Maternal PCOS status and metformin in pregnancy: Steroid hormones in 5–10 years old children from the PregMet randomized controlled study
Polycystic ovary syndrome (PCOS) is a common endocrine disorder, with potential effects on offspring both genetically and through altered intrauterine environment. Metformin, which ameliorate hormonal disturbances in non-pregnant women with PCOS is increasingly used in pregnancy. It passes the place...
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Published in | PloS one Vol. 16; no. 9; p. e0257186 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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Abstract | Polycystic ovary syndrome (PCOS) is a common endocrine disorder, with potential effects on offspring both genetically and through altered intrauterine environment. Metformin, which ameliorate hormonal disturbances in non-pregnant women with PCOS is increasingly used in pregnancy. It passes the placenta, and the evidence on potential consequences for offspring endocrine development is scarce. We explore the potential effects of maternal PCOS status and intrauterine metformin exposure on offspring steroid hormone levels. This is a follow-up study of 5-10 years old children from the PregMet-study-a randomized controlled trial comparing metformin (2000 mg/day) to placebo during PCOS pregnancies. Of the 255 children invited, 117 (46%) were included. There was no intervention in this follow-up study. Outcomes were serum levels of androstenedione, testosterone, SHBG, cortisol, 17-hydroxyprogesterone, 11-deoxycortisol and calculated free testosterone converted to gender-and age adjusted z-scores from a Norwegian reference population. These were compared in i) placebo-exposed children versus children from the reference population (z-score zero) by the deviation in z-score by one-sample t-tests and ii) metformin versus placebo-exposed children by two-sample t-tests. Holm-Bonferroni adjustments were performed to account for multiple endpoints. Girls of mothers with PCOS (n = 30) had higher mean z-scores of androstenedione (0.73 (95% confidence interval (CI) 0.41 to 1.06), p<0.0001), testosterone (0.76 (0.51 to 1.00), p<0.0001), and free testosterone (0.99 (0.67 to 1.32), p<0.0001) than the reference population. Metformin-exposed boys (n = 31) tended to have higher 11-deoxycortisol z-score than placebo-exposed boys (n = 24) (mean difference 0.65 (95% CI 0.14-1.17), p = 0.014). Maternal PCOS status was associated with elevated androgens in 5- to 10-year-old daughters, which might indicate earlier maturation and increased risk of developing PCOS. An impact of metformin in pregnancy on steroidogenesis in children born to mothers with PCOS cannot be excluded. Our findings need confirmation in studies that include participants that have entered puberty. |
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AbstractList | Objective
Polycystic ovary syndrome (PCOS) is a common endocrine disorder, with potential effects on offspring both genetically and through altered intrauterine environment. Metformin, which ameliorate hormonal disturbances in non-pregnant women with PCOS is increasingly used in pregnancy. It passes the placenta, and the evidence on potential consequences for offspring endocrine development is scarce. We explore the potential effects of maternal PCOS status and intrauterine metformin exposure on offspring steroid hormone levels.
Design
This is a follow-up study of 5–10 years old children from the PregMet-study–a randomized controlled trial comparing metformin (2000 mg/day) to placebo during PCOS pregnancies. Of the 255 children invited, 117 (46%) were included.
Methods
There was no intervention in this follow-up study. Outcomes were serum levels of androstenedione, testosterone, SHBG, cortisol, 17-hydroxyprogesterone, 11-deoxycortisol and calculated free testosterone converted to gender-and age adjusted z-scores from a Norwegian reference population. These were compared in i) placebo-exposed children versus children from the reference population (z-score zero) by the deviation in z-score by one-sample t-tests and ii) metformin versus placebo-exposed children by two-sample t-tests. Holm-Bonferroni adjustments were performed to account for multiple endpoints.
Results
Girls of mothers with PCOS (n = 30) had higher mean z-scores of androstenedione (0.73 (95% confidence interval (CI) 0.41 to 1.06), p<0.0001), testosterone (0.76 (0.51 to 1.00), p<0.0001), and free testosterone (0.99 (0.67 to 1.32), p<0.0001) than the reference population. Metformin-exposed boys (n = 31) tended to have higher 11-deoxycortisol z-score than placebo-exposed boys (n = 24) (mean difference 0.65 (95% CI 0.14–1.17), p = 0.014).
Conclusion
Maternal PCOS status was associated with elevated androgens in 5- to 10-year-old daughters, which might indicate earlier maturation and increased risk of developing PCOS. An impact of metformin in pregnancy on steroidogenesis in children born to mothers with PCOS cannot be excluded. Our findings need confirmation in studies that include participants that have entered puberty. Polycystic ovary syndrome (PCOS) is a common endocrine disorder, with potential effects on offspring both genetically and through altered intrauterine environment. Metformin, which ameliorate hormonal disturbances in non-pregnant women with PCOS is increasingly used in pregnancy. It passes the placenta, and the evidence on potential consequences for offspring endocrine development is scarce. We explore the potential effects of maternal PCOS status and intrauterine metformin exposure on offspring steroid hormone levels. This is a follow-up study of 5-10 years old children from the PregMet-study-a randomized controlled trial comparing metformin (2000 mg/day) to placebo during PCOS pregnancies. Of the 255 children invited, 117 (46%) were included. There was no intervention in this follow-up study. Outcomes were serum levels of androstenedione, testosterone, SHBG, cortisol, 17-hydroxyprogesterone, 11-deoxycortisol and calculated free testosterone converted to gender-and age adjusted z-scores from a Norwegian reference population. These were compared in i) placebo-exposed children versus children from the reference population (z-score zero) by the deviation in z-score by one-sample t-tests and ii) metformin versus placebo-exposed children by two-sample t-tests. Holm-Bonferroni adjustments were performed to account for multiple endpoints. Girls of mothers with PCOS (n = 30) had higher mean z-scores of androstenedione (0.73 (95% confidence interval (CI) 0.41 to 1.06), p<0.0001), testosterone (0.76 (0.51 to 1.00), p<0.0001), and free testosterone (0.99 (0.67 to 1.32), p<0.0001) than the reference population. Metformin-exposed boys (n = 31) tended to have higher 11-deoxycortisol z-score than placebo-exposed boys (n = 24) (mean difference 0.65 (95% CI 0.14-1.17), p = 0.014). Maternal PCOS status was associated with elevated androgens in 5- to 10-year-old daughters, which might indicate earlier maturation and increased risk of developing PCOS. An impact of metformin in pregnancy on steroidogenesis in children born to mothers with PCOS cannot be excluded. Our findings need confirmation in studies that include participants that have entered puberty. OBJECTIVEPolycystic ovary syndrome (PCOS) is a common endocrine disorder, with potential effects on offspring both genetically and through altered intrauterine environment. Metformin, which ameliorate hormonal disturbances in non-pregnant women with PCOS is increasingly used in pregnancy. It passes the placenta, and the evidence on potential consequences for offspring endocrine development is scarce. We explore the potential effects of maternal PCOS status and intrauterine metformin exposure on offspring steroid hormone levels. DESIGNThis is a follow-up study of 5-10 years old children from the PregMet-study-a randomized controlled trial comparing metformin (2000 mg/day) to placebo during PCOS pregnancies. Of the 255 children invited, 117 (46%) were included. METHODSThere was no intervention in this follow-up study. Outcomes were serum levels of androstenedione, testosterone, SHBG, cortisol, 17-hydroxyprogesterone, 11-deoxycortisol and calculated free testosterone converted to gender-and age adjusted z-scores from a Norwegian reference population. These were compared in i) placebo-exposed children versus children from the reference population (z-score zero) by the deviation in z-score by one-sample t-tests and ii) metformin versus placebo-exposed children by two-sample t-tests. Holm-Bonferroni adjustments were performed to account for multiple endpoints. RESULTSGirls of mothers with PCOS (n = 30) had higher mean z-scores of androstenedione (0.73 (95% confidence interval (CI) 0.41 to 1.06), p<0.0001), testosterone (0.76 (0.51 to 1.00), p<0.0001), and free testosterone (0.99 (0.67 to 1.32), p<0.0001) than the reference population. Metformin-exposed boys (n = 31) tended to have higher 11-deoxycortisol z-score than placebo-exposed boys (n = 24) (mean difference 0.65 (95% CI 0.14-1.17), p = 0.014). CONCLUSIONMaternal PCOS status was associated with elevated androgens in 5- to 10-year-old daughters, which might indicate earlier maturation and increased risk of developing PCOS. An impact of metformin in pregnancy on steroidogenesis in children born to mothers with PCOS cannot be excluded. Our findings need confirmation in studies that include participants that have entered puberty. Objective Polycystic ovary syndrome (PCOS) is a common endocrine disorder, with potential effects on offspring both genetically and through altered intrauterine environment. Metformin, which ameliorate hormonal disturbances in non-pregnant women with PCOS is increasingly used in pregnancy. It passes the placenta, and the evidence on potential consequences for offspring endocrine development is scarce. We explore the potential effects of maternal PCOS status and intrauterine metformin exposure on offspring steroid hormone levels. Design This is a follow-up study of 5–10 years old children from the PregMet-study–a randomized controlled trial comparing metformin (2000 mg/day) to placebo during PCOS pregnancies. Of the 255 children invited, 117 (46%) were included. Methods There was no intervention in this follow-up study. Outcomes were serum levels of androstenedione, testosterone, SHBG, cortisol, 17-hydroxyprogesterone, 11-deoxycortisol and calculated free testosterone converted to gender-and age adjusted z-scores from a Norwegian reference population. These were compared in i) placebo-exposed children versus children from the reference population (z-score zero) by the deviation in z-score by one-sample t-tests and ii) metformin versus placebo-exposed children by two-sample t-tests. Holm-Bonferroni adjustments were performed to account for multiple endpoints. Results Girls of mothers with PCOS (n = 30) had higher mean z-scores of androstenedione (0.73 (95% confidence interval (CI) 0.41 to 1.06), p<0.0001), testosterone (0.76 (0.51 to 1.00), p<0.0001), and free testosterone (0.99 (0.67 to 1.32), p<0.0001) than the reference population. Metformin-exposed boys (n = 31) tended to have higher 11-deoxycortisol z-score than placebo-exposed boys (n = 24) (mean difference 0.65 (95% CI 0.14–1.17), p = 0.014). Conclusion Maternal PCOS status was associated with elevated androgens in 5- to 10-year-old daughters, which might indicate earlier maturation and increased risk of developing PCOS. An impact of metformin in pregnancy on steroidogenesis in children born to mothers with PCOS cannot be excluded. Our findings need confirmation in studies that include participants that have entered puberty. |
Audience | Academic |
Author | Vanky, Eszter Salvesen, Øyvind Carlsen, Sven Magnus Sagen, Jørn V Hanem, Liv Guro Engen Madsen, André Ødegård, Rønnaug Mellgren, Gunnar Juliusson, Petur Benedikt |
AuthorAffiliation | 11 Centre for Obesity Research, Dept. of Surgery St. Olav University Hospital, Trondheim, Norway 2 Children’s clinic, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway 9 Department of Endocrinology, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway Pennington Biomedical Research Center, UNITED STATES 7 KG Jebsen Centre for Diabetes Research, University of Bergen, Bergen, Norway 1 Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway 5 Department of Clinical Science, University of Bergen, Bergen, Norway 4 Hormone Laboratory, Haukeland University Hospital, Bergen, Norway 10 Department of Obstetrics and Gynecology, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway 6 Department of Pediatrics, Haukeland University Hospital, Bergen, Norway 8 Department of Health Registries, Norwegian Institute of Public Health, Bergen, Norway 3 Department of Public |
AuthorAffiliation_xml | – name: 5 Department of Clinical Science, University of Bergen, Bergen, Norway – name: 11 Centre for Obesity Research, Dept. of Surgery St. Olav University Hospital, Trondheim, Norway – name: 8 Department of Health Registries, Norwegian Institute of Public Health, Bergen, Norway – name: Pennington Biomedical Research Center, UNITED STATES – name: 3 Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway – name: 10 Department of Obstetrics and Gynecology, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway – name: 1 Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway – name: 9 Department of Endocrinology, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway – name: 6 Department of Pediatrics, Haukeland University Hospital, Bergen, Norway – name: 7 KG Jebsen Centre for Diabetes Research, University of Bergen, Bergen, Norway – name: 2 Children’s clinic, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway – name: 4 Hormone Laboratory, Haukeland University Hospital, Bergen, Norway |
Author_xml | – sequence: 1 fullname: Hanem, Liv Guro Engen – sequence: 2 fullname: Salvesen, Øyvind – sequence: 3 fullname: Madsen, André – sequence: 4 fullname: Sagen, Jørn V – sequence: 5 fullname: Mellgren, Gunnar – sequence: 6 fullname: Juliusson, Petur Benedikt – sequence: 7 fullname: Carlsen, Sven Magnus – sequence: 8 fullname: Vanky, Eszter – sequence: 9 fullname: Ødegård, Rønnaug |
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References | IS Bruserud (pone.0257186.ref038) 2020; 105 L Aksglaede (pone.0257186.ref023) 2009; 4 LGE Hanem (pone.0257186.ref015) 2018; 103 M Maliqueo (pone.0257186.ref009) 2009; 94 T Sir-Petermann (pone.0257186.ref008) 2009; 94 W van Weelden (pone.0257186.ref021) 2018; 9 PB Juliusson (pone.0257186.ref032) 2013; 40 RB Barnes (pone.0257186.ref045) 1989; 320 DA Dumesic (pone.0257186.ref003) 2020; 159 F Courant (pone.0257186.ref040) 2010; 95 G HOMMEL (pone.0257186.ref042) 1988; 75 A Auzéby (pone.0257186.ref051) 1995; 80 JM Tanner (pone.0257186.ref031) 1976; 51 R Voutilainen (pone.0257186.ref043) 2015; 145 TJ Cole (pone.0257186.ref037) 1990; 44 A Madsen (pone.0257186.ref036) 2020; 105 K Tertti (pone.0257186.ref026) 2016; 13 S Palomba (pone.0257186.ref006) 2015; 21 T Sir-Petermann (pone.0257186.ref046) 2006; 91 MN Gunning (pone.0257186.ref004) 2020; 26 S Franks (pone.0257186.ref001) 1995; 333 E Diamanti-Kandarakis (pone.0257186.ref016) 2010; 162 NHB Oehme (pone.0257186.ref039) 2020; 109 B Brannsether (pone.0257186.ref033) 2011 A la Marca (pone.0257186.ref017) 1999; 72 RS Legro (pone.0257186.ref013) 2017; 102 S Holm (pone.0257186.ref041) 1979; 6 T Sir-Petermann (pone.0257186.ref011) 2007; 92 P Methlie (pone.0257186.ref034) 2013; 2 A Madsen (pone.0257186.ref035) 2020; 105 B Echiburú (pone.0257186.ref002) 2020; 15 TS Løvvik (pone.0257186.ref019) 2019 N Crisosto (pone.0257186.ref048) 2007; 92 LGE Hanem (pone.0257186.ref014) 2019 Q Xu (pone.0257186.ref020) 2019; 299 DA Dumesic (pone.0257186.ref005) 2014; 32 Rotterdam ESHRE/ASRM-Sponsored PCOS Consensus Workshop Group (pone.0257186.ref030) 2004; 19 MR Caanen (pone.0257186.ref012) 2016; 174 E Vanky (pone.0257186.ref018) 2010; 95 E Vanky (pone.0257186.ref025) 2012; 97 SE Recabarren (pone.0257186.ref050) 2008; 93 P Tartarin (pone.0257186.ref054) 2012; 27 L Ibanez (pone.0257186.ref044) 2017; 88 MF Alotaibi (pone.0257186.ref027) 2019; 71 DA Doherty (pone.0257186.ref007) 2015; 125 H Bratke (pone.0257186.ref024) 2017; 17 B Aydin (pone.0257186.ref028) 2016; 8 LS Adair (pone.0257186.ref022) 2001; 107 N Crisosto (pone.0257186.ref049) 2017; 6 JW Honour (pone.0257186.ref052) 2014; 51 C Battaglia (pone.0257186.ref010) 2002; 17 ML Marcovecchio (pone.0257186.ref029) 2013; 106 G Noppe (pone.0257186.ref053) 2016; 40 T Sir-Petermann (pone.0257186.ref047) 2012; 19 |
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Snippet | Objective
Polycystic ovary syndrome (PCOS) is a common endocrine disorder, with potential effects on offspring both genetically and through altered... Objective Polycystic ovary syndrome (PCOS) is a common endocrine disorder, with potential effects on offspring both genetically and through altered... Polycystic ovary syndrome (PCOS) is a common endocrine disorder, with potential effects on offspring both genetically and through altered intrauterine... OBJECTIVEPolycystic ovary syndrome (PCOS) is a common endocrine disorder, with potential effects on offspring both genetically and through altered intrauterine... ObjectivePolycystic ovary syndrome (PCOS) is a common endocrine disorder, with potential effects on offspring both genetically and through altered intrauterine... |
SourceID | plos doaj pubmedcentral proquest gale crossref |
SourceType | Open Website Open Access Repository Aggregation Database |
StartPage | e0257186 |
SubjectTerms | Androgens Androstenedione Antidiabetics Biology and Life Sciences Body mass index Children Complications and side effects Confidence intervals Cortisol Exposure Health aspects Hormones Insulin resistance Intrauterine exposure Medicine and Health Sciences Metformin Offspring People and Places Placebos Placenta Polycystic ovary syndrome Pregnancy Pregnant women Puberty Serum levels Stein-Leventhal syndrome Steroid hormones Steroidogenesis Steroids Testosterone Womens health |
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Title | Maternal PCOS status and metformin in pregnancy: Steroid hormones in 5–10 years old children from the PregMet randomized controlled study |
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