Agnusdei D, Civitelli R, Camporeale A, Gennari C
Istituto di Semeiotica Medica, Università di Siena, Italy.
J Endocrinol Invest. 1990 Sep;13(8):625-30. doi: 10.1007/BF03349583.
Estrogen deficiency is thought to be the main factor leading to postmenopausal osteoporosis (PMO). A role for calcitonin (CT) has been proposed as mediator of estrogen action on bone, and therefore, as pathogenetic factor of PMO. However, this hypothesis is still controversial. To further analyze the relationships between estrogens and CT in PMO, we studied the effects of one-year estro/progesterone therapy on CT secretory reserve, evaluated by a calcium infusion test in 12 postmenopausal women, as compared to 12 placebo treated subjects. In the hormone treated group, blood levels of CT showed a progressive increase during the study and a plateau was reached at 9 months, indicating that CT production achieved a new steady state. Hormonal therapy also significantly improved the CT response to calcium stimulation test. A concomitant increase of vertebral bone mass was observed in the hormone treated women, who also maintained initial bone density of femoral dyaphyses. On the contrary, the placebo treated group continued to lose bone mineral at both sites. Our study demonstrates that estrogens regulate CT secretion in postmenopausal women; thus, CT may be considered a mediator of estrogen action on bone.
雌激素缺乏被认为是导致绝经后骨质疏松症(PMO)的主要因素。有人提出降钙素(CT)作为雌激素对骨骼作用的介质,因此也是PMO的致病因素。然而,这一假说仍存在争议。为了进一步分析PMO中雌激素与CT之间的关系,我们研究了为期一年的雌二醇/孕酮治疗对CT分泌储备的影响,通过对12名绝经后女性进行钙输注试验进行评估,并与12名接受安慰剂治疗的受试者进行比较。在激素治疗组中,CT的血液水平在研究期间逐渐升高,并在9个月时达到平台期,表明CT的产生达到了一个新的稳态。激素治疗还显著改善了CT对钙刺激试验的反应。在接受激素治疗的女性中观察到椎骨骨量同时增加,她们还维持了股骨骨干的初始骨密度。相反,安慰剂治疗组在这两个部位继续丢失骨矿物质。我们的研究表明,雌激素调节绝经后女性的CT分泌;因此,CT可被视为雌激素对骨骼作用的介质。