Anorexia Nervosa
Conditions
Keywords
Eating Disorders, Osteopenia
Brief summary
Women with Anorexia Nervosa have been found to have low bone density. The study will determine whether administration of low doses of a natural hormone, testosterone and/or risedronate, a medication to help prevent bone breakdown will improve or prevent bone loss in this condition.
Detailed description
II. SPECIFIC AIMS Severe osteopenia is a prevalent complication of anorexia nervosa (AN), affecting over half of all women with this disease. Loss of 25-50% of total bone mass occurs frequently and is often permanent. Although anorexia nervosa affects from 0.5-1.0% of college age women, no successful therapeutic interventions have been developed for osteoporosis in this population. Bone loss in anorexia nervosa is characterized by reduced bone formation coupled with increased bone resorption. Anorexia nervosa results in a deficiency of testosterone. Testosterone administration reduces bone resorption and data suggest that low-dose testosterone replacement therapy can increase surrogate markers of bone formation. Bisphosphonates are now well established to decrease bone resorption and improve bone density in severely osteopenic postmenopausal women. However, there are few data regarding the use of this antiresorptive therapy in women with severe pre-menopausal bone loss. Our preliminary data demonstrate that administration of a bisphosphonate decreases bone resorption and increases bone mass in women with AN after 6 and 9 months. These are the first data to demonstrate a striking increase in bone density in such women. We will test the hypothesis that a combined strategy to increase bone formation and decrease bone resorption by combining testosterone with a bisphosphonate will increase bone mass in anorexia nervosa. The following hypotheses will be tested: Specific Aim 1. Testosterone, a nutritionally dependent bone trophic factor, is a critical determinant of decreased bone formation in anorexia nervosa, and administration of physiologic testosterone will increase bone formation and lean body mass in this disease We will investigate in women with anorexia nervosa whether: A. Bone formation is reduced in association with low serum testosterone B. Testosterone deficiency is due to a combination of ovarian and adrenal defects resulting from undernutrition C. Testosterone administration reverses testosterone deficiency leading to an acute and sustained increase in bone formation and a decrease in bone resorption D. Administration of physiologic testosterone replacement stimulates increases in IGF-I levels in women with anorexia nervosa, a mechanism for increased bone formation and bone density E. Administration of physiologic testosterone replacement increases lean body mass, a major determinant of bone density Specific Aim 2. Long-term (12 months) physiologic testosterone administration combined with a bisphosphonate increases bone density by a dual anabolic and anti-resorptive strategy We will investigate in women with anorexia nervosa whether: A. Physiologic testosterone administration increases bone density B. Administration of a bisphosphonate decreases the excessive state of bone resorption and increases bone density C. Co-administration of physiologic testosterone replacement and a bisphosphonate increases bone density to a greater degree than testosterone or a bisphosphonate alone by increasing bone formation and decreasing bone resorption
Interventions
Testosterone patch 150mcg daily
Actonel (risedronate) 35mg PO one time weekly
Placebo tablet identical in appearance to active Actonel (risedronate) tablet
Placebo patch identical in appearance to testosterone patch
Sponsors
Study design
Eligibility
Inclusion criteria
* Anorexia Nervosa, * Over 18, * Female, * Decreased bone density
Exclusion criteria
* Medications to increase bone density
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Bone Mineral Density | Baseline and 12 months | Percent change in postero-anterior (PA) spine bone mineral density as measured by dual energy x-ray absorptiometry (DXA)over a 12-month period. The differences in log-transformed values are reported as percent change. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Markers of Bone Metabolism | Baseline to 12 months | type 1 collagen C-telopeptide(CTX); The differences in log-transformed values are reported as percent change. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Placebo Actonel and Active Testosterone Patch Placebo Actonel tablet weekly and active testosterone patch (starting dose 150 mcg daily; increased to 300 mcg daily in subjects whose levels remained below the median on the initial dose) | 19 |
| Active Actonel and Active Testosterone Patch Active Actonel tablet (35 mg weekly) and Active Testosterone patch (starting dose 150 mcg daily; increased to 300 mcg daily in subjects whose levels remained below the median on the initial dose) | 20 |
| Active Actonel and Placebo Testosterone Active Actonel tablet (35 mg weekly) and Placebo Testosterone Patch | 20 |
| Placebo Testosterone Patch and Placebo Actonel Placebo Testosterone Patch and placebo Actonel tablet | 18 |
| Total | 77 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 | FG002 | FG003 |
|---|---|---|---|---|---|
| Overall Study | Physician Decision | 1 | 0 | 0 | 1 |
| Overall Study | Withdrawal by Subject | 1 | 4 | 5 | 6 |
Baseline characteristics
| Characteristic | Active Actonel and Active Testosterone Patch | Active Actonel and Placebo Testosterone | Placebo Actonel and Active Testosterone Patch | Placebo Testosterone Patch and Placebo Actonel | Total |
|---|---|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical Between 18 and 65 years | 20 Participants | 20 Participants | 19 Participants | 18 Participants | 77 Participants |
| Age, Continuous | 25.2 years STANDARD_DEVIATION 6.2 | 25.3 years STANDARD_DEVIATION 6.3 | 27.1 years STANDARD_DEVIATION 7.3 | 26.9 years STANDARD_DEVIATION 7.2 | 26.1 years STANDARD_DEVIATION 6.7 |
| Region of Enrollment United States | 20 participants | 20 participants | 19 participants | 18 participants | 77 participants |
| Sex: Female, Male Female | 20 Participants | 20 Participants | 19 Participants | 18 Participants | 77 Participants |
| Sex: Female, Male Male | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk | EG003 affected / at risk |
|---|---|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — | — / — | — / — |
| other Total, other adverse events | 12 / 19 | 16 / 20 | 16 / 20 | 12 / 18 |
| serious Total, serious adverse events | 6 / 19 | 1 / 20 | 5 / 20 | 2 / 18 |
Outcome results
Bone Mineral Density
Percent change in postero-anterior (PA) spine bone mineral density as measured by dual energy x-ray absorptiometry (DXA)over a 12-month period. The differences in log-transformed values are reported as percent change.
Time frame: Baseline and 12 months
Population: 1 subject was excluded from analysis. A factorial analysis was performed and determines the effect of each intervention separately, whether or not a subject received the 2nd intervention. Therefore, data from all 76 subjects who participated were used to determine the effect of each intervention on our endpoints.
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Actonel (Risedronate) 35 mg Weekly | Bone Mineral Density | 3.2 percent change |
| Testosterone | Bone Mineral Density | -0.6 percent change |
Markers of Bone Metabolism
type 1 collagen C-telopeptide(CTX); The differences in log-transformed values are reported as percent change.
Time frame: Baseline to 12 months
Population: 1 subject was excluded from analysis. A factorial analysis was performed and determines the effect of each intervention separately, whether or not a subject received the 2nd intervention. Therefore, data from all 76 subjects who participated were used to determine the effect of each intervention on our endpoints.
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Actonel (Risedronate) 35 mg Weekly | Markers of Bone Metabolism | -41 percent change of CTX |
| Testosterone | Markers of Bone Metabolism | -11 percent change of CTX |