Buchanan J R, Santen R J, Cavaliere A, Cauffman S W, Greer R B, Demers L M
Metabolism. 1986 Jun;35(6):489-94. doi: 10.1016/0026-0495(86)90003-x.
It has been hypothesized that estrogens conserve bone substance by blocking the resorbing effect of parathyroid hormone (PTH). We evaluated this hypothesis by examining the relation of circulating PTH to endogenous estrogen fluctuation during four quarters of a single menstrual cycle in 20 normal women. The hypothesis predicts that PTH should vary directly with estrogen, since PTH should increase following estrogen elevation to satisfy physiologic demands for calcium. Contrary to the predicted direct variation, PTH remained constant throughout the menstrual cycle despite sharply fluctuating estrogen levels. Furthermore, PTH was negatively associated with estrone during the early follicular (r = -.65, P less than 0.005) and late follicular (r = -.84, P less than 0.0001) phases. We attempted to determine whether this unexpected relationship between estrone and PTH signified a direct physiologic link, by excluding factors which could have spuriously engendered the inverse correlation. Stepwise multiple regression and partial correlation showed that estrone contributed significantly to circulating PTH independent of the effects of dietary calcium, 25-hydroxyvitamin D, serum calcium, 1,25-dihydroxyvitamin D, phosphate, estradiol, progesterone, and body weight. Therefore, it is possible that the inverse correlation between estrone and PTH signified a direct physiologic link, as an artifactual cause for the relationship could not be identified. These data imply that estrone interacts with PTH, but not by blocking PTH-mediated bone resorption. We conclude that estrone is associated with reduced circulating PTH through an as yet undetermined mechanism.
有人提出假说,认为雌激素通过阻断甲状旁腺激素(PTH)的重吸收作用来保存骨质。我们通过检测20名正常女性在一个月经周期的四个阶段中循环PTH与内源性雌激素波动之间的关系来评估这一假说。该假说预测PTH应与雌激素呈直接变化关系,因为雌激素升高后PTH应增加,以满足对钙的生理需求。与预测的直接变化关系相反,尽管雌激素水平急剧波动,但在整个月经周期中PTH保持恒定。此外,在卵泡早期(r = -0.65,P < 0.005)和卵泡晚期(r = -0.84,P < 0.0001),PTH与雌酮呈负相关。我们试图通过排除可能虚假产生这种负相关的因素,来确定雌酮与PTH之间这种意外的关系是否意味着直接的生理联系。逐步多元回归和偏相关分析表明,独立于膳食钙、25-羟维生素D、血清钙、1,25-二羟维生素D、磷酸盐、雌二醇、孕酮和体重的影响,雌酮对循环PTH有显著贡献。因此,雌酮与PTH之间的负相关可能意味着直接的生理联系,因为无法确定这种关系的人为原因。这些数据表明雌酮与PTH相互作用,但不是通过阻断PTH介导的骨质吸收。我们得出结论,雌酮通过一种尚未确定的机制与循环PTH降低有关。