Evidence map›Paper›PMID 42649843›Full record

ArticleBioengineering (Basel, Switzerland)2026

Estimation of Blood Velocity from TOF-MRA Arterial Centerlines: Theory, Simulation, and Inverse Solution.

Abrar Faiyaz, Md Nasir Uddin, Giovanni Schifitto

Abstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 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
0cells of the map it votes in
0citing 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

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.

Abrar FaiyazDepartment of Neurology, University of Rochester, Rochester, NY 14609, USA.ORCID 0000-0003-0666-3051
Md Nasir UddinDepartment of Neurology, University of Rochester, Rochester, NY 14609, USA.ORCID 0000-0002-5887-1322
Giovanni SchifittoDepartment of Neurology, University of Rochester, Rochester, NY 14609, USA.ORCID 0000-0002-2115-4143

Funding

Brain signature of SARS-CoV-2 Infection and its impact on long-term cognitive functioning in older adultsR01AG077156 · NIA · UNIVERSITY OF ROCHESTER · PI GIOVANNI SCHIFITTO · 2022 to 2026
$3.7M
Automated Machine Learning-Based Brain Artery Segmentation, Anatomical Prior Labeling, and Feature Extraction on MR AngiographyR03NS134395 · NINDS · UNIVERSITY OF ROCHESTER · PI UDDIN, MD NASIR · 2023 to 2023
$154k
NIA NIH HHS R01 AG077156NIA NIH HHS R01AG077156-01A1NINDS NIH HHS R03 NS134395NINDS NIH HHS R03NS134395-01
6 · The paper itself

Abstract

Time-of-flight magnetic resonance angiography (TOF-MRA) is widely used for noninvasive visualization of arterial anatomy, but extracting hemodynamics like blood velocity typically requires supplementary phase-contrast scans, tagging or multi-TE images. This study proposes a novel, physics-informed computational framework to extract variable fluid velocity directly from standard TOF-MRA signal profiles. We analytically expand the approach-to-steady-state Bloch equations to include convective flow, establishing a mathematical relationship between the spatial decay of longitudinal magnetization and fluid velocity. The velocity derivation was further extended to pointwise estimation over a 1-D centerline, overcoming the limitations of constant-velocity assumptions. To validate and solve this problem, a MATLAB (R2025b) simulation framework was developed to model fluid flow in two variable-geometry flowing tube cases, i.e., continuous narrowing and focal stenosis, under synthetic scanner noise. A global inverse optimization approach utilizing Dual-Tikhonov regularization was applied to stably invert the ill-posed transit time integral, actively penalizing high-frequency numerical ringing while preserving structural curves. The computational simulations successfully recovered ground-truth point-wise velocities, tracking gradual hemodynamic accelerations and sharp stenotic jets. This theoretical framework and the example centerline TOF-MRA signal intensity provide a robust mathematical proof-of-concept that quantitative, localized functional hemodynamic metrics can be extracted from standard structural MRA imaging, establishing a foundation for advanced flow quantification without requiring additional scan time.

Indexed as

ArteryXbloch equationsblood velocitycerebrovascular morphometrycomputational hemodynamicsCSVDTOF-MRA

Identifiers

PMID42649843
PMCPMC13509243

What OpenQuestion holds

Textmetadata
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.