Xingfeng Li

Dr. Xingfeng Li

orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 January 2018 in NeuroImage: Clinical
Verified
Journal Article
Open access
XLXingfeng Li
Xingfeng Li
YXYue Xing
Yue Xing
Antonio Martin-BastidaAntonio Martin-Bastida
Antonio Martin-Bastida
PPPaola Piccini
Paola Piccini
DADorothee P. Auer
Dorothee P. Auer
Classical motor symptoms of Parkinson's disease (PD) such as tremor, rigidity, bradykinesia, and axial symptoms are graded in the Movement Disorders Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS) III. It is yet to be ascertained whether parkinsonian motor symptoms are associated with different anatomical patterns of neurodegeneration as reflected by brain grey matter (GM) alteration. This study aimed to investigate associations between motor subscores and brain GM at voxel level. High resolution structural MRI T1 scans from the Parkinson's Progression Markers Initiative (PPMI) repository were employed to estimate brain GM intensity of PD subjects. Correlations between GM intensity and total MDS-UPDRS III and its four subscores were computed. The total MDS-UPDRS III score was significantly negatively correlated bilaterally with putamen and caudate GM density. Lower anterior striatal GM intensity was significantly associated with higher rigidity subscores, whereas left-sided anterior striatal and precentral cortical GM reduction were correlated with severity of axial symptoms. No significant morphometric associations were demonstrated for tremor subscores. In conclusion, we provide evidence for neuroanatomical patterns underpinning motor symptoms in early PD.

27 November 2010 in Neuroradiology
Verified
Journal Article
Closed access
PDF file
XLXingfeng Li
Xingfeng Li
DCDamien Coyle
Damien Coyle
LMLiam Maguire
Liam Maguire
DWDavid R Watson
David R Watson
TMThomas Martin McGinnity
Thomas Martin McGinnity

8 April 2023 in Cancers
Verified
Journal Article
Open access
PDF file
XLXingfeng Li
Xingfeng Li
MDMichele Dessi
Michele Dessi
Diana MarcusDiana Marcus
Diana Marcus
JRJames Russell
James Russell
EAEric Ofori Aboagye
Eric Ofori Aboagye
ARAnd Andrea G. Rockall
And Andrea G. Rockall
Purpose: To predict deep myometrial infiltration (DMI), clinical risk category, histological type, and lymphovascular space invasion (LVSI) in women with endometrial cancer using machine learning classification methods based on clinical and image signatures from T2-weighted MR images. Methods: A training dataset containing 413 patients and an independent testing dataset consisting of 82 cases were employed in this retrospective study. Manual segmentation of the whole tumor volume on sagittal T2-weighted MRI was performed. Clinical and radiomic features were extracted to predict: (i) DMI of endometrial cancer patients, (ii) endometrial cancer clinical high-risk level, (iii) histological subtype of tumor, and (iv) presence of LVSI. A classification model with different automatically selected hyperparameter values was created. The area under the curve (AUC) of the receiver operating characteristic (ROC) curve, F1 score, average recall, and average precision were calculated to evaluate different models. Results: Based on the independent external testing dataset, the AUCs for DMI, high-risk endometrial cancer, endometrial histological type, and LVSI classification were 0.79, 0.82, 0.91, and 0.85, respectively. The corresponding 95% confidence intervals (CI) of the AUCs were [0.69, 0.89], [0.75, 0.91], [0.83, 0.97], and [0.77, 0.93], respectively. Conclusion: It is possible to classify endometrial cancer DMI, risk, histology type, and LVSI using different machine learning methods.

12 October 2024 in Laser & Photonics Reviews
Verified
Journal Article
Closed access
JSJian Shen
Jian Shen
YZYong Zhang
Yong Zhang
LZLei Zhang
Lei Zhang
Jingchi LiJingchi Li
Jingchi Li
CFChenglong Feng
Chenglong Feng
YSYikai Su
Yikai Su

2 May 2017 in Human Brain Mapping
Verified
Journal Article
Open access
PDF file
XLXingfeng Li
Xingfeng Li
YXYue Xing
Yue Xing
SSStefan T Schwarz
Stefan T Schwarz
DADorothee P. Auer
Dorothee P. Auer
The purpose of this study was to investigate local and network‐related changes of limbic grey matter in early Parkinson's disease (PD) and their inter‐relation with non‐motor symptom severity. We applied voxel‐based morphometric methods in 538 T1 MRI images retrieved from the Parkinson's Progression Markers Initiative website. Grey matter densities and cross‐sectional estimates of age‐related grey matter change were compared between subjects with early PD (n = 366) and age‐matched healthy controls (n = 172) within a regression model, and associations of grey matter density with symptoms were investigated. Structural brain networks were obtained using covariance analysis seeded in regions showing grey matter abnormalities in PD subject group. Patients displayed focally reduced grey matter density in the right amygdala, which was present from the earliest stages of the disease without further advance in mild‐moderate disease stages. Right amygdala grey matter density showed negative correlation with autonomic dysfunction and positive with cognitive performance in patients, but no significant interrelations were found with anxiety scores. Patients with PD also demonstrated right amygdala structural disconnection with less structural connectivity of the right amygdala with the cerebellum and thalamus but increased covariance with bilateral temporal cortices compared with controls. Age‐related grey matter change was also increased in PD preferentially in the limbic system. In conclusion, detailed brain morphometry in a large group of early PD highlights predominant limbic grey matter deficits with stronger age associations compared with controls and associated altered structural connectivity pattern. This provides in vivo evidence for early limbic grey matter pathology and structural network changes that may reflect extranigral disease spread in PD. Hum Brain Mapp 38:3566–3578, 2017. © 2017 The Authors Human Brain Mapping Published by Wiley Periodicals, Inc.

9 December 2022 in Journal of Magnetic Resonance Imaging
Verified
Journal Article
Open access
XLXingfeng Li
Xingfeng Li
Diana MarcusDiana Marcus
Diana Marcus
JRJames Russell
James Russell
EAEric Ofori Aboagye
Eric Ofori Aboagye
LELaura Burney Ellis
Laura Burney Ellis
ARAnd Andrea G. Rockall
And Andrea G. Rockall
Background: Determination of survival time in women with endometrial cancer using clinical features remains imprecise. Features from MRI may improve the survival estimation allowing improved treatment planning.Purpose: To identify clinical features and imaging signatures on T2‐weighted MRI that can be used in an integrated model to estimate survival time for endometrial cancer subjects.Study Type: Retrospective.Population: Four hundred thirteen patients with endometrial cancer as training (N = 330, 66.41 ± 11.42 years) and validation (N = 83, 67.60 ± 11.89 years) data and an independent set of 82 subjects as testing data (63.26 ± 12.38 years).Field Strength/Sequence: 1.5‐T and 3‐T scanners with sagittal T2‐weighted spin echo sequence.Assessment: Tumor regions were manually segmented on T2‐weighted images. Features were extracted from segmented masks, and clinical variables including age, cancer histologic grade and risk score were included in a Cox proportional hazards (CPH) model. A group least absolute shrinkage and selection operator method was implemented to determine the model from the training and validation datasets.Statistical Tests: A likelihood‐ratio test and decision curve analysis were applied to compare the models. Concordance index (CI) and area under the receiver operating characteristic curves (AUCs) were calculated to assess the model.Results: Three radiomic features (two image intensity and volume features) and two clinical variables (age and cancer grade) were selected as predictors in the integrated model. The CI was 0.797 for the clinical model (includes clinical variables only) and 0.818 for the integrated model using training and validation datasets, the associated mean AUC value was 0.805 and 0.853. Using the testing dataset, the CI was 0.792 and 0.882, significantly different and the mean AUC was 0.624 and 0.727 for the clinical model and integrated model, respectively.Data Conclusion: The proposed CPH model with radiomic signatures may serve as a tool to improve estimated survival time in women with endometrial cancer.Evidence Level: 4Technical Efficacy: Stage 2