA · UNIVERSITY OF MARYLAND BALTIMORE · PI WANG, ZE · 2022 to 2022
$442k
NCATS NIH HHS UL1 TR003098NIA NIH HHS R01 AG060054NIA NIH HHS R01 AG070227NIA NIH HHS R21 AG080518NIA NIH HHS R21 AG082345NIBIB NIH HHS P41 EB029460NIBIB NIH HHS R01 EB031080
6 · The paper itself

Abstract

Cerebral blood flow (CBF) indicates both vascular integrity and brain function. Regional CBF can be non-invasively measured with arterial spin labeling (ASL) perfusion MRI. By repeating the same ASL MRI sequence several times, each with a different post-labeling delay (PLD), another important neurovascular index, the arterial transit time (ATT) can be estimated by fitting the acquired ASL signal to a kinetic model. This process however faces two challenges: one is the multiplicatively prolonged scan time, making it impractically for clinical use due to the escalated risk of motions; the other is the reduced signal-to-noise-ratio (SNR) in the long PLD scans due to the T1 decay of the labeled spins. Increasing SNR needs more repetitions which will further increase the total scan time. Currently, there lacks a way to accurately estimate ATT from a parsimonious number of PLDs. In this paper, we proposed a deep learning-based algorithm to reduce the number of PLDs and to accurately estimate ATT and CBF. Two separate deep networks were trained: one is designed to estimate CBF and ATT from ASL data with a single PLD; the other is to estimate CBF and ATT from ASL data with two PLDs. The models were trained and tested using the large Human Connectome Project multiple-PLD ASL MRI. Performance of the DL-based approach was compared to the traditional full dataset-based data fitting approach. Our results showed that ATT and CBF can be reliably estimated using deep networks even with one PLD.

Indexed as

Cerebrovascular CirculationMagnetic Resonance ImagingBrainHumansMotionPerfusionSignal-To-Noise RatioSpin LabelsSpin Labels

Identifiers

PMID37812536
PMCPMC10841663

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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.