Bone Loss in Women With Anorexia Nervosa
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
Anorexia Nervosa |
Drug: Testosterone Drug: Actonel (risedronate) Drug: Placebo Actonel (risedronate) Drug: Placebo testosterone |
Phase 2 Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Factorial Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | IGF-1 and Bone Loss in Women Anorexia Nervosa |
- Bone Mineral Density [ Time Frame: Baseline and 12 months ] [ Designated as safety issue: No ]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.
- Markers of Bone Metabolism [ Time Frame: Baseline to 12 months ] [ Designated as safety issue: No ]type 1 collagen C-telopeptide(CTX); The differences in log-transformed values are reported as percent change.
| Enrollment: | 77 |
| Study Start Date: | June 2003 |
| Study Completion Date: | April 2008 |
| Primary Completion Date: | April 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: 2
Placebo Actonel (risedronate) and active testosterone patch
|
Drug: Testosterone
Testosterone patch 150mcg daily
Other Name: Intrinsa
Drug: Placebo Actonel (risedronate)
Placebo tablet identical in appearance to active Actonel (risedronate) tablet
|
|
Active Comparator: 3
Active Actonel (risedronate) and active testosterone patch
|
Drug: Testosterone
Testosterone patch 150mcg daily
Other Name: Intrinsa
Drug: Actonel (risedronate)
Actonel (risedronate) 35mg PO one time weekly
Other Name: Actonel
|
|
Active Comparator: 4
Active Actonel (risedronate) and placebo testosterone
|
Drug: Actonel (risedronate)
Actonel (risedronate) 35mg PO one time weekly
Other Name: Actonel
Drug: Placebo testosterone
Placebo patch identical in appearance to testosterone patch
|
|
Placebo Comparator: 1
Placebo testosterone patch and placebo Actonel (risedronate)
|
Drug: Placebo Actonel (risedronate)
Placebo tablet identical in appearance to active Actonel (risedronate) tablet
Drug: Placebo testosterone
Placebo patch identical in appearance to testosterone patch
|
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
Eligibility| Ages Eligible for Study: | 18 Years to 45 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Anorexia Nervosa,
- Over 18,
- Female,
- Decreased bone density
Exclusion Criteria:
- Medications to increase bone density
Contacts and Locations| United States, Massachusetts | |
| Massachusetts General Hospital | |
| Boston, Massachusetts, United States, 02114 | |
| Principal Investigator: | Anne Klibanski, M.D. | Massachusetts General Hospital |
More Information
No publications provided by Massachusetts General Hospital
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Anne Klibanski, MD, Principal Investigator, Massachusetts General Hospital |
| ClinicalTrials.gov Identifier: | NCT00089843 History of Changes |
| Other Study ID Numbers: | 5 R01 DK052625 (completed), R01DK052625, 1UL1RR025758 |
| Study First Received: | August 16, 2004 |
| Results First Received: | November 9, 2011 |
| Last Updated: | May 1, 2012 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by Massachusetts General Hospital:
|
Eating Disorders Osteopenia |
Additional relevant MeSH terms:
|
Anorexia Anorexia Nervosa Signs and Symptoms, Digestive Signs and Symptoms Eating Disorders Mental Disorders Testosterone Testosterone enanthate Testosterone undecanoate Testosterone 17 beta-cypionate Methyltestosterone Risedronic acid Etidronic Acid Androgens |
Hormones Hormones, Hormone Substitutes, and Hormone Antagonists Physiological Effects of Drugs Pharmacologic Actions Antineoplastic Agents, Hormonal Antineoplastic Agents Therapeutic Uses Anabolic Agents Bone Density Conservation Agents Calcium Channel Blockers Membrane Transport Modulators Molecular Mechanisms of Pharmacological Action Cardiovascular Agents |
ClinicalTrials.gov processed this record on June 17, 2013