Ipriflavone prevents the bone mass reduction in premenopausal women treated with gonadotropin hormone-releasing hormone agonists

Marco Gambacciani , Adriana Spinetti , Laura Piaggesi , Barbara Cappagli , Fabio Taponeco , Pietro Manetti , Carlo Weiss , Gian Carlo Teti , Paolo La Commare , Virgilio Facchini
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引用次数: 31

Abstract

In the present study we assessed the effects of ipriflavone in the prevention of increased bone turnover and the rapid bone loss that follows medical induced hypogonadism caused by the administration of a gonadotropin hormone-releasing hormone agonist (GnRH-A). In a double blind, placebo-controlled study, ipriflavone (600 mg/day, tdd (three divided doses)) or identical placebo tablets were given with 500 mg/day of calcium to patients treated with 3.75 mg leuproreline acetate every 30 days, for 6 months. In placebo-treated subjects (n = 39), urinary hydroxyproline excretion and plasma bone GLA protein levels showed a substantial (P < 0.01) increase, while spine bone density and total body bone density significantly (P < 0.01) decreased after 3 and 6 months of GnRH-A administration. Conversely, in ipriflavone treated group (n = 39), no significant difference in bone markers and bone density was evidenced. These data indicate that ipriflavone can restrain the bone remodeling processes and prevent the rapid bone loss that follows medical induced hypogonadism. Thus, ipriflavone administration can be of value in the prevention of osteopenia in women treated with GnRH-A.

依普利酮可防止绝经前妇女接受促性腺激素释放激素激动剂治疗时骨量减少
在本研究中,我们评估了伊普利黄酮在预防骨转换增加和骨质流失的作用,骨质流失是由服用促性腺激素激素释放激素激动剂(GnRH-A)引起的药物性性腺功能减退引起的。在一项双盲、安慰剂对照研究中,对每30天服用3.75 mg leuproreline acetate的患者,给予ipriflavone (600 mg/天,tdd(三次分剂量))或相同的安慰剂片剂500 mg/天钙,持续6个月。在安慰剂治疗的受试者中(n = 39),尿羟脯氨酸排泄和血浆骨GLA蛋白水平显示出显著的(P <0.01),脊柱骨密度和全身骨密度显著升高(P <0.01),给药3个月和6个月后下降。相反,依普利黄酮治疗组(n = 39)骨标志物和骨密度无显著差异。这些数据表明,伊普利黄酮可以抑制骨重塑过程,防止药物性性腺功能减退后的快速骨质流失。因此,在接受GnRH-A治疗的妇女中,给予伊普利酮对预防骨质减少有价值。
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