Perspective on post-menopausal osteoporosis: establishing an interdisciplinary understanding of the sequence of events from the molecular level to whole bone fractures

被引:101
|
作者
McNamara, L. M. [1 ]
机构
[1] Natl Univ Ireland Galway, Dept Mech & Biomed Engn, Galway, Ireland
关键词
bone; post-menopausal osteoporosis; tissue composition; biomechanics; cell biology; GROWTH-FACTOR-BETA; OSTEOBLAST-LIKE CELLS; HUMAN TRABECULAR BONE; ILIAC CREST BIOPSIES; MECHANICAL-PROPERTIES; CANCELLOUS BONE; GENE-EXPRESSION; MESSENGER-RNA; MINERAL DENSITY; TRANSFORMING GROWTH-FACTOR-BETA-1;
D O I
10.1098/rsif.2009.0282
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Current drug treatments for post-menopausal osteoporosis cannot eliminate bone fractures, possibly because the mechanisms responsible for bone loss are not fully understood. Although research within various disciplines has significantly advanced the state of knowledge, fundamental findings are not widely understood between different disciplines. For that reason, this paper presents noteworthy experimental findings from discrete disciplines focusing on post-menopausal osteoporosis. These studies have established that, in addition to bone loss, significant changes in bone micro-architecture, tissue composition and micro-damage occur. Cellular processes and molecular signalling pathways governing pathological bone resorption have been identified to a certain extent. Ongoing studies endeavour to determine how such changes are initiated at the onset of oestrogen deficiency. It emerges that, because of the discrete nature of previous research studies, the sequence of events that lead to bone fracture is not fully understood. In this paper, two sequences of multi-scale changes are proposed and the experimental challenges that need to be overcome to fully de. ne this sequence are outlined. Future studies must comprehensively characterize the time sequence of molecular, cellular-and tissue-level changes to attain a coherent understanding of the events that ultimately lead to bone fracture and inform the future development of treatments for post-menopausal osteoporosis.
引用
收藏
页码:353 / 372
页数:20
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