Consumer and Clinical Radiation Protection Bureau, Health Canada, Ottawa, Ontario, Canada.
Hospital for Special Surgery Research Institute, New York City, New York, USA.
Environ Mol Mutagen. 2024 Oct;65 Suppl 3:85-111. doi: 10.1002/em.22631. Epub 2024 Oct 10.
Bone loss, commonly seen in osteoporosis, is a condition that entails a progressive decline of bone mineral density and microarchitecture, often seen in post-menopausal women. Bone loss has also been widely reported in astronauts exposed to a plethora of stressors and in patients with osteoporosis following radiotherapy for cancer. Studies on mechanisms are well documented but the causal connectivity of events to bone loss development remains incompletely understood. Herein, the adverse outcome pathway (AOP) framework was used to organize data and develop a qualitative AOP beginning from deposition of energy (the molecular initiating event) to bone loss (the adverse outcome). This qualitative AOP was developed in collaboration with bone loss research experts to aggregate relevant findings, supporting ongoing efforts to understand and mitigate human system risks associated with radiation exposures. A literature review was conducted to compile and evaluate the state of knowledge based on the modified Bradford Hill criteria. Following review of 2029 studies, an empirically supported AOP was developed, showing the progression to bone loss through many factors affecting the activities of bone-forming osteoblasts and bone-resorbing osteoclasts. The structural, functional, and quantitative basis of each proposed relationship was defined, for inference of causal changes between key events. Current knowledge and its gaps relating to dose-, time- and incidence-concordance across the key events were identified, as well as modulating factors that influence linkages. The new priorities for research informed by the AOP highlight areas for improvement to enable development of a quantitative AOP used to support risk assessment strategies for space travel or cancer radiotherapy.
骨质疏松症常见的骨质流失是一种骨矿物质密度和微结构逐渐下降的情况,常见于绝经后妇女。骨质流失也在暴露于大量应激源的宇航员和接受癌症放射治疗后的骨质疏松症患者中广泛报道。对机制的研究有充分的记录,但事件与骨质流失发展之间的因果关系仍不完全清楚。在此,使用不良结局途径(AOP)框架来组织数据并开发从能量沉积(分子起始事件)到骨质流失(不良结局)的定性 AOP。这个定性 AOP 是与骨质流失研究专家合作开发的,以汇总相关发现,支持正在努力理解和减轻与辐射暴露相关的人体系统风险。进行了文献综述,以根据修改后的布拉德福德·希尔标准编译和评估知识状况。在审查了 2029 项研究后,开发了一个经验支持的 AOP,显示了通过许多因素影响骨形成成骨细胞和骨吸收破骨细胞的活性,导致骨质流失的进展。定义了每个提议关系的结构、功能和定量基础,以推断关键事件之间的因果变化。确定了与关键事件的剂量、时间和发生率一致性相关的当前知识及其差距,以及影响联系的调节因素。AOP 提供的新研究重点突出了改进领域,以支持用于支持太空旅行或癌症放射治疗风险评估策略的定量 AOP 的开发。