Evidence map›Paper›PMID 39148028›Full record

ArticleBMC medical imaging2024

A radiomics nomogram based on multiparametric MRI for diagnosing focal cortical dysplasia and initially identifying laterality.

Shi-Qi Chen, Liang Wei, Keng He, Ya-Wen Xiao, Zhao-Tao Zhang, Jian-Kun Dai, Ting Shu, Xiao-Yu Sun, Di Wu, Yi Luo and 2 more

Abstract read
In one paragraph

Article in BMC medical imaging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

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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.

Shi-Qi ChenDepartment of Radiology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, China.
Liang WeiDepartment of Pediatrics, The Affiliated Hospital of Jinggangshan University, Jinggangshan, Jiangxi Province, China.
Keng HeDepartment of Radiology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, China.
Ya-Wen XiaoDepartment of Radiology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, China.
Zhao-Tao ZhangDepartment of Radiology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, China.
Jian-Kun DaiGE Healthcare, MR Research China, Beijing, China.
Ting ShuDepartment of Radiology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, China.
Xiao-Yu SunDepartment of Radiology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, China.
Di WuDepartment of Radiology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, China.
Yi LuoDepartment of Radiology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, China.
Yi-Fei GuiDepartment of Radiology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, China.
Xin-Lan XiaoDepartment of Radiology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, China. jx_xiaoxinlan@sina.com.

Funding

youth research project of Jiangxi science and technology department 20171BAB215049
6 · The paper itself

Abstract

backgroundFocal cortical dysplasia (FCD) is the most common epileptogenic developmental malformation. The diagnosis of FCD is challenging. We generated a radiomics nomogram based on multiparametric magnetic resonance imaging (MRI) to diagnose FCD and identify laterality early.

methodsForty-three patients treated between July 2017 and May 2022 with histopathologically confirmed FCD were retrospectively enrolled. The contralateral unaffected hemispheres were included as the control group. Therefore, 86 ROIs were finally included. Using January 2021 as the time cutoff, those admitted after January 2021 were included in the hold-out set (n = 20). The remaining patients were separated randomly (8:2 ratio) into training (n = 55) and validation (n = 11) sets. All preoperative and postoperative MR images, including T1-weighted (T1w), T2-weighted (T2w), fluid-attenuated inversion recovery (FLAIR), and combined (T1w + T2w + FLAIR) images, were included. The least absolute shrinkage and selection operator (LASSO) was used to select features. Multivariable logistic regression analysis was used to develop the diagnosis model. The performance of the radiomic nomogram was evaluated with an area under the curve (AUC), net reclassification improvement (NRI), integrated discrimination improvement (IDI), calibration and clinical utility.

resultsThe model-based radiomics features that were selected from combined sequences (T1w + T2w + FLAIR) had the highest performances in all models and showed better diagnostic performance than inexperienced radiologists in the training (AUCs: 0.847 VS. 0.664, p = 0.008), validation (AUC: 0.857 VS. 0.521, p = 0.155), and hold-out sets (AUCs: 0.828 VS. 0.571, p = 0.080). The positive values of NRI (0.402, 0.607, 0.424) and IDI (0.158, 0.264, 0.264) in the three sets indicated that the diagnostic performance of Model-Combined improved significantly. The radiomics nomogram fit well in calibration curves (p > 0.05), and decision curve analysis further confirmed the clinical usefulness of the nomogram. Additionally, the contrast (the radiomics feature) of the FCD lesions not only played a crucial role in the classifier but also had a significant correlation (r = -0.319, p < 0.05) with the duration of FCD.

conclusionThe radiomics nomogram generated by logistic regression model-based multiparametric MRI represents an important advancement in FCD diagnosis and treatment.

Indexed as

Focal Cortical DysplasiaMultiparametric Magnetic Resonance ImagingNomogramsRadiomicsAdolescentAdultChildChild, PreschoolFemaleFunctional LateralityHumansMaleRetrospective StudiesYoung AdultEpilepsyFCDNomogramPrecision medicineRadiomics

Identifiers

PMID39148028
PMCPMC11325615

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LicenceCC BY-NC-ND
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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.