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Diabetes: Is There a Future for Pharmacogenomics Guided Treatment?

Diabetes is a disease defined on the basis of hyperglycemia. There are monogenic forms of diabetes where defining the genetic cause has a dramatic impact on treatment—with patients being able to transition from insulin to sulfonylureas. However, the majority of diabetes is type 2 diabetes. This revi...

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Autor principal: Pearson, Ewan R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771467/
https://www.ncbi.nlm.nih.gov/pubmed/31012484
http://dx.doi.org/10.1002/cpt.1484
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author Pearson, Ewan R.
author_facet Pearson, Ewan R.
author_sort Pearson, Ewan R.
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description Diabetes is a disease defined on the basis of hyperglycemia. There are monogenic forms of diabetes where defining the genetic cause has a dramatic impact on treatment—with patients being able to transition from insulin to sulfonylureas. However, the majority of diabetes is type 2 diabetes. This review outlines the robust evidence accrued to date for pharmacogenetics of metformin, sulfonylureas, thiazolidinediones, and dipeptidyl peptidase‐4 inhibitors but highlights that these variants will only be of clinical utility when the genotype is already known at the point of prescribing. The future of pharmacogenetics in diabetes and other common complex disease relies on a paradigm shift—that of preemptive panel genotyping and use of clinical decision support tools to assimilate this genetic information with other clinical phenotypic data and to present this information simply to the prescriber. Given the recent dramatic fall in genotyping costs, this future is not far off.
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spelling pubmed-67714672019-10-07 Diabetes: Is There a Future for Pharmacogenomics Guided Treatment? Pearson, Ewan R. Clin Pharmacol Ther Reviews Diabetes is a disease defined on the basis of hyperglycemia. There are monogenic forms of diabetes where defining the genetic cause has a dramatic impact on treatment—with patients being able to transition from insulin to sulfonylureas. However, the majority of diabetes is type 2 diabetes. This review outlines the robust evidence accrued to date for pharmacogenetics of metformin, sulfonylureas, thiazolidinediones, and dipeptidyl peptidase‐4 inhibitors but highlights that these variants will only be of clinical utility when the genotype is already known at the point of prescribing. The future of pharmacogenetics in diabetes and other common complex disease relies on a paradigm shift—that of preemptive panel genotyping and use of clinical decision support tools to assimilate this genetic information with other clinical phenotypic data and to present this information simply to the prescriber. Given the recent dramatic fall in genotyping costs, this future is not far off. John Wiley and Sons Inc. 2019-07-12 2019-08 /pmc/articles/PMC6771467/ /pubmed/31012484 http://dx.doi.org/10.1002/cpt.1484 Text en © 2019 The Author Clinical Pharmacology & Therapeutics published by Wiley Periodicals, Inc. on behalf of American Society for Clinical Pharmacology and Therapeutics This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Pearson, Ewan R.
Diabetes: Is There a Future for Pharmacogenomics Guided Treatment?
title Diabetes: Is There a Future for Pharmacogenomics Guided Treatment?
title_full Diabetes: Is There a Future for Pharmacogenomics Guided Treatment?
title_fullStr Diabetes: Is There a Future for Pharmacogenomics Guided Treatment?
title_full_unstemmed Diabetes: Is There a Future for Pharmacogenomics Guided Treatment?
title_short Diabetes: Is There a Future for Pharmacogenomics Guided Treatment?
title_sort diabetes: is there a future for pharmacogenomics guided treatment?
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771467/
https://www.ncbi.nlm.nih.gov/pubmed/31012484
http://dx.doi.org/10.1002/cpt.1484
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