Evidence map›Paper›PMID 42233513›Full record

ArticleJournal of magnetic resonance imaging : JMRI2026

A Data-Driven Normalization Framework for Subject-Specific Cerebrovascular Reactivity Assessment in Cerebrovascular Disease.

Yihui Zhu, Siddhant Dogra, Xiuyuan Wang, Jonathan R Polimeni, Seena Dehkharghani

Abstract read
In one paragraph

Article in Journal of magnetic resonance imaging : JMRI, 2026. 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.

Yihui ZhuDepartment of Radiology, Stanford University School of Medicine, Palo Alto, California, USA.ORCID https://orcid.org/0009-0003-3987-6624
Siddhant DograDepartment of Radiology, New York University Grossman School of Medicine, New York, New York, USA.ORCID https://orcid.org/0000-0003-2386-7849
Xiuyuan WangDepartment of Radiology, Weill Cornell Medical College, New York, New York, USA.
Jonathan R PolimeniDepartment of Radiology, Stanford University School of Medicine, Palo Alto, California, USA.
Seena DehkharghaniDepartment of Radiology, Stanford University School of Medicine, Palo Alto, California, USA.ORCID https://orcid.org/0000-0002-3141-1094

Funding

TR&D 4: Revealing Microstructure: Biophysical modeling and validation for discovery and clinical careP41EB017183 · NIBIB · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Daniel K Sodickson · 2014 to 2026
$19.3M
Random Matrix Theory-Based Noise Removal in MRIR01EB027075 · NIBIB · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI FIEREMANS, ELS, NOVIKOV, DMITRY S · 2019 to 2022
$2.7M
NIBIB NIH HHS P41 EB017183NIBIB NIH HHS P41EB017183NIBIB NIH HHS R01 EB027075NIBIB NIH HHS R01EB027075
6 · The paper itself

Abstract

backgroundAssessment of cerebrovascular reactivity (CVR) has been reported using acetazolamide-augmented blood oxygenation level-dependent (BOLD) MRI; however, wide intersubject baseline variability can complicate interpretation. PURPOSE: To develop an integrated normalization framework combining machine learning-guided identification of healthy voxels for subject-specific baseline rescaling with atlas-based assessment. STUDY TYPE: Retrospective. POPULATION: 26 subjects (age 51 ± 13 at first scan, 50% women, 34 exams) with unilateral steno-occlusive disease (SOD) and 9 subjects with bilateral disease (age 55 ± 12, 4/9 women) underwent acetazolamide-augmented BOLD-MRI. FIELD STRENGTH/SEQUENCE: T1-weighted MPRAGE (1 mm isotropic) and gradient-echo EPI at 3 T. ASSESSMENT: Machine learning models (random forest, XGBoost, LightGBM, and neural networks) were trained to identify healthy candidate voxels using a previously reported pipeline based on baseline resting-state BOLD temporal shift features derived from 32 arterial territories. A healthy reference CVR atlas was constructed from unaffected hemispheres. Individual CVR maps were rescaled using predicted healthy voxels and converted to Z-scores and risk index maps using the reference atlas. STATISTICAL TESTS: Coefficient of variation (CV) within normal hemispheres, lesion contrast-to-noise ratio (CNR), Lesion ROC AUC, asymmetry index (AI) in unilateral patients, and chi-square distance between thresholded normal and abnormal CVR distributions across all patients were compared between atlas-based group normalization alone and the proposed integrated normalization using paired t-tests. (cutoff p = 0.05).

resultsCV within normal hemispheres significantly decreased (1.07 ± 0.15 vs. 0.45 ± 0.09), indicating improved inter-subject stability. Lesion CNR and ROC AUC improved across all impairment thresholds (CNR: 0.73-1.12 vs. 0.79-1.19; AUC: 0.76-0.89 vs. 0.81-0.90). AI increased significantly at higher risk thresholds (≥ 0.78), with no significant difference at the lowest threshold (p = 0.181). Chi-square analysis demonstrated significantly increased separation between CVR distributions at intermediate thresholds. DATA

conclusionThe proposed integrated normalization improves the stability, discriminability, and interpretability of acetazolamide-augmented BOLD-CVR for detection of cerebrovascular impairment. EVIDENCE LEVEL: 3. TECHNICAL EFFICACY: Stage 2.

Indexed as

BrainCerebrovascular CirculationCerebrovascular DisordersMagnetic Resonance ImagingAcetazolamideAdultAgedBoosting Machine Learning AlgorithmsFemaleHumansImage Interpretation, Computer-AssistedImage Processing, Computer-AssistedMachine LearningMaleMiddle AgedOxygenAcetazolamideOxygenacetazolamideBOLD MRIcerebrovascular reactivitynormalizationsteno‐occlusive diseasestroke

Identifiers

PMID42233513
PMCPMC13466569

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.