User:Sqkatz/sandbox

This is Spencer Katz's Sandbox

Project 1 (Edit existing article) – Patrick Brown https://wiki.riteme.site/wiki/Patrick_O._Brown

Description: Added the following 2 sentences to the career section of Patrick Brown’s page:

In 2001, Brown helped lead the Public Library of Science (PLOS) initiative to make published scientific research open access and freely available to researchers in the scientific community. He and Michael Eisen of Lawrence Berkeley National Laboratory advocated for designing alternative systems to fund for scientific publishing.

Personal Genomics.

https://wiki.riteme.site/wiki/Personal_genomics#Use_of_personal_genomics_in_predictive_and_precision_medicine

Description: Added or edited the info on the following sections of the Personal genomics page

Personal Genomics

Add:

The emerging market of direct-to-consumer genome sequencing services has brought new questions about both the medical efficacy and the ethical dilemmas associated with widespread knowledge of individual genetic information.

Personal Genomics in Personalized Medicine

Personalized Medicine is a medical method that targets treatment structures and medicinal decisions based on a patient’s predicted response or risk of disease. The National Cancer Institute or NCI, an arm of the National Institutes of Health, lists a patient’s genes, proteins, and environment as the primarily factors analyzed to prevent, diagnose, and treat disease through personalized medicine.

There are various subcategories of the concept of Personalized Medicine such as Predictive Medicine, Precision Medicine and Stratified Medicine. Although these terms are used interchangeably to describe this practice, each carries individual nuances. Predictive Medicine describes the field of medicine that utilizes information, often obtained through personal genomics techniques, to both predict the possibility of disease, and institute preventative measures for a particular individual. Precision Medicine is a term extremely similar to Personalized Medicine in that it focuses on a patient’s genes, environment, and lifestyle, however, is utilized by National Research Council to avoid any confusion or misinterpretations associated with the broader term. Stratified Medicine is a version of Personalized Medicine which focuses on dividing patients into subgroups based on specific responses to treatment, and identifying effective treatments for the particular group.

Examples of the use of personalized medicine include Oncogenomics and Pharmacogenomics. Oncogenomics is a field of study focused on the characterization of cancer–related genes. With cancer, specific information about a tumor is used to help create a personalized diagnosis and treatment plan.  Pharmacogenomics is the study of how a person’s genome affects their response to drugs. This field is relatively new but growing fast due in part to an increase in funding for the NIH Pharmacogenomics Research Network. Since 2001, there has been an almost 550% increase in the number of research papers in PubMed related to the search terms pharmacogenomics and pharmacogenetics. This field allows researchers to better understand how genetic differences will influence the body’s response to a drug and inform which medicine is most appropriate for the patient. These treatment plans will be able to prevent or at least minimize the adverse drug reactions which are a, “significant cause of hospitalizations and deaths in the United States.” Overall, researchers believe pharmacogenomics will allow physicians to better tailor medicine to the needs of the individual patient. As of November 2016, the FDA has approved 204 drugs with pharmacogenetics information in its labeling. These labels may describe genotype-specific dosing instructions and risk for adverse events amongst other information.

Cost of sequencing an individual's genome

The National Human Genome Research Institute, an arm of the U.S. National Institutes of Health, has reported that the cost to sequence a whole human-sized genome has dropped from about $14 million in 2006, to below $1,500” by late 2015.

Ethical issues

The passage of the Affordable Care Act in 2010, strengthened the GINA protections by prohibiting health insurance companies from denying coverage because of patient’s ‘pre-existing conditions’ and removing insurance issuers ability to adjust premium costs based on certain factors such as genetic diseases.

There are also concerns regarding human genome research in developing countries. The tools for conducting whole genome analyses are generally found in high income nations, necessitating partnerships between developed and developing countries in order to study the patients afflicted with certain diseases. The relevant tools for sharing access to the collected data are not equally accessible across low-income nations and without an established standard for this type of research, concerns over fairness to local researchers remain unsettled.

Another ethical consideration with regards to personal genomics that as of 2016 appears remote, yet, remains important to contemplate, is the impact of whole genome sequencing on non-consenting family members. While an individual's familial consent is not required for genome-sequencing research, information personal to genetically related people may end up being revealed against their wishes.

Other Issues

Genetic Privacy:

In the United States, biomedical research containing human subjects is governed by a baseline standard of ethics known as The Common Rule, which aims to protect a subject's privacy by requiring “identifiers” such as name or address to be removed from collected data.  A 2012 report by the Presidential Commission for the Study of Bioethical Issues stated, however, that “what constitutes ‘identifiable’ and ‘de-identified’ data is fluid and that evolving technologies and the increasing accessibility of data could allow de-identified data to become re-identified.” In fact, research has already shown that it is “possible to discover a study participant’s identity by cross-referencing research data about him and his DNA sequence … [with] genetic genealogy and public-records databases.” This has led to calls for policy-makers to establish consistent guidelines and best practices for the accessibility and usage of individual genomic data collected by researchers.

There is also controversy regarding the concerns with companies testing individual DNA. There are issues such as "leaking" information, the right to privacy and what responsibility the company has to ensure this does not happen. Regulation rules are not clearly laid out. What is still not determined is who legally owns the genome information: the company or the individual whose genome has been read. There have been published examples of personal genome information being exploited. Additional privacy concerns, related to, e.g., genetic discrimination, loss of anonymity, and psychological impacts, have been increasingly pointed out by the academic community  as well as government agencies.

Personalized Genome Utility

Full genome sequencing holds large promise in the world of healthcare in the potential of precise and personalized medical treatments. This use of genetic information to select appropriate drugs is known as pharmacogenomics. This technology may allow treatments to be catered to the individual and the certain genetic predispositions they may have (such as personalized chemotherapy).

At the same time, full sequencing of the genome can identify polymorphisms that are so rare that no conclusions may be drawn about their impact, creating uncertainty in the analysis of individual genomes, particularly in the context of clinical care. Czech medical geneticist Eva Machácková writes: "In some cases it is difficult to distinguish if the detected sequence variant is a causal mutation or a neutral (polymorphic) variation without any effect on phenotype. The interpretation of rare sequence variants of unknown significance detected in disease-causing genes becomes an increasingly important problem." ^{In fact, the average person is a carrier of 54 genetic mutations that are classified as lethal, yet presents no negative effect on their health.}

Doctors are currently conducting tests for which some are not correctly trained to interpret the results. Many are unaware of how SNPs respond to one another. This results in presenting the client with potentially misleading and worrisome results which could strain the already overloaded health care system. This may antagonize the individual to make uneducated decisions such as unhealthy lifestyle choices and family planning modifications. Moreover, negative results which may potentially be inaccurate, theoretically decrease the quality of life and mental health of the individual (such as increased depression and extensive anxiety).

Direct to Consumer Genetics

There are also three potential problems associated with the validity of personal genome kits. The first issue is the test’s validity. Handling errors of the sample increases the likelihood for errors which could affect the test results and interpretation. The second affects the clinical validity, which could affect the test’s ability to detect or predict associated disorders. The third problem is the clinical utility of personal genome kits and associated risks, and the benefits of introducing them into clinical practices.

Patients will need to be educated on interpreting their results and what they should be rationally taking from the experience. It is not only the average person who needs to be educated in the dimensions of their own genomic sequence but also professionals, including physicians and science journalists, who must be provided with the knowledge required to inform and educate their patients and the public  Examples of such efforts include the Personal Genetics Education Project (pgEd) and the Smithsonian collaboration with NHGRI