Concept: Pharmacogenetics can be defined as the study of
hereditary factors contributing to variability in human drug response.
Essentially, this branch of genetics studies the how an individual reacts to
drugs and other pharmacological products to further understand genetic
differences between different humans. This in turn leads to personalized
medicine for various genetic disorders, or to help researchers understand how
different drugs and pharmaceuticals affect different genetic or
chromosome-linked disorders. Another strong concept in this field would be that
the driving force for such studies was the suggestion, made over half a century
ago, that many abnormal responses to drugs might be due to genetically determined
variation.
Based on
DNA: With the unravelling of the structure of DNA3,
and subsequent development of molecular biology, it soon became possible to
study associations between genotype (DNA mutations) and phenotype (observable
or measurable traits including clinical presentation). As the scale of the
investigations became more ambitious to find other genetic patterns and the
enabling technologies more sophisticated, the term ‘pharmacogenomics’ was
coined to allow association studies on a genome-wide basis. In the clinical
arena, both terms can be used interchangeably.
Basic Science: The study of pharmacogenetics promises to hold a
lot of potential. Pharmacists have had to deal with the various ailments of
people for a long time, while looking to understand the concept of their
problems. When they would try to understand why these genetic disorders occur
and which drugs or compounds would remedy the situation, they would
inadvertently dabble in this field. As years have gone past, we have learned to
associate certain drugs and the implications of their affects and our
understanding of genetic altering grew. With this approach we should
theoretically be able to predict response to an increasing array of drugs and
thereby personalise therapy with appropriate pharmacogenetic testing.
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