McKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Key Laboratory of Biorheological Science and Technology, Ministry of Education and Bioengineering College, Chongqing University, Chongqing, China.
J Bone Miner Res. 2018 Dec;33(12):2165-2176. doi: 10.1002/jbmr.3559. Epub 2018 Aug 13.
The female skeleton undergoes substantial structural changes during the course of reproduction. Although bone mineral density recovers postweaning, reproduction may induce permanent alterations in maternal bone microarchitecture. However, epidemiological studies suggest that a history of pregnancy and/or lactation does not increase the risk of postmenopausal osteoporosis or fracture and may even have a protective effect. Our study aimed to explain this paradox by using a rat model, combined with in vivo micro-computed tomography (μCT) imaging and bone histomorphometry, to track the changes in bone structure and cellular activities in response to estrogen deficiency following ovariectomy (OVX) in rats with and without a reproductive history. Our results demonstrated that a history of reproduction results in an altered skeletal response to estrogen-deficiency-induced bone loss later in life. Prior to OVX, rats with a reproductive history had lower trabecular bone mass, altered trabecular microarchitecture, and more robust cortical structure at the proximal tibia when compared to virgins. After OVX, these rats underwent a lower rate of trabecular bone loss than virgins, with minimal structural deterioration. As a result, by 12 weeks post-OVX, rats with a reproductive history had similar trabecular bone mass, elevated trabecular thickness, and increased robustness of cortical bone when compared to virgins, resulting in greater bone stiffness. Further evaluation suggested that reproductive-history-induced differences in post-OVX trabecular bone loss were likely due to differences in baseline trabecular microarchitecture, particularly trabecular thickness. Rats with a reproductive history had a larger population of thick trabeculae, which may be protective against post-OVX trabecular connectivity deterioration and bone loss. Taken together, these findings indicate that reproduction-associated changes in bone microarchitecture appear to reduce the rate of bone loss induced by estrogen deficiency later in life, and thereby exert a long-term protective effect on bone strength. © 2018 American Society for Bone and Mineral Research.
女性骨骼在生殖过程中会发生实质性的结构变化。尽管产后骨矿物质密度会恢复,但生殖可能会导致母体骨微观结构发生永久性改变。然而,流行病学研究表明,妊娠和/或哺乳史并不会增加绝经后骨质疏松症或骨折的风险,甚至可能具有保护作用。我们的研究旨在通过使用大鼠模型来解释这一悖论,结合体内微计算机断层扫描(μCT)成像和骨组织形态计量学,来跟踪骨结构和细胞活性的变化,以响应去卵巢(OVX)后大鼠的雌激素缺乏,这些大鼠有或没有生殖史。我们的研究结果表明,生殖史会导致骨对雌激素缺乏引起的骨丢失的反应发生改变。在 OVX 之前,与处女大鼠相比,有生殖史的大鼠胫骨近端的小梁骨量较低,小梁微观结构改变,皮质结构更健壮。OVX 后,这些大鼠的小梁骨丢失速度比处女大鼠低,结构恶化最小。因此,在 OVX 后 12 周,与处女大鼠相比,有生殖史的大鼠的小梁骨量相似,小梁厚度增加,皮质骨的健壮性增加,导致骨刚度增加。进一步评估表明,生殖史引起的 OVX 后小梁骨丢失差异可能是由于基线小梁微观结构的差异,特别是小梁厚度的差异所致。有生殖史的大鼠有更多的厚小梁,这可能对 OVX 后小梁连通性恶化和骨丢失具有保护作用。总之,这些发现表明,与生殖相关的骨微观结构变化似乎会降低晚年雌激素缺乏引起的骨丢失率,从而对骨强度产生长期的保护作用。