Does Spironolactone Normalize Sleep-wake Luteinizing Hormone Pulse Frequency in Pubertal Girls With Hyperandrogenism?

Launched by UNIVERSITY OF VIRGINIA · Jan 20, 2021

Keywords

ClinConnect Summary

This clinical trial is exploring whether a medication called spironolactone can help normalize the sleep-wake patterns of a hormone called luteinizing hormone (LH) in teenage girls who have a condition known as hyperandrogenism, which is characterized by higher levels of certain male hormones. The study is specifically looking at girls aged 10 to 17 who are in mid to late puberty and exhibit signs of hyperandrogenism, such as excess hair growth or elevated testosterone levels.

Eligible participants must be in good health overall, except for their hyperandrogenism, and should be willing to avoid pregnancy during the study. If a girl joins the trial, she will receive spironolactone and will be monitored to see how it affects her hormone levels and sleep patterns. It’s important to note that this study is focused solely on females, as hyperandrogenism primarily affects them. The trial aims to better understand how this medication could potentially help manage symptoms related to conditions like polycystic ovary syndrome (PCOS) in adolescents.

Gender

FEMALE

Eligibility criteria

• Inclusion Criteria:
• • Mid- to late pubertal adolescent girls as signified by either (a) post-menarcheal status (Tanner breast stages 2-5) or (b) Tanner breast stage of 4 or 5 (whether pre-menarcheal or post-menarcheal) ages 10-17 years.
• • Hyperandrogenism, defined as a serum (calculated) free testosterone concentration greater than the Tanner stage-specific reference range and/or clinical hirsutism
• • General good health (excepting obesity, hyperandrogenism, PCOS, and adequately-treated hypothyroidism)
• • Willing to strictly avoid pregnancy with use of reliable non-hormonal methods during the study period.
• Exclusion Criteria:
• • Inability/incapacity to provide informed consent
• • Males will be excluded (hyperandrogenism is unique to females)
• • Age \< 10 or \> 17 years (this study is designed to elucidate mechanisms underlying emerging PCOS in mid- to late pubertal adolescent girls
• • Post-menarcheal by \> 4 years
• • Obesity resulting from a well-defined endocrinopathy, or genetic syndrome
• • To ensure that blood withdrawal is within safe limits, weight \< 21.5 kg is an exclusion criterion.
• • Since underweight can alter pulsatile LH secretion, BMI-for-age percentile \< 5 is an exclusion criterion.
• • Positive pregnancy test or current lactation. Subjects with a positive pregnancy test will be informed of the result by the screening physician. Under Virginia law, parental notification is not required for minors. However, the screening physician will encourage the subject to tell her parent(s). We will counsel the adolescent about the importance of appropriate prenatal care/counseling. We will offer appropriate follow-up at the Teen Health Clinic at UVA and/or encourage the adolescent to secure prompt care via their primary care physician's office.
• • Evidence for non-physiologic or non-PCOS causes of hyperandrogenism and/or anovulation
• • Evidence of virilization (e.g., rapidly progressive hirsutism, deepening of the voice, clitoromegaly)
• • Total testosterone \> 150 ng/dl, which suggests the possibility of virilizing ovarian or adrenal tumor.
• • DHEA-S elevation \> 1.5 times the upper reference range limit. Mild elevations may be seen in adolescent HA and in PCOS, and will be accepted in these groups.
• • Early morning 17-hydroxyprogesterone \> 300 ng/dl measured in the follicular phase, which suggests the possibility of congenital adrenal hyperplasia (if elevated during the luteal phase, the 17-hydroxyprogesterone will be repeated during the follicular phase). NOTE: if a 17-hydorxyprogesterone \> 300 ng/dl is confirmed on repeat testing, an ACTH stimulated 17-hydroxyprogesterone \< 1000 ng/dl performed by the subject's personal physician will be required for study participation.
• • Any abnormal TSH concentration will trigger repeat testing. In many cases when TSH is initially abnormal, a repeat TSH will be normal. These subjects will be permitted to continue study. If TSH remains abnormal on repeat testing, the subject will be referred to her primary medical provider. In some cases, a participant's primary medical provider will elect to simply observe a mildly low (\> 0.1) or mildly elevated (\< 10) if stable. In such cases, we will accept a TSH between 0.3 and 7 (inclusive) if it has remained stable for at least 6 months-such TSH values are exceedingly unlikely to influence the central reproductive axis or to influence the risks of the study. Notably, subjects with reasonably-treated primary hypothyroidism-reflected by TSH values between 0.3 and 7-on a stable dose of thyroid hormone (i.e., same dose for at least 2 months) will not be excluded.
• • Prolactin concentration \> 30 ng/mL (confirmed on repeat). Mild prolactin elevations may be seen in adolescents and women with HA/PCOS or obesity.
• • History and/or physical exam findings suggestive of Cushing's syndrome, adrenal insufficiency, or acromegaly.
• • History and/or physical exam findings suggestive of hypogonadotropic hypogonadism (e.g., symptoms of estrogen deficiency) including functional hypothalamic amenorrhea (which may be suggested by a constellation of symptoms including restrictive eating patterns, excessive exercise, psychological stress, etc.)
• • Persistent hemoglobin \< 11.5 g/dL for non-African American subjects; hemoglobin \< 11.0 g/dL for African American subjects (confirmed on repeat). Importantly, documentation of a hemoglobin ≥ 11.0 g/dL for African American subjects or ≥ 11.5 g/dL for non-African American subjects in the month prior to the CRU admission is required for frequent sampling protocol in the CRU.
• • Severe thrombocytopenia (platelets \< 50,000 cells/microliter) or leukopenia (total white blood count \< 4,000 cells/microliter)
• • Previous diagnosis of diabetes, fasting glucose ≥ 126 mg/dl, or a hemoglobin A1c ≥ 6.5%
• • Persistently abnormal sodium or potassium concentration. Bicarbonate concentrations \< 20 or \> 30.
• • Liver test abnormalities, with two exceptions: (1) mild bilirubin elevations will be accepted in the setting of known Gilbert's syndrome or when the subject's primary care provider provides a presumptive diagnosis of Gilbert's syndrome and has no plans for further work-up; (2) mild transaminase (ALT, AST) elevations may be seen in obese/HA/PCOS girls, so stable elevations \< 1.5 times the upper limit of normal will be accepted in this group.
• • Absolute contraindications to spironolactone use include history of allergy to spironolactone, anuria, acute renal insufficiency, significant impairment of renal excretory function, hyperkalemia, primary adrenal insufficiency (Addison's disease), and concomitant use of eplerenone
• • Significant history of cardiac or pulmonary dysfunction (e.g., known or suspected congestive heart failure, asthma requiring intermittent systemic corticosteroids, etc.)
• • Decreased renal function evidenced by GFR \< 60 ml/min/1.73m2
• • History of cancer diagnosis and/or treatment (with the exception of basal cell or squamous cell skin carcinoma) unless they have remained clinically disease free (based on appropriate surveillance) for five years.