他莫昔芬和雌激素可降低健康绝经后妇女的循环脂蛋白(a)浓度。

D A Shewmon, J L Stock, C J Rosen, K M Heiniluoma, M M Hogue, A Morrison, E M Doyle, T Ukena, V Weale, S Baker
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引用次数: 149

摘要

文献数据表明,循环脂蛋白(a) [Lp(a)]和胰岛素样生长因子I (IGF-I)水平对生长激素、雌激素或他莫昔芬治疗的反应相似。为了更清楚地证明这些关系,我们设计了一项随机、双盲、安慰剂对照研究,研究他莫昔芬和持续雌激素对健康绝经后妇女血液中Lp(a)、IGF- i和IGF结合蛋白3 (IGFBP-3)水平的影响。在治疗3个月期间,雌激素和他莫昔芬均使血清igf - 1水平降低至比基线低30%,而IGFBP-3水平不变。使用雌激素或他莫昔芬治疗1个月后,血浆Lp(a)水平降至比基线低24%(仅使用雌激素组P < 0.05);3个月后,他莫昔芬组的Lp(a)下降到比基线低34% (P < 0.05),而雌激素组的Lp(a)仅比基线低16%。Lp(a)与IGF-I的相关性非常显著(P < 0.0001)。我们得出结论:(1)他莫昔芬降低健康绝经后妇女血浆Lp(a)水平,(2)他莫昔芬和雌激素对循环Lp(a)浓度的抑制作用在治疗的第一个月后出现分歧,(3)循环Lp(a)和IGF-I水平相互强烈相关,表明它们可能具有共同的调节作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tamoxifen and estrogen lower circulating lipoprotein(a) concentrations in healthy postmenopausal women.

Data in the literature suggest that circulating levels of lipoprotein(a) [Lp(a)] and insulinlike growth factor I (IGF-I) respond similarly to therapy with growth hormone, estrogen, or tamoxifen. To more clearly document these relations, we designed a randomized, double-blind, placebo-controlled study of the effects of tamoxifen and continuous estrogen on circulating levels of Lp(a), IGF-I, and IGF binding protein 3 (IGFBP-3) in healthy postmenopausal women. Both estrogen and tamoxifen decreased serum levels of IGF-I to 30% below baseline during the 3 months of treatment, while IGFBP-3 levels were unchanged. Plasma Lp(a) levels decreased to 24% below baseline after 1 month of treatment with either estrogen or tamoxifen (P < .05 for estrogen only); after 3 months Lp(a) decreased to 34% below baseline with tamoxifen therapy (P < .05) but returned to only 16% below baseline with estrogen. The correlation between Lp(a) and IGF-I was highly significant (P < .0001). We conclude that (1) tamoxifen lowers plasma Lp(a) levels in healthy postmenopausal women, (2) the suppressive effects of tamoxifen and estrogen on circulating Lp(a) concentration diverge after the first month of therapy, and (3) circulating levels of Lp(a) and IGF-I are strongly correlated with each other, an indication that they may share regulatory influences.

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