Issue Concerning Genetic Testing And Insurance Companies example essay topic
It was announced on April 14, 2003 that the HGP was successfully complete, with 99.99% accuracy of the 99% of the genome sequenced. As mentioned above, the project has been marked by criticism from many social groups the world over. Due to the obvious social implications of such research, a sub-division was set up within the HGP. The Ethical, Legal and Social Implications Research Program (ELSE) was established to address concerns that relate to the privacy of genetic information, protection of human subjects, and possibility of criminal action with the usage of data being produced by the HGP.
The Human Genome Project will greatly affect human welfare in many ways once the information that has been discovered, and put into practice. Issues relating to the understanding of human genetics, evolution, gene therapy and manipulation, improvements into health, and the downfalls of genetic testing will all be discussed below in terms of future human welfare. With the completion of the HGP, scientists will be more easily able to explain how genes are expressed, how they mutate and how they are inherited. A better understanding of the interaction between genes will also be known. Mapping the human genome may also help to determine the role of the non-coding nucleotide regions - the in trons, and the unknown functions of some genes may also be discovered. However with the vast amounts of knowledge gained, questions remain as to how it is to be used, and who can have access to the information.
Whether private organisations have the rights to patent genes, gene fragments, proteins, stem cells etc, whether governments will be able to collect and use the genetic information gained from genetic testing. All these issues need to be addressed with stringent laws as to protect human welfare. The completed human genome can be compared with genomes of other species and the similarities and differences of their evolutionary pathways can be compared. These comparisons may provide evidence to support current evolutionary theories or provide evidence to refute these theories.
Therefore finally putting to rest the question as to the evolution of humanity. The HGP provides a map of the chromosomes of a human, within this map it may determine the precise location of mutant genes, which have the potential to cause an inherited disorder in the individual, using this information, scientists may be able to initiate gene therapy to provide prevention form the disorder for the individuals. Gene therapy involves the insertion of healthy therapeutic cells into the cells of genes with the potential to cause an inherited disease. This treatment can be targeted at both the somatic or germ line cells. Genetic engineering is one of many issues concerning human welfare.
The human genome provides information that will eventually allow diagnosis and treatment of many diseases. The mapping of the human genome will also allow for the determination of what genes produce physical and psychological qualities. From the information found out from the HGP, people today may start to remove the genes known to cause debilitating and fatal diseases, which would not cause (presumably) any problems to future generations. However if enhancement engineering continued on into the aesthetic traits such as height, skin colour etc, the future generations may feel that their self-identity has been manipulated in favour of trends of the particular time. Parents may have the possibility to dictate the physical characteristics of their unborn children. Further research needs to be done into this field before the public are able to do such acts, as the effects of such gene modification on the human gene pool are unknown.
This kind of manipulation to the genes, may also lead to the creation of a "super" race, similar to that of the proposed Aryan race in Nazi Germany. It has also been suggested that due to the events that occurred during Nazi Germany, and more recent "ethnic cleansing's"- humans may not be ready for the genetic knowledge we are pursuing (Cohen). Social scientists also feel that genetic research will also lessen the social diversity we currently have in society, and encourage bias and prejudice among one another. The data derived from the HGP will help scientists associate specific traits and inherited diseases with particular genes at their precise chromosome location. This knowledge may lead to new tests to determine whether or not an individual is carrying 'faulty genes' for a particular disease before the disorder develops. However the identification of said 'faulty genes' might lead to the discrimination of individuals by insurance companies and employers and the development of a society constantly living in fear of what may be.
Genetic testing resulting from the completion of the HGP, may lead to society developing a constant state of fear for their health and well being". Genetic analysis can tell whether someone is at a slightly higher or slightly lower risk of colon cancer: it cannot say whether the person will get the disease, at what age it will strike, how quickly it will be diagnosed, and whether treatment will be successful". (Spangerburg & Moser, Open for Debate Genetic Engineering pg 171). The population could be over come by hypochondriacs constantly wrestling with the possibility that they may or may not develop certain diseases, therefore causing an increased stress on the health care systems. The issue concerning genetic testing and insurance companies has received much media attention.
It is a great concern that insurance companies may use the new genetic information to discriminate against those needing medical coverage the most. When applying for insurance policies a family medical history along with urine and blood samples is required. However insurance companies may be allowed in the future to request genetic testing of candidates if no laws are put in place to prevent this. A balance needs to be attained between the rights of the individual and the rights of the insurance companies; .".. comprehensive law would need to say that no insurance company may deny coverage or raise rates based on an individual's past, present or predicted health status".
(Mark A. Rothstein Protecting the Genetic Privacy: Why It is So Hard to Do). Employers may also seek to use genetic testing as a form of discrimination against potential employees. If an employer is allowed to view the information obtained from genetic testing, they may decide not to employ a suitable candidate due to the identification of a potential 'bad gene' that may lead to extended periods of leave, heavier financial burdens on the company, or the replacement of the person within a short period of time. The employer may also seek to see the information attained from other family members that have been tested, of the prospective employee.
If it is found that family members may cause the potential employee to need extended period of time off work, variations in working patterns, or once again cause financial burden on the company, the person may be overlooked for the position available. The costing of the HGP was enormous, and continues to be funded. Since the initiation of the project millions of dollars have been spent on the project. However the health care research funding all over the world are in dire need of more funding.
The HGP has taken away vital funding from health care system which has further depleted the welfare of humans around the world. The lack in funding has left many diseases, which affect the overall populations, unfunded instead focussing on the funding of specific diseases that the overall population is not affected by. The Human Genome Project will cause more harm than good for human welfare. This is evident through the social, ethical and legalities involved with the Human Genome Project and its associated findings. This is evident through the apparent availability of manipulating genes to produce socially physically accepted person, the potential for governments, insurance companies and employers to use genetic testing as a mode of direct discrimination, and the removal of funding from various health care research projects. The completions of the Human Genome Project and the further studies into the findings has taken away another chunk of the already diminishing natural selection process that had worked flawlessly for thousands of years.
As this area of science is relatively new, reliability is questionable; if we test positive for an adult-onset disease, will we definitely get it, or does environment play a role? How can we be sure that genetic tests are reliable? If some terrible news was given to someone based on genetic predisposition, and the illness or condition never occurred, there are ethical and legal issues arising. The amount that is not known in this new field is certainly more than what is known, especially about the social impact. There need to be universal standards and enforcement of international regulations for ethics in genetic testing, as is the mere reliability.
Bibliography
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