Quantitative modeling of lenticulostriate arteries on 7-T TOF-MRA for cerebral small vessel disease.

Eur Radiol Exp

State Key Laboratory of Brain and Cognitive Science, Institute of Biophysics, Chinese Academy of Sciences, 100101, Beijing, China.

Published: November 2024

AI Article Synopsis

  • Researchers created a framework to segment and model lenticulostriate arteries using advanced MRI techniques, specifically targeting patients with CADASIL and comparing them to healthy controls.
  • The framework involves a small-patch convolutional neural network for accurate segmentation, supported by a random forest model for further analysis, with performance evaluated against manual segmentation methods.
  • Results showed that the framework achieved high accuracy in artery measurements, demonstrating better reliability than manual methods, suggesting it could be beneficial for diagnosing and studying CADASIL.

Article Abstract

Background: We developed a framework for segmenting and modeling lenticulostriate arteries (LSAs) on 7-T time-of-flight magnetic resonance angiography and tested its performance on cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) patients and controls.

Methods: We prospectively included 29 CADASIL patients and 21 controls. The framework includes a small-patch convolutional neural network (SP-CNN) for fine segmentation, a random forest for modeling LSAs, and a screening model for removing wrong branches. The segmentation performance of our SP-CNN was compared to competitive networks. External validation with different resolution was performed on ten patients with aneurysms. Dice similarity coefficient (DSC) and Hausdorff distance (HD) between each network and manual segmentation were calculated. The modeling results of the centerlines, diameters, and lengths of LSAs were compared against manual labeling by four neurologists.

Results: The SP-CNN achieved higher DSC (92.741 ± 2.789, mean ± standard deviation) and lower HD (0.610 ± 0.141 mm) in the segmentation of LSAs. It also outperformed competitive networks in the external validation (DSC 82.6 ± 5.5, HD 0.829 ± 0.143 mm). The framework versus manual difference was lower than the manual inter-observer difference for the vessel length of primary branches (median -0.040 mm, interquartile range -0.209 to 0.059 mm) and secondary branches (0.202 mm, 0.016-0.537 mm), as well as for the offset of centerlines of primary branches (0.071 mm, 0.065-0.078 mm) and secondary branches (0.072, 0.064-0.080 mm), with p < 0.001 for all comparisons.

Conclusion: Our framework for LSAs modeling/quantification demonstrated high reliability and accuracy when compared to manual labeling.

Trial Registration: NCT05902039 ( https://clinicaltrials.gov/study/NCT05902039?cond=NCT05902039 ).

Relevance Statement: The proposed automatic segmentation and modeling framework offers precise quantification of the morphological parameters of lenticulostriate arteries. This innovative technology streamlines diagnosis and research of cerebral small vessel disease, eliminating the burden of manual labeling, facilitating cohort studies and clinical diagnosis.

Key Points: The morphology of LSAs is important in the diagnosis of CSVD but difficult to quantify. The proposed algorithm achieved the performance equivalent to manual labeling by neurologists. Our method can provide standardized quantitative results, reducing radiologists' workload in cohort studies.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11538103PMC
http://dx.doi.org/10.1186/s41747-024-00512-7DOI Listing

Publication Analysis

Top Keywords

modeling lenticulostriate
8
lenticulostriate arteries
8
cadasil patients
8
competitive networks
8
networks external
8
external validation
8
primary branches
8
secondary branches
8
branches
5
quantitative modeling
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!