Background:Genetic research has become an indispensable instrument for medical research, and the subjects involved have both divergent and convergent interests.
Objective:The possibility of having more detailed genetic information undoubtedly offers benefits for the health of the subject, but could also pose risks and make the subject vulnerable to discrimination.
Methods:The scientific community has viewed very favorably the public health utility of family history, in which data from a family whose members suffer from chronic pathologies is collected and filed, in order to develop a sort of "stratification of family risk."Even though in the last decade the scientific and juridical literature has contributed greatly to the topic of biobanks, the perplexities that continue to surround this theme give the idea that current ethical protocols on research are inadequate.
Results:Researchers, citizens, International stakeholders, mass media, Public Health and Governments play a key role in genetic research. It is obvious that the methods used for genetic research do not present intrinsic risks; they are much less dangerous than other activities of diagnosis and research.We believe that the highest priority need is to develop a common language on the theme, as is the case in the sphere of clinical experimentation where rules of good clinical practice, albeit at times conflicting, have led to uniform convergences in the scientific world on the points to be actuated. possibility that may occur. It is easy to obtain, and can be of interest to third parties [2] such as family members, insurance companies and employers.Therefore, there is great interest in this information, especially since genetic predisposition has been clearly demonstrated for various diseases such as cardiovascular pathologies [3,4] diabetes [5], late onset Alzheimer [6], schizophrenia [7]