Evidence map›Paper›PMID 30828660›Full record

ArticleHeliyon2019

Robust, atlas-free, automatic segmentation of brain MRI in health and disease.

Kartiga Selvaganesan, Emily Whitehead, Paba M DeAlwis, Matthew K Schindler, Souheil Inati, Ziad S Saad, Joan E Ohayon, Irene C M Cortese, Bryan Smith, Steven Jacobson and 4 more

Open access · goldAbstract read
In one paragraph

Article in Heliyon, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

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  15. Leptomeningeal enhancement in multiple sclerosis demonstrates posterior predilection and TMultiple sclerosis journal - experimental, translational and clinical
    Article
  16. High-Field-Blinded Assessment of Portable Ultra-Low-Field Brain MRI for Multiple Sclerosis.Journal of neuroimaging : official journal of the American Society of Neuroimaging
    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

14 authors at 2 institutions in 1 country.

Kartiga SelvaganesanNational Institute of Neurological Disorders and Stroke (NINDS), Bethesda, MD, 20893, USA.
Emily WhiteheadNational Institute of Neurological Disorders and Stroke (NINDS), Bethesda, MD, 20893, USA.
Paba M DeAlwisNational Institute of Neurological Disorders and Stroke (NINDS), Bethesda, MD, 20893, USA.
Matthew K SchindlerNational Institute of Neurological Disorders and Stroke (NINDS), Bethesda, MD, 20893, USA.
Souheil InatiInati Analytics, Potomac, MD 20854, USA.
Ziad S SaadNational Institute of Mental Health, National Institutes of Health, Bethesda, MD, 20893, USA.
Joan E OhayonNational Institute of Neurological Disorders and Stroke (NINDS), Bethesda, MD, 20893, USA.
Irene C M CorteseNational Institute of Neurological Disorders and Stroke (NINDS), Bethesda, MD, 20893, USA.
Bryan SmithNational Institute of Neurological Disorders and Stroke (NINDS), Bethesda, MD, 20893, USA.
Steven JacobsonNational Institute of Neurological Disorders and Stroke (NINDS), Bethesda, MD, 20893, USA.
Avindra NathNational Institute of Neurological Disorders and Stroke (NINDS), Bethesda, MD, 20893, USA.
Daniel S ReichNational Institute of Neurological Disorders and Stroke (NINDS), Bethesda, MD, 20893, USA.
Sara InatiNational Institute of Neurological Disorders and Stroke (NINDS), Bethesda, MD, 20893, USA.
Govind NairNational Institute of Neurological Disorders and Stroke (NINDS), Bethesda, MD, 20893, USA.
National Institute of Neurological Disorders and Stroke · USNational Institutes of Health · US

Funding

Multimodal MRI in Multiple SclerosisZIANS003119 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI REICH, DANIEL · 2010 to 2025
$53.4M
6 · The paper itself

Abstract

backgroundBrain- and lesion-volumes derived from magnetic resonance images (MRI) serve as important imaging markers of disease progression in neurodegenerative diseases and aging. While manual segmentation of these volumes is both tedious and impractical in large cohorts of subjects, automated segmentation methods often fail in accurate segmentation of brains with severe atrophy or high lesion loads. The purpose of this study was to develop an atlas-free brain Classification using DErivative-based Features (C-DEF), which utilizes all scans that may be acquired during the course of a routine MRI study at any center.

methodsProton-density, T

resultsC-DEF algorithm was optimized using leave-one-out cross validation on five healthy subjects (age 36 ± 11 years), and five subjects infected with HIV (age 57 ± 2.6 years) in cohort one. The optimized C-DEF algorithm outperformed FreeSurfer and Lesion-TOADS segmentation in 49 other subjects infected with HIV (cohort two, age 54 ± 6 years) in qualitative and quantitative comparisons. Although trained only on HIV brains, sensitivity to detect lesions using C-DEF increased by 45% in HTLV-I-associated myelopathy/tropical spastic paraparesis (n = 5; age 58 ± 7 years), 33% in multiple sclerosis (n = 5; 42 ± 9 years old), and 4% in subjects with polymorphism of the cytotoxic T-lymphocyte-associated protein 4 gene (n = 5; age 24 ± 12 years) compared to Lesion-TOADS.

conclusionC-DEF outperformed other segmentation algorithms in the various neurological diseases explored herein, especially in lesion segmentation. While the results reported are from routine images acquired at the NIH, the algorithm can be easily trained and optimized for any set of contrasts and protocols for wider application. We are currently exploring various technical aspects of optimal implementation of CDEF in a clinical setting and evaluating a larger cohort of patients with other neurological diseases. Improving the accuracy of brain segmentation methodology will help better understand the relationship of imaging abnormalities to clinical and neuropsychological markers in disease.

Indexed as

Medical imaging

Identifiers

PMID30828660
PMCPMC6383003
OpenAlexW2916497546

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.