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Evaluation of DNA variants associated with androgenetic alopecia and their potential to predict male pattern baldness.
Marcinska, Magdalena; Pospiech, Ewelina; Abidi, Sarah; Andersen, Jeppe Dyrberg; van den Berge, Margreet; Carracedo, Ángel; Eduardoff, Mayra; Marczakiewicz-Lustig, Anna; Morling, Niels; Sijen, Titia; Skowron, Malgorzata; Söchtig, Jens; Syndercombe-Court, Denise; Weiler, Natalie; Schneider, Peter M; Ballard, David; Børsting, Claus; Parson, Walther; Phillips, Chris; Branicki, Wojciech.
Afiliação
  • Marcinska M; Institute of Forensic Research, Section of Forensic Genetics, Krakow, Poland.
  • Pospiech E; Department of Genetics and Evolution, Jagiellonian University, Krakow, Poland.
  • Abidi S; Faculty of Life Sciences, King's College, London, United Kingdom.
  • Andersen JD; Section of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.
  • van den Berge M; Department of Human Biological Traces, Netherlands Forensic Institute, The Hague, The Netherlands.
  • Carracedo Á; Forensic Genetics Unit, Institute of Forensic Medicine, Faculty of Medicine, University of Santiago de Compostela, Santiago de Compostela, Spain; Genomic Medicine Group, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Institute of Health Carlos III, Madrid, Spain.
  • Eduardoff M; Institute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria.
  • Marczakiewicz-Lustig A; Department of Analytical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
  • Morling N; Section of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.
  • Sijen T; Department of Human Biological Traces, Netherlands Forensic Institute, The Hague, The Netherlands.
  • Skowron M; Department of Dermatology, Medical College of Jagiellonian University, Krakow, Poland.
  • Söchtig J; Forensic Genetics Unit, Institute of Forensic Medicine, Faculty of Medicine, University of Santiago de Compostela, Santiago de Compostela, Spain.
  • Syndercombe-Court D; Faculty of Life Sciences, King's College, London, United Kingdom.
  • Weiler N; Department of Human Biological Traces, Netherlands Forensic Institute, The Hague, The Netherlands.
  • Schneider PM; Institute of Legal Medicine, Medical Faculty, University of Cologne, Cologne, Germany.
  • Ballard D; Faculty of Life Sciences, King's College, London, United Kingdom.
  • Børsting C; Section of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.
  • Parson W; Institute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria; Forensic Science Program, The Pennsylvania State University, University Park, Pennsylvania, United States of America.
  • Phillips C; Forensic Genetics Unit, Institute of Forensic Medicine, Faculty of Medicine, University of Santiago de Compostela, Santiago de Compostela, Spain.
  • Branicki W; Institute of Forensic Research, Section of Forensic Genetics, Krakow, Poland; Department of Genetics and Evolution, Jagiellonian University, Krakow, Poland.
PLoS One ; 10(5): e0127852, 2015.
Article em En | MEDLINE | ID: mdl-26001114
ABSTRACT
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Alopecia Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged Idioma: En Revista: PLoS One Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Alopecia Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged Idioma: En Revista: PLoS One Ano de publicação: 2015 Tipo de documento: Article