Androgen Receptor CAG Repeat Length Is Associated With Body Fat and Serum SHBG in Boys: A Prospective Cohort Study

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Standard

Androgen Receptor CAG Repeat Length Is Associated With Body Fat and Serum SHBG in Boys : A Prospective Cohort Study. / Mouritsen, Annette; Hagen, Casper P; Sørensen, Kaspar; Aksglaede, Lise; Mieritz, Mikkel G; Main, Katharina M; Almstrup, Kristian; Rajpert-De Meyts, Ewa; Juul, Anders.

I: Journal of Clinical Endocrinology and Metabolism, Bind 98, Nr. 3, 2013, s. E605-9.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Mouritsen, A, Hagen, CP, Sørensen, K, Aksglaede, L, Mieritz, MG, Main, KM, Almstrup, K, Rajpert-De Meyts, E & Juul, A 2013, 'Androgen Receptor CAG Repeat Length Is Associated With Body Fat and Serum SHBG in Boys: A Prospective Cohort Study', Journal of Clinical Endocrinology and Metabolism, bind 98, nr. 3, s. E605-9. https://doi.org/10.1210/jc.2012-3778

APA

Mouritsen, A., Hagen, C. P., Sørensen, K., Aksglaede, L., Mieritz, M. G., Main, K. M., Almstrup, K., Rajpert-De Meyts, E., & Juul, A. (2013). Androgen Receptor CAG Repeat Length Is Associated With Body Fat and Serum SHBG in Boys: A Prospective Cohort Study. Journal of Clinical Endocrinology and Metabolism, 98(3), E605-9. https://doi.org/10.1210/jc.2012-3778

Vancouver

Mouritsen A, Hagen CP, Sørensen K, Aksglaede L, Mieritz MG, Main KM o.a. Androgen Receptor CAG Repeat Length Is Associated With Body Fat and Serum SHBG in Boys: A Prospective Cohort Study. Journal of Clinical Endocrinology and Metabolism. 2013;98(3):E605-9. https://doi.org/10.1210/jc.2012-3778

Author

Mouritsen, Annette ; Hagen, Casper P ; Sørensen, Kaspar ; Aksglaede, Lise ; Mieritz, Mikkel G ; Main, Katharina M ; Almstrup, Kristian ; Rajpert-De Meyts, Ewa ; Juul, Anders. / Androgen Receptor CAG Repeat Length Is Associated With Body Fat and Serum SHBG in Boys : A Prospective Cohort Study. I: Journal of Clinical Endocrinology and Metabolism. 2013 ; Bind 98, Nr. 3. s. E605-9.

Bibtex

@article{6b19b2a6345f4cb6a92306a996a80ccb,
title = "Androgen Receptor CAG Repeat Length Is Associated With Body Fat and Serum SHBG in Boys: A Prospective Cohort Study",
abstract = "Background: Longer androgen receptor gene CAG trinucleotide repeats, AR (CAG)n, have been associated with reduced sensitivity of the androgen receptor (AR) in vitro as well as in humans. Furthermore, short AR (CAG)n have been associated with premature adrenarche. Objective: The aim of the study was to evaluate associations between the AR (CAG)n polymorphism and development of pubic hair, levels of androgens, and body fat content in healthy boys. Methods: A longitudinal study of 78 healthy boys (age 6.2-12.4 years at inclusion) from the COPENHAGEN Puberty Study was conducted with clinical examinations and blood samples drawn every 6 months. The AR (CAG)n length was established by direct DNA sequencing and reproductive hormones were measured in serum by standardized analyses. Results: Median AR (CAG)n length was 22 (range, 17-30). Before puberty (at 10 years of age), boys with long CAG repeats (CAG ≥24) had lower levels of SHBG (88 vs 125 nmol/L) (P <.05) and a nonsignificant trend toward higher median skinfold thickness (41 vs 31 mm) (P = .06) compared with boys with an average number of CAG repeats (CAG 21-23). In contrast, the inverse association was observed at puberty (at 12 years of age) in boys with short CAG repeats (CAG 17-20) (P <.05). Serum levels of LH and testosterone (at 12 years) were significantly higher in boys with long CAG repeats compared with boys with an average number of CAG repeats (P = .05). Conclusion: The observed associations between AR (CAG)n and peripubertal fat accumulation and serum SHBG concentrations indicate that this genetic polymorphism may influence the androgen-dependent fine-tuning of metabolic and reproductive factors at a young age.",
author = "Annette Mouritsen and Hagen, {Casper P} and Kaspar S{\o}rensen and Lise Aksglaede and Mieritz, {Mikkel G} and Main, {Katharina M} and Kristian Almstrup and {Rajpert-De Meyts}, Ewa and Anders Juul",
year = "2013",
doi = "10.1210/jc.2012-3778",
language = "English",
volume = "98",
pages = "E605--9",
journal = "Journal of Clinical Endocrinology and Metabolism",
issn = "0021-972X",
publisher = "Oxford University Press",
number = "3",

}

RIS

TY - JOUR

T1 - Androgen Receptor CAG Repeat Length Is Associated With Body Fat and Serum SHBG in Boys

T2 - A Prospective Cohort Study

AU - Mouritsen, Annette

AU - Hagen, Casper P

AU - Sørensen, Kaspar

AU - Aksglaede, Lise

AU - Mieritz, Mikkel G

AU - Main, Katharina M

AU - Almstrup, Kristian

AU - Rajpert-De Meyts, Ewa

AU - Juul, Anders

PY - 2013

Y1 - 2013

N2 - Background: Longer androgen receptor gene CAG trinucleotide repeats, AR (CAG)n, have been associated with reduced sensitivity of the androgen receptor (AR) in vitro as well as in humans. Furthermore, short AR (CAG)n have been associated with premature adrenarche. Objective: The aim of the study was to evaluate associations between the AR (CAG)n polymorphism and development of pubic hair, levels of androgens, and body fat content in healthy boys. Methods: A longitudinal study of 78 healthy boys (age 6.2-12.4 years at inclusion) from the COPENHAGEN Puberty Study was conducted with clinical examinations and blood samples drawn every 6 months. The AR (CAG)n length was established by direct DNA sequencing and reproductive hormones were measured in serum by standardized analyses. Results: Median AR (CAG)n length was 22 (range, 17-30). Before puberty (at 10 years of age), boys with long CAG repeats (CAG ≥24) had lower levels of SHBG (88 vs 125 nmol/L) (P <.05) and a nonsignificant trend toward higher median skinfold thickness (41 vs 31 mm) (P = .06) compared with boys with an average number of CAG repeats (CAG 21-23). In contrast, the inverse association was observed at puberty (at 12 years of age) in boys with short CAG repeats (CAG 17-20) (P <.05). Serum levels of LH and testosterone (at 12 years) were significantly higher in boys with long CAG repeats compared with boys with an average number of CAG repeats (P = .05). Conclusion: The observed associations between AR (CAG)n and peripubertal fat accumulation and serum SHBG concentrations indicate that this genetic polymorphism may influence the androgen-dependent fine-tuning of metabolic and reproductive factors at a young age.

AB - Background: Longer androgen receptor gene CAG trinucleotide repeats, AR (CAG)n, have been associated with reduced sensitivity of the androgen receptor (AR) in vitro as well as in humans. Furthermore, short AR (CAG)n have been associated with premature adrenarche. Objective: The aim of the study was to evaluate associations between the AR (CAG)n polymorphism and development of pubic hair, levels of androgens, and body fat content in healthy boys. Methods: A longitudinal study of 78 healthy boys (age 6.2-12.4 years at inclusion) from the COPENHAGEN Puberty Study was conducted with clinical examinations and blood samples drawn every 6 months. The AR (CAG)n length was established by direct DNA sequencing and reproductive hormones were measured in serum by standardized analyses. Results: Median AR (CAG)n length was 22 (range, 17-30). Before puberty (at 10 years of age), boys with long CAG repeats (CAG ≥24) had lower levels of SHBG (88 vs 125 nmol/L) (P <.05) and a nonsignificant trend toward higher median skinfold thickness (41 vs 31 mm) (P = .06) compared with boys with an average number of CAG repeats (CAG 21-23). In contrast, the inverse association was observed at puberty (at 12 years of age) in boys with short CAG repeats (CAG 17-20) (P <.05). Serum levels of LH and testosterone (at 12 years) were significantly higher in boys with long CAG repeats compared with boys with an average number of CAG repeats (P = .05). Conclusion: The observed associations between AR (CAG)n and peripubertal fat accumulation and serum SHBG concentrations indicate that this genetic polymorphism may influence the androgen-dependent fine-tuning of metabolic and reproductive factors at a young age.

U2 - 10.1210/jc.2012-3778

DO - 10.1210/jc.2012-3778

M3 - Journal article

C2 - 23393169

VL - 98

SP - E605-9

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

SN - 0021-972X

IS - 3

ER -

ID: 48484684