Nutrigenomics and Nutrigenetics and the Medicinal Values of Vegetables and Fruits

2018 ◽  
pp. 52-67
Author(s):  
E. William Ebomoyi

Since the accomplishment of the human genome sequencing project by March 25, 2003, nutritionists, biochemists, and modern genome epidemiologists became involved in genome-based nutritional research studies. In fact, the completion of a high-quality, comprehensive sequencing of the human genome derived from the discovery of the double-helical structure of the DNA became a landmark event that has influenced several realms of academic research disciplines and their applications to maximize public health and minimize harm to health care consumers.

Since the accomplishment of the human genome sequencing project by March 25, 2003, nutritionists, biochemists, and modern genome epidemiologists became involved in genome-based nutritional research studies. In fact, the completion of a high-quality, comprehensive sequencing of the human genome derived from the discovery of the double-helical structure of the DNA became a landmark event that has influenced several realms of academic research disciplines and their applications to maximize public health and minimize harm to health care consumers.


2011 ◽  
pp. 51-84 ◽  
Author(s):  
Richard A. Stein

The 1953 discovery of the DNA double-helical structure by James Watson, Francis Crick, Maurice Wilkins, and Rosalind Franklin, represented one of the most significant advances in the biomedical world (Watson and Crick 1953; Maddox 2003). Almost half a century after this landmark event, in February 2001, the initial draft sequences of the human genome were published (Lander et al., 2001; Venter et al., 2001) and, in April 2003, the International Human Genome Sequencing Consortium reported the completion of the Human Genome Project, a massive international collaborative endeavor that started in 1990 and is thought to represent the most ambitious undertaking in the history of biology (Collins et al., 2003; Thangadurai, 2004; National Human Genome Research Institute). The Human Genome Project provided a plethora of genetic and genomic information that significantly changed our perspectives on biomedical and social sciences. The sequencing of the first human genome was a 13-year, 2.7-billion-dollar effort that relied on the automated Sanger (dideoxy or chain termination) method, which was developed in 1977, around the same time as the Maxam-Gilbert (chemical) sequencing, and subsequently became the most frequently used approach for several decades (Sanger et al., 1975; Maxam & Gilbert, 1977; Sanger et al., 1977). The new generations of DNA sequencing technologies, known as next-generation (second generation) and next-next-generation (third generation) sequencing, which started to be commercialized in 2005, enabled the cost-effective sequencing of large chromosomal regions during progressively shorter time frames, and opened the possibility for new applications, such as the sequencing of single-cell genomes (Service, 2006; Blow, 2008; Morozova and Marra, 2008; Metzker, 2010).


This project focused on the return on investment from the Human Genome Sequencing Project, and we characterized the quality of life indices and economic resources in the G8 nations. The research team explored the existing scientific infrastructures already in place in the industrialized nations, even before the completion of the human genome sequencing by March 2003. Their authentic and well-established technological workforce developed a new generation of innovative technologies for inexpensive, spontaneous, and precise genomic sequencing. The project team not only discussed the medical, public health and economic benefits derived from genomic research, but also compiled the fledging careers in bioscience and genetics in the G8 nations.


2006 ◽  
Vol 2006 ◽  
pp. 1-11 ◽  
Author(s):  
Ahmet Kara

This paper demonstrates the existence, in a particular subset of the Turkish public health care sector, of equilibria moving towards a low-quality trap over time. The dynamics of the movement in question hinges, in part, on the socially necessary but demographically asymmetric burden, on some public health care institutions, of providing affordable health care to certain sections of the population. The paper formulates a policy option that could help the sector to escape the trap, moving the sector towards high quality-high welfare equilibria.


2013 ◽  
Vol 12 (1) ◽  
pp. 6-9 ◽  
Author(s):  
Charles J.M. Bell

PurposePatient‐defined spiritual aspects of mental health care are an understudied and potentially important aspect to non‐pharmaceutical treatments. A review of this area will lead to improved rigorous research and better patient outcomes. The purpose of this paper is to examine the public health implications of spiritual healing practice, in conditions such as depression.Design/methodology/approachThe current research into spiritual healing was reviewed, and in particular its use in depression. Scientific and anecdotal evidence was considered, and areas of improvement were identified.FindingsThe attitudes of physicians and patients may affect the efficacy of patient‐defined spiritual healing, which is currently lacking in rigorous academic research. A better scientific understanding may aid in a cost‐benefit analysis of such treatments in the future.Originality/valueThis paper should aid those involved in public health‐care planning or who practice psychotherapeutic methods to ensure they utilise all possible methods, whilst working within a rigorous evidence‐based framework.


Author(s):  
Gustavo Camps-Valls ◽  
Alistair Morgan Chalk

Bioinformatics is a new, rapidly expanding field that uses computational approaches to answer biological questions (Baxevanis, 2005). These questions are answered by means of analyzing and mining biological data. The field of bioinformatics or computational biology is a multidisciplinary research and development environment, in which a variety of techniques from computer science, applied mathematics, linguistics, physics, and, statistics are used. The terms bioinformatics and computational biology are often used interchangeably (Baldi, 1998; Pevzner, 2000). This new area of research is driven by the wealth of data from high throughput genome projects, such as the human genome sequencing project (International Human Genome Sequencing Consortium, 2001; Venter, 2001). As of early 2006, 180 organisms have been sequenced, with the capacity to sequence constantly increasing. Three major DNA databases collaborate and mirror over 100 billion base pairs in Europe (EMBL), Japan (DDBJ) and the USA (Genbank.) The advent of high throughput methods for monitoring gene expression, such as microarrays (Schena, 1995) detecting the expression level of thousands of genes simultaneously. Such data can be utilized to establish gene function (functional genomics) (DeRisi, 1997). Recent advances in mass spectrometry and proteomics have made these fields high-throughput. Bioinformatics is an essential part of drug discovery, pharmacology, biotechnology, genetic engineering and a wide variety of other biological research areas. In the context of these proceedings, we emphasize that machine learning approaches, such as neural networks, hidden Markov models, or kernel machines, have emerged as good mathematical methods for analyzing (i.e. classifying, ranking, predicting, estimating and finding regularities on) biological datasets (Baldi, 1998). The field of bioinformatics has presented challenging problems to the machine learning community and the algorithms developed have resulted in new biological hypotheses. In summary, with the huge amount of information a mutually beneficial knowledge feedback has developed between theoretical disciplines and the life sciences. As further reading, we recommend the excellent “Bioinformatics: A Machine Learning Approach” (Baldi, 1998), which gives a thorough insight into topics, methods and common problems in Bioinformatics. The next section introduces the most important subfields of bioinformatics and computational biology. We go on to discuss current issues in bioinformatics and what we see are future trends.


2017 ◽  
Vol 2017 ◽  
pp. 1-11 ◽  
Author(s):  
Lolemo Kelbiso ◽  
Admasu Belay ◽  
Mirkuzie Woldie

Background. A high quality of work life (QWL) is a crucial issue for health care facilities to have qualified, dedicated, and inspired employees. Among different specialties in health care settings, nurses have a major share among other health care providers. So, they should experience a better QWL to deliver high-quality holistic care to those who need help. Objective. To assess the level of quality of work life and its predictors among nurses working in Hawassa town public health facilities, South Ethiopia. Methods. A facility based cross-sectional study was conducted on 253 nurses of two hospitals and nine health centers. The total sample size was allocated to each facility based on the number of nurses in each facility. Data were collected using a structured questionnaire. The interitem consistency of the scale used to measure QWL had Cronbach’s alpha value of 0.86. A multinomial logistic regression model was fitted to identify significant predictors of quality of work life using SPSS version 20. Results. The study showed that 67.2% of the nurses were dissatisfied with the quality of their work life. We found that educational status, monthly income, working unit, and work environment were strong predictors of quality of work life among nurses (p<0.05). Conclusion. Significant proportions of the nurses were dissatisfied with the quality of their work life. The findings in this study and studies reported from elsewhere pinpoint that perception of nurses about the quality of their work life can be modified if health care managers are considerate of the key issues surrounding QWL.


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