Hyperandrogenism and Hyperinsulinism in Children of Women with Polycystic Ovary Syndrome: A Controlled Study (original) (raw)

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1Departments of Obstetrics and Gynecology (S.C.K., C.L.G., R.S.L.), Penn State College of Medicine, Hershey, Pennsylvania 17033

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1Departments of Obstetrics and Gynecology (S.C.K., C.L.G., R.S.L.), Penn State College of Medicine, Hershey, Pennsylvania 17033

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2Departments of Public Health Sciences (A.R.K.), Penn State College of Medicine, Hershey, Pennsylvania 17033

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3Departments of Pathology (L.M.D.), Penn State College of Medicine, Hershey, Pennsylvania 17033

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4Departments of Pediatrics (P.A.L.), Penn State College of Medicine, Hershey, Pennsylvania 17033

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1Departments of Obstetrics and Gynecology (S.C.K., C.L.G., R.S.L.), Penn State College of Medicine, Hershey, Pennsylvania 17033

*Address all correspondence and requests for reprints to: Richard S. Legro, M.D., Department of Obstetrics and Gynecology, Penn State College of Medicine, 500 University Drive, Hershey, Pennsylvania 17033.

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Received:

04 September 2007

Accepted:

06 February 2008

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Sarah C. Kent, Carol L. Gnatuk, Allen R. Kunselman, Laurence M. Demers, Peter A. Lee, Richard S. Legro, Hyperandrogenism and Hyperinsulinism in Children of Women with Polycystic Ovary Syndrome: A Controlled Study, The Journal of Clinical Endocrinology & Metabolism, Volume 93, Issue 5, 1 May 2008, Pages 1662–1669, https://doi.org/10.1210/jc.2007-1958
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Abstract

Objective: Hyperandrogenia and insulin resistance are heritable family traits, likely to cluster in children of polycystic ovary syndrome (PCOS) mothers.

Design: We performed a case control study of PCOS children (n = 32) compared with children from control women (n = 38) for reproductive and metabolic abnormalities, stratifying results by three Tanner stage groupings. The children underwent history and physical examinations, a 3-h timed urine collection, a 2-h oral glucose tolerance test, and abdominal ultrasound examination (females only). Serum was obtained in older children (age > 8 yr) who consented.

Results: Urine LH levels were significantly lower in the Tanner IV–V PCOS girls compared with controls (P = 0.04). Urine testosterone levels were significantly elevated in Tanner II–III PCOS boys compared with controls (P = 0.007). There were no significant differences in dehydroepiandrosterone levels. We validated the correlation between salivary and serum levels of insulin (insulin areas under the curve) in an adult population [n =30, Pearson correlation coefficient (r) = 0.67; P < 0.0001], which also replicated in the children (2-h insulin r = 0.57; P = 0.0004). Mean area under the curve salivary insulin levels were significantly higher in the Tanner IV–V PCOS girls in the later stages of puberty when compared with controls (3625 ± 1372 vs. 1766 ± 621 min × μU/ml, 95% confidence interval 475-3242; P < 0.02).

Conclusions: Hyperinsulinism may be a familial characteristic of PCOS children (or at least girls) but does not appear until the later stages of puberty. Other reproductive abnormalities that characterize PCOS may develop later.

Copyright © 2008 by The Endocrine Society

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