Pharmacogenetics of Antiplatelet Drugs

Pharmacogenetics refers to the genetic factors that influence the response to a drug, often involving genetic variations in drug metabolizing enzymes. The pharmacogenetics of antiplatelet agents is in its infancy and largely reflects variations in drug targets or related genes. One particular gene v...

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Main Authors: Ronan Curtin, Desmond J. Fitzgerald
Format: Article
Language:English
Published: Hindawi Limited 2002-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1100/tsw.2002.153
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spelling doaj-3286cdbb1ae94239886b407d55adeaa62020-11-25T00:59:44ZengHindawi LimitedThe Scientific World Journal1537-744X2002-01-01279180010.1100/tsw.2002.153Pharmacogenetics of Antiplatelet DrugsRonan Curtin0Desmond J. Fitzgerald1Department of Clinical Pharmacology, Royal College of Surgeons in Ireland, 123 St. Stephen’s Green, Dublin 2, IrelandDepartment of Clinical Pharmacology, Royal College of Surgeons in Ireland, 123 St. Stephen’s Green, Dublin 2, IrelandPharmacogenetics refers to the genetic factors that influence the response to a drug, often involving genetic variations in drug metabolizing enzymes. The pharmacogenetics of antiplatelet agents is in its infancy and largely reflects variations in drug targets or related genes. One particular gene variant, the PlA2 polymorphism of the glycoprotein (GP) IIb/IIIa receptor, is now emerging as a probable determinant of the response to antiplatelet agents including GPIIb/IIIa antagonists. This variant may in part explain the heterogeneity in the response to GPIIb/IIIa antagonists. The PlA2 genotype appears to be associated with an adverse outcome in patients treated with an oral GPIIb/IIIa antagonist and may be a factor in the observed failure of these agents in unselected populations. However, there are preliminary indications that other antiplatelet agents may have an enhanced effect in PlA2 subjects. Further clinical trials in particular are required to definitively characterize the pharmacogenetic effect of PlA2. Other polymorphisms are also likely to contribute to the pharmacogenetics of antiplatelet agents, but these await investigation.http://dx.doi.org/10.1100/tsw.2002.153
collection DOAJ
language English
format Article
sources DOAJ
author Ronan Curtin
Desmond J. Fitzgerald
spellingShingle Ronan Curtin
Desmond J. Fitzgerald
Pharmacogenetics of Antiplatelet Drugs
The Scientific World Journal
author_facet Ronan Curtin
Desmond J. Fitzgerald
author_sort Ronan Curtin
title Pharmacogenetics of Antiplatelet Drugs
title_short Pharmacogenetics of Antiplatelet Drugs
title_full Pharmacogenetics of Antiplatelet Drugs
title_fullStr Pharmacogenetics of Antiplatelet Drugs
title_full_unstemmed Pharmacogenetics of Antiplatelet Drugs
title_sort pharmacogenetics of antiplatelet drugs
publisher Hindawi Limited
series The Scientific World Journal
issn 1537-744X
publishDate 2002-01-01
description Pharmacogenetics refers to the genetic factors that influence the response to a drug, often involving genetic variations in drug metabolizing enzymes. The pharmacogenetics of antiplatelet agents is in its infancy and largely reflects variations in drug targets or related genes. One particular gene variant, the PlA2 polymorphism of the glycoprotein (GP) IIb/IIIa receptor, is now emerging as a probable determinant of the response to antiplatelet agents including GPIIb/IIIa antagonists. This variant may in part explain the heterogeneity in the response to GPIIb/IIIa antagonists. The PlA2 genotype appears to be associated with an adverse outcome in patients treated with an oral GPIIb/IIIa antagonist and may be a factor in the observed failure of these agents in unselected populations. However, there are preliminary indications that other antiplatelet agents may have an enhanced effect in PlA2 subjects. Further clinical trials in particular are required to definitively characterize the pharmacogenetic effect of PlA2. Other polymorphisms are also likely to contribute to the pharmacogenetics of antiplatelet agents, but these await investigation.
url http://dx.doi.org/10.1100/tsw.2002.153
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