Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Objective: To explore the potential of radiomics features derived from T2-weighted fluid-attenuated inversion recovery (T2W FLAIR) images to distinguish idiopathic Parkinson's disease (PD) patients from healthy controls (HCs).

Methods: T2W FLAIR images from 1727 subjects were retrospectively obtained from five cohorts and divided into a training set (395 PD/574 HC), an internal test set (99 PD/144 HC) and an external test set (295 PD/220 HC). Regions of interest (ROIs), including bilateral globus pallidus (GP), putamen (PU), substantia nigra (SN), and red nucleus (RN), were manually delineated. The radiomics features were extracted from ROIs. Six independent machine learning (ML) classifiers were trained on the training set, and validated on the internal and external test sets.

Results: A selection of five, two, three, and ten highly correlated diagnostic features were identified from SN, RN, GP, and PU regions, respectively. Six ML classifiers were implemented based on the combined 20 radiomics features. In the internal test cohort, the six models achieved AUC of 0.96-0.98 with the accuracy ranging from 0.80 to 0.90. In the external test cohort, the multilayer perceptron model demonstrated the highest AUC of 0.85 (95% CI: 0.80-0.89) with an accuracy of 0.78.

Conclusion: ML models based on the conventional T2W FLAIR images demonstrated promising diagnostic performance for PD and those models may serve as a basis for future investigations on PD diagnosis with the aid of ML methods.

Critical Relevance Statement: Our study confirmed that early screening of Parkinson's Disease based on the conventional T2W FLAIR images was feasible with the aid of machine learning algorithms in a large multicenter cohort and those models had certain generalization.

Key Points: Conventional head MRI is routinely performed in Parkinson's disease (PD) but exhibits inadequate specificity for diagnosis. Machine learning (ML) models based on conventional T2W FLAIR images showed favorable accuracy for PD diagnosis. ML algorithm enables early screening of PD on routine T2W FLAIR sequence.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12033128PMC
http://dx.doi.org/10.1186/s13244-025-01961-3DOI Listing

Publication Analysis

Top Keywords

t2w flair
24
flair images
20
parkinson's disease
16
machine learning
16
early screening
12
radiomics features
12
external test
12
based conventional
12
conventional t2w
12
screening parkinson's
8

Similar Publications

To assess amide proton transfer weighted (APTw) MR imaging capabilities in differentiating high-grade glial tumors across alpha-thalassemia/mental retardation X-linked (ATRX) expression, tumor-suppressor protein p53 expression (p53), O6-methylguanine-DNA methyltransferase promoter (MGMTp) methylation, isocitrate dehydrogenase (IDH) status, and proliferation marker Ki-67 (Ki-67 index) as a preoperative diagnostic aid. A total of 42 high-grade glioma WHO grade 4 (HGG) patients were evaluated prospectively (30 males and 12 females). All patients were examined using conventional MRI, including the following: T1w-MPRAGE pre- and post-contrast administration, conventional T2w and 3D FLAIR, and APTw imaging with a 3T MR scanner.

View Article and Find Full Text PDF

Classification of glioma grade and Ki-67 level prediction in MRI data: A SHAP-driven interpretation.

Comput Med Imaging Graph

September 2025

Center for Magnetic Resonance Research, University of Illinois Chicago, Chicago, 60612, IL, USA; Department of Biomedical Engineering, University of Illinois Chicago, Chicago, 60607, IL, USA; Departments of Radiology and Neurosurgery, University of Illinois College of Medicine at Chicago, Chicago, 6

This study focuses on artificial intelligence-driven classification of glioma and Ki-67 leveling using T2w-FLAIR MRI, exploring the association of Ki-67 biomarkers with deep learning (DL) features through explainable artificial intelligence (XAI) and SHapley Additive exPlanations (SHAP). This IRB-approved study included 101 patients with glioma brain tumor acquired MR images with the T2W-FLAIR sequence. We extracted DL bottleneck features using ResNet50 from glioma MR images.

View Article and Find Full Text PDF

Introduction And Importance: Progressive multifocal leukoencephalopathy (PML) is a rare demyelinating disease of the central nervous system caused by substantial damage to oligodendrocytes. It clinically presents as movement impairment, cognitive disability, language aphasia, dysarthria, and visual impairments. It was first identified in 1958.

View Article and Find Full Text PDF

Objectives: Evaluating response to epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) is crucial in non-small cell lung cancer (NSCLC) patients with brain metastases (BM). To explore values of multi-sequence MRI in early assessing response to EGFR-TKIs in non-small cell lung cancer (NSCLC) patients with BM.

Approach: A primary cohort of 133 patients (January 2018 to March 2024) from center one and an external cohort of 52 patients (May 2017 to December 2022) from center two were established.

View Article and Find Full Text PDF

Deep Learning Auto-segmentation of Diffuse Midline Glioma on Multimodal Magnetic Resonance Images.

J Imaging Inform Med

May 2025

Biomedical Imaging Research Group (GIBI230), Instituto de Investigación Sanitaria La Fe, Av. Fernando Abril Martorell, 106 Torre A, Planta 7ª, Despacho 7.22, Valencia, 46026, Spain.

Diffuse midline glioma (DMG) H3 K27M-altered is a rare pediatric brainstem cancer with poor prognosis. To advance the development of predictive models to gain a deeper understanding of DMG, there is a crucial need for seamlessly integrating automatic and highly accurate tumor segmentation techniques. There is only one method that tries to solve this task in this cancer; for that reason, this study develops a modified CNN-based 3D-Unet tool to automatically segment DMG in an accurate way in magnetic resonance (MR) images.

View Article and Find Full Text PDF