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女性老龄化:当翻译模型无法翻译时
Gabrielle Gilmer1,2,3,4, Zachary R Hettinger1,2,5,6, Yetsa Tuakli-Wosornu7,8
1Discovery Center for Musculoskeletal Recovery, Schoen Adams Research Institute at Spaulding Rehabilitation, Boston, MA, USA.
老龄化研究模型往往排除了女性特有的生殖变化,如更年期,导致对女性年龄相关疾病的理解不佳. 纳入这些因素对于推进衰老生物学至关重要.
科学领域:
- 老年学是指老年学的学科.
- 生殖生物学 生殖生物学
- 临床前研究模型 临床前研究模型
背景情况:
- 与男性相比,女性患者在与衰老相关的病理中表现出更高的发病率和不良治疗事件.
- 目前的临床前老龄化模型不充分代表女性老龄化轨迹,特别是生殖衰老.
- 不到1%的衰老生物学研究包括更年期的表型,尽管生殖衰老影响了70%以上的与年龄相关的疾病.
研究的目的:
- 总结关于女性生物学常用的临床前衰老模型的局限性.
- 为将更年期,怀孕和性别考虑纳入衰老研究提供建议.
- 为研究人员,期刊,资助机构和动物供应商概述可行的步骤,以解决这些差距.
主要方法:
- 对当前临床前衰老模型的文献综述和分析.
- 确定老龄化研究中关于女性生殖生理学的关键遗漏.
- 制定建议和行动项目,以改善老龄化研究中的性别包容性.
主要成果:
- 普遍存在的衰老模型未能纳入女性衰老的关键方面,例如更年期过渡和怀孕,分娩和母乳养的影响.
- 这种遗漏导致了对了解女性年龄相关疾病的重大知识差距.
- 现有的研究主要利用不反映女性衰老生物现实的模型.
结论:
- 有必要加强临床前衰老模型,以准确反映女性衰老轨迹,包括生殖因素.
- 实施将性别因素纳入考虑的建议对于推进衰老生物学和改善妇女健康结果至关重要.
- 需要涉及研究人员,机构和资助机构的协作努力,以解决女性老龄化表型在研究中的不足.
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