Hormone Replacement Therapy to Treat Turner Syndrome
Status:
Completed
Trial end date:
2002-12-01
Target enrollment:
Participant gender:
Summary
This study will evaluate the effects of hormone replacement therapy on patients with Turner
syndrome (TS)-a genetic disorder in females in which part or all of one X chromosome is
missing. Most girls and women with TS have underdeveloped ovaries-the female reproductive
organs that produce the female sex hormones estrogen and progesterone, and smaller amounts of
the male sex hormone, testosterone. These hormones affect muscle and bone strength, sex
drive, energy, and an overall sense of well being. Estrogen may also play a role in memory
and mood and have a protective effect against heart disease. Women with TS have a much higher
risk of developing osteoporosis (loss of bone density), high blood pressure, high cholesterol
and diabetes than women without this disorder.
Girls and women with Turner syndrome between the ages of 14 and 50 years may be eligible for
this 2-year study. Three months before beginning treatment, all patients will wear an
estrogen patch and take a progesterone tablet daily for 10 days each month. They will then be
randomly assigned to one of two treatment groups to compare the effects of estrogen alone
with estrogen plus testosterone on bone strength, muscle and fat mass and psychosocial well
being. Both groups will wear an estrogen patch and take oral progesterone. One group will
also wear a testosterone patch while the other group will wear a placebo patch (a patch that
does not contain any testosterone). Neither study participants nor the doctors will know who
is getting the testosterone until the study is complete. Patients will undergo the following
procedures before beginning treatment and at 6, 12 and 24 months after starting treatment:
- Physical examination.
- DEXA scans (dual energy X-ray absorptiometry) to measure body composition and bone
thickness. Low radiation X-rays scan the whole body to measure fat, muscle and bone
mineral content..
- Magnetic resonance imaging (MRI) scan of the abdomen to measure the amount of fat around
the internal organs. The patient lies on a stretcher in a large tube surrounded by a
magnetic field during the scanning. The procedure uses a strong magnet and radio waves
to produce the images.
- Heel ultrasound to measure bone thickness. The heel is placed in a chamber and sound
waves pass through it to produce images.
- Oral glucose tolerance test (OGTT) for diabetes and problems with carbohydrate
metabolism. The patient drinks a sugary substance. A small amount of blood is drawn
before taking the drink and four times afterwards.
- Blood and urine tests to measure blood counts, liver and kidney function, ovarian
hormones, growth factors, thyroid function, blood lipids, bone strength markers, and to
test for pregnancy.
- Blood pressure measurements.
- Psychological testing for the effect of treatment on mood, self-esteem, quality of life,
social shyness, anxiety and sexual function.
- Neurocognitive tests (at first inpatient visit and 1 and 2 years after starting
treatment) to measure nonverbal memory and visual-perceptual abilities.
During the hospital admissions, patients will be given a "metabolic diet" that contains
specific amounts of salt and carbohydrates to ensure accurate blood pressure and sugar
metabolism measurements. Patients will keep a record of their menstrual periods and physical
activity throughout the treatment period.
Phase:
Phase 2
Details
Lead Sponsor:
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)