Evidence map›Paper›PMID 36258783›Full record

ArticleNeuroimage. Reports2022

Harmonization of Multi-Center Diffusion Tensor Tractography in Neonates with Congenital Heart Disease: Optimizing Post-Processing and Application of ComBat.

Benjamin Meyers, Vincent K Lee, Lauren Dennis, Julia Wallace, Vanessa Schmithorst, Jodie K Votava-Smith, Vidya Rajagopalan, Elizabeth Herrup, Tracy Baust, Nhu N Tran and 6 more

Open access · goldAbstract read
In one paragraph

Article in Neuroimage. Reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. 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

16 authors at 4 institutions in 1 country.

Benjamin MeyersDepartment of Radiology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Vincent K LeeDepartment of Radiology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Lauren DennisDepartment of Radiology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Julia WallaceDepartment of Radiology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Vanessa SchmithorstDepartment of Radiology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Jodie K Votava-SmithDivision of Cardiology, Department of Pediatrics, Children's Hospital of Los Angeles and Keck School of Medicine University of Southern California, Los Angeles, CA.
Vidya RajagopalanDepartment of Radiology, Children's Hospital of Los Angeles and Keck School of Medicine University of Southern California Los Angeles, CA.
Elizabeth HerrupDepartment of Critical Care Medicine, University of Pittsburgh, Pittsburgh, PA.
Tracy BaustDepartment of Critical Care Medicine, University of Pittsburgh, Pittsburgh, PA.
Nhu N TranDivision of Cardiology, Department of Pediatrics, Children's Hospital of Los Angeles and Keck School of Medicine University of Southern California, Los Angeles, CA.
Jill HunterDepartment of Radiology, Texas Children's Hospital, Houston, TX.
Daniel J LichtDepartment of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA.
J William GaynorDepartment of Surgery, Children's Hospital of Philadelphia, Philadelphia, PA.
Dean B AndropoulosDepartment of Anesthesiology, Texas Children's Hospital, Houston, TX.
Ashok PanigrahyDepartment of Radiology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Rafael CeschinDepartment of Radiology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
University of Pittsburgh · USUniversity of Southern California · USChildren's Hospital of Philadelphia · USTexas Children's Hospital · US

Funding

Southern California Clinical and Translational Science InstituteUL1TR001855 · NCATS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Thomas A Buchanan, Michele D. Kipke · 2016 to 2026
$81.3M
SVRIII: Brain Connectome and Neurodevelopment OutcomesR01HL128818 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PANIGRAHY, ASHOK · 2015 to 2019
$3.5M
Modeling Cerebral Microbleeds and Striatal Brain Iron in Adult Congenital Heart Disease in Relationship to Differential Genetic Risk for Alzheimer DiseaseR01HL152740 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CESCHIN, RAFAEL C, GURVITZ, MICHELLE · 2020 to 2023
$2.2M
Influence of placental impairments and maternal-fetal environment on neurodevelopmental outcomes in Congenital Heart DiseaseK01HL153942 · NHLBI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI RAJAGOPALAN, VIDYA · 2020 to 2024
$735k
Longitudinal Assessment of Cerebrovascular Autoregulation (CA) and Associations to Neurodevelopmental Delays in Infants and Toddlers with and without Congenital Heart Disease (CHD)K23NR019121 · NINR · CHILDREN'S HOSPITAL OF LOS ANGELES · PI TRAN, NHU · 2021 to 2023
$497k
NCATS NIH HHS UL1 TR001855NHLBI NIH HHS K01 HL153942NHLBI NIH HHS R01 HL128818NHLBI NIH HHS R01 HL152740NINR NIH HHS K23 NR019121
6 · The paper itself

Abstract

Advanced brain imaging of neonatal macrostructure and microstructure, which has prognosticating importance, is more frequently being incorporated into multi-center trials of neonatal neuroprotection. Multicenter neuroimaging studies, designed to overcome small sample sized clinical cohorts, are essential but lead to increased technical variability. Few harmonization techniques have been developed for neonatal brain microstructural (diffusion tensor) analysis. The work presented here aims to remedy two common problems that exist with the current state of the art approaches: 1) variance in scanner and protocol in data collection can limit the researcher's ability to harmonize data acquired under different conditions or using different clinical populations. 2) The general lack of objective guidelines for dealing with anatomically abnormal anatomy and pathology. Often, subjects are excluded due to subjective criteria, or due to pathology that could be informative to the final analysis, leading to the loss of reproducibility and statistical power. This proves to be a barrier in the analysis of large multi-center studies and is a particularly salient problem given the relative scarcity of neonatal imaging data. We provide an objective, data-driven, and semi-automated neonatal processing pipeline designed to harmonize compartmentalized variant data acquired under different parameters. This is done by first implementing a search space reduction step of extracting the along-tract diffusivity values along each tract of interest, rather than performing whole-brain harmonization. This is followed by a data-driven outlier detection step, with the purpose of removing unwanted noise and outliers from the final harmonization. We then use an empirical Bayes harmonization algorithm performed at the along-tract level, with the output being a lower dimensional space but still spatially informative. After applying our pipeline to this large multi-site dataset of neonates and infants with congenital heart disease (n= 398 subjects recruited across 4 centers, with a total of n=763 MRI pre-operative/post-operative time points), we show that infants with single ventricle cardiac physiology demonstrate greater white matter microstructural alterations compared to infants with bi-ventricular heart disease, supporting what has previously been shown in literature. Our method is an open-source pipeline for delineating white matter tracts in subject space but provides the necessary modular components for performing atlas space analysis. As such, we validate and introduce Diffusion Imaging of Neonates by Group Organization (DINGO), a high-level, semi-automated framework that can facilitate harmonization of subject-space tractography generated from diffusion tensor imaging acquired across varying scanners, institutions, and clinical populations. Datasets acquired using varying protocols or cohorts are compartmentalized into subsets, where a cohort-specific template is generated, allowing for the propagation of the tractography mask set with higher spatial specificity. Taken together, this pipeline can reduce multi-scanner technical variability which can confound important biological variability in relation to neonatal brain microstructure.

Indexed as

Congenital Heart DiseaseDiffusion Tensor ImagingNeonatal Imaging

Identifiers

PMID36258783
PMCPMC9575513
OpenAlexW4283156000

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.