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Developing precision medicine for people of East Asian descent

The goal of precision medicine is to separate patient populations into groups to ultimately provide customized care tailored to patients. In terms of precision medicine, ~540 million people in the world have a genetic variant of the aldehyde dehydrogenase 2 (ALDH2) enzyme causing a flushing response...

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Detalles Bibliográficos
Autores principales: McAllister, Stacy L., Sun, Katherine, Gross, Eric R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5106841/
https://www.ncbi.nlm.nih.gov/pubmed/27835996
http://dx.doi.org/10.1186/s12929-016-0299-3
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author McAllister, Stacy L.
Sun, Katherine
Gross, Eric R.
author_facet McAllister, Stacy L.
Sun, Katherine
Gross, Eric R.
author_sort McAllister, Stacy L.
collection PubMed
description The goal of precision medicine is to separate patient populations into groups to ultimately provide customized care tailored to patients. In terms of precision medicine, ~540 million people in the world have a genetic variant of the aldehyde dehydrogenase 2 (ALDH2) enzyme causing a flushing response and tachycardia after alcohol consumption. The genetic variant is identified as ALDH2*2 and originates from East Asian descendants of the Han Chinese. The variant is particularly important to consider when discussing lifestyle choices with patients in terms of risk for developing specific diseases, preventative screening, and selection of medications for treatment. Here we provide examples why patients with an ALDH2*2 variant need more individualized medical management which is becoming a more standard practice in the precision medicine era.
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spelling pubmed-51068412016-11-25 Developing precision medicine for people of East Asian descent McAllister, Stacy L. Sun, Katherine Gross, Eric R. J Biomed Sci Review The goal of precision medicine is to separate patient populations into groups to ultimately provide customized care tailored to patients. In terms of precision medicine, ~540 million people in the world have a genetic variant of the aldehyde dehydrogenase 2 (ALDH2) enzyme causing a flushing response and tachycardia after alcohol consumption. The genetic variant is identified as ALDH2*2 and originates from East Asian descendants of the Han Chinese. The variant is particularly important to consider when discussing lifestyle choices with patients in terms of risk for developing specific diseases, preventative screening, and selection of medications for treatment. Here we provide examples why patients with an ALDH2*2 variant need more individualized medical management which is becoming a more standard practice in the precision medicine era. BioMed Central 2016-11-11 /pmc/articles/PMC5106841/ /pubmed/27835996 http://dx.doi.org/10.1186/s12929-016-0299-3 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
McAllister, Stacy L.
Sun, Katherine
Gross, Eric R.
Developing precision medicine for people of East Asian descent
title Developing precision medicine for people of East Asian descent
title_full Developing precision medicine for people of East Asian descent
title_fullStr Developing precision medicine for people of East Asian descent
title_full_unstemmed Developing precision medicine for people of East Asian descent
title_short Developing precision medicine for people of East Asian descent
title_sort developing precision medicine for people of east asian descent
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5106841/
https://www.ncbi.nlm.nih.gov/pubmed/27835996
http://dx.doi.org/10.1186/s12929-016-0299-3
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