Ecogenetics
{{Short description|Branch of genetics}}
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Ecogenetics is a branch of genetics that studies genetic traits related to the response to environmental substances.{{cite book|last=Cummings|first=Michael R.|title=Human Heredity: Principles and Issues |pages=264–265 }} Or, a contraction of ecological genetics, the study of the relationship between a natural population and its genetic structure.{{citation needed|date=December 2011}}
Ecogenetics principally deals with effects of preexisting genetically-determined variability on the response to environmental agents.{{cite web |url=http://www.akhilautismfoundation.org/UserFiles/Image/Ecogenetics_Model.jpg |title=Ecogenetics Model |website=akhilautismfoundation.org |format=image |access-date=19 April 2018 |archive-date=5 July 2016 |archive-url=https://web.archive.org/web/20160705202422/http://akhilautismfoundation.org/UserFiles/Image/Ecogenetics_Model.jpg |url-status=dead }} The word environmental is defined broadly to include the physical, chemical, biological, atmospheric, and climate agents. Ecogenetics, therefore, is an all-embracing term, and concepts such as pharmacogenetics are seen as subcomponents of ecogenetics. This work grew logically from the book entitled Pollutants and High Risk Groups (1978), which presented an overview of the various host factors i.e. age, heredity, diet, preexisting diseases, and lifestyles which affect environmentally-induced disease.
The primary intention of ecogenetics is to provide an objective and critical evaluation of the scientific literature pertaining to genetic factors and differential susceptibility to environmental agents, with particular emphasis on those agents typically considered pollutants. It is important to realize though that ones genetic makeup, while important, is but one of an array of host factors contributing to overall adaptive capacity of the individual. In many instances, it is possible for such factors to interact in ways that may enhance or offset the effect of each other.
Red blood cell conditions
There is a broad group of genetic diseases that result in either producing or predisposing affected individuals to the development of hemolytic anemias. These diseases include abnormal haemoglobin, inability to manufacture one or the other of the peptide globin chains of the haemoglobin, and deficiencies of the Embden-Meyerhoff monophosphate.
Liver metabolism
Individuals lacking the ability to detoxify and excrete PCB's may have a high risk of total liver failure in conjunction with certain ecological conditions.
Cardiovascular diseases
The pathologic lesion of atherosclerosis is a plaque-like substance that thickens the innermost and middle of the three layers of the artery wall. The thickening of the intimal and medial layers results from the accumulation of the proliferating smooth muscle cells that are encompassed by interstitial substances such as collagen, elastin, glycosaminoglycans, and fibrin.
Respiratory diseases
There are three genetically-based respiratory diseases that can directly correspond with ecological functions and induce disease. These include lung cancer and the upper and lower respiratory tract associated with a serum Ig A deficiency.
See also
References
:*van Zyl, Jay. [https://www.academia.edu/2053628/Built_to_Thrive_Using_Innovation_to_Make_Your_Mark_in_a_Connected_World Built to Thrive: Using Innovation to Make Your Mark in a Connected World]. Chapter 5: Ecogenetics. San Francisco. 2011
:*Calabrese, Edward J. Ecogenetics: Genetic Variation in Susceptibility to Environmental Agents. Environmental Science and Technology. New York. 1984.