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Is Serum Anti-Mullerian Hormone (AMH) Level Associated With Body Weight, Glycemic and Lipidemic Markers in Adolescent Girls With Polycystic Ovaries?


N/A
12 Years
20 Years
Open (Enrolling)
Female
Polycystic Ovary Syndrome

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Trial Information

Is Serum Anti-Mullerian Hormone (AMH) Level Associated With Body Weight, Glycemic and Lipidemic Markers in Adolescent Girls With Polycystic Ovaries?


In this study the investigators aimed to investigate whether there is a relation between
body weight and serum anti mullerian hormone levels in adults with polycystic ovary
syndrome. For this purpose the investigators designed a prospective study including three
groups. The diagnosis of polycystic ovary syndrome was made in the presence of ;oligo-
and/or anovulation,clinical and/or biochemical signs of hyperandrogenism and polycystic
ovaries. Clinical hyperandrogenism was defined by the presence of hirsutism , acne, or the
presence of androgenic alopecia , biochemical hyperandrogenemia was defined as a serum level
of total testosterone higher than 2.60 nmol/L, body mass index (BMI) was calculated as
weight in kilograms divided by the square of height in meters. The patients were classified
as obese with BMI ≥ 25 kg/m2 , adolescent patients were diagnosed 2 years after menarche in
order to avoid the misdiagnosis of transitory functional hyperandrogenism and menstrual
disorders during puberty. The all three groups are compared considering their serum AMH
levels,lipid profiles, sex steroids and glycemic analyses.


Inclusion Criteria:



The participants with the following findings;oligo- and/or anovulation, clinical and/or
biochemical signs of hyperandrogenism and polycystic ovaries, presence in each ovary of 12
or more follicles measuring 2-9 mm in diameter and/or increased ovarian volume (> 10 mL).

Exclusion Criteria:

The participants with the following findings;pregnancy,breastfeeding,known liver disease
or alanine aminotransferase (60 IU/l), creatinine (130 mmol/l), known alcohol abuse,
diabetes mellitus and treatment with oral glucocorticoids or hormonal contraceptives.

Patients could be included if hormonal contraception had been discontinued at least 1
month previously.

Type of Study:

Observational

Study Design:

Observational Model: Case Control, Time Perspective: Prospective

Outcome Measure:

Ovarian reserve, as measured by basal follicle stimulating hormone/anti-Mullerian hormone/antral follicle count

Outcome Time Frame:

Three months

Safety Issue:

No

Principal Investigator

Hüseyin Cengiz, M.D.

Investigator Role:

Study Director

Investigator Affiliation:

Bakirkoy Dr Sadi Konuk Teaching and Research Hospital, Department of Obstetrics and Gynecology

Authority:

Turkey: Ministry of Health

Study ID:

PCODHC

NCT ID:

NCT01856894

Start Date:

May 2013

Completion Date:

August 2013

Related Keywords:

  • Polycystic Ovary Syndrome
  • polycystic ovary syndrome
  • Anti-Mullerian Hormone
  • obesity
  • Polycystic Ovary Syndrome

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