Effects of the phytoestrogen genistein on bone metabolism in osteopenic postmenopausal women - A randomized trial

被引:232
作者
Marini, Herbert [1 ]
Minutoli, Letteria [1 ]
Polito, Francesca [1 ]
Bitto, Alessandra [1 ]
Altavilla, Domenica [1 ]
Atteritano, Marco [1 ]
Gaudio, Agostino [1 ]
Mazzaferro, Susanna [1 ]
Frisina, Alessia [1 ]
Frisina, Nicola [1 ]
Lubrano, Carla [1 ]
Bonaiuto, Michele [1 ]
D'Anna, Rosario [1 ]
Cannata, Maria Letizia [1 ]
Corrado, Francesco [1 ]
Adamo, Elena Bianca [1 ]
Wilson, Steven [1 ]
Squadrito, Francesco [1 ]
机构
[1] Univ Messina, Dept Expt & Clin Med & Pharmacol, Pharmacol Sect, Azienda Osped,Policlin G Martino, I-98125 Messina, Italy
关键词
D O I
10.7326/0003-4819-146-12-200706190-00005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Observational studies and small trials of short duration suggest that the isoflavone phytoestrogen genistein reduces bone loss, but the evidence is not definitive. Objective: To assess the effects of genistein on bone metabolism in osteopenic postmenopausal women. Design: Randomized, double-blind, placebo-controlled trial. Setting: 3 university medical centers in Italy. Patients: 389 postmenopausal women with a bone mineral density (BMD) less than 0.795 g/cm(2) at the femoral neck and no significant comorbid conditions. Intervention: After a 4-week stabilization period during which participants received a low-soy, reduced-fat diet, participants were randomly assigned to receive placebo (n = 191) or 54 mg of genistein (n = 198) daily for 24 months. Both the genistein and placebo tablets contained calcium and vitamin D. Measurements: The primary outcome was BMD at the anteroposterior lumbar spine and femoral neck at 24 months. Secondary outcomes were serum levels of bone-specific alkaline phosphatase and insulin-like growth factor 1, urinary excretion of pyridinoline and deoxypyridinoline, and endometrial thickness. Data on adverse events were also collected. Results: At 24 months, BMD had increased in genistein recipients and decreased in placebo recipients at the anteroposterior lumbar spine (change, 0.049 g/cm(2) [95% CI, 0.035 to 0.059] vs. -0.053 g/cm(2) [CI, -0.058 to -0.035]; difference, 0.10 g/cm(2) [CI, 0.08 to 0.121; P < 0.001) and the femoral neck (change, 0.035 g/cm(2) [Cl, 0.025 to 0.0421 vs. -0.037 g/cm(2) [CI, -0.044 to -0.0271; difference, 0.062 g/cm(2) [CI, 0.049 to 0.073]; P < 0.001). Genistein statistically significantly decreased urinary excretion of pyridinoline and deoxypyriclinoline, increased levels of bone-specific alkaline phosphatase and insulin-like growth factor 1, and did not change endometrial thickness compared with placebo. More genistein recipients than placebo recipients experienced gastrointestinal side effects (19% vs. 8%; P = 0.002) and discontinued the study. Limitations: The study did not measure fractures and had limited power to evaluate adverse effects. Conclusion: Twenty-four months of treatment with genistein has positive effects on BMD in osteopenic postmenopausal women.
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页码:839 / 847
页数:9
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