help button home button Endocrine Society JCEM
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a related Letter to the Editor
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Calvo, R. M.
Right arrow Articles by Escobar-Morreale, H. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Calvo, R. M.
Right arrow Articles by Escobar-Morreale, H. F.
The Journal of Clinical Endocrinology & Metabolism Vol. 85, No. 4 1735-1740
Copyright © 2000 by The Endocrine Society


Comments

The Role of the CAG Repeat Polymorphism in the Androgen Receptor Gene and of Skewed X-Chromosome Inactivation, in the Pathogenesis of Hirsutism1

Rosa M. Calvo, Miryam Asunción, José Sancho, José L. San Millán and Héctor F. Escobar-Morreale

Departments of Endocrinology (R.M.C., M.A., J.S., H.F.E.-M.) and Molecular Genetics (J.L.S.M.), Hospital Ramón y Cajal, 28034 Madrid, Spain

Address correspondence and requests for reprints to: Héctor F. Escobar-Morreale, M.D., Ph.D., Department of Endocrinology, Hospital Ramón y Cajal, Carretera de Colmenar km. 9,100, 28034 Madrid, Spain. E-mail: hector.escobar{at}uam.es

Abstract

The human androgen receptor (AR) gene contains a variable number of CAG repeats within exon 1. Shorter AR alleles, by increasing transactivation, may result in augmented AR-mediated sensitivity of the hair follicle. We have evaluated whether the number of CAG repeats, or if skewed inactivation of X-chromosome, favoring the presence of shorter AR alleles, influence hirsutism in women with and without hyperandrogenemia. Twenty-eight women with idiopathic hirsutism (normal serum androgens), 34 women with hyperandrogenic hirsutism (increased serum androgens), and 15 healthy control women were analyzed by evaluating the number of CAG repeats in genomic DNA, as well as the methylation pattern (after DNA digestion with HpaII), which allows identification of which allele is inactive. Despite marked differences among the groups in serum androgens, which were markedly increased in women with hyperandrogenic hirsutism as compared with women with idiopathic hirsutism and to controls, there were no significant differences among the groups in the number of CAG repeats. Moreover, skewed X-chromosome inactivation was found in 10 subjects (3 with idiopathic hirsutism, 5 with hyperandrogenic hirsutism, and 2 controls; P = 0.746) of the 67 women (14.9%) who were heterozygous for the AR gene. In several of these subjects, it was the shorter allele that was preferentially inactivated.

In conclusion, neither the CAG repeat polymorphism in the AR gene, nor skewed X-chromosome inactivation, seem to play a significant role in the pathogenesis of hirsutism.




This article has been cited by other articles:


Home page
J. Clin. Endocrinol. Metab.Home page
N. A. Shah, H. J. Antoine, M. Pall, K. D. Taylor, R. Azziz, and M. O. Goodarzi
Association of Androgen Receptor CAG Repeat Polymorphism and Polycystic Ovary Syndrome
J. Clin. Endocrinol. Metab., May 1, 2008; 93(5): 1939 - 1945.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
S. Lappalainen, P. Utriainen, T. Kuulasmaa, R. Voutilainen, and J. Jaaskelainen
Androgen Receptor Gene CAG Repeat Polymorphism and X-Chromosome Inactivation in Children with Premature Adrenarche
J. Clin. Endocrinol. Metab., April 1, 2008; 93(4): 1304 - 1309.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
N. Xita, I. Georgiou, L. Lazaros, V. Psofaki, G Kolios, and A. Tsatsoulis
The role of sex hormone-binding globulin and androgen receptor gene variants in the development of polycystic ovary syndrome
Hum. Reprod., March 1, 2008; 23(3): 693 - 698.
[Abstract] [Full Text] [PDF]


Home page
Exp. Biol. Med.Home page
Y. Wang, H. Zhang, J. Ding, and F. Wang
Correlation Between mRNA Expression Level of the Mutant COL4A5 Gene and Phenotypes of XLAS Females
Experimental Biology and Medicine, May 1, 2007; 232(5): 638 - 642.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
N. Xita and A. Tsatsoulis
Fetal Programming of Polycystic Ovary Syndrome by Androgen Excess: Evidence from Experimental, Clinical, and Genetic Association Studies
J. Clin. Endocrinol. Metab., May 1, 2006; 91(5): 1660 - 1666.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
A. Vottero, M. Capelletti, S. Giuliodori, I. Viani, M. Ziveri, T. M. Neri, S. Bernasconi, and L. Ghizzoni
Decreased Androgen Receptor Gene Methylation in Premature Pubarche: A Novel Pathogenetic Mechanism?
J. Clin. Endocrinol. Metab., March 1, 2006; 91(3): 968 - 972.
[Abstract] [Full Text] [PDF]


Home page
Endocr. Rev.Home page
H. F. Escobar-Morreale, M. Luque-Ramirez, and J. L. San Millan
The Molecular-Genetic Basis of Functional Hyperandrogenism and the Polycystic Ovary Syndrome
Endocr. Rev., April 1, 2005; 26(2): 251 - 282.
[Abstract] [Full Text] [PDF]


Home page
Reproductive SciencesHome page
I. S. Brum, P. M. Spritzer, F. Paris, M. A. Maturana, F. Audran, and C. Sultan
Association Between Androgen Receptor Gene CAG Repeat Polymorphism and Plasma Testosterone Levels in Postmenopausal Women
Reproductive Sciences, February 1, 2005; 12(2): 135 - 141.
[Abstract] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
M. Zitzmann, M. Depenbusch, J. Gromoll, and E. Nieschlag
X-Chromosome Inactivation Patterns and Androgen Receptor Functionality Influence Phenotype and Social Characteristics as Well as Pharmacogenetics of Testosterone Therapy in Klinefelter Patients
J. Clin. Endocrinol. Metab., December 1, 2004; 89(12): 6208 - 6217.
[Abstract] [Full Text] [PDF]


Home page
Obstet GynecolHome page
R. Azziz
The Evaluation and Management of Hirsutism
Obstet. Gynecol., May 1, 2003; 101(5): 995 - 1007.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
B. Peral, J. L. San Millan, R. Castello, P. Moghetti, and H. F. Escobar-Morreale
The Methionine 196 Arginine Polymorphism in Exon 6 of the TNF Receptor 2 Gene (TNFRSF1B) Is Associated with the Polycystic Ovary Syndrome and Hyperandrogenism
J. Clin. Endocrinol. Metab., August 1, 2002; 87(8): 3977 - 3983.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
Y. L. Giwercman, A. Nordenskjold, E. M. Ritzen, K. O. Nilsson, S.-A. Ivarsson, U. Grandell, and A. Wedell
An Androgen Receptor Gene Mutation (E653K) in a Family with Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency as well as in Partial Androgen Insensitivity
J. Clin. Endocrinol. Metab., June 1, 2002; 87(6): 2623 - 2628.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
T. Hickey, A. Chandy, and R. J. Norman
The Androgen Receptor CAG Repeat Polymorphism and X-Chromosome Inactivation in Australian Caucasian Women with Infertility Related to Polycystic Ovary Syndrome
J. Clin. Endocrinol. Metab., January 1, 2002; 87(1): 161 - 165.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
H. F. Escobar-Morreale, R. M. Calvo, J. Sancho, and J. L. San Millan
TNF-{alpha} and Hyperandrogenism: A Clinical, Biochemical, and Molecular Genetic Study
J. Clin. Endocrinol. Metab., August 1, 2001; 86(8): 3761 - 3767.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
R. M. Calvo, M. Asunción, D. Tellería, J. Sancho, J. L. San Millán, and H. F. Escobar-Morreale
Screening for Mutations in the Steroidogenic Acute Regulatory Protein and Steroidogenic Factor-1 Genes, and in CYP11A and Dosage-Sensitive Sex Reversal-Adrenal Hypoplasia Gene on the X Chromosome, Gene-1 (DAX-1), in Hyperandrogenic Hirsute Women
J. Clin. Endocrinol. Metab., April 1, 2001; 86(4): 1746 - 1749.
[Abstract] [Full Text]


Home page
Endocr. Rev.Home page
D. Deplewski and R. L. Rosenfield
Role of Hormones in Pilosebaceous Unit Development
Endocr. Rev., August 1, 2000; 21(4): 363 - 392.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 2000 by The Endocrine Society