Osteoporosis Clinical Trial
Official title:
Transdermal Estrogen in Older Premenopausal Women With Anorexia Nervosa
Decreased bone strength is a common and serious medical problem present in many women with
anorexia nervosa. Women with decreased bone strength are more likely to suffer broken bones
than women with normal bone strength.
This study will investigate whether the use of transdermal estrogen can improve bone mineral
density (BMD) and bone microarchitecture in women with anorexia nervosa anorexia nervosa when
used for 6 months.
Anorexia nervosa (AN) is a prevalent psychiatric disorder affecting up to 1% of college-aged
women in the US and an increasing number of women over 30 years of age. Among the many
medical co-morbidities associated with AN, the most common is significant bone loss, which
can persist despite weight recovery. Nearly 50% of women with AN have osteopenia with an
additional 30% meeting WHO criteria for osteoporosis. Importantly, this severe bone loss is
associated with an increased fracture risk. Nearly 30% of women with AN report a history of a
fracture and a prospective study demonstrated a 7-fold increased risk of fracture in women
with AN compared to age-matched controls. Because AN is a chronic disease that can persist
despite psychiatric and nutritional counseling, the bone loss and increased fracture risk can
persist and lead to lifelong morbidity. Therefore, finding a treatment for bone loss
associated with AN is of critical importance.
This 6 month open-label study will investigate in women (ages 25 to 50 years old) with AN
whether treatment with transdermal estrogen replacement will increase bone mineral density
(BMD), improve parameters of bone microarchitecture as assessed by high-resolution peripheral
quantitative computed tomography (HR-pQCT), and improve bone strength as estimated by
microfinite element analysis.
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