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Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness

Androgenetic alopecia, known in men as male pattern baldness (MPB), is a very conspicuous condition that is particularly frequent among European men and thus contributes markedly to variation in physical appearance traits amongst Europeans. Recent studies have revealed multiple genes and polymorphis...

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Autores principales: Marcińska, Magdalena, Pośpiech, Ewelina, Abidi, Sarah, Andersen, Jeppe Dyrberg, van den Berge, Margreet, Carracedo, Ángel, Eduardoff, Mayra, Marczakiewicz-Lustig, Anna, Morling, Niels, Sijen, Titia, Skowron, Małgorzata, Söchtig, Jens, Syndercombe-Court, Denise, Weiler, Natalie, Schneider, Peter M., Ballard, David, Børsting, Claus, Parson, Walther, Phillips, Chris, Branicki, Wojciech
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4441445/
https://www.ncbi.nlm.nih.gov/pubmed/26001114
http://dx.doi.org/10.1371/journal.pone.0127852
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author Marcińska, Magdalena
Pośpiech, Ewelina
Abidi, Sarah
Andersen, Jeppe Dyrberg
van den Berge, Margreet
Carracedo, Ángel
Eduardoff, Mayra
Marczakiewicz-Lustig, Anna
Morling, Niels
Sijen, Titia
Skowron, Małgorzata
Söchtig, Jens
Syndercombe-Court, Denise
Weiler, Natalie
Schneider, Peter M.
Ballard, David
Børsting, Claus
Parson, Walther
Phillips, Chris
Branicki, Wojciech
author_facet Marcińska, Magdalena
Pośpiech, Ewelina
Abidi, Sarah
Andersen, Jeppe Dyrberg
van den Berge, Margreet
Carracedo, Ángel
Eduardoff, Mayra
Marczakiewicz-Lustig, Anna
Morling, Niels
Sijen, Titia
Skowron, Małgorzata
Söchtig, Jens
Syndercombe-Court, Denise
Weiler, Natalie
Schneider, Peter M.
Ballard, David
Børsting, Claus
Parson, Walther
Phillips, Chris
Branicki, Wojciech
author_sort Marcińska, Magdalena
collection PubMed
description Androgenetic alopecia, known in men as male pattern baldness (MPB), is a very conspicuous condition that is particularly frequent among European men and thus contributes markedly to variation in physical appearance traits amongst Europeans. Recent studies have revealed multiple genes and polymorphisms to be associated with susceptibility to MPB. In this study, 50 candidate SNPs for androgenetic alopecia were analyzed in order to verify their potential to predict MPB. Significant associations were confirmed for 29 SNPs from chromosomes X, 1, 5, 7, 18 and 20. A simple 5-SNP prediction model and an extended 20-SNP model were developed based on a discovery panel of 305 males from various European populations fitting one of two distinct phenotype categories. The first category consisted of men below 50 years of age with significant baldness and the second; men aged 50 years or older lacking baldness. The simple model comprised the five best predictors: rs5919324 near AR, rs1998076 in the 20p11 region, rs929626 in EBF1, rs12565727 in TARDBP and rs756853 in HDAC9. The extended prediction model added 15 SNPs from five genomic regions that improved overall prevalence-adjusted predictive accuracy measured by area under the receiver characteristic operating curve (AUC). Both models were evaluated for predictive accuracy using a test set of 300 males reflecting the general European population. Applying a 65% probability threshold, high prediction sensitivity of 87.1% but low specificity of 42.4% was obtained in men aged <50 years. In men aged ≥50, prediction sensitivity was slightly lower at 67.7% while specificity reached 90%. Overall, the AUC=0.761 calculated for men at or above 50 years of age indicates these SNPs offer considerable potential for the application of genetic tests to predict MPB patterns, adding a highly informative predictive system to the emerging field of forensic analysis of externally visible characteristics.
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spelling pubmed-44414452015-05-28 Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness Marcińska, Magdalena Pośpiech, Ewelina Abidi, Sarah Andersen, Jeppe Dyrberg van den Berge, Margreet Carracedo, Ángel Eduardoff, Mayra Marczakiewicz-Lustig, Anna Morling, Niels Sijen, Titia Skowron, Małgorzata Söchtig, Jens Syndercombe-Court, Denise Weiler, Natalie Schneider, Peter M. Ballard, David Børsting, Claus Parson, Walther Phillips, Chris Branicki, Wojciech PLoS One Research Article Androgenetic alopecia, known in men as male pattern baldness (MPB), is a very conspicuous condition that is particularly frequent among European men and thus contributes markedly to variation in physical appearance traits amongst Europeans. Recent studies have revealed multiple genes and polymorphisms to be associated with susceptibility to MPB. In this study, 50 candidate SNPs for androgenetic alopecia were analyzed in order to verify their potential to predict MPB. Significant associations were confirmed for 29 SNPs from chromosomes X, 1, 5, 7, 18 and 20. A simple 5-SNP prediction model and an extended 20-SNP model were developed based on a discovery panel of 305 males from various European populations fitting one of two distinct phenotype categories. The first category consisted of men below 50 years of age with significant baldness and the second; men aged 50 years or older lacking baldness. The simple model comprised the five best predictors: rs5919324 near AR, rs1998076 in the 20p11 region, rs929626 in EBF1, rs12565727 in TARDBP and rs756853 in HDAC9. The extended prediction model added 15 SNPs from five genomic regions that improved overall prevalence-adjusted predictive accuracy measured by area under the receiver characteristic operating curve (AUC). Both models were evaluated for predictive accuracy using a test set of 300 males reflecting the general European population. Applying a 65% probability threshold, high prediction sensitivity of 87.1% but low specificity of 42.4% was obtained in men aged <50 years. In men aged ≥50, prediction sensitivity was slightly lower at 67.7% while specificity reached 90%. Overall, the AUC=0.761 calculated for men at or above 50 years of age indicates these SNPs offer considerable potential for the application of genetic tests to predict MPB patterns, adding a highly informative predictive system to the emerging field of forensic analysis of externally visible characteristics. Public Library of Science 2015-05-22 /pmc/articles/PMC4441445/ /pubmed/26001114 http://dx.doi.org/10.1371/journal.pone.0127852 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Marcińska, Magdalena
Pośpiech, Ewelina
Abidi, Sarah
Andersen, Jeppe Dyrberg
van den Berge, Margreet
Carracedo, Ángel
Eduardoff, Mayra
Marczakiewicz-Lustig, Anna
Morling, Niels
Sijen, Titia
Skowron, Małgorzata
Söchtig, Jens
Syndercombe-Court, Denise
Weiler, Natalie
Schneider, Peter M.
Ballard, David
Børsting, Claus
Parson, Walther
Phillips, Chris
Branicki, Wojciech
Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness
title Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness
title_full Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness
title_fullStr Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness
title_full_unstemmed Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness
title_short Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness
title_sort evaluation of dna variants associated with androgenetic alopecia and their potential to predict male pattern baldness
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4441445/
https://www.ncbi.nlm.nih.gov/pubmed/26001114
http://dx.doi.org/10.1371/journal.pone.0127852
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