Leuprolide acetate‐stimulated androgen response during female puberty. (26th January 2015)

• Record Type: Journal Article
• Authors: Hernandez, María Isabel; Martinez‐Aguayo, Alejandro; Cavada, Gabriel; Avila, Alejandra; Iñiguez, German; Mericq, Veronica
• Is Part Of: Clinical endocrinology. Volume 83:Number 2(2015:Aug.)
• Page Start: 205
• Page End: 211
• Publication Date: 2015-01-26
• Subjects: Endocrinology -- Periodicals; 616.4005
• DOI: 10.1111/cen.12690
• Languages: English
• ISSNs: 0300-0664

Abstract

<abstract abstract-type="main" id="cen12690-abs-0001"> <title>Summary</title> <sec id="cen12690-sec-0001" sec-type="section"> <title>Background</title> <p>A physiological increase in androgen levels occurs during adolescence. Measuring androgen concentrations is the best method to distinguish normal evolution processes from hyperandrogenic disorders.</p> </sec> <sec id="cen12690-sec-0002" sec-type="section"> <title>Hypothesis</title> <p>The increase in circulating androgens during puberty is inversely associated with insulin sensitivity in normal weight girls.</p> </sec> <sec id="cen12690-sec-0003" sec-type="section"> <title>Objective</title> <p>To assess circulating levels of ovarian androgens and anti‐Müllerian hormone (AMH) at baseline and after GnRH analogue (GnRH‐a) stimulation in normal pubertal girls across different Tanner stages. We also studied the association between this response and insulin sensitivity.</p> </sec> <sec id="cen12690-sec-0004" sec-type="section"> <title>Design</title> <p>Prospective study of healthy girls (6–12 years) from the local community (<italic>n </italic>=<italic> </italic>63).</p> </sec> <sec id="cen12690-sec-0005" sec-type="section"> <title>Methods</title> <p>Tanner I (<italic>n </italic>=<italic> </italic>23) subjects were assessed cross‐sectionally, and Tanner II girls (<italic>n </italic>=<italic> </italic>40) were evaluated every 6 months until they reached Tanner V. Early morning dehydroepiandrosterone sulphate (DHEA‐S), AMH, sex hormone‐binding globulin (SHBG), androstenedione, glucose and insulin levels were measured. A GnRH‐a test (500 μg/m<sup>2</sup>; sc) and oral glucose intolerance test (OGTT) were performed. Differences throughout puberty were evaluated.</p> </sec> <sec id="cen12690-sec-0006" sec-type="section"> <title>Results</title> <p>Basal and/or stimulated Testosterone DHEA‐S and 17‐hydroxyprogesterone (17OHP) were inversely associated with insulin sensitivity (WIBSI) from the beginning of puberty, whereas androstenedione was directly associated with gonadotrophins. AMH was inversely associated with basal and stimulated gonadotrophins and directly with insulin area under the curve (AUC) only in the early stages of puberty. 17OHP and testosterone responsiveness increased significantly during puberty in all subjects, whereas testosterone levels changed less consistently. This pattern of ovarian‐steroidogenic response was most evident during mid‐ and late puberty. Moreover, during late puberty only, basal 17OHP, testosterone and DHEA‐S were positively associated with gonadotrophins.</p> </sec> <sec id="cen12690-sec-0007" sec-type="section"> <title>Conclusion</title> <p>In normal nonobese girls born appropriate for gestational age, androgen synthesis was associated with insulin sensitivity in early puberty and with LH only in late puberty.</p> </sec> </abstract>