Evidence map›Paper›PMID 39231612›Full record

ArticleAJNR. American journal of neuroradiology2025

Quantitative Susceptibility Mapping with Source Separation in Normal Brain Development of Newborns.

MinJung Jang, Alexey V Dimov, Kushal Kapse, Jonathan Murnick, Zachary Grinspan, Alan Wu, Arindam RoyChoudhury, Yi Wang, Pascal Spincemaille, Thanh D Nguyen and 2 more

Abstract read
In one paragraph

Article in AJNR. American journal of neuroradiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Vessel segmentation forMagnetic resonance in medicine · 2026
    Article
  4. Rapid, high-resolution and distortion-freeMagnetic resonance in medicine · 2025
    Article
  5. Article
  6. 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

12 authors.

MinJung JangFrom the Department of Radiology (M.J., A.V.D., Y.W., P.S., T.D.N., Z.Z.), Weill Cornell Medicine, New York, New York.
Alexey V DimovFrom the Department of Radiology (M.J., A.V.D., Y.W., P.S., T.D.N., Z.Z.), Weill Cornell Medicine, New York, New York.
Kushal KapseInstitute for the Developing Brain (K.K., J.M., C.L.), Division of Diagnostic Imaging and Radiology, Children's National Hospital, Washington, DC.ORCID 0000-0001-8363-5404
Jonathan MurnickInstitute for the Developing Brain (K.K., J.M., C.L.), Division of Diagnostic Imaging and Radiology, Children's National Hospital, Washington, DC.ORCID 0000-0003-0582-428X
Zachary GrinspanDepartment of Pediatrics (Z.G.), Weill Cornell Medicine, New York, New York.
Alan WuDepartment of Population Health Sciences (A.W., A.R.), Weill Cornell Medicine, New York, New York.
Arindam RoyChoudhuryDepartment of Population Health Sciences (A.W., A.R.), Weill Cornell Medicine, New York, New York.
Yi WangFrom the Department of Radiology (M.J., A.V.D., Y.W., P.S., T.D.N., Z.Z.), Weill Cornell Medicine, New York, New York.ORCID 0000-0003-1404-8526
Pascal SpincemailleFrom the Department of Radiology (M.J., A.V.D., Y.W., P.S., T.D.N., Z.Z.), Weill Cornell Medicine, New York, New York.ORCID 0000-0002-8821-1341
Thanh D NguyenFrom the Department of Radiology (M.J., A.V.D., Y.W., P.S., T.D.N., Z.Z.), Weill Cornell Medicine, New York, New York.ORCID 0000-0002-1411-7694
Catherine LimperopoulosInstitute for the Developing Brain (K.K., J.M., C.L.), Division of Diagnostic Imaging and Radiology, Children's National Hospital, Washington, DC.ORCID 0000-0003-1735-0069
Zungho ZunFrom the Department of Radiology (M.J., A.V.D., Y.W., P.S., T.D.N., Z.Z.), Weill Cornell Medicine, New York, New York zuz4001@med.cornell.edu.

Funding

Clinical and Translational Science AwardUL1TR001873 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI REILLY, MUREDACH P · 2016 to 2025
$99.0M
Disparities in COVID Disease Severity and Outcomes in New York CityUL1TR002384 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI JULIANNE L IMPERATO-MCGINLEY · 2017 to 2026
$86.2M
Antecedents of Impaired Brain Development in Fetuses with Heart DiseaseR01HL116585 · NHLBI · CHILDREN'S RESEARCH INSTITUTE · PI LIMPEROPOULOS, CATHERINE · 2013 to 2017
$3.8M
Assessment of placental perfusion and oxygenation using novel MRI approaches.R01HD100012 · NICHD · WEILL MEDICAL COLL OF CORNELL UNIV · PI ZUN, ZUNGHO · 2019 to 2022
$2.4M
NCATS NIH HHS UL1 TR001873NCATS NIH HHS UL1 TR002384NHLBI NIH HHS R01 HL116585NICHD NIH HHS R01 HD100012
6 · The paper itself

Abstract

background and purposeQuantitative susceptibility mapping is an emerging method for characterizing tissue composition and studying myelination and iron deposition. However, accurate assessment of myelin and iron content in the neonate brain using this method is challenging because these 2 susceptibility sources of opposite signs (myelin, negative; iron, positive) occupy the same voxel, with minimal and comparable content in both sources. In this study, susceptibilities were measured in the healthy neonate brain using susceptibility source separation. MATERIALS AND

methodsSixty-nine healthy neonates without clinical indications were prospectively recruited for MRI. All neonates underwent gradient-echo imaging for quantitative susceptibility mapping. Positive (paramagnetic) and negative (diamagnetic) susceptibility sources were separated using additional information from R2* with linear modeling performed for the neonate brain. Average susceptibility maps were generated by normalizing all susceptibility maps to an atlas space. Mean regional susceptibility measurements were obtained in the cortical GM, WM, deep GM, caudate nucleus, putamen, globus pallidus, thalamus, and the 4 brain lobes.

resultsA total of 65 healthy neonates (mean postmenstrual age, 42.8 [SD, 2.3] weeks; 34 females) were studied. The negative susceptibility maps visually demonstrated high signals in the thalamus, brainstem, and potentially myelinated WM regions, whereas the positive susceptibility maps depicted high signals in the GM compared with all WM regions, including both myelinated and unmyelinated WM. The WM exhibited significantly lower mean positive susceptibility and significantly higher mean negative susceptibility than cortical GM and deep GM. Within the deep GM, the thalamus showed a significantly lower mean negative susceptibility than the other nuclei, and the putamen and globus pallidus showed significant associations with neonate age in positive and/or negative susceptibility. Among the 4 brain lobes, the occipital lobe showed a significantly higher mean positive susceptibility and a significantly lower mean negative susceptibility than the frontal lobe.

conclusionsThis study demonstrates regional variations and temporal changes in positive and negative susceptibilities of the neonate brain, potentially associated with myelination and iron deposition patterns in normal brain development. It suggests that quantitative susceptibility mapping with source separation may be used for early identification of delayed myelination or iron deficiency.

Indexed as

BrainBrain MappingMagnetic Resonance ImagingFemaleHumansInfant, NewbornIronMaleMyelin SheathReference ValuesReproducibility of ResultsSensitivity and SpecificityIron

Identifiers

PMID39231612
PMCPMC11878958

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.