{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,8,29]],"date-time":"2025-08-29T10:36:31Z","timestamp":1756463791737},"reference-count":26,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2015,7,14]],"date-time":"2015-07-14T00:00:00Z","timestamp":1436832000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J of Cosmetic Dermatology"],"published-print":{"date-parts":[[2015,12]]},"abstract":"<jats:title>Summary<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Androgenetic alopecia (<jats:styled-content style=\"fixed-case\">AGA<\/jats:styled-content>) or common baldness is the most prevalent form of hair loss in males. Familial predisposition has been recognized, and heritability estimated in monozygotic twins suggests an important genetic predisposition. Several studies indicate that the numbers of <jats:styled-content style=\"fixed-case\">CAG<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">GGC<\/jats:styled-content> repeats in exon 1 of the androgen receptor gene <jats:italic>(<jats:styled-content style=\"fixed-case\">AR<\/jats:styled-content>)<\/jats:italic> maybe associated with <jats:styled-content style=\"fixed-case\">AGA<\/jats:styled-content> susceptibility.<\/jats:p><\/jats:sec><jats:sec><jats:title>Aims<\/jats:title><jats:p>To investigate a possible correlation between <jats:italic><jats:styled-content style=\"fixed-case\">AR<\/jats:styled-content><\/jats:italic> <jats:styled-content style=\"fixed-case\">CAG<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">GGC<\/jats:styled-content> haplotypes and the presence or not of alopecia in sibships with two or more brothers among them at least one of them has <jats:styled-content style=\"fixed-case\">AGA<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Patients\/Methods<\/jats:title><jats:p>Thirty\u2010two trios including an alopecic man, one brother alopecic or not, and their mother were enrolled. Sanger sequencing of the exon 1 of the <jats:italic><jats:styled-content style=\"fixed-case\">AR<\/jats:styled-content><\/jats:italic> gene was conducted to ascertain the number of <jats:styled-content style=\"fixed-case\">CAG<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">GGC<\/jats:styled-content> repeats in each individual. Heterozygous mother for the <jats:styled-content style=\"fixed-case\">CAG<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">GGC<\/jats:styled-content> haplotypes was an inclusion criterion to analyze the segregation haplotype patterns in the family. Concordance for the number of repeats and <jats:styled-content style=\"fixed-case\">AGA<\/jats:styled-content> among brothers was evaluated using kappa coefficient and the probability of association in the presence of genetic linkage between <jats:styled-content style=\"fixed-case\">CAG<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">GGC<\/jats:styled-content> repeats and <jats:styled-content style=\"fixed-case\">AGA<\/jats:styled-content> estimated by means of the family\u2010based association test (<jats:styled-content style=\"fixed-case\">FBAT<\/jats:styled-content>).<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>The median for the <jats:styled-content style=\"fixed-case\">CAG<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">GGC<\/jats:styled-content> repeats in the <jats:italic><jats:styled-content style=\"fixed-case\">AR<\/jats:styled-content><\/jats:italic> is similar to that reported in other populations. The <jats:styled-content style=\"fixed-case\">CAG<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">GGC<\/jats:styled-content> haplotypes were less polymorphic than that reported in other studies, especially due to the <jats:styled-content style=\"fixed-case\">GGC<\/jats:styled-content> number of repeats found. <jats:italic>Kappa<\/jats:italic> coefficient resulted in a concordance of 37.3% (<jats:styled-content style=\"fixed-case\">IC<\/jats:styled-content> 95%, 5.0\u201369.0%) for the <jats:styled-content style=\"fixed-case\">AGA<\/jats:styled-content> phenotype and identical <jats:styled-content style=\"fixed-case\">CAG<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">GGC<\/jats:styled-content> haplotypes. There was no evidence of linkage disequilibrium.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Our results do not confirm a possible correlation or linkage disequilibrium between the <jats:styled-content style=\"fixed-case\">CAG<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">GGC<\/jats:styled-content> haplotypes of the <jats:italic><jats:styled-content style=\"fixed-case\">AR<\/jats:styled-content><\/jats:italic> gene and androgenetic alopecia in Mexican brothers.<\/jats:p><\/jats:sec>","DOI":"10.1111\/jocd.12159","type":"journal-article","created":{"date-parts":[[2015,7,14]],"date-time":"2015-07-14T20:48:00Z","timestamp":1436906880000},"page":"268-273","source":"Crossref","is-referenced-by-count":2,"title":["Lack of concordance and linkage disequilibrium among brothers for androgenetic alopecia and <scp>CAG<\/scp>\/<scp>GGC<\/scp> haplotypes of the androgen receptor gene in Mexican families"],"prefix":"10.1111","volume":"14","author":[{"given":"Jazm\u00edn","family":"Arteaga\u2010V\u00e1zquez","sequence":"first","affiliation":[{"name":"Departamento de Gen\u00e9tica Instituto Nacional de Ciencias M\u00e9dicas y Nutrici\u00f3n \u201cSalvador Zubir\u00e1n\u201d M\u00e9xico D.F. M\u00e9xico"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mar\u00eda A.","family":"L\u00f3pez\u2010Hern\u00e1ndez","sequence":"additional","affiliation":[{"name":"Departamento de Gen\u00e9tica Instituto Nacional de Ciencias M\u00e9dicas y Nutrici\u00f3n \u201cSalvador Zubir\u00e1n\u201d M\u00e9xico D.F. M\u00e9xico"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yevgeniya","family":"Svyryd","sequence":"additional","affiliation":[{"name":"Departamento de Gen\u00e9tica Instituto Nacional de Ciencias M\u00e9dicas y Nutrici\u00f3n \u201cSalvador Zubir\u00e1n\u201d M\u00e9xico D.F. M\u00e9xico"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Osvaldo M.","family":"Mutchinick","sequence":"additional","affiliation":[{"name":"Departamento de Gen\u00e9tica Instituto Nacional de Ciencias M\u00e9dicas y Nutrici\u00f3n \u201cSalvador Zubir\u00e1n\u201d M\u00e9xico D.F. 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