Genetic and prenatal testing are powerful tools that can provide valuable information to patients and healthcare providers about a person’s health, the likelihood of their developing certain conditions, and the potential health risks to their offspring. These tests, however, also bring up challenging ethical questions that demand careful thought.
The potential for discrimination based on genetic information is one of the main issues with genetic testing. In the past, insurance companies and employers have denied coverage or employment based on a person’s genetic makeup. To address this issue, the Genetic Information Nondiscrimination Act (GINA) was passed in 2008, which prohibits genetic discrimination in employment and health insurance.
Another ethical concern is the potential psychological impact of genetic testing. While some individuals may feel empowered by knowing their genetic risks, others may experience anxiety or depression, and some may even experience stigma or discrimination as a result of their genetic makeup.
Prenatal testing, which is often used to identify genetic abnormalities or developmental issues in the fetus, also raises ethical questions. One concern is the possibility of terminating a pregnancy based on the results of the test. Although the choice to have a selective abortion is up to the individual or couple, some may argue that this type of selective abortion raises ethical concerns and moral questions about the value of human life and the possibilities for eugenics.
A second concern surrounding prenatal testing is the potential for false positives or false negatives. A false positive can lead to unnecessary stress and interventions, while a false negative can result in missed opportunities for treatment or preparation for the birth of a child with special needs.
Despite these ethical concerns, genetic and prenatal testing can also have numerous benefits. For example, identifying genetic risks can help individuals and families make informed decisions about their health, including lifestyle changes, preventative measures, or early interventions.
Ultimately, the ethical considerations surrounding genetic and prenatal testing highlight the importance of informed consent and the need for patients and healthcare providers to have access to accurate and unbiased information about the risks, benefits, and limitations of these tests. By balancing the potential benefits with the ethical concerns, we can ensure that these powerful tools are used responsibly and with the utmost consideration for human dignity and autonomy.
~ Saathvika Diviti `25