Evolution of metabolic alterations 5 Years after early puberty in a cohort of girls predisposed to polycystic ovary syndrome

Abstract Background We and others have observed that young girls predisposed to polycystic ovary syndrome (PCOS) display defective insulin sensitivity, beta-cell function and non-esterified fatty acids (NEFA) suppressibility during early pubertal years, compared to controls. Our objective is to asse...

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Main Authors: Soren Harnois-Leblanc, Andréanne Trottier, Samuel Leblanc, Marie-Claude Battista, David H. Geller, Jean-Patrice Baillargeon
Format: Article
Language:English
Published: BMC 2017-07-01
Series:Reproductive Biology and Endocrinology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12958-017-0275-0
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author Soren Harnois-Leblanc
Andréanne Trottier
Samuel Leblanc
Marie-Claude Battista
David H. Geller
Jean-Patrice Baillargeon
author_facet Soren Harnois-Leblanc
Andréanne Trottier
Samuel Leblanc
Marie-Claude Battista
David H. Geller
Jean-Patrice Baillargeon
author_sort Soren Harnois-Leblanc
collection DOAJ
description Abstract Background We and others have observed that young girls predisposed to polycystic ovary syndrome (PCOS) display defective insulin sensitivity, beta-cell function and non-esterified fatty acids (NEFA) suppressibility during early pubertal years, compared to controls. Our objective is to assess whether these differences in glucose and NEFA metabolisms persist after 5 years in late/post-puberty. Methods We conducted a prospective cohort study between 2007 and 2015 with 4–6 years of follow-up in an academic institution research center. We compared 8 daughters and sisters of PCOS women (PCOSr) to 8 age-matched girls unrelated to PCOS (±1.5 years). Girls were assessed initially at 8–14 years old and re-assessed after a median follow-up of 5.4 years, at 13–21 years old. Our main measures were a frequently sampled intravenous glucose tolerance test (FSivGTT)-derived insulin sensitivity (IS) and beta-cell function (disposition index, DIFSivGTT); and indices of NEFA suppression during FSivGTT (logn-linear slope of NEFA and T50 of NEFA suppression). Results At follow-up, both PCOSr and controls had similar results: IS = 3.2 vs 3.4 (p = 0.88), DIFSivGTT = 1926 vs 1380 (p = 0.44), logn-linear slope = −0.032 vs −0.032 (p = 0.88) and T50NEFA = 18.1 vs 20.8 min (p = 0.57). IS, DIFSivGTT and NEFA suppressibility were stable in PCOSr after 5 years, but decreased significantly in controls (all p < 0.05). Conclusions Impaired metabolism observed during early puberty in girls predisposed to PCOS remains stable after 5 years whereas control girls deteriorated their metabolic parameters. Therefore, both groups become comparable in late/post-puberty. Early puberty may thus represent a window during which metabolic alterations are transiently apparent in girls at risk of PCOS.
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spelling doaj.art-3f8d2bb6b5404aae9ccb23899cceb0072022-12-21T23:43:12ZengBMCReproductive Biology and Endocrinology1477-78272017-07-011511910.1186/s12958-017-0275-0Evolution of metabolic alterations 5 Years after early puberty in a cohort of girls predisposed to polycystic ovary syndromeSoren Harnois-Leblanc0Andréanne Trottier1Samuel Leblanc2Marie-Claude Battista3David H. Geller4Jean-Patrice Baillargeon5Division of Endocrinology, Department of Medicine, Faculty of Medicine and Health Sciences, Université de SherbrookeDivision of Endocrinology, Department of Medicine, Faculty of Medicine and Health Sciences, Université de SherbrookeDivision of Endocrinology, Department of Medicine, Faculty of Medicine and Health Sciences, Université de SherbrookeResearch Center, Centre Hospitalier Universitaire de SherbrookeDepartment of Pediatrics, Cedars-Sinai Medical CenterDivision of Endocrinology, Department of Medicine, Faculty of Medicine and Health Sciences, Université de SherbrookeAbstract Background We and others have observed that young girls predisposed to polycystic ovary syndrome (PCOS) display defective insulin sensitivity, beta-cell function and non-esterified fatty acids (NEFA) suppressibility during early pubertal years, compared to controls. Our objective is to assess whether these differences in glucose and NEFA metabolisms persist after 5 years in late/post-puberty. Methods We conducted a prospective cohort study between 2007 and 2015 with 4–6 years of follow-up in an academic institution research center. We compared 8 daughters and sisters of PCOS women (PCOSr) to 8 age-matched girls unrelated to PCOS (±1.5 years). Girls were assessed initially at 8–14 years old and re-assessed after a median follow-up of 5.4 years, at 13–21 years old. Our main measures were a frequently sampled intravenous glucose tolerance test (FSivGTT)-derived insulin sensitivity (IS) and beta-cell function (disposition index, DIFSivGTT); and indices of NEFA suppression during FSivGTT (logn-linear slope of NEFA and T50 of NEFA suppression). Results At follow-up, both PCOSr and controls had similar results: IS = 3.2 vs 3.4 (p = 0.88), DIFSivGTT = 1926 vs 1380 (p = 0.44), logn-linear slope = −0.032 vs −0.032 (p = 0.88) and T50NEFA = 18.1 vs 20.8 min (p = 0.57). IS, DIFSivGTT and NEFA suppressibility were stable in PCOSr after 5 years, but decreased significantly in controls (all p < 0.05). Conclusions Impaired metabolism observed during early puberty in girls predisposed to PCOS remains stable after 5 years whereas control girls deteriorated their metabolic parameters. Therefore, both groups become comparable in late/post-puberty. Early puberty may thus represent a window during which metabolic alterations are transiently apparent in girls at risk of PCOS.http://link.springer.com/article/10.1186/s12958-017-0275-0Polycystic ovary syndromeDaughtersPubertyInsulin sensitivityNon-esterified fatty acidsGlucose homeostasis
spellingShingle Soren Harnois-Leblanc
Andréanne Trottier
Samuel Leblanc
Marie-Claude Battista
David H. Geller
Jean-Patrice Baillargeon
Evolution of metabolic alterations 5 Years after early puberty in a cohort of girls predisposed to polycystic ovary syndrome
Reproductive Biology and Endocrinology
Polycystic ovary syndrome
Daughters
Puberty
Insulin sensitivity
Non-esterified fatty acids
Glucose homeostasis
title Evolution of metabolic alterations 5 Years after early puberty in a cohort of girls predisposed to polycystic ovary syndrome
title_full Evolution of metabolic alterations 5 Years after early puberty in a cohort of girls predisposed to polycystic ovary syndrome
title_fullStr Evolution of metabolic alterations 5 Years after early puberty in a cohort of girls predisposed to polycystic ovary syndrome
title_full_unstemmed Evolution of metabolic alterations 5 Years after early puberty in a cohort of girls predisposed to polycystic ovary syndrome
title_short Evolution of metabolic alterations 5 Years after early puberty in a cohort of girls predisposed to polycystic ovary syndrome
title_sort evolution of metabolic alterations 5 years after early puberty in a cohort of girls predisposed to polycystic ovary syndrome
topic Polycystic ovary syndrome
Daughters
Puberty
Insulin sensitivity
Non-esterified fatty acids
Glucose homeostasis
url http://link.springer.com/article/10.1186/s12958-017-0275-0
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