Obesity Clinical Trial
Official title:
Adrenal Hyperplasia Among Young Patients With Polycystic Ovarian Syndrome
Background:
- Polycystic ovarian syndrome (PCOS) is a group of disorders related to problems with the
secretion of certain hormones, which can lead to reproductive and other issues in women.
Frequent complications of PCOS include irregular menstruation, development of ovarian cysts,
and insulin resistance. The adrenal glands, which sit on top of the kidney, are involved in
the production of certain hormones and the regulation of steroid levels in the blood, and may
be affected in women with PCOS. Researchers are interested in studying possible connections
between the adrenal glands and PCOS in young women who have been diagnosed with PCOS and
healthy volunteers with normal menstrual function.
Objectives:
- To investigate possible connections between adrenal gland steroid hormone secretion and
polycystic ovarian syndrome.
Eligibility:
- Women between 16 and 29 years of age who have been diagnosed with PCOS, or who are
healthy volunteers with normal menstrual function.
- Participants must be willing to discontinue the use of oral contraceptives or any other
medications that alter steroid hormone production for at least 1 month before the start
of the study.
Design:
- Participants will be screened with a physical examination, medical history, and blood
and urine tests. All participants will also have a pelvic (ovarian) ultrasound.
- All participants will be admitted to the hospital for a 1-week testing period, which
will involve the following tests:
- Regular blood draws for two 2-hour periods (late evening and early morning) to measure
hormone levels
- Fasting blood draws with a dose of corticotropin to test the body's adrenal function
- Hormone level measurement following regular doses of dexamethasone (a drug that controls
the function of the adrenal gland)
- Daily urine collection for 6 days.
- Other studies, such as imaging studies of the adrenal glands, may be conducted as
required by the study researchers.
Polycystic ovarian syndrome (PCOS) is a heterogeneous group of disorders presenting with
hyperandrogenism in adolescents and young women. The etiology of this condition remains
unknown, despite its many identified links to insulin resistance, hypertension and metabolic
syndrome, as well as its potential connection to the various forms of congenital adrenal
hyperplasia (CAH).
The adrenal glands are the only source in the body of adrenocortical steroids. In normal
physiology, the pituitary hormone ACTH regulates the secretion of glucocorticoids, while the
secretion of mineralocorticoids is controlled by the renin-angiotensin system. In addition to
these two steroids, the adrenal gland secretes lesser amounts of intermediate metabolites of
these steroids, as well as the sex-steroids DHEA, DHEAS, androstenedione, testosterone,
estrogen, and estrone. Dysregulated secretion of any of these hormones can be caused by the
development of hyperplasia of the adrenocortical tissue, which may be mild and lead to
specific clinical syndromes depending on the identity of the secreted hormones. Bilateral
adrenocortical hyperplasia (BAH) is now an increasingly diagnosed cause of adrenal
dysfunction.
We propose that there is a subgroup of patients with PCOS who actually have non-CAH primary
forms of BAH. To investigate this possibility, we propose to study the
hypothalamic-pituitary-adrenal axis (HPAA) over the next 2 years in 120 young girls and women
(ages 16 to 25 years) that we will compare to 30 age- and race-matched normal females.
Patients will be recruited primarily (although not exclusively) from a busy New York City
clinic run by the Pediatric Endocrine Division at the Infants and Children's Hospital of
Brooklyn at Maimonides and SUNY Downstate. All patients will undergo standard testing of the
HPAA including oral low- and high-dose dexamethasone (DEX)-suppression testing (Liddle s
test). Paradoxical rise of cortisol and/or other steroid metabolites in response to DEX is
considered a sensitive test for the diagnosis of BAH. Patients with such responses will be
molecularly investigated for the known causes of BAH (GNAS, PRKAR1A, PDE11A, PDE8B and other
mutations).
The first goal of this study is to identify any possible contributions of the BAH phenotypes
and genotypes to the pathophysiology of PCOS, a yet unknown factor in the etiology of this
multifaceted disorder. The second goal is to perform a comparative analysis of the expression
of large sets of genes in cells of these patients using gene arrays and other genetic
analyses. This study will generate important information about the molecular pathways that
are affected in this subgroup of patients with PCOS. Thirdly, this study will also allow for
the collection of DNA from affected and non-affected relatives of the patients to perform
genetic studies and identify causative genetic defects. Finally, the study is expected to
lead to new diagnostic and therapeutic methods for at least certain forms of PCOS.
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