Circulating MKRN3 levels decline prior to pubertal onset and through puberty: a longitudinal study of healthy girls

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Standard

Circulating MKRN3 levels decline prior to pubertal onset and through puberty : a longitudinal study of healthy girls. / Hagen, Casper P; Sørensen, Kaspar; Mieritz, Mikkel G; Johannsen, Trine Holm; Almstrup, Kristian; Juul, Anders.

I: Journal of Clinical Endocrinology and Metabolism, Bind 100, Nr. 5, 2015, s. 1920-6.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Hagen, CP, Sørensen, K, Mieritz, MG, Johannsen, TH, Almstrup, K & Juul, A 2015, 'Circulating MKRN3 levels decline prior to pubertal onset and through puberty: a longitudinal study of healthy girls', Journal of Clinical Endocrinology and Metabolism, bind 100, nr. 5, s. 1920-6. https://doi.org/10.1210/jc.2014-4462

APA

Hagen, C. P., Sørensen, K., Mieritz, M. G., Johannsen, T. H., Almstrup, K., & Juul, A. (2015). Circulating MKRN3 levels decline prior to pubertal onset and through puberty: a longitudinal study of healthy girls. Journal of Clinical Endocrinology and Metabolism, 100(5), 1920-6. https://doi.org/10.1210/jc.2014-4462

Vancouver

Hagen CP, Sørensen K, Mieritz MG, Johannsen TH, Almstrup K, Juul A. Circulating MKRN3 levels decline prior to pubertal onset and through puberty: a longitudinal study of healthy girls. Journal of Clinical Endocrinology and Metabolism. 2015;100(5):1920-6. https://doi.org/10.1210/jc.2014-4462

Author

Hagen, Casper P ; Sørensen, Kaspar ; Mieritz, Mikkel G ; Johannsen, Trine Holm ; Almstrup, Kristian ; Juul, Anders. / Circulating MKRN3 levels decline prior to pubertal onset and through puberty : a longitudinal study of healthy girls. I: Journal of Clinical Endocrinology and Metabolism. 2015 ; Bind 100, Nr. 5. s. 1920-6.

Bibtex

@article{de88a1003f814dc9a78e7f5d71a4a3ae,
title = "Circulating MKRN3 levels decline prior to pubertal onset and through puberty: a longitudinal study of healthy girls",
abstract = "CONTEXT: Puberty is initiated by a complex interaction of suppressing and stimulating factors. Genetic studies of familial central precocious puberty have suggested makorin ring finger protein 3 (MKRN3) as a major inhibitor of GnRH secretion during childhood. Furthermore, genetic variation near MKRN3 (rs12148769) affects age at menarche in healthy girls.OBJECTIVE: The purpose of this study was to evaluate whether serum levels of MKRN3 declined before pubertal onset in healthy girls.DESIGN: This was a population-based longitudinal study of healthy Danish girls and a cohort study of early maturing girls.SETTING: The study was performed in the general community and in a tertiary referral center for pediatric endocrinology.PATIENTS OR OTHER PARTICIPANTS: Healthy girls (n = 38) aged 9.3 years (range, 5.9-11.3 years) at baseline and followed for 6.0 years (2.7-7.6 years) (2006-2014) with blood sampling every 6 months and early maturing girls (n = 13) with breast development ay <8.3 years of age were included.MAIN OUTCOME MEASURES: Serum levels of MKRN3 were measured in 354 samples (median, 9 per girl; range, 2-14 per girl), and genotyping of variants near MKRN3 (rs12148769 and rs12439354) was performed.RESULTS: MKRN3 concentrations declined preceding pubertal onset; the geometric mean (95% confidence interval) 3 years before pubertal onset vs the last visit before pubertal onset was 304 pg/mL (264-350 pg/mL) vs 257 pg/mL (243-273 pg/mL), corresponding to a reduction of 15% (1-27%) (P = .033). In prepubertal girls, circulating MKRN3 correlated negatively with gonadotropin levels: for FSH, r = -0.262 (P = .015) and for LH, r = -0.226 (P = .037). After adjustment, MKRN3 levels were lower in early maturing girls than in age-matched prepubertal girls: 171 pg/mL (<25-333 pg/mL) vs 262 pg/mL (94-624 pg/mL) (P = .051). Genetic variants near MKRN3 did not correlate with serum levels of MKRN3.CONCLUSIONS: Declining levels of circulating MKRN3 preceded pubertal onset. The negative correlation between MKRN3 and gonadotropins further supports MKRN3 as a major regulator of hypothalamic GnRH secretion during childhood. Undetectable or low MKRN3 levels were observed in a subgroup of patients with early onset of puberty.",
keywords = "Adolescent, Child, Child, Preschool, Female, Follicle Stimulating Hormone, Genotype, Healthy Volunteers, Humans, Longitudinal Studies, Luteinizing Hormone, Prospective Studies, Puberty, Puberty, Precocious, Ribonucleoproteins",
author = "Hagen, {Casper P} and Kaspar S{\o}rensen and Mieritz, {Mikkel G} and Johannsen, {Trine Holm} and Kristian Almstrup and Anders Juul",
year = "2015",
doi = "10.1210/jc.2014-4462",
language = "English",
volume = "100",
pages = "1920--6",
journal = "Journal of Clinical Endocrinology and Metabolism",
issn = "0021-972X",
publisher = "Oxford University Press",
number = "5",

}

RIS

TY - JOUR

T1 - Circulating MKRN3 levels decline prior to pubertal onset and through puberty

T2 - a longitudinal study of healthy girls

AU - Hagen, Casper P

AU - Sørensen, Kaspar

AU - Mieritz, Mikkel G

AU - Johannsen, Trine Holm

AU - Almstrup, Kristian

AU - Juul, Anders

PY - 2015

Y1 - 2015

N2 - CONTEXT: Puberty is initiated by a complex interaction of suppressing and stimulating factors. Genetic studies of familial central precocious puberty have suggested makorin ring finger protein 3 (MKRN3) as a major inhibitor of GnRH secretion during childhood. Furthermore, genetic variation near MKRN3 (rs12148769) affects age at menarche in healthy girls.OBJECTIVE: The purpose of this study was to evaluate whether serum levels of MKRN3 declined before pubertal onset in healthy girls.DESIGN: This was a population-based longitudinal study of healthy Danish girls and a cohort study of early maturing girls.SETTING: The study was performed in the general community and in a tertiary referral center for pediatric endocrinology.PATIENTS OR OTHER PARTICIPANTS: Healthy girls (n = 38) aged 9.3 years (range, 5.9-11.3 years) at baseline and followed for 6.0 years (2.7-7.6 years) (2006-2014) with blood sampling every 6 months and early maturing girls (n = 13) with breast development ay <8.3 years of age were included.MAIN OUTCOME MEASURES: Serum levels of MKRN3 were measured in 354 samples (median, 9 per girl; range, 2-14 per girl), and genotyping of variants near MKRN3 (rs12148769 and rs12439354) was performed.RESULTS: MKRN3 concentrations declined preceding pubertal onset; the geometric mean (95% confidence interval) 3 years before pubertal onset vs the last visit before pubertal onset was 304 pg/mL (264-350 pg/mL) vs 257 pg/mL (243-273 pg/mL), corresponding to a reduction of 15% (1-27%) (P = .033). In prepubertal girls, circulating MKRN3 correlated negatively with gonadotropin levels: for FSH, r = -0.262 (P = .015) and for LH, r = -0.226 (P = .037). After adjustment, MKRN3 levels were lower in early maturing girls than in age-matched prepubertal girls: 171 pg/mL (<25-333 pg/mL) vs 262 pg/mL (94-624 pg/mL) (P = .051). Genetic variants near MKRN3 did not correlate with serum levels of MKRN3.CONCLUSIONS: Declining levels of circulating MKRN3 preceded pubertal onset. The negative correlation between MKRN3 and gonadotropins further supports MKRN3 as a major regulator of hypothalamic GnRH secretion during childhood. Undetectable or low MKRN3 levels were observed in a subgroup of patients with early onset of puberty.

AB - CONTEXT: Puberty is initiated by a complex interaction of suppressing and stimulating factors. Genetic studies of familial central precocious puberty have suggested makorin ring finger protein 3 (MKRN3) as a major inhibitor of GnRH secretion during childhood. Furthermore, genetic variation near MKRN3 (rs12148769) affects age at menarche in healthy girls.OBJECTIVE: The purpose of this study was to evaluate whether serum levels of MKRN3 declined before pubertal onset in healthy girls.DESIGN: This was a population-based longitudinal study of healthy Danish girls and a cohort study of early maturing girls.SETTING: The study was performed in the general community and in a tertiary referral center for pediatric endocrinology.PATIENTS OR OTHER PARTICIPANTS: Healthy girls (n = 38) aged 9.3 years (range, 5.9-11.3 years) at baseline and followed for 6.0 years (2.7-7.6 years) (2006-2014) with blood sampling every 6 months and early maturing girls (n = 13) with breast development ay <8.3 years of age were included.MAIN OUTCOME MEASURES: Serum levels of MKRN3 were measured in 354 samples (median, 9 per girl; range, 2-14 per girl), and genotyping of variants near MKRN3 (rs12148769 and rs12439354) was performed.RESULTS: MKRN3 concentrations declined preceding pubertal onset; the geometric mean (95% confidence interval) 3 years before pubertal onset vs the last visit before pubertal onset was 304 pg/mL (264-350 pg/mL) vs 257 pg/mL (243-273 pg/mL), corresponding to a reduction of 15% (1-27%) (P = .033). In prepubertal girls, circulating MKRN3 correlated negatively with gonadotropin levels: for FSH, r = -0.262 (P = .015) and for LH, r = -0.226 (P = .037). After adjustment, MKRN3 levels were lower in early maturing girls than in age-matched prepubertal girls: 171 pg/mL (<25-333 pg/mL) vs 262 pg/mL (94-624 pg/mL) (P = .051). Genetic variants near MKRN3 did not correlate with serum levels of MKRN3.CONCLUSIONS: Declining levels of circulating MKRN3 preceded pubertal onset. The negative correlation between MKRN3 and gonadotropins further supports MKRN3 as a major regulator of hypothalamic GnRH secretion during childhood. Undetectable or low MKRN3 levels were observed in a subgroup of patients with early onset of puberty.

KW - Adolescent

KW - Child

KW - Child, Preschool

KW - Female

KW - Follicle Stimulating Hormone

KW - Genotype

KW - Healthy Volunteers

KW - Humans

KW - Longitudinal Studies

KW - Luteinizing Hormone

KW - Prospective Studies

KW - Puberty

KW - Puberty, Precocious

KW - Ribonucleoproteins

U2 - 10.1210/jc.2014-4462

DO - 10.1210/jc.2014-4462

M3 - Journal article

C2 - 25695892

VL - 100

SP - 1920

EP - 1926

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

SN - 0021-972X

IS - 5

ER -

ID: 162373403