User:Sh1539/Genetic discrimination

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Genetic discrimination occurs when people treat others (or are treated) differently because they have or are perceived to have a gene mutation(s) that causes or increases the risk of an inherited disorder. It may also refer to any and all discrimination based on the genotype of a person rather than their individual merits, including that related to race. Some legal scholars have argued for a more precise and broader definition of genetic discrimination: "Genetic discrimination should be defined as when an individual is subjected to negative treatment, not as a result of the individual's physical manifestation of disease or disability, but solely because of the individual's genetic composition." Genetic discrimination is considered to have its foundations in genetic determinism and genetic essentialism, and is based on the concept of genism, i.e. distinctive human characteristics and capacities are determined by genes.

Genetic discrimination takes different forms depending on the country and the protections that have been taken to limit genetic discrimination, such as GINA in the United States that protects people from being barred from working or from receiving healthcare as a result of their genetic makeup. The umbrella of genetic discrimination also includes the notion of informed consent, which refers to an individual's right to make a decision about their participation in research with complete comprehension of the research study. '''Within the United States, genetic discrimination is an ever-evolving concept that remains prominent across different domains. Emerging technology such as direct-to-consumer genetic tests have allowed for broad genetic health information to be more accessible to the public, but raises concerns about privacy. In addition, the COVID-19 pandemic has exacerbated difficulties of those with genetic conditions as they have faced discrimination within the U.S. healthcare system.'''

The idea of genetic discrimination has been combatted since the 1947 Nuremberg Code that was created shortly after WWII, during which thousands of racialized and disabled victims died in tests conducted in Germany. Since then, new issues of racialized genetic discrimination have come to light involving sharing of genetic information to genomic biobanks and subsequent novel treatments. Many countries are still developing policies to combat genetic discrimination in science, law, and everyday life.

United States[edit]
There are multiple legal protections in place in the United States, such as Genetic Information Nondiscrimination Act (GINA), the Americans with Disabilities Act (ADA), and the Affordable Care Act (ACA), which all help to prevent genetic discrimination in the workplace, public services, and provide some insurance protection. Therefore, by law, those with genetic conditions are protected from possible discrimination and have a right to receive equitable care.

Genetic discrimination is illegal in the U.S. after passage of the Genetic Information Nondiscrimination Act (GINA) on May 21, 2008. It was signed into law by President George W. Bush, and passed in the US Senate by a vote of 95–0 and in the House of Representatives by 414–1. The legislation bars employers from using individuals' genetic information when making hiring, firing, job placement, or promotion decisions. GINA also protects individuals from genetic discrimination in healthcare; however, GINA itself does not define what genetic information is, leaving it up for debate. Prior to the 2008 GINA Act, individuals could be denied insurance, either partially or fully, based on genetic tests they had received.

Although it was passed in 2008 there were 201 cases that cited GINA in 2010 and 333 in 2014. It wasn't until 2013 that a company actually faced penalties under GINA.

Genetic Discrimination During COVID-19
COVID-19, or a coronavirus labeled SARS-CoV-2, is a highly-transmittable, respiratory virus first identified in Wuhan, China in December 2019 and the virus has since spread globally and reached a pandemic status. Individuals with co-morbidities, such as pre-existing conditions and disabilities like cardiovascular disease, diabetes, immunocompromised conditions, obesity, etc, are more likely to experience severe COVID-19 symptoms and have greater risk of worse outcomes, such as death. Genetic conditions are among some of the causes of these co-morbid conditions. While the body of knowledge surrounding COVID-19 and genetic susceptibilities to the virus is continually growing with new research, there is a preliminary understanding that genetic conditions or inherited mutations can increase one's likelihood of experiencing severe symptoms. Due to this increased potential of contraction and subsequent severe symptoms, individuals with genetic conditions are among those with co-morbidities that have received cautionary advisories from the CDC and preferential designation for the rollout of COVID-19 vaccines.

During the beginning months of the pandemic, existing legal protections, like GINA and the ADA, were put to the test. With scarce resources, including PPE, ventilators, and other crucial equipment, doctors and heath care systems were put under incredible stress to treat an ever-increasing number of patients and in some places still continue to battle high numbers of cases. Due to the overwhelming surge in COVID-19 cases, hospital systems needed to enact triage protocols, or a system of guidelines meant to help direct resources and help health care professionals make choices about limited supplies. There were instances across the country early in the pandemic, where hospitals were accused of enacting discriminatory triage protocols which excluded those with genetic conditions, such as in Tennessee, where those with spinal muscular atrophy, a autosomal recessive disease, or other disabilities were prevented from receiving ventilators or other scarce resources. In other states for example, like Washington and Alabama, hospitals were accused of more broad discriminatory allocation policies which prevented larger groups of individuals with genetic conditions under categorizations of "chronic conditions" or "intellectual disabilities," from receiving life saving treatments, such as ventilators. Many advocacy groups raised complaints about these triage protocols to the Department of Health and Human Services Office of Civil Rights, and after the complaints the guidelines have been swiftly removed. These examples of triage protocols which had complaints raised against them are just a few of many across the country.

These instances may now call into question the efficacy of current legal protections and their ability to prohibit genetic discrimination, opening up discussions of whether they might need to reformed in order to continue to protect individuals' genetic privacy and autonomy, but also to account for instances like a pandemic, where individuals with genetic conditions might be at greater risk. Further, the COVID-19 pandemic may have uncovered possible gaps among existent legal protections, like GINA, which may leave room for discrimination in longterm care and disability insurance, or the ADA, which more so covers ongoing disabilities, rather than susceptibility to conditions. Additionally conversations have turned to how to protect DNA and genetic privacy during a pandemic like COVID-19. According to Hollenstein et al., in a preprint of their research on preserving genetic privacy, they address the possible issue of mass-scale detections and numerous samples being collected through COVID-19 tests and contact-tracing and what that means in terms of who then has access or owns this genetic information. While the exact solutions or changes to be made remain unknown, some solutions could possibly arise from research into equity-first preemption frameworks, which could help eliminate inequities in access to proper healthcare.

Direct-to-consumer genetic testing
Main article: Direct-to-consumer genetic testing

Background
A genetic test is considered a direct-to-consumer test if it is presented to the consumer separate from a health care provider. These tests are easily accessible on the market and popularized by companies such as 23andMe and Ancestry.com. These genetic kits are expensive and disproportionately serve wealthy individuals. The Food and Drug Administration (FDA) additionally halted all 23andMe marketing in 2013 over unsubstantiated claims 23andMe made regarding disease diagnosis and prevention. After an investigation, the FDA approved 23andMe to begin carrier screening in 2015 and to resume genetic health risk screening in 2017. This has led the way for an expansion of the market of direct-to-consumer genetic tests.

Controversy
As technology has progressed, genetic testing has become a more wide scale practice, potentially affecting the privacy of consumers as a result. While some providers of DTC testing destroy the samples after giving the consumer their data, others keep the samples for future data use. The way in which samples that are sent to DTC genetic testing companies are used after analysis is an important point of ethical controversy, as many worry that the creation of biobanks form DTC data creates increased possibility for genetic discrimination. Genomic information is playing an increasingly important role in medical practice and progress. As DTC companies continue to grow, a large obstacle they face is creating a sense of trust with the public in promising to uphold nondiscrimination standards as consumer health data is not currently regulated. Some argue that the clinical utility of results from DTC tests is extremely limited and thus the risk of genetic discrimination is not worth the utility of DTC tests. However, DTC companies argue that the lack of regulation for these companies equip them at a unique position to provide important health related data for contributions to personalized medicine.

One current example of this ethical controversy was demonstrated in the 2018 announcement of 23andMe's partnership with the pharmaceutical company GlaxoSmithKline. In this deal, GlaxoSmithKline purchased a $300 million stake in 23andMe and in return 23andMe would allow the pharmaceutical company access to its biobank of genomic data for their pharmaceutical research. While these companies made this announcement in celebration of the opportunity for progress in pharmacogenomics and drug development, others were wary of the possible breaches of privacy that selling customer's personal genomic data may entail. Privacy concerns include incidental data sharing to third party companies, such as insurance companies or employers. Privacy concerns with genetic information also extend to family members of DTC customers, having similar genetic make-up to their family member who did consent to data sharing, although these individuals did not consent themselves. GINA protects against genetic discrimination in health insurance and employment; however, there are circumstances of exception. For example, GINA does not protect individuals from genetic discrimination in life insurance, disability insurance, and long term care or employees in companies with fewer than 15 individuals or in the military. DTC companies are not regulated in the same way as physician genetic testing and the disclaimers of data sharing in DTC companies is not as clear as medical biobanks, such as the All of Us project sponsored by the NIH. However, this does not necessarily mean that the intentions of DTC companies are nefarious. According to a qualitative study published in the Journal of Personalized Medicine, these companies can prevent the feared genetic discrimination from privacy breaches by advocating for updated policy to regulate data privacy and being intentional about only sharing genetic information to sources who intend to contribute to medical discovery with the appropriate ethical standards.

Race and Genetic Discrimination
See also: Race and genetics

Race and Genetics
Researchers emphasize that race is not a scientifically valid concept and cannot accurately describe biological variation. Attempts to do using genetics may lead down a slippery slope toward scientific racism, the pseudoscientific practice of justifying racism using empirical evidence. Though the human genome is extremely complex, humans share 99.9% of their DNA and differences among people cannot be attributed to social categories of race.

Some cases, however, have found statistical evidence of genetic differences between human populations, such as mutations within the Duffy blood group. Yet research looking at 109 genetic markers across 16 populations by Guido Barbujani "does not suggest that the racial subdivision of our species reflects any major discontinuity in our genome". As genomic research continues to investigate human genetic variation on a large scale, racial genetic discrimination remains a concern for many.

Linking Genetic Conditions and Treatments to Race
See also: Race and health

State governments in the United States have attempted to combat racial discrimination by barring instances of discrimination by insurers that involve linking specific genetic conditions to race, such as the sickle cell trait in African Americans. Further, therapeutic interventions or treatments based on genetic variants associated with race can sometimes be inaccurate and lead to negative health outcomes. An example of this has been doctors prescribing an improper dosage of a drug called warfarin prescribed to African American populations, despite research disproving they require a higher dose than white populations. The medical community recognizes that genetic variants -- such as predisposition to drug metabolism among others -- make up only one facet of a person’s health, which is also impacted by their environment and lifestyle.

Genetic Privacy
In addition, many non-white individuals are concerned with their genetic privacy and worry that they will face discrimination based on their genetic information. These worries may include loss of confidentiality, risk of information being shared with insurance providers, risk of genetic samples being used without their consent, and health-based discrimination more broadly.

Genomic Biobanks
Contributing to genomic biobanks can be an additional source of concern for minority populations. Biobanks are collections of biological samples which can include blood, tissue, or DNA from many people. Despite the utility of biobanks to furthering genomic research, minority groups fear that their samples may be used improperly or even be used to strike down an entire culture. Such was the case when genetic samples were taken from the Havasupai people, a Native American tribe in Arizona. They consented for their samples to provide insight into the prevalence of diabetes in their community, but did not consent to them to investigate links to schizophrenia or provide evolutionary genetic analysis to discredit the tribe’s origin beliefs. Misuse of genetic data may create long-lasting distrust towards the medical community.

Diversity in Genomics
Some efforts have been made to use genetic testing for reconciliation projects involving people of African descent, which attempt to make social reparations based upon genetic genealogy. Though genetic ancestry testing can be a valuable source of information for those seeking connections to their heritage or recognize a new identity, African Americans may feel coerced into genetic testing or unknowingly face discrimination. Participants also have very little control over how their data will be used, including within the medical sphere or the criminal justice system. As such, increased circulation of genetic genealogical data may be harmful for African Americans.

As minority populations are hesitant to contribute their DNA to genomic research, there continues to be a lack of inclusive health information being disseminated and incorporated in medical treatments. Genomic research has been predominantly based upon DNA samples with European heritage, which fails to holistically and accurately describe the complexity of all people’s genetics.

Other confounding factors related to diversity such as age, gender, or socioeconomic status may also influence genetic discrimination in addition to race.