Background: Classifying T1-weighted Magnetic Resonance brain scans into cerebrospinal fluid, gray matter and white matter is one of the most critical tasks in neurodegenerative disease analysis. Since manual delineation is a labor-intensive and time-consuming process, automated methods have been widely adopted for this purpose. One group of commonly used method by biomedical researchers are based on Gaussian mixture model. The main drawbacks of this model include complex computational cost and parameter selection with the presence of imaging defects such as intensity inhomogeneity and noise.

Objective: To alleviate these aspects, an improved Gaussian mixture model-based method is proposed in this work.

Methods: Standard mixture model was used to formulate individual voxel intensity. A set of spatial weightings were created to represent local tissue characteristics. The emphasis of this method is its "lite" and robust implementation mode highlighted by a dedicated entropy term. The Expectation-Maximization algorithm was then iteratively executed to estimate model parameters. The Maximum a Posteriori criterion was employed to determine for each voxel if it belongs to a certain tissue.

Results: The proposed method was validated on both simulated and real MR scans. The averaged Dice coefficient of segmented brain tissues on each dataset ranged between [66.41, 87.42] for cerebrospinal fluid, [80.57, 85.35] for gray matter, and [83.17, 85.63] for white matter.

Conclusions: Experiments illustrated the effectiveness and reliability in tissue classification against imaging defects compared with manually constructed reference standard.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9028685PMC
http://dx.doi.org/10.3233/THC-228008DOI Listing

Publication Analysis

Top Keywords

gaussian mixture
12
mixture model
12
tissue classification
8
cerebrospinal fluid
8
gray matter
8
imaging defects
8
model
5
brain tissue
4
classification based
4
based spatial
4

Similar Publications

Simple quantitation and spatial characterization of label free cellular images.

Heliyon

December 2024

Human and Animal Physiology, Department Animal Sciences, Wageningen University, De Elst 1, 6708WD, Wageningen, the Netherlands.

Label-free imaging is routinely used during cell culture because of its minimal interference with intracellular biology and capability of observing cells over time. However, label-free image analysis is challenging due to the low contrast between foreground signals and background. So far various deep learning tools have been developed for label-free image analysis and their performance depends on the quality of training data.

View Article and Find Full Text PDF

Active transportation, such as cycling, improves mobility and general health. However, statistics reveal that in low- and middle-income countries, male and female cycling participation rates differ significantly. Existing literature highlights that women's willingness to use bicycles is significantly influenced by their perception of security.

View Article and Find Full Text PDF

The derivation of water quality criteria (WQC) for antibiotics is influenced by the inclusion of various organisms' toxicity data, including microbial data, though no definitive conclusions have been reached. This study focuses on sulfonamide antibiotics, common in the Yangtze River Delta (YRD), to assess the influences of different organisms' toxicity data on determining WQCs and subsequent evaluation of ecological risks. A total of 263 toxicity data points from eight sulfonamides, including sulfamethoxazole (SMX) and sulfamethazine (SM2), were selected to derive WQCs using Species Sensitivity Distribution (SSD) methods.

View Article and Find Full Text PDF

Basic Science and Pathogenesis.

Alzheimers Dement

December 2024

Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, TN, USA.

Background: Genome-wide association studies (GWAS) in Alzheimer's disease (AD) leveraging endophenotypes beyond case/control diagnosis, such as brain amyloid β pathology, have shown promise in identifying novel variants and understanding their potential functional impact. In this study, we leverage two brain amyloid β pathology measurement modalities, PET imaging and neuropathology, to address sample size limitations and to discover novel genetic drivers of disease.

Method: We conducted a meta-analysis on an amyloid PET imaging GWAS (N = 7,036, 35% amyloid positive, 53.

View Article and Find Full Text PDF

Background: New methods developed to estimate when AD biomarkers became abnormal in individuals have shown considerable heterogeneity in amyloid and tau pathology onset age. This work used polygenic scores (PGS) generated from CSF Aβ and ptau GWAS, individual-level genetic data, and estimated tau onset age (ETOA) to identify genetic influences on tau onset beyond APOE.

Method: Participants from the Alzheimer's Disease Neuroimaging Initiative (ADNI) with genetic data, CSF biomarkers (Aβ and ptau), and longitudinal [F]Flortaucipir (FTP) tau PET were analyzed (N = 462).

View Article and Find Full Text PDF

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!