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Sex-specific estrogen levels and reference intervals from infancy to late adulthood determined by LC-MS/MS

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@article{16c2892f8f3c46c8b3f273c68f3b5c7a,
title = "Sex-specific estrogen levels and reference intervals from infancy to late adulthood determined by LC-MS/MS",
abstract = "CONTEXT: The lack of sensitive and robust analytical methods has hindered the reliable quantification of estrogen metabolites in subjects with low concentrations.OBJECTIVE: To establish sex-specific reference ranges for estrone (E1) and estradiol (E2) throughout life and to evaluate sex-differences using the state-of-the-art liquid chromatography tandem mass spectrometry (LC-MS/MS) method for quantification of E1, E2, and estriol (E3).DESIGN: LC-MS/MS method development and construction of estrogen reference ranges.SETTINGS: Population-based cross-sectional cohorts from the greater Copenhagen and Aarhus areas.PARTICIPANTS: Healthy participants aged 3 months to 61 years (n = 1838).RESULTS: An isotope diluted LC-MS/MS method was developed and validated for measurements of serum E1, E2, and E3. Limits of detections (LODs) were 3 pmol/L (E1), 4 pmol/L (E2), and 12 pmol/L (E3), respectively. This sensitive method made it possible to differentiate between male and female concentration levels of E1 and E2 in children. In girls, E2 levels ranged from <LOD to 100 pmol/L during mini-puberty, whereas it was ≤20 pmol/L during childhood. E1 and E2 increased with age and pubertal breast stage and varied during the menstrual cycle; E1 was lower than E2 in girls and premenopausal women, and higher than E2 in postmenopausal women. In boys, E1 and E2 increased with age and pubertal stage, whereas little changes with age were observed in men. High E3 concentrations were confirmed in pregnant women.CONCLUSION: Reference ranges of simultaneous quantification of E1 and E2 by this novel specific and highly sensitive LC-MS/MS method provide an invaluable tool in clinical practice and in future research studies.",
keywords = "childhood, estradiol, estrone, LC-MS/MS, menopause, menstrual cycle, mini-puberty, pubertal development, reference range",
author = "Hanne Frederiksen and Johannsen, {Trine Holm} and Andersen, {Stine Ehlern} and Jakob Albrethsen and Landersoe, {Selma Kl{\o}ve} and Petersen, {J{\o}rgen Holm} and Andersen, {Anders Nyboe} and Vestergaard, {Esben Thyssen} and Schorring, {Mia Elbek} and Allan Linneberg and Main, {Katharina M} and Anna-Maria Andersson and Anders Juul",
note = "{\circledC} Endocrine Society 2019.",
year = "2020",
month = "3",
day = "1",
doi = "10.1210/clinem/dgz196",
language = "English",
volume = "105",
pages = "1--15",
journal = "Journal of Clinical Endocrinology and Metabolism",
issn = "0021-972X",
publisher = "The/Endocrine Society",
number = "3",

}

RIS

TY - JOUR

T1 - Sex-specific estrogen levels and reference intervals from infancy to late adulthood determined by LC-MS/MS

AU - Frederiksen, Hanne

AU - Johannsen, Trine Holm

AU - Andersen, Stine Ehlern

AU - Albrethsen, Jakob

AU - Landersoe, Selma Kløve

AU - Petersen, Jørgen Holm

AU - Andersen, Anders Nyboe

AU - Vestergaard, Esben Thyssen

AU - Schorring, Mia Elbek

AU - Linneberg, Allan

AU - Main, Katharina M

AU - Andersson, Anna-Maria

AU - Juul, Anders

N1 - © Endocrine Society 2019.

PY - 2020/3/1

Y1 - 2020/3/1

N2 - CONTEXT: The lack of sensitive and robust analytical methods has hindered the reliable quantification of estrogen metabolites in subjects with low concentrations.OBJECTIVE: To establish sex-specific reference ranges for estrone (E1) and estradiol (E2) throughout life and to evaluate sex-differences using the state-of-the-art liquid chromatography tandem mass spectrometry (LC-MS/MS) method for quantification of E1, E2, and estriol (E3).DESIGN: LC-MS/MS method development and construction of estrogen reference ranges.SETTINGS: Population-based cross-sectional cohorts from the greater Copenhagen and Aarhus areas.PARTICIPANTS: Healthy participants aged 3 months to 61 years (n = 1838).RESULTS: An isotope diluted LC-MS/MS method was developed and validated for measurements of serum E1, E2, and E3. Limits of detections (LODs) were 3 pmol/L (E1), 4 pmol/L (E2), and 12 pmol/L (E3), respectively. This sensitive method made it possible to differentiate between male and female concentration levels of E1 and E2 in children. In girls, E2 levels ranged from <LOD to 100 pmol/L during mini-puberty, whereas it was ≤20 pmol/L during childhood. E1 and E2 increased with age and pubertal breast stage and varied during the menstrual cycle; E1 was lower than E2 in girls and premenopausal women, and higher than E2 in postmenopausal women. In boys, E1 and E2 increased with age and pubertal stage, whereas little changes with age were observed in men. High E3 concentrations were confirmed in pregnant women.CONCLUSION: Reference ranges of simultaneous quantification of E1 and E2 by this novel specific and highly sensitive LC-MS/MS method provide an invaluable tool in clinical practice and in future research studies.

AB - CONTEXT: The lack of sensitive and robust analytical methods has hindered the reliable quantification of estrogen metabolites in subjects with low concentrations.OBJECTIVE: To establish sex-specific reference ranges for estrone (E1) and estradiol (E2) throughout life and to evaluate sex-differences using the state-of-the-art liquid chromatography tandem mass spectrometry (LC-MS/MS) method for quantification of E1, E2, and estriol (E3).DESIGN: LC-MS/MS method development and construction of estrogen reference ranges.SETTINGS: Population-based cross-sectional cohorts from the greater Copenhagen and Aarhus areas.PARTICIPANTS: Healthy participants aged 3 months to 61 years (n = 1838).RESULTS: An isotope diluted LC-MS/MS method was developed and validated for measurements of serum E1, E2, and E3. Limits of detections (LODs) were 3 pmol/L (E1), 4 pmol/L (E2), and 12 pmol/L (E3), respectively. This sensitive method made it possible to differentiate between male and female concentration levels of E1 and E2 in children. In girls, E2 levels ranged from <LOD to 100 pmol/L during mini-puberty, whereas it was ≤20 pmol/L during childhood. E1 and E2 increased with age and pubertal breast stage and varied during the menstrual cycle; E1 was lower than E2 in girls and premenopausal women, and higher than E2 in postmenopausal women. In boys, E1 and E2 increased with age and pubertal stage, whereas little changes with age were observed in men. High E3 concentrations were confirmed in pregnant women.CONCLUSION: Reference ranges of simultaneous quantification of E1 and E2 by this novel specific and highly sensitive LC-MS/MS method provide an invaluable tool in clinical practice and in future research studies.

KW - childhood

KW - estradiol

KW - estrone

KW - LC-MS/MS

KW - menopause

KW - menstrual cycle

KW - mini-puberty

KW - pubertal development

KW - reference range

U2 - 10.1210/clinem/dgz196

DO - 10.1210/clinem/dgz196

M3 - Journal article

VL - 105

SP - 1

EP - 15

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

SN - 0021-972X

IS - 3

ER -

ID: 58366501