Pub Date : 2025-08-13eCollection Date: 2025-01-01DOI: 10.3389/fninf.2025.1616981
Jose Arturo Santisteban, David Rotenberg, Stefan Kloiber, Marta M Maslej, Adeel Ansari, Bahar Amani, Darren Courtney, Farhat Farrokhi, Natalie Freeman, Masooma Hassan, Lucia Kwan, Mindaugas Mozuraitis, Michael Lau, Natalia Potapova, Farhad Qureshi, Nicole Schoer, Nelson Shen, Joanna Yu, Noelle Coombe, Kimberly Hunter, Peter Selby, Nicole Thomson, Damian Jankowicz, Sean L Hill
Introduction: Mental health care is undermined by fragmented data collection, as incomplete datasets can compromise treatment efficacy and research. The BrainHealth Databank (BHDB) at the Centre for Addiction and Mental Health (CAMH) establishes the governance and infrastructure for a Learning Mental Health System that integrates digital tools, measurement-based care, artificial intelligence (AI), and open science to deliver personalized, data-driven care.
Methods: Central to the BHDB's approach is its comprehensive governance framework, which actively engages clinicians, researchers, data scientists, privacy and ethics experts, and patient and family partners. This codesigned approach ensures that digital health technologies are deployed ethically, securely, and effectively within clinical settings.
Results: By aligning data collection with clinical and research goals and harmonizing over 12 million data points from 33,000 patient trajectories, the BHDB enhances data quality, enables real-time decision support, and fosters continuous improvement.
Discussion: The BHDB provides a model for integrating AI and digital tools into mental health care, as well as research data collection, analyses, storage, and sharing through the BHDB Portal (https://bhdb.camh.ca).
{"title":"The BrainHealth Databank: a systems approach to data-driven mental health care and research.","authors":"Jose Arturo Santisteban, David Rotenberg, Stefan Kloiber, Marta M Maslej, Adeel Ansari, Bahar Amani, Darren Courtney, Farhat Farrokhi, Natalie Freeman, Masooma Hassan, Lucia Kwan, Mindaugas Mozuraitis, Michael Lau, Natalia Potapova, Farhad Qureshi, Nicole Schoer, Nelson Shen, Joanna Yu, Noelle Coombe, Kimberly Hunter, Peter Selby, Nicole Thomson, Damian Jankowicz, Sean L Hill","doi":"10.3389/fninf.2025.1616981","DOIUrl":"10.3389/fninf.2025.1616981","url":null,"abstract":"<p><strong>Introduction: </strong>Mental health care is undermined by fragmented data collection, as incomplete datasets can compromise treatment efficacy and research. The BrainHealth Databank (BHDB) at the Centre for Addiction and Mental Health (CAMH) establishes the governance and infrastructure for a Learning Mental Health System that integrates digital tools, measurement-based care, artificial intelligence (AI), and open science to deliver personalized, data-driven care.</p><p><strong>Methods: </strong>Central to the BHDB's approach is its comprehensive governance framework, which actively engages clinicians, researchers, data scientists, privacy and ethics experts, and patient and family partners. This codesigned approach ensures that digital health technologies are deployed ethically, securely, and effectively within clinical settings.</p><p><strong>Results: </strong>By aligning data collection with clinical and research goals and harmonizing over 12 million data points from 33,000 patient trajectories, the BHDB enhances data quality, enables real-time decision support, and fosters continuous improvement.</p><p><strong>Discussion: </strong>The BHDB provides a model for integrating AI and digital tools into mental health care, as well as research data collection, analyses, storage, and sharing through the BHDB Portal (https://bhdb.camh.ca).</p>","PeriodicalId":12462,"journal":{"name":"Frontiers in Neuroinformatics","volume":"19 ","pages":"1616981"},"PeriodicalIF":2.5,"publicationDate":"2025-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12392782/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144948997","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-12eCollection Date: 2025-01-01DOI: 10.3389/fninf.2025.1625279
Paulina Tarara, Iwona Przybył, Julius Schöning, Artur Gunia
Introduction: Enhancing the command capacity of motor imagery (MI)-based brain-computer interfaces (BCIs) remains a significant challenge in neuroinformatics, especially for real-world assistive applications. This study explores a multiclass BCI system designed to classify multiple MI tasks using a low-cost EEG device.
Methods: A BCI system was developed to classify six mental states: resting state, left and right hand movement imagery, tongue movement, and left and right lateral bending, using EEG data collected with the Emotiv EPOC X headset. Seven participants underwent a body awareness training protocol integrating mindfulness and physical exercises to improve MI performance. Machine learning techniques were applied to extract discriminative features from the EEG signals.
Results: Post-training assessments indicated modest improvements in participants' MI proficiency. However, classification performance was limited due to inter- and intra-subject signal variability and the technical constraints of the consumer-grade EEG hardware.
Discussion: These findings highlight the value of combining user training with MI-based BCIs and the need to optimize signal quality for reliable performance. The results support the feasibility of scalable, multiclass MI paradigms in low-cost, user-centered neurotechnology applications, while pointing to critical areas for future system enhancement.
{"title":"Motor imagery-based brain-computer interfaces: an exploration of multiclass motor imagery-based control for Emotiv EPOC X.","authors":"Paulina Tarara, Iwona Przybył, Julius Schöning, Artur Gunia","doi":"10.3389/fninf.2025.1625279","DOIUrl":"10.3389/fninf.2025.1625279","url":null,"abstract":"<p><strong>Introduction: </strong>Enhancing the command capacity of motor imagery (MI)-based brain-computer interfaces (BCIs) remains a significant challenge in neuroinformatics, especially for real-world assistive applications. This study explores a multiclass BCI system designed to classify multiple MI tasks using a low-cost EEG device.</p><p><strong>Methods: </strong>A BCI system was developed to classify six mental states: resting state, left and right hand movement imagery, tongue movement, and left and right lateral bending, using EEG data collected with the Emotiv EPOC X headset. Seven participants underwent a body awareness training protocol integrating mindfulness and physical exercises to improve MI performance. Machine learning techniques were applied to extract discriminative features from the EEG signals.</p><p><strong>Results: </strong>Post-training assessments indicated modest improvements in participants' MI proficiency. However, classification performance was limited due to inter- and intra-subject signal variability and the technical constraints of the consumer-grade EEG hardware.</p><p><strong>Discussion: </strong>These findings highlight the value of combining user training with MI-based BCIs and the need to optimize signal quality for reliable performance. The results support the feasibility of scalable, multiclass MI paradigms in low-cost, user-centered neurotechnology applications, while pointing to critical areas for future system enhancement.</p>","PeriodicalId":12462,"journal":{"name":"Frontiers in Neuroinformatics","volume":"19 ","pages":"1625279"},"PeriodicalIF":2.5,"publicationDate":"2025-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12378764/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144949052","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Computational-neuroscience simulators have traditionally been constrained by tightly coupled simulation engines and modeling languages, limiting their flexibility and scalability. Retrofitting these platforms to accommodate new backends is often costly, and sharing models across simulators remains cumbersome. This paper puts forward an alternative approach based on the EDEN neural simulator, which introduces a modular stack that decouples abstract model descriptions from execution. This architecture enhances flexibility and extensibility by enabling seamless integration of multiple backends, including hardware accelerators, without extensive reprogramming. Through the use of NeuroML, simulation developers can focus on high-performance execution, while model users benefit from improved portability without the need to implement custom simulation engines. Additionally, the proposed method for incorporating arbitrary simulation platforms-from model-optimized code kernels to custom hardware devices-as backends offers a more sustainable and adaptable framework for the computational-neuroscience community. The effectiveness of EDEN's approach is demonstrated by integrating two distinct backends: flexHH, an FPGA-based accelerator for extended Hodgkin-Huxley networks, and SpiNNaker, the well-known, neuromorphic platform for large-scale spiking neural networks. Experimental results show that EDEN integrates the different backends with minimal effort while maintaining competitive performance, reaffirming it as a robust, extensible platform that advances the design paradigm for neural simulators by achieving high generality, performance, and usability.
{"title":"Decoupling model descriptions from execution: a modular paradigm for extensible neurosimulation with EDEN.","authors":"Sotirios Panagiotou, Rene Miedema, Dimitrios Soudris, Christos Strydis","doi":"10.3389/fninf.2025.1572782","DOIUrl":"10.3389/fninf.2025.1572782","url":null,"abstract":"<p><p>Computational-neuroscience simulators have traditionally been constrained by tightly coupled simulation engines and modeling languages, limiting their flexibility and scalability. Retrofitting these platforms to accommodate new backends is often costly, and sharing models across simulators remains cumbersome. This paper puts forward an alternative approach based on the EDEN neural simulator, which introduces a modular stack that decouples abstract model descriptions from execution. This architecture enhances flexibility and extensibility by enabling seamless integration of multiple backends, including hardware accelerators, without extensive reprogramming. Through the use of NeuroML, simulation developers can focus on high-performance execution, while model users benefit from improved portability without the need to implement custom simulation engines. Additionally, the proposed method for incorporating arbitrary simulation platforms-from model-optimized code kernels to custom hardware devices-as backends offers a more sustainable and adaptable framework for the computational-neuroscience community. The effectiveness of EDEN's approach is demonstrated by integrating two distinct backends: flexHH, an FPGA-based accelerator for extended Hodgkin-Huxley networks, and SpiNNaker, the well-known, neuromorphic platform for large-scale spiking neural networks. Experimental results show that EDEN integrates the different backends with minimal effort while maintaining competitive performance, reaffirming it as a robust, extensible platform that advances the design paradigm for neural simulators by achieving high generality, performance, and usability.</p>","PeriodicalId":12462,"journal":{"name":"Frontiers in Neuroinformatics","volume":"19 ","pages":"1572782"},"PeriodicalIF":2.5,"publicationDate":"2025-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12367680/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144949023","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-05eCollection Date: 2025-01-01DOI: 10.3389/fninf.2025.1628030
Liya Li, Ying Hu, Xiaojun Wang, Pei Sun, Tingwei Quan
Neuron reconstruction is a critical step in quantifying neuronal structures from imaging data. Advances in molecular labeling techniques and optical imaging technologies have spurred extensive research into the patterns of long-range neuronal projections. However, mapping these projections incurs significant costs, as large-scale reconstruction of individual axonal arbors remains time-consuming. In this study, we present a dataset comprising axon imaging volumes along with corresponding annotations to facilitate the evaluation and development of axon reconstruction algorithms. This dataset, derived from 11 mouse brain samples imaged using fluorescence micro-optical sectioning tomography, contains carefully selected 852 volume images sized at 192 × 192 × 192 voxels. These images exhibit substantial variations in terms of axon density, image intensity, and signal-to-noise ratios, even within localized regions. Conventional methods often struggle when processing such complex data. To address these challenges, we propose a distance field-supervised segmentation network designed to enhance image signals effectively. Our results demonstrate significantly improved axon detection rates across both state-of-the-art and traditional methodologies. The released dataset and benchmark algorithm provide a data foundation for advancing novel axon reconstruction methods and are valuable for accelerating the reconstruction of long-range axonal projections.
{"title":"A neuronal imaging dataset for deep learning in the reconstruction of single-neuron axons.","authors":"Liya Li, Ying Hu, Xiaojun Wang, Pei Sun, Tingwei Quan","doi":"10.3389/fninf.2025.1628030","DOIUrl":"10.3389/fninf.2025.1628030","url":null,"abstract":"<p><p>Neuron reconstruction is a critical step in quantifying neuronal structures from imaging data. Advances in molecular labeling techniques and optical imaging technologies have spurred extensive research into the patterns of long-range neuronal projections. However, mapping these projections incurs significant costs, as large-scale reconstruction of individual axonal arbors remains time-consuming. In this study, we present a dataset comprising axon imaging volumes along with corresponding annotations to facilitate the evaluation and development of axon reconstruction algorithms. This dataset, derived from 11 mouse brain samples imaged using fluorescence micro-optical sectioning tomography, contains carefully selected 852 volume images sized at 192 × 192 × 192 voxels. These images exhibit substantial variations in terms of axon density, image intensity, and signal-to-noise ratios, even within localized regions. Conventional methods often struggle when processing such complex data. To address these challenges, we propose a distance field-supervised segmentation network designed to enhance image signals effectively. Our results demonstrate significantly improved axon detection rates across both state-of-the-art and traditional methodologies. The released dataset and benchmark algorithm provide a data foundation for advancing novel axon reconstruction methods and are valuable for accelerating the reconstruction of long-range axonal projections.</p>","PeriodicalId":12462,"journal":{"name":"Frontiers in Neuroinformatics","volume":"19 ","pages":"1628030"},"PeriodicalIF":2.5,"publicationDate":"2025-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12361129/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144949067","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-31eCollection Date: 2025-01-01DOI: 10.3389/fninf.2025.1633196
Geoffrey Chern-Yee Tan, Ziying Wang, Ethel Siew Ee Tan, Rachel Jing Min Ong, Pei En Ooi, Danan Lee, Nikita Rane, Sheryl Yu Xuan Tey, Si Ying Chua, Nicole Goh, Glynis Weibin Lam, Atlanta Chakraborty, Anthony Khye Loong Yew, Sin Kee Ong, Jin Lin Kee, Xin Ying Lim, Nawal Hashim, Sharon Huixian Lu, Michael Meany, Serenella Tolomeo, Christopher Lee Asplund, Hong Ming Tan, Jussi Keppo
[This corrects the article DOI: 10.3389/fninf.2023.1244347.].
[这更正了文章DOI: 10.3389/fninf.2023.1244347.]。
{"title":"Correction: Transdiagnostic clustering of self-schema from self-referential judgements identifies subtypes of healthy personality and depression.","authors":"Geoffrey Chern-Yee Tan, Ziying Wang, Ethel Siew Ee Tan, Rachel Jing Min Ong, Pei En Ooi, Danan Lee, Nikita Rane, Sheryl Yu Xuan Tey, Si Ying Chua, Nicole Goh, Glynis Weibin Lam, Atlanta Chakraborty, Anthony Khye Loong Yew, Sin Kee Ong, Jin Lin Kee, Xin Ying Lim, Nawal Hashim, Sharon Huixian Lu, Michael Meany, Serenella Tolomeo, Christopher Lee Asplund, Hong Ming Tan, Jussi Keppo","doi":"10.3389/fninf.2025.1633196","DOIUrl":"10.3389/fninf.2025.1633196","url":null,"abstract":"<p><p>[This corrects the article DOI: 10.3389/fninf.2023.1244347.].</p>","PeriodicalId":12462,"journal":{"name":"Frontiers in Neuroinformatics","volume":"19 ","pages":"1633196"},"PeriodicalIF":2.5,"publicationDate":"2025-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12351648/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144872317","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-23eCollection Date: 2025-01-01DOI: 10.3389/fninf.2025.1590968
Seyedadel Moravveji, Halima Sadia, Nicolas Doyon, Simon Duchesne
Introduction: Mathematical models serve as essential tools to investigate brain aging, the onset of Alzheimer's disease (AD) and its progression. By studying the representation of the complex dynamics of brain aging processes, such as amyloid beta (Aβ) deposition, tau tangles, neuro-inflammation, and neuronal death. Sensitivity analyses provide a powerful framework for identifying the underlying mechanisms that drive disease progression. In this study, we present the first local sensitivity analysis of a recent and comprehensive multiscale ODE-based model of Alzheimer's Disease (AD) that originates from our group. As such, it is one of the most complex model that captures the multifactorial nature of AD, incorporating neuronal, pathological, and inflammatory processes at the nano, micro and macro scales. This detailed framework enables realistic simulation of disease progression and identification of key biological parameters that influence system behavior. Our analysis identifies the key drivers of disease progression across patient profiles, providing insight into targeted therapeutic strategies.
Methods: We investigated a recent ODE-based model composed of 19 variables and 75 parameters, developed by our group, to study Alzheimer's disease dynamics. We performed single- and paired-parameter sensitivity analyses, focusing on three key outcomes: neural density, amyloid beta plaques, and tau proteins.
Results: Our findings suggest that the parameters related to glucose and insulin regulation could play an important role in neurodegeneration and cognitive decline. Second, the parameters that have the most important impact on cognitive decline are not completely the same depending on sex and APOE status.
Discussion: These results underscore the importance of incorporating a multifactorial approach tailored to demographic characteristics when considering strategies for AD treatment. This approach is essential to identify the factors that contribute significantly to neural loss and AD progression.
{"title":"Sensitivity analysis of a mathematical model of Alzheimer's disease progression unveils important causal pathways.","authors":"Seyedadel Moravveji, Halima Sadia, Nicolas Doyon, Simon Duchesne","doi":"10.3389/fninf.2025.1590968","DOIUrl":"10.3389/fninf.2025.1590968","url":null,"abstract":"<p><strong>Introduction: </strong>Mathematical models serve as essential tools to investigate brain aging, the onset of Alzheimer's disease (AD) and its progression. By studying the representation of the complex dynamics of brain aging processes, such as amyloid beta (Aβ) deposition, tau tangles, neuro-inflammation, and neuronal death. Sensitivity analyses provide a powerful framework for identifying the underlying mechanisms that drive disease progression. In this study, we present the first local sensitivity analysis of a recent and comprehensive multiscale ODE-based model of Alzheimer's Disease (AD) that originates from our group. As such, it is one of the most complex model that captures the multifactorial nature of AD, incorporating neuronal, pathological, and inflammatory processes at the nano, micro and macro scales. This detailed framework enables realistic simulation of disease progression and identification of key biological parameters that influence system behavior. Our analysis identifies the key drivers of disease progression across patient profiles, providing insight into targeted therapeutic strategies.</p><p><strong>Methods: </strong>We investigated a recent ODE-based model composed of 19 variables and 75 parameters, developed by our group, to study Alzheimer's disease dynamics. We performed single- and paired-parameter sensitivity analyses, focusing on three key outcomes: neural density, amyloid beta plaques, and tau proteins.</p><p><strong>Results: </strong>Our findings suggest that the parameters related to glucose and insulin regulation could play an important role in neurodegeneration and cognitive decline. Second, the parameters that have the most important impact on cognitive decline are not completely the same depending on sex and APOE status.</p><p><strong>Discussion: </strong>These results underscore the importance of incorporating a multifactorial approach tailored to demographic characteristics when considering strategies for AD treatment. This approach is essential to identify the factors that contribute significantly to neural loss and AD progression.</p>","PeriodicalId":12462,"journal":{"name":"Frontiers in Neuroinformatics","volume":"19 ","pages":"1590968"},"PeriodicalIF":2.5,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12325246/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144793928","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
This study demonstrates the effectiveness of integrating cloud computing platforms with Course-based Undergraduate Research Experiences (CUREs) to broaden access to neuroscience education. Over four consecutive spring semesters (2021-2024), a total of 42 undergraduate students at Lawrence Technological University participated in computational neuroscience CUREs using brainlife.io, a cloud-computing platform. Students conducted anatomical and functional brain imaging analyses on openly available datasets, testing original hypotheses about brain structure variations. The program evolved from initial data processing to hypothesis-driven research exploring the influence of age, gender, and pathology on brain structures. By combining open science and big data within a user-friendly cloud environment, the CURE model provided hands-on, problem-based learning to students with limited prior knowledge. This approach addressed key limitations of traditional undergraduate research experiences, including scalability, early exposure, and inclusivity. Students consistently worked with MRI datasets, focusing on volumetric analysis of brain structures, and developed scientific communication skills by presenting findings at annual research days. The success of this program demonstrates its potential to democratize neuroscience education, enabling advanced research without extensive laboratory facilities or prior experience, and promoting original undergraduate research using real-world datasets.
{"title":"Breaking barriers: broadening neuroscience education via cloud platforms and course-based undergraduate research.","authors":"Franco Delogu, Chantol Aspinall, Kimberly Ray, Anibal Solon Heinsfeld, Conner Victory, Franco Pestilli","doi":"10.3389/fninf.2025.1608900","DOIUrl":"10.3389/fninf.2025.1608900","url":null,"abstract":"<p><p>This study demonstrates the effectiveness of integrating cloud computing platforms with Course-based Undergraduate Research Experiences (CUREs) to broaden access to neuroscience education. Over four consecutive spring semesters (2021-2024), a total of 42 undergraduate students at Lawrence Technological University participated in computational neuroscience CUREs using brainlife.io, a cloud-computing platform. Students conducted anatomical and functional brain imaging analyses on openly available datasets, testing original hypotheses about brain structure variations. The program evolved from initial data processing to hypothesis-driven research exploring the influence of age, gender, and pathology on brain structures. By combining open science and big data within a user-friendly cloud environment, the CURE model provided hands-on, problem-based learning to students with limited prior knowledge. This approach addressed key limitations of traditional undergraduate research experiences, including scalability, early exposure, and inclusivity. Students consistently worked with MRI datasets, focusing on volumetric analysis of brain structures, and developed scientific communication skills by presenting findings at annual research days. The success of this program demonstrates its potential to democratize neuroscience education, enabling advanced research without extensive laboratory facilities or prior experience, and promoting original undergraduate research using real-world datasets.</p>","PeriodicalId":12462,"journal":{"name":"Frontiers in Neuroinformatics","volume":"19 ","pages":"1608900"},"PeriodicalIF":2.5,"publicationDate":"2025-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12307389/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144752882","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-08eCollection Date: 2025-01-01DOI: 10.3389/fninf.2025.1563893
Karina J Maciejewska
Introduction: This paper describes an experimental work using machine learning (ML) as a "decoding for interpretation" to understand the brain's physiology better.
Methods: Multivariate pattern analysis (MVPA) was used to decode the patterns of event-related potentials (ERPs, brain responses to stimuli) in a visual oddball task. The ERPs were measured before (run 1) and after (30 min-run 2, 90 min-run 3) a single dose of an energy dietary supplement with only a small amount of caffeine.
Results: Its effect on ERPs was successfully decoded. Above-chance decoding accuracies were obtained between ∼350 and 450 ms (corresponds to P3 peak) after stimulus onset for both the placebo and study groups, whereas between ∼200 and 260 ms (corresponds to P2 waveform) only in the placebo group. Moreover, the decoding accuracies were significantly higher in the placebo than in the study group in the 200-250 ms and 450-500 ms time bins. Our previously reported findings showed an increase in P3 amplitude among the runs only in the placebo group, indicating a reduction of mental fatigue caused by the supplementation.
Discussion: Thus, this paper extends these results, showing that the dietary supplement affected the brain's neural activity related to the attention-related processing of the visual stimuli in the oddball task already at the early processing stage. This implies that inhibiting the fatigue-related brain changes after only a single dose of a dietary neurostimulant acts on early and late processing stages. This emphasizes the value of decoding for interpretation in ERP research. The results also point out the necessity of controlling the uptake of dietary supplements before the neurophysiological examinations.
{"title":"Decoding event-related potentials: single-dose energy dietary supplement acts on earlier brain processes than we thought.","authors":"Karina J Maciejewska","doi":"10.3389/fninf.2025.1563893","DOIUrl":"10.3389/fninf.2025.1563893","url":null,"abstract":"<p><strong>Introduction: </strong>This paper describes an experimental work using machine learning (ML) as a \"decoding for interpretation\" to understand the brain's physiology better.</p><p><strong>Methods: </strong>Multivariate pattern analysis (MVPA) was used to decode the patterns of event-related potentials (ERPs, brain responses to stimuli) in a visual oddball task. The ERPs were measured before (run 1) and after (30 min-run 2, 90 min-run 3) a single dose of an energy dietary supplement with only a small amount of caffeine.</p><p><strong>Results: </strong>Its effect on ERPs was successfully decoded. Above-chance decoding accuracies were obtained between ∼350 and 450 ms (corresponds to P3 peak) after stimulus onset for both the placebo and study groups, whereas between ∼200 and 260 ms (corresponds to P2 waveform) only in the placebo group. Moreover, the decoding accuracies were significantly higher in the placebo than in the study group in the 200-250 ms and 450-500 ms time bins. Our previously reported findings showed an increase in P3 amplitude among the runs only in the placebo group, indicating a reduction of mental fatigue caused by the supplementation.</p><p><strong>Discussion: </strong>Thus, this paper extends these results, showing that the dietary supplement affected the brain's neural activity related to the attention-related processing of the visual stimuli in the oddball task already at the early processing stage. This implies that inhibiting the fatigue-related brain changes after only a single dose of a dietary neurostimulant acts on early and late processing stages. This emphasizes the value of decoding for interpretation in ERP research. The results also point out the necessity of controlling the uptake of dietary supplements before the neurophysiological examinations.</p>","PeriodicalId":12462,"journal":{"name":"Frontiers in Neuroinformatics","volume":"19 ","pages":"1563893"},"PeriodicalIF":2.5,"publicationDate":"2025-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12279804/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144689712","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-01eCollection Date: 2025-01-01DOI: 10.3389/fninf.2025.1549916
Rachele Fabbri, Ermes Botte, Arti Ahluwalia, Chiara Magliaro
Introduction: Computational models are valuable tools for understanding and studying a wide range of characteristics and mechanisms of the brain. Furthermore, they can also be exploited to explore biological neural networks from neuronal cultures. However, few of the current in silico approaches consider the energetic demand of neurons to sustain their electrophysiological functions, specifically their well-known oxygen-dependent firing.
Methods: In this work, we introduce Digitoids, a computational platform which integrates a Hodgkin-Huxley-like model to describe the time-dependent oscillations of the neuronal membrane potential with oxygen dynamics in the culture environment. In Digitoids, neurons are connected to each other according to Small-World topologies observed in cell cultures, and oxygen consumption by cells is modeled as limited by diffusion through the culture medium. The oxygen consumed is used to fuel their basal metabolism and the activity of Na+-K+-ATP membrane pumps, thus it modulates neuronal firing.
Results: Our simulations show that the characteristics of neuronal firing predicted throughout the network are related to oxygen availability. In addition, the average firing rate predicted by Digitoids is statistically similar to that measured in neuronal networks in vitro, further proving the relevance of this platform.
Dicussion: Digitoids paves the way for a new generation of in silico models of neuronal networks, establishing the oxygen dependence of electrophysiological dynamics as a fundamental requirement to improve their physiological relevance.
{"title":"Digitoids: a novel computational platform for mimicking oxygen-dependent firing of neurons <i>in vitro</i>.","authors":"Rachele Fabbri, Ermes Botte, Arti Ahluwalia, Chiara Magliaro","doi":"10.3389/fninf.2025.1549916","DOIUrl":"10.3389/fninf.2025.1549916","url":null,"abstract":"<p><strong>Introduction: </strong>Computational models are valuable tools for understanding and studying a wide range of characteristics and mechanisms of the brain. Furthermore, they can also be exploited to explore biological neural networks from neuronal cultures. However, few of the current in silico approaches consider the energetic demand of neurons to sustain their electrophysiological functions, specifically their well-known oxygen-dependent firing.</p><p><strong>Methods: </strong>In this work, we introduce Digitoids, a computational platform which integrates a Hodgkin-Huxley-like model to describe the time-dependent oscillations of the neuronal membrane potential with oxygen dynamics in the culture environment. In Digitoids, neurons are connected to each other according to Small-World topologies observed in cell cultures, and oxygen consumption by cells is modeled as limited by diffusion through the culture medium. The oxygen consumed is used to fuel their basal metabolism and the activity of Na<sup>+</sup>-K<sup>+</sup>-ATP membrane pumps, thus it modulates neuronal firing.</p><p><strong>Results: </strong>Our simulations show that the characteristics of neuronal firing predicted throughout the network are related to oxygen availability. In addition, the average firing rate predicted by Digitoids is statistically similar to that measured in neuronal networks <i>in vitro</i>, further proving the relevance of this platform.</p><p><strong>Dicussion: </strong>Digitoids paves the way for a new generation of <i>in silico</i> models of neuronal networks, establishing the oxygen dependence of electrophysiological dynamics as a fundamental requirement to improve their physiological relevance.</p>","PeriodicalId":12462,"journal":{"name":"Frontiers in Neuroinformatics","volume":"19 ","pages":"1549916"},"PeriodicalIF":2.5,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12259620/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144642248","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-06-27eCollection Date: 2025-01-01DOI: 10.3389/fninf.2025.1583428
Denise Alonso-Vázquez, Omar Mendoza-Montoya, Ricardo Caraza, Hector R Martinez, Javier M Antelis
Introduction: Imagined speech decoding using EEG holds promising applications for individuals with motor neuron diseases, although its performance remains limited due to small dataset sizes and the absence of sensory feedback. Here, we investigated whether incorporating EEG data from overt (pronounced) speech could enhance imagined speech classification.
Methods: Our approach systematically compares four classification scenarios by modifying the training dataset: intra-subject (using only imagined speech, combining overt and imagined speech, and using only overt speech) and multi-subject (combining overt speech data from different participants with the imagined speech of the target participant). We implemented all scenarios using the convolutional neural network EEGNet. To this end, twenty-four healthy participants pronounced and imagined five Spanish words.
Results: In binary word-pair classifications, combining overt and imagined speech data in the intra-subject scenario led to accuracy improvements of 3%-5.17% in four out of 10 word pairs, compared to training with imagined speech only. Although the highest individual accuracy (95%) was achieved with imagined speech alone, the inclusion of overt speech data allowed more participants to surpass 70% accuracy, increasing from 10 (imagined only) to 15 participants. In the intra-subject multi-class scenario, combining overt and imagined speech did not yield statistically significant improvements over using imagined speech exclusively.
Discussion: Finally, we observed that features such as word length, phonological complexity, and frequency of use contributed to higher discriminability between certain imagined word pairs. These findings suggest that incorporating overt speech data can improve imagined speech decoding in individualized models, offering a feasible strategy to support the early adoption of brain-computer interfaces before speech deterioration occurs in individuals with motor neuron diseases.
{"title":"From pronounced to imagined: improving speech decoding with multi-condition EEG data.","authors":"Denise Alonso-Vázquez, Omar Mendoza-Montoya, Ricardo Caraza, Hector R Martinez, Javier M Antelis","doi":"10.3389/fninf.2025.1583428","DOIUrl":"10.3389/fninf.2025.1583428","url":null,"abstract":"<p><strong>Introduction: </strong><i>Imagined speech</i> decoding using EEG holds promising applications for individuals with motor neuron diseases, although its performance remains limited due to small dataset sizes and the absence of sensory feedback. Here, we investigated whether incorporating EEG data from <i>overt</i> (pronounced) speech could enhance <i>imagined speech</i> classification.</p><p><strong>Methods: </strong>Our approach systematically compares four classification scenarios by modifying the training dataset: intra-subject (using only <i>imagined speech</i>, combining <i>overt</i> and <i>imagined speech</i>, and using only <i>overt speech</i>) and multi-subject (combining <i>overt speech</i> data from different participants with the <i>imagined speech</i> of the target participant). We implemented all scenarios using the convolutional neural network EEGNet. To this end, twenty-four healthy participants pronounced and imagined five Spanish words.</p><p><strong>Results: </strong>In binary word-pair classifications, combining <i>overt</i> and <i>imagined speech</i> data in the intra-subject scenario led to accuracy improvements of 3%-5.17% in four out of 10 word pairs, compared to training with <i>imagined speech</i> only. Although the highest individual accuracy (95%) was achieved with <i>imagined speech</i> alone, the inclusion of <i>overt speech</i> data allowed more participants to surpass 70% accuracy, increasing from 10 (<i>imagined only</i>) to 15 participants. In the intra-subject multi-class scenario, combining <i>overt</i> and <i>imagined speech</i> did not yield statistically significant improvements over using <i>imagined speech</i> exclusively.</p><p><strong>Discussion: </strong>Finally, we observed that features such as word length, phonological complexity, and frequency of use contributed to higher discriminability between certain <i>imagined</i> word pairs. These findings suggest that incorporating <i>overt speech</i> data can improve <i>imagined speech</i> decoding in individualized models, offering a feasible strategy to support the early adoption of brain-computer interfaces before speech deterioration occurs in individuals with motor neuron diseases.</p>","PeriodicalId":12462,"journal":{"name":"Frontiers in Neuroinformatics","volume":"19 ","pages":"1583428"},"PeriodicalIF":2.5,"publicationDate":"2025-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12245923/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144625885","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}