2018 3rd International Conference on Public Health and Medical Sciences
May 29-31, 2018, Hangzhou, China
中文版 More Conferences
Days to the Submission Deadline
Important Dates
SubmissionJan. 20, 2018
    Extended to Apr. 20, 2018
Notification20-40 days after the submission
Publication15-20 days after the final edition
ConferenceMay 29-31, 2018
Keynote Speakers

The information about the Keynote Speakers of ICPHMS2018 are as follows, which will be updated regularly.

Dr. Xingyi Guo, Assistant Professor
Division of Epidemiology, Department of Medicine, Vanderbilt University Medical Center, USA

Biography: Dr. Xingyi Guo obtained his PhD in bioinformatics from Zhejiang University in 2008, and completed his postdoctoral training in functional genomics and bioinformatics lab, at Albert Einstein College of Medicine from 2008 to 2013. After postdoctoral training, he joined Vanderbilt as a Research Assistant Professor in the Department of Biomedical Informatics in March of 2013, and then joined the Division of Epidemiology in November of 2013. He was then converted to the tenure-track as an Assistant Professor in 2017. Dr. Guo has a strong track record on studies of bioinformatics, genetics and cancer epidemiology. He has more than 40 peer-reviewed publications in these fields. His research currently concentrates on genetic epidemiological studies aiming to identify putative causative genetic and epigenetic factors for cancer risk and outcome using bioinformatics and functional genomics approaches.

Topic: Identifying Putative Causative Variants and Genes for Cancer Risk Using Functional Genomics Approaches

Abstract: Previous genome-wide association studies (GWAS), have identified approximately 150 genetic susceptibility loci associated with breast cancer risk. However, the target genes and underlying mechanisms for the large majority of the identified associations remain unknown. We recently completed studies to systematically identify potential target genes for GWAS-identified single nucleotide polymorphisms (index SNPs) using a cis-expression quantitative trait loci (cis-eQTL) analysis based on genetic and transcriptome datasets from tumor tissue samples from the Genotype-Tissue Expression (GTEx), The Cancer Genome Atlas (TCGA), and the Molecular Taxonomy of Breast Cancer International Consortium (METABRIC). A total of 101 potential eQTL target genes were identified at Benjamini-Hochberg adjusted P < 0.05. Using various functional genomics data from ENCODE, ROADMAP and literature, we further demonstrated that many identified target genes showed evidence of cis-regulation by putative functional SNPs (in strong linkage disequilibrium with the index SNPs) via promoter or enhancer-promoter interactions. We next performed in vitro functional assays for multiple genes, and confirmed that they play a vital role in beast carcinogenesis via disruption of cell behavior. In summary, our findings revealed novel biological mechanisms for understanding genetic susceptibility risk loci and provided additional insight into understanding the pathogenesis of breast cancer.

Dr. Ruoling Chen, Professor
Faculty of Education, Health and Wellbeing, University of Wolverhampton, UK

Biography: Dr. Ruoling Chen is the Professor of Public Health and Medical Statistics at the University of Wolverhampton, UK. He was awarded a PhD degree from the University of Aberdeen, UK in 1997, after studying medicine and medical statistics in China. Dr. Chen worked at the Universities of Liverpool, Dundee and London (UCL and KCL) as a lecturer, senior lecturer and principle investigator respectively, for 20 years. His research areas and expertise include epidemiology and global public health. Dr. Chen is the Lead for Global Health and Epidemiology at the University of Wolverhampton. Currently he supervises four PhD students and leads a research group including post-doc researchers and senior academic staff to work on new risk factors and care for dementia. Dr. Chen has published widely in epidemiology and public health research fields.

Topic: Air Pollution and Dementia Risk – where is evidence?

Abstract: Objectives. Air pollution is associated with increased risk of respiratory and cardiovascular diseases, but it’s a/ssociation with dementia is unclear. The aim of this study is to assess the evidence of impacts of air pollution on the development of dementia, and its possible pathological mechanisms.
Methods. We systematically searched literature and identified seven population-based studies on the topic and a number of articles on the mechanisms.
Results. In seven studies one was case-control and six were cohort studies with 11-16 years follow-up, and the number of participants varied from 871 to 2,165,268. Six studies measured at least one of air pollutants of nitrogen oxide(s), nitrogen dioxide, small/larger particulate matter, Ozone and carbon monoxide, while one study investigated the residential distance from the nearest major road as pollution indices. Although there were variations in pollutants assessment and in data analysis methods, all studies showed a significant association of air pollution with the risk of dementia, except for one measuring ozone exposure (adjusted hazard ratio 0.98, 95%CI 0.96-1.00). Our meta-analysis demonstrated significant associations of different air pollutants with increasedrisk of dementia. There are several hypotheses about the impacts of air pollution on dementia, and the neuroinflammation is a main focus to be studied.
Conclusions. The evidence to date is coherent in that exposure to a range of air pollutants has increased the risk of dementia. There is insufficient evidence at present to comment on consistency, in view of the different indices of pollution, the limited number of studies, and the probability at this stage of publication bias. However, plausible neuroinflammatory mechanisms have been demonstrated and the evidence as a whole suggests that ambient air pollution contributes to the development of dementia.

Dr. Yi Wang, Assistant Professor
Department of Environmental Health, Indiana University Richard M. Fairbanks School of Public Health, USA

Biography: Dr. Yi Wang is an environmental epidemiologist, who enjoys working with community and on project with community and policy impact. His research focuses on health effects of air pollution, environmental justice in local community and local impact of climate change on health. Dr. Wang is an Assistant Professor of Environmental Health at Indiana University Richard M Fairbanks School of Public Health. He received his PhD in Environmental Health Sciences from University of Michigan School of Public Health, followed by postdoctoral training in environmental epidemiology at Brown University School of Public Health.

Topic: Health, Air Pollution and Environmental Equity in Community

Abstract: Millions around the world are chronically exposed to environmental hazards including air pollution, solid waste, hazardous waste discharge and drinking water contamination, as a result of the legacy of industrial development and processes. Environmental equity across residents and communities became an increasingly important issue especially for disadvantaged communities. Using Indiana and City of Indianapolis as examples, the Multi-layered Data Community Action Tool (MDCAT) was created to provide vulnerability index of environmental burden across local communities (http://hecap.net/). Dr. Wang’s research team leveraged MDCAT to successfully convince Indianapolis Office of Metro Development to include environmental equity in Indy2020 Indy Land Use Plan. The expansion of this tool for scenarios under the threat of climate change has also been archived by the US Climate Resilience Toolkit. Dr. Wang has shared his insights of impact-oriented research with a US-China State Government sponsored delegation of Chinese universities and CDC researchers in 2017.

Dr. Serena Kuang, Assistant Professor
Department of Biomedical Sciences, Oakland University William Beaumont School of Medicine (OUWB), USA

Biography: Dr. Serena Kuang received her PhD in Neuroengineering at Clemson University in 2014. She is an assistant professor in the Department of Biomedical Sciences at Oakland University William Beaumont School of Medicine. She teaches M1 and M2 medical students Physiology and Neuroscience I courses and conducts research in the field of electrophysiology. She is specialized in the study of the behavior of the cultured neuronal network and the microelectrode array (MEA) technology. The coupling of the two establishes an in vitro neuronal network platform, which enables research studies with a wide spectrum of purposes involving multiple disciplines such as pharmacology, neurotoxicology, neuroscience, and neuron-based biosensor development. She and her coworkers pioneered the investigation of a rarely used but abundant and economic cortical neuron resource, chick forebrain neurons (C-FBNs), conducting fundamental works to characterize the morphology, development, and function of the neuronal networks formed from dissociated C-FBNs and cultured on the MEA chips. Their work demonstrated that the C-FBNs are able to achieve long-term lifespan with both stability in the electrophysiology and sensibility toward environmental changes, thus are a valuable, convenient cortical neuron resource to be utilized as a novel model of an in vitro neuronal network.

Topic: Chick Forebrain Neurons on A Microelectrode Array: A Novel Functional Platform for a Wide Spectrum of Research Purposes

Abstract: The development of the microelectrode array (MEA) technology has remarkably accelerated in vitro electrophysiological studies using the cultured neuronal networks. The most widely used animal neurons are rodent cortical neurons. However, the cost of rodent cortical neurons limits the use of rodent neuronal cultures in a large scale. We have explored an abundant economic cortical neuron resource - chick forebrain neurons. In this presentation, we will report that we have 1) successfully established a long-term stable chick forebrain neuronal network on the MEA platform; 2) characterized it morphologically, functionally, and developmentally; 3) tested its responsiveness toward several classic neuroactive agents; 4) partially compared its physiology and pharmacology with the rodent counterparts; and finally, 5) partially evaluated its sensitivity and stability, and its potential as a novel functional platform for a wide spectrum of research purposes.

Dr. Stephen Hsu, Professor
Department of Oral Biology, Department of Oral Health & Diagnostic Sciences, Dental College of Georgia, Augusta University (Formerly the Medical College of Georgia), USA

Biography: Dr. Stephen Hsu earned a bachelor’s degree in biochemistry from Wuhan University, a Master of Arts degree in molecular biology from Montclair State University and a Ph.D. in cell biology and anatomy from the University of Cincinnati, College of Medicine. He completed a postdoctoral fellowship at Memorial Sloan-Kettering Cancer Center in New York City. Dr. Hsu joined the Augusta University, formerly the Medical College of Georgia, in 1999 and is currently a tenured professor. He is a world-renowned expert in green tea polyphenol research and inventor of green tea technology-derived products and medications, which treat dry mouth, dandruff, hair loss, cold sores, and viral infections with natural ingredients. Dr. Hsu received the Ruth L. Kirstein Research Service Award from the National Cancer Institute. His most recent NIH project is to test the virucidal activity of lipophilic EGCG against norovirus. He was awarded a number of patents on novel technologies targeting autoimmune diseases, herpes simplex virus, virus-induced infections, and salivary dysfunction (xerostomia or dry mouth). Dr. Hsu has been selected as a TED Talk speaker in 2014. He received the International Association for Dental Research (IADR)/GSK Innovation in Oral Care Award in 2011. In 2015, he received Georgia Bio Innovation Award for his unique inventions. Also in 2015, Dr. Hsu received Oral Discoveries & Inventions Award from Georgia Dental Association. Dr. Hsu is also a recipient of two overseas talent awards (Wuhan 3551, and Hubei Chu-Tian Scholar) from China.

Topic: Persistent Virucidal Activity in a Novel Alcohol-Based Sanitizer Formulation Containing EGCG for Potential Use Against Norovirus

Abstract: Norovirus is a major cause of acute gastroenteritis. Alcohol sanitization is ineffective, and currently used alcohol-based hand sanitizers are not recommended by the CDC for norovirus in healthcare settings. The current study evaluated virucidal and bactericidal activity and surface persistence of a novel alcohol-based hand sanitizer formulation, ProtecTeaV, containing lipophilic epigallocatechin-3-gallate (EGCG-p) against a human norovirus surrogate and two bacterial strains. Virucidal capacity against feline calicivirus (FCV) was tested using a standard 50% Tissue Culture Infective Dose (TCID50) suspension assay. Persistence of residual virucidal activity after application on a clean surface was determined through 12 hours. Controls included the formulation without EGCG-p, popular alcohol-based sanitizers, and antibacterial liquid hand soap (LHS). Statistical analysis employed one-way ANOVA (alpha=0.05). Suspension assay results demonstrated that the ProtecTeaV formulation effectively reduced FCV viral infectivity >log10 4 (10,000 fold). Surface applied residue activity remained strong (reduction of infectivity by > log10 3) through 12 hours. In comparison, LHS did not show virucidal activity without washing with water, and other controls failed to reduce infectivity by more than log10 3 (1,000 fold). Results from bactericidal suspension tests demonstrated that ProtecTeaV formulation reduced colony forming united (CFU) of Escherichia coli and Staphylococcus aureus by more than log10 6 (1 million fold). In conclusion, this non-toxic hand sanitizer/surface disinfectant demonstrated effective and prolonged virucidal activities against a norovirus surrogate. Therefore, the EGCG-p formulation is potentially a novel and effective approach to prevent norovirus outbreaks.

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