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The role of input imaging combination and ADC threshold on segmentation of acute ischemic stroke lesion using U-Net

European Radiology 2023年第9期33卷 6157-6167页

作者： Li, Ya-Hui Lin, Shao-Chieh Chung, Hsiao-Wen Chang, Chia-Ching Peng, Hsu-Hsia Huang, Teng-Yi Shen, Wu-Chung Tsai, Chon-Haw Lo, Yu-Chien Lee, Tung-Yang Juan, Cheng-Hsuan Juan, Cheng-En Chang, Hing-Chiu Liu, Yi-Jui Juan, Chun-Jung Graduate Institute of Biomedical Electronics and Bioinformatics National Taiwan University Taipei Taiwan Department of Medical Imaging China Medical University Hsinchu Hospital No. 199 Sec. 1 Xinglong Rd. Zhubei City Hsinchu County 302 Hsinchu Taiwan Ph.D. Program in Electrical and Communication Engineering Feng Chia University Taichung Taiwan Department of Electrical Engineering National Taiwan University Taipei Taiwan Department of Management Science National Yang Ming Chiao Tung University Hsinchu Taiwan Department of Biomedical Engineering and Environmental Sciences National Tsing Hua University Hsinchu Taiwan Department of Electrical Engineering National Taiwan University of Science and Technology Taipei Taiwan Department of Radiology School of Medicine College of Medicine China Medical University Taichung Taiwan Department of Medical Imaging Medical University Hospital Taichung Taiwan Department of Neurology China Medical University Hospital Taichung Taiwan Cheng Ching Hospital Taichung Taiwan Master’s Program of Biomedical Informatics and Biomedical Engineering Feng Chia University Taichung Taiwan Department of Automatic Control Engineering Feng Chia University No. 100 Wenhwa Rd. Seatwen Taichung 40724 Taiwan Department of Biomedical Engineering The Chinese University of Hong Kong ERB1112 11/F William M.W. Mong Engineering Building N.T Shatin Hong Kong Multi-Scale Medical Robotics Center The Chinese University of Hong Kong N.T Shatin Hong Kong Department of Biomedical Engineering National Defense Medical Center Taipei Taiwan Department of Computer Science and Information Engineering National Taiwan University Taipei Taiwan

Background: To evaluate the effect of the weighting of input imaging combo and ADC threshold on the performance of the U-Net and to find an optimized input imaging combo and ADC threshold in segmenting acute ischemic stroke (AIS) lesion. Methods: This study retrospectively enrolled a total of 212 patients having AIS. Four combos, including ADC-ADC-ADC (AAA), DWI-ADC-ADC (DAA), DWI-DWI-ADC (DDA), and DWI-DWI-DWI (DDD), were used as input images, respectively. Three ADC thresholds including 0.6, 0.8 and 1.8 × 10^–3 mm²/s were applied. Dice similarity coefficient (DSC) was used to evaluate the segmentation performance of U-Nets. Nonparametric Kruskal–Wallis test with Tukey–Kramer post-hoc tests were used for comparison. A p <.05 was considered statistically significant. Results: The DSC significantly varied among different combos of images and different ADC thresholds. Hybrid U-Nets outperformed uniform U-Nets at ADC thresholds of 0.6 × 10^–3 mm²/s and 0.8 × 10^–3 mm²/s (p <.001). The U-Net with imaging combo of DDD had segmentation performance similar to hybrid U-Nets at an ADC threshold of 1.8 × 10^–3 mm²/s (p =.062 to 1). The U-Net using the imaging combo of DAA at the ADC threshold of 0.6 × 10^–3 mm²/s achieved the highest DSC in the segmentation of AIS lesion. Conclusions: The segmentation performance of U-Net for AIS varies among the input imaging combos and ADC thresholds. The U-Net is optimized by choosing the imaging combo of DAA at an ADC threshold of 0.6 × 10^–3 mm²/s in segmentating AIS lesion with highest DSC. Key Points: • Segmentation performance of U-Net for AIS differs among input imaging combos. • Segmentation performance of U-Net for AIS differs among ADC thresholds. • U-Net is optimized using DAA with ADC = 0.6 × 10^–3mm²/s. © 2023, The Author(s), under exclusive licence to European Society of Radiology.

关键词： Deep Learning Diffusion Magnetic Resonance Imaging Ischemic Stroke Neural Networks, Computer Retrospective Study

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Graph AI in Medicine

arXiv

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arXiv 2023年

作者： Johnson, Ruth Li, Michelle M. Noori, Ayush Queen, Owen Zitnik, Marinka Department of Biomedical Informatics Harvard Medical School BostonMA02115 United States Berkowitz Family Living Laboratory Harvard Medical School BostonMA02115 United States Bioinformatics and Integrative Genomics Program Harvard Medical School BostonMA02115 United States Harvard College CambridgeMA02138 United States Broad Institute of MIT and Harvard CambridgeMA02142 United States Harvard Data Science Initiative CambridgeMA02138 United States Kempner Institute for the Study of Natural and Artificial Intelligence Harvard University AllstonMA United States

In clinical artificial intelligence (AI), graph representation learning, mainly through graph neural networks and graph transformer architectures, stands out for its capability to capture intricate relationships and structures within clinical datasets. With diverse data-from patient records to imaging-graph AI models process data holistically by viewing modalities and entities within them as nodes interconnected by their relationships. Graph AI facilitates model transfer across clinical tasks, enabling models to generalize across patient populations without additional parameters or minimal to no re-training. However, the importance of human-centered design and model interpretability in clinical decision-making cannot be overstated. Since graph AI models capture information through localized neural transformations defined on relational datasets, they offer both an opportunity and a challenge in elucidating model rationale. Knowledge graphs can enhance interpretability by aligning model-driven insights with medical knowledge. Emerging graph AI models integrate diverse data modalities through pre-training, facilitate interactive feedback loops, and foster human-AI collaboration, paving the way to clinically meaningful predictions. © 2023, CC BY.

关键词： Knowledge graph

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Graph Artificial Intelligence in Medicine

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Biomedical Data Science 1000年第1期7卷 345-368页

作者： Ruth Johnson Michelle M. Li Ayush Noori Owen Queen Marinka Zitnik 1Department of Biomedical Informatics Harvard Medical School Boston Massachusetts USA email: marinka@hms.harvard.edu 2Berkowitz Family Living Laboratory Harvard Medical School Boston Massachusetts USA 3Bioinformatics and Integrative Genomics Program Harvard Medical School Boston Massachusetts USA 4Department of Computer Science Harvard John A. Paulson School of Engineering and Applied Sciences Allston Massachusetts USA 5Broad Institute of MIT and Harvard Cambridge Massachusetts USA 7Kempner Institute for the Study of Natural and Artificial Intelligence Harvard University Allston Massachusetts USA 6Harvard Data Science Initiative Cambridge Massachusetts USA

In clinical artificial intelligence (AI), graph representation learning, mainly through graph neural networks and graph transformer architectures, stands out for its capability to capture intricate relationships and structures within clinical datasets. With diverse data—from patient records to imaging—graph AI models process data holistically by viewing modalities and entities within them as nodes interconnected by their relationships. Graph AI facilitates model transfer across clinical tasks, enabling models to generalize across patient populations without additional parameters and with minimal to no retraining. However, the importance of human-centered design and model interpretability in clinical decision-making cannot be overstated. Since graph AI models capture information through localized neural transformations defined on relational datasets, they offer both an opportunity and a challenge in elucidating model rationale. Knowledge graphs can enhance interpretability by aligning model-driven insights with medical knowledge. Emerging graph AI models integrate diverse data modalities through pretraining, facilitate interactive feedback loops, and foster human–AI collaboration, paving the way toward clinically meaningful predictions.

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Multimodal learning with graphs

arXiv

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arXiv 2022年

作者： Ektefaie, Yasha Dasoulas, George Noori, Ayush Farhat, Maha Zitnik, Marinka Bioinformatics and Integrative Genomics Program Harvard Medical School BostonMA02115 United States Department of Biomedical Informatics Harvard University BostonMA02115 United States Harvard College CambridgeMA02138 United States Broad Institute of MIT and Harvard CambridgeMA02142 United States Harvard Data Science Initiative CambridgeMA02138 United States Division of Pulmonary and Critical Care Department of Medicine Massachusetts General Hospital BostonMA United States

Artificial intelligence for graphs has achieved remarkable success in modeling complex systems, ranging from dynamic networks in biology to interacting particle systems in physics. However, the increasingly heterogeneous graph datasets call for multimodal methods that can combine different inductive biases—the set of assumptions that algorithms use to make predictions for inputs they have not encountered during training. Learning on multimodal datasets presents fundamental challenges because the inductive biases can vary by data modality and graphs might not be explicitly given in the input. To address these challenges, multimodal graph AI methods combine different modalities while leveraging cross-modal dependencies using graphs. Diverse datasets are combined using graphs and fed into sophisticated multimodal architectures, specified as image-intensive, knowledge-grounded and language-intensive models. Using this categorization, we introduce a blueprint for multimodal graph learning, use it to study existing methods and provide guidelines to design new models. © 2022, CC BY.

关键词： Blueprints

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Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma

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Frontiers of Medicine 2021年第2期15卷 275-291页

作者： Na Qin Yuancheng Li Cheng Wang Meng Zhu Juncheng Dai Tongtong Hong Demetrius Albanes Stephen Lam Adonina Tardon Chu Chen Gary Goodman Stig EBojesen Maria Teresa Landi Mattias Johansson Angela Risch H-Erich Wichmann Heike Bickeboller Gadi Rennert Susanne Arnold Paul Brennan John KField Sanjay Shete Loic Le Marchand Olle Melander Hans Brunnstrom Geoffrey Liu Rayjean JHung Angeline Andrew Lambertus AKiemeney Shan Zienolddiny Kjell Grankvist Mikael Johansson Neil Caporaso Penella Woll Philip Lazarus Matthew BSchabath Melinda CAldrich Victoria LStevens Guangfu Jin David CChristiani Zhibin Hu Christopher IAmos Hongxia Ma Hongbing Shen Department of Epidemiology Center for Global HealthSchool of Public HealthNanjing Medical UniversityNanjing 211166China State Key Laboratory of Reproductive Medicine Center for Global HealthNanjing Medical UniversityNanjing 211166China Department of Bioinformatics School of Biomedical Engineering and InformaticsNanjing Medical UniversityNanjing 211166China Jiangsu Key Lab of Cancer Biomarkers Prevention and TreatmentCollaborative Innovation Center for Cancer MedicineNanjing Medical UniversityNanjing 211166China China International Cooperation Center for Environment and Human Health School of Public HealthNanjing Medical UniversityNanjing 211166China Division of Cancer Epidemiology and Genetics National Cancer InstituteBethesdaMD 20892-9304USA Department of Integrative Oncology British Columbia Cancer AgencyVancouverBC V5Z 1L3Canada Faculty of Medicine University of Oviedo and CIBERESPOviedo 33006Spain Program in Epidemiology Public Health Sciences DivisionFred Hutchinson Cancer Research CenterSeattleWA 98109-1024USA Public Health Sciences Division Swedish Cancer InstituteSeattleWA 98026USA Department of Clinical Biochemistry Copenhagen University HospitalCopenhagen DK-1017Denmark National Cancer Institute BethesdaMD 20892-9304USA Genetic Epidemiology Group International Agency for Research on CancerLyon 69372France Cancer Center Cluster Salzburg at PLUS Department of Molecular BiologyUniversity of SalzburgHeidelberg 5020Austria Institute of Medical Informatics Biometry and EpidemiologyChair of EpidemiologyLudwig Maximilians UniversityMunichBavaria 80539Germany Department of Genetic Epidemiology University Medical Center GoettingenGoettingen 37075Germany Technion Faculty of Medicine Carmel Medical CenterHaifa 3448516Israel Markey Cancer Center University of KentuckyLexingtonKY 40506-0054USA Department of Molecular and Clinical Cancer Medicine Roy Castle Lung Cancer Research ProgrammeThe University of Liverpool Institute of Translational MedicineLiverpool L697Z

Although genome-wide association studies have identified more than eighty genetic variants associated with non-small cell lung cancer(NSCLC)risk,biological mechanisms of these variants remain largely *** integrating a large-scale genotype data of 15581 lung adenocarcinoma(AD)cases,8350 squamous cell carcinoma(SqCC)cases,and 27355 controls,as well as multiple transcriptome and epigenomic databases,we conducted histology-specific meta-analyses and functional annotations of both reported and novel susceptibility *** identified 3064 credible risk variants for NSCLC,which were overrepresented in enhancer-like and promoter-like histone modification peaks as well as DNase I hypersensitive *** factor enrichment analysis revealed that USF1 was AD-specific while CREB1 was *** annotation and genebased analysis implicated 894 target genes,including 274 specifics for AD and 123 for SqCC,which were overrepresented in somatic driver genes(ER=1.95,P=0.005).Pathway enrichment analysis and Gene-Set Enrichment Analysis revealed that AD genes were primarily involved in immune-related pathways,while SqCC genes were homologous recombination deficiency *** results illustrate the molecular basis of both wellstudied and new susceptibility loci of NSCLC,providing not only novel insights into the genetic heterogeneity between AD and SqCC but also a set of plausible gene targets for post-GWAS functional experiments.

关键词： lung cancer genome-wide association study function annotation immune homologous recombination repair deficiency genetic heterogeneity

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The cell surface marker CD36 selectively identifies matured,mitochondria-rich hPSC-cardiomyocytes

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细胞研究（英文版） 2020年第7期30卷 626-629页

作者： Ellen Ngar-Yun Poon Xiao-ling Luo Sarah E.Webb Bin Yan Rui Zhao Stanley Chun Ming Wu Yong Yang Peng Zhang Huajun Bai Jiaofang Shao Ching Man Chan Godfrey Chi-Fung Chan Suk Ying Tsang Rebekah L.Gundry Huang-Tian Yang Kenneth R.Boheler Department of Medicine and Therapeutics and Centre for Cardiovascular Genomics and Medicine The Chinese University of Hong Kong (CUHK) HKSAR China CAS Key Laboratory of Tissue Microenvironment and Tumor Laboratory of Molecular CardiologyShanghai Institute of Nutrition and Health University of Chinese Academy of Sciences (CAS) CAS Shanghai China Division of Life Science and State Key Laboratory of Molecular Neuroscience The Hong Kong University of Science and Technology HKSAR China Department of Computer Science The University of Hong Kong (HKU) HKSAR China Intervention and Cell Therapy Center Peking University Shenzhen Hospital Shenzhen China School of Life Sciences CUHK HKSAR China Department of Paediatrics and Adolescent Medicine HKU HKSAR China School of Biomedical Sciences HKU HKSAR China SUSTech Academy for Advanced Interdisciplinary Studies Southern University of Science and Technology (SUSTech) Shenzhen China Department of Bioinformatics School of Biomedical Engineering and InformaticsNanjing Medical University Nanjing Jiangsu China State Key Laboratory of Agrobiotechnology CUHK HKSAR China Department of Biochemistry and Center for Biomedical Mass Spectrometry Research Medical College of Wisconsin Milwaukee WIUSA CardiOmics Program Center for Heart and Vascular Research Division of Cardiovascular Medicine and Department of Cellular and Integrative Physiology University of Nebraska Medical Center Omaha NE USA Institute for Stem Cell and Regeneration Medicine CASBeijing China Division of Cardiology Department of Medicineand Department of Biomedical Engineering The Johns Hopkins University Baltimore MD USA

Dear Editor,Human pluripotent stem cell (hPSC)-derived cardiomyocytes (CMs) are of significant translational value to in vitro studies of human cardiac development, drug and cardiotoxicity testing and cardiac disease *** of hPSCs to CMs,however, yields mixed cultures of atrial-, ventricular-, and pacemaker-like cells as well as non-CMs in variable proportions.1

关键词： Stem-cell differentiation Stem cells

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Genetically-Defined Diffuse Large B-Cell Lymphoma Subsets Arise By Distinct Pathogenetic Mechanisms and Predict Outcome

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BLOOD 2017年 130卷 38-38页

作者： Chapuy, Bjoern Stewart, Chip Dunford, Andrew Kim, Jaegil Kamburow, Atanas Redd, Robert A. Lawrence, Michael Roemer, Margaretha G. M. Li, Amy Ziepert, Marita Staiger, Annette M. Wala, Jeremiah Ducar, Matthew D. Leshchiner, Ignaty Rheinbay, Esther Taylor-Weiner, Amaro Coughlin, Caroline Hess, Julian Pedamallu, Chandra Livitz, Dimitri Rosebrock, Daniel Rosenberg, Mara Tracy, Adam Horn, Heike van Hummelen, Paul Feldman, Andrew L. Link, Brian K. Novak, Anne J. Cerhan, James R. Habermann, Thomas M. Siebert, Reiner Rosenwald, Andreas Thorner, Aaron R. Meyerson, Matthew Golub, Todd R. Beroukhim, Rameen Wulf, Gerald Ott, German Rodig, Scott J. Monti, Stefano Neuberg, Donna S. Loeffler, Markus Pfreundschuh, Michael Trumper, Lorenz Getz, Gad Shipp, Margaret A. Dana-Farber Cancer Institute Boston MA Broad Institute Cambridge MA Section of Computational Biomedicine Boston University School of Medicine Boston MA Bioinformatics Program Boston University Boston MA Institute for Medical Informatics Statistics and Epidemiology University of Leipzig Leipzig Germany Department of Clinical Pathology Robert-Bosch-Krankenhaus Stuttgart Germany Dr Margarete Fischer-Bosch Institute of Clinical Pharmacology Stuttgart and University of Tuebingen Stuttgart Germany Center for Cancer Genome Discovery Dana-Farber Cancer Institute Boston MA

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Genomic, transcriptomic, and immunogenomic landscape of over 1300 sarcomas of diverse histology subtypes

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Nature communications 2025年第1期16卷 4206-4206页

作者： Soupir, Alex Ospina, Oscar E. Hampton, Oliver Churchman, Michelle Radmacher, Michael Hedges, Dale McKean, David Agius, Phaedra Zeeshan, Saman Seligson, Nathan D. Pollock, Raphael Liebner, David Chen, James L. Tinoco, Gabriel Salhia, Bodour McCarter, Martin Wilky, Breelyn A. Miller, Benjamin J. Cavnar, Michael J. Groundland, John S. Schneider, Bryan P. Riedlinger, Gregory Edge, Stephen B. Moskaluk, Christopher A. Cardona, Kenneth Naqash, Abdul Rafeh Gonzalez, Ricardo J. Mullinax, John E. Joyce, David M. Binitie, Odion Douglas Letson, G. Naghavi, Arash O. Druta, Mihaela Reed, Damon R. Siegel, Erin M. Teer, Jamie K. Fridley, Brooke L. Brohl, Andrew S. Department of Biostatistics and Bioinformatics Moffitt Cancer Center Tampa FL United States Hudson FL United States Department of Biomedical and Health Informatics School of Medicine University of Missouri Kansas City MO United States Department of Pharmacotherapy and Translational Research College of Pharmacy University of Florida Jacksonville FL United States Division of Surgical Oncology Ohio State University Comprehensive Cancer Center College of Medicine Ohio State University Wexner Medical Center Columbus OH United States Division of Medical Oncology Ohio State University Comprehensive Cancer Center College of Medicine Ohio State University Wexner Medical Center Columbus OH United States Department of Biology Norris Comprehensive Cancer Center Keck School of Medicine University of Southern California Los Angeles CA United States University of Colorado School of Medicine Aurora CO United States Department of Orthopaedics and Rehabilitation University of Iowa IO Iowa City United States Department of Surgery University of Kentucky Lexington KY United States University of Utah Huntsman Cancer Institute Salt Lake City UT United States Indiana University Simon Comprehensive Cancer Center Indianapolis 46202 IN United States Rutgers Cancer Institute of New Jersey New Brunswick NJ USA Roswell Park Comprehensive Cancer Center Buffalo NY United States Department of Pathology University of Virginia Charlottesville VA United States Division of Surgical Oncology Emory University Atlanta GA United States Medical Oncology/Phase 1 program Stephenson Cancer Center University of Oklahoma Health Sciences Oklahoma City OK United States Sarcoma Department Moffitt Cancer Center Tampa FL United States Department of Radiation Oncology Moffitt Cancer Center Tampa FL United States Department of Individualized Cancer Management Moffitt Cancer Center Tampa FL United States Department of Cancer Epidemiology Moffitt Cancer Center Tampa FL United State

Given their rarity and diversity, a fundamental understanding of the genomic underpinnings for many sarcoma subtypes is still lacking. To better define the molecular landscape of this group of diseases, we perform matched whole exome sequencing and RNA sequencing on a cohort of 1340 sarcoma tumor specimens. We identify recurrent somatic mutations and observe an increased mutational burden in metastatic vs. primary samples (p < 0.001). We observe frequent copy number alterations including whole genome doubling, with this feature being more common in metastatic tumors (p = 0.026). Estimation of immune cell abundances followed by hierarchical clustering identifies five immune subtypes ranging from low to high and we observe inferior overall survival in immune deplete clusters compared to immune enriched (p < 0.01). Interestingly, GIST predominantly form a distinct "immune intermediate" cluster that is marked by a specific enrichment for NK cells (FDR < 0.01). © 2025. The Author(s).

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Estimating Classification Confidence Using Kernel Densities

arXiv

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arXiv 2022年

作者： Salamon, Peter Salamon, David Cantu, V. Adrian An, Michelle Perry, Tyler Edwards, Robert A. Segall, Anca M. The Department of Mathematics and Statistics The Computational Science Research Center The Viral Information Institute San Diego State University San DiegoCA92182 United States The Department of Mathematics and Statistics San Diego State University San DiegoCA92182 United States The Computational Science Research Center The Department of Biology San Diego State University San DiegoCA92182 United States The Perelman School of Medicine The University of Pennsylvania 425 Johnson Pavilion 3610 Hamilton Walk PhiladelphiaPA19104 United States The Computational Science Research Center San Diego State University San DiegoCA92182 United States Google 1600 Amphitheater Parkway Mountain ViewCA94043 United States The Bioinformatics and Medical Informatics Program San Diego State University San DiegoCA92182 United States Helix 9875 Towne Center Drive San DiegoCA92121 United States The Department of Biology The Computational Science Research Center The Viral Information Institute The Bioinformatics and Medical Informatics Program San Diego State University San DiegoCA92182 United States

This paper investigates the post-hoc calibration of confidence for "exploratory" machine learning classification problems. The difficulty in these problems stems from the continuing desire to push the boundaries of which categories have enough examples to generalize from when curating datasets, and confusion regarding the validity of those categories. We argue that for such problems the "one-versus-all" approach (top-label calibration) must be used rather than the "calibrate-the-full-response-matrix" approach advocated elsewhere in the literature. We introduce and test four new algorithms designed to handle the idiosyncrasies of category-specific confidence estimation. Chief among these methods is the use of kernel density ratios for confidence calibration including a novel, bulletproof algorithm for choosing the bandwidth. We test our claims and explore the limits of calibration on a bioinformatics application (PhANNs) [1], [2] as well as the classic MNIST benchmark [3]. Finally, our analysis argues that post-hoc calibration should always be performed, should be based only on the test dataset, and should be sanity-checked visually. Copyright © 2022, The Authors. All rights reserved.

关键词： Calibration

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A transcriptome meta-analysis of ethanol embryonic exposure: Implications in neurodevelopment and neuroinflammatory genes

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Neuroscience informatics 2022年第3期2卷 100094-100094页

作者： Lord, Vinícius Oliveira Giudicelli, Giovanna Câmara Recamonde-Mendoza, Mariana Vianna, Fernanda Sales Luiz Kowalski, Thayne Woycinck Laboratory of Genomic Medicine Center of Experimental Research Hospital de Clínicas de Porto Alegre (HCPA) Porto Alegre Brazil Centro Universitário CESUCA Cachoeirinha Brazil Post-Graduation Program in Genetics and Molecular Biology Genetics Department Universidade Federal do Rio Grande do Sul (UFRGS) Porto Alegre Brazil Institute of Informatics Universidade Federal do Rio Grande do Sul (UFRGS) Porto Alegre Brazil Bioinformatics Core Hospital de Clínicas de Porto Alegre (HCPA) Porto Alegre Brazil National Institute of Medical Population Genetics (INAGEMP) Porto Alegre Brazil Post-Graduation Program in Medical Sciences Medical College Universidade Federal do Rio Grande do Sul (UFRGS) Porto Alegre Brazil

Fetal Alcohol Spectrum Disorder (FASD) comprises the phenotypes induced by prenatal alcohol exposure. Understanding the molecular mechanisms of FASD is needed since it is a public health problem. This study aimed to evaluate the impact of ethanol in the differential gene expression (DGE) of embryonic cells and fetal tissues by performing a transcriptome meta-analysis in microarrays datasets publicly available. The datasets were obtained in the GEO database and DGE was evaluated, followed by meta-analysis. DGE was also analyzed in a RNA-Seq dataset, although it was not included in the meta-analysis. To filter the main candidate genes, a database and literature review was performed, followed by ontologies enrichment analyses. In the meta-analysis, 1,938 genes were deregulated and 487 were perturbed in the RNA-Seq. Calcium homeostasis and neuroinflammation genes were overrepresented in the meta-analysis and RNA-Seq, respectively. After the database and literature review, DOCK8, FOXG1, IL1RN, and PRKN genes were proposed as new candidates for FASD;they are associated with neurodevelopment and neuroinflammation. BDNF and SLC2A1, previously associated to FASD, were also suggested in meta-analysis as candidate genes. It is known neuroinflammation reduction might help to minimize the alcohol damage. Hence, there is an urgent need to understand FASD molecular mechanisms to help in strategies aimed at preventing ethanol-induced neurologic damage. © 2022 The Authors

关键词： bioinformatics Differential gene expression Fetal alcohol spectrum disorder Microarray Neurophenotypes Ontology Prenatal ethanol exposure Random effect model RNA-Seq

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