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Dennis T. Villareal, MD; Ellen F. Binder, MD; Daniel
B. Williams, MD; Kenneth B. Schechtman, PhD; Kevin E. Yarasheski, PhD;
Wendy M. Kohrt, PhD
JAMA. 2001;286:815-820.
ABSTRACT
Context Although hormone replacement therapy
(HRT) is an established approach for osteoporosis prevention, little is
known about the osteoprotective effects of HRT in frail elderly women.
Objective To determine whether HRT increases
bone mineral density (BMD) in frail elderly women.
Design and Setting Randomized, double-blind,
placebo-controlled trial conducted in a US university-based research center
from September 1995 to August 2000.
Participants Sixty-seven women aged 75 years
or older with mild-to-moderate physical frailty.
Intervention Participants were randomly assigned
to receive conjugated estrogens, 0.625 mg/d, plus trimonthly medroxyprogesterone
acetate, 5 mg/d for 13 days (n = 45), or matching placebo (n = 22), for
9 months.
Main Outcome Measures The primary outcome measure
was 9-month change in BMD of the lumbar spine and hip, measured by dual-energy
x-ray absorptiometry. Secondary outcomes were changes in markers of bone
turnover.
Results Based on intention-to-treat analyses,
HRT resulted in significantly larger increases in BMD of the lumbar spine
than placebo (mean change, 4.3% vs 0.4%; between-group difference, 3.9%;
95% confidence interval [CI], 3.5%-4.3%) and total hip (mean change, 1.7%
vs -0.1%; between-group difference, 1.8%; 95% CI, 1.5%-2.1%). Compared
with placebo, HRT resulted in significant decreases in serum bone-specific
alkaline phosphatase levels (mean change, -24% vs 6%; between-group difference,
-30%; 95% CI, -26% to -33%) and urine N-telopeptide levels (mean change,
-48% vs 4%; between-group difference, -52%; 95% CI, -47% to -55%).
Conclusions In physically frail elderly
women, 9 months of HRT significantly increased BMD compared with placebo
in clinically important skeletal regions. Further studies are needed to
determine whether these osteogenic effects of HRT in elderly women are
associated with a reduction in osteoporotic fractures.
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