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Prediction and visualization of CYP2D6 genotype-based phenotype using clustering algorithms

This study focused on the role of cytochrome P450 2D6 (CYP2D6) genotypes to predict phenotypes in the metabolism of dextromethorphan. CYP2D6 genotypes and metabolic ratios (MRs) of dextromethorphan were determined in 201 Koreans. Unsupervised clustering algorithms, hierarchical and k-means clusterin...

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Autores principales: Kim, Eun-Young, Shin, Sang-Goo, Shin, Jae-Gook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Clinical Pharmacology and Therapeutics 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033374/
https://www.ncbi.nlm.nih.gov/pubmed/32095466
http://dx.doi.org/10.12793/tcp.2017.25.3.147
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author Kim, Eun-Young
Shin, Sang-Goo
Shin, Jae-Gook
author_facet Kim, Eun-Young
Shin, Sang-Goo
Shin, Jae-Gook
author_sort Kim, Eun-Young
collection PubMed
description This study focused on the role of cytochrome P450 2D6 (CYP2D6) genotypes to predict phenotypes in the metabolism of dextromethorphan. CYP2D6 genotypes and metabolic ratios (MRs) of dextromethorphan were determined in 201 Koreans. Unsupervised clustering algorithms, hierarchical and k-means clustering analysis, and color visualizations of CYP2D6 activity were performed on a subset of 130 subjects. A total of 23 different genotypes were identified, five of which were observed in one subject. Phenotype classifications were based on the means, medians, and standard deviations of the log MR values for each genotype. Color visualization was used to display the mean and median of each genotype as different color intensities. Cutoff values were determined using receiver operating characteristic curves from the k-means analysis, and the data were validated in the remaining subset of 71 subjects. Using the two highest silhouette values, the selected numbers of clusters were three (the best) and four. The findings from the two clustering algorithms were similar to those of other studies, classifying *5/*5 as a lowest activity group and genotypes containing duplicated alleles (i.e., CYP2D6*1/*2N) as a highest activity group. The validation of the k-means clustering results with data from the 71 subjects revealed relatively high concordance rates: 92.8% and 73.9% in three and four clusters, respectively. Additionally, color visualization allowed for rapid interpretation of results. Although the clustering approach to predict CYP2D6 phenotype from CYP2D6 genotype is not fully complete, it provides general information about the genotype to phenotype relationship, including rare genotypes with only one subject.
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spelling pubmed-70333742020-02-24 Prediction and visualization of CYP2D6 genotype-based phenotype using clustering algorithms Kim, Eun-Young Shin, Sang-Goo Shin, Jae-Gook Transl Clin Pharmacol Original Article This study focused on the role of cytochrome P450 2D6 (CYP2D6) genotypes to predict phenotypes in the metabolism of dextromethorphan. CYP2D6 genotypes and metabolic ratios (MRs) of dextromethorphan were determined in 201 Koreans. Unsupervised clustering algorithms, hierarchical and k-means clustering analysis, and color visualizations of CYP2D6 activity were performed on a subset of 130 subjects. A total of 23 different genotypes were identified, five of which were observed in one subject. Phenotype classifications were based on the means, medians, and standard deviations of the log MR values for each genotype. Color visualization was used to display the mean and median of each genotype as different color intensities. Cutoff values were determined using receiver operating characteristic curves from the k-means analysis, and the data were validated in the remaining subset of 71 subjects. Using the two highest silhouette values, the selected numbers of clusters were three (the best) and four. The findings from the two clustering algorithms were similar to those of other studies, classifying *5/*5 as a lowest activity group and genotypes containing duplicated alleles (i.e., CYP2D6*1/*2N) as a highest activity group. The validation of the k-means clustering results with data from the 71 subjects revealed relatively high concordance rates: 92.8% and 73.9% in three and four clusters, respectively. Additionally, color visualization allowed for rapid interpretation of results. Although the clustering approach to predict CYP2D6 phenotype from CYP2D6 genotype is not fully complete, it provides general information about the genotype to phenotype relationship, including rare genotypes with only one subject. Korean Society for Clinical Pharmacology and Therapeutics 2017-09 2017-09-15 /pmc/articles/PMC7033374/ /pubmed/32095466 http://dx.doi.org/10.12793/tcp.2017.25.3.147 Text en Copyright © 2017 Translational and Clinical Pharmacology http://creativecommons.org/licenses/by-nc/3.0/ It is identical to the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/).
spellingShingle Original Article
Kim, Eun-Young
Shin, Sang-Goo
Shin, Jae-Gook
Prediction and visualization of CYP2D6 genotype-based phenotype using clustering algorithms
title Prediction and visualization of CYP2D6 genotype-based phenotype using clustering algorithms
title_full Prediction and visualization of CYP2D6 genotype-based phenotype using clustering algorithms
title_fullStr Prediction and visualization of CYP2D6 genotype-based phenotype using clustering algorithms
title_full_unstemmed Prediction and visualization of CYP2D6 genotype-based phenotype using clustering algorithms
title_short Prediction and visualization of CYP2D6 genotype-based phenotype using clustering algorithms
title_sort prediction and visualization of cyp2d6 genotype-based phenotype using clustering algorithms
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033374/
https://www.ncbi.nlm.nih.gov/pubmed/32095466
http://dx.doi.org/10.12793/tcp.2017.25.3.147
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