激素替代疗法、绝经年龄和生活方式变量与随访时更好的认知表现相关,但与老年成年妇女的认知能力无关,而与APOE4携带者状态和合并症无关。

Frontiers in dementia Pub Date : 2025-01-17 eCollection Date: 2024-01-01 DOI:10.3389/frdem.2024.1496051
Tamlyn J Watermeyer, Sarah Gregory, Emmi Leetham, Chinedu T Udeh-Momoh, Graciela Muniz-Terrera
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引用次数: 0

摘要

激素替代疗法(HRT)对绝经后妇女认知功能的影响仍然是一个相当有争议的话题。尽管雌激素的神经保护作用暗示了潜在的认知益处,但实证结果却喜忧参半。方法:本研究使用来自威尔士认知功能和衰老研究(CFAS Wales)队列的数据,探讨老年成年女性HRT使用、绝经年龄、APOE4携带者状态、生活方式因素、合并症和认知结局之间的关系。采用了两种回归模型:一种分析随访时的认知表现,另一种检查认知得分随时间的变化。结果:结果表明,虽然年龄、受教育程度、HRT使用、绝经年龄、饮酒和饮食在一个较晚的时间点与认知功能相关,但当随着时间的推移建立认知模型时,只有年龄仍然是一个重要的预测因子。讨论:这些发现表明,虽然激素替代疗法、绝经年龄和生活方式因素可能支持认知稳定性,但它们并不一定预测绝经后老年妇女的认知能力下降。目前工作的一个主要限制是缺乏关于激素替代疗法使用的细节,例如配方、时间和持续时间;未来研究应解决的问题。该研究强调需要更长的随访期,考虑其他女性特有的风险因素,以及更全面的生活方式和健康评估,以阐明激素替代疗法使用、生殖史、生活方式、合并症和女性认知衰老之间复杂的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hormone replacement therapy, menopausal age and lifestyle variables are associated with better cognitive performance at follow-up but not cognition over time in older-adult women irrespective of APOE4 carrier status and co-morbidities.

Introduction: The impact of Hormone Replacement Therapy (HRT) on cognitive function in postmenopausal women remains a topic of considerable debate. Although estrogen's neuroprotective effects suggest potential cognitive benefits, empirical findings are mixed.

Methods: This study uses data from the Cognitive Function and Ageing Study Wales (CFAS Wales) cohort to explore the relationships between HRT use, age at menopause, APOE4 carrier status, lifestyle factors, comorbidities, and cognitive outcomes in older adult women. Two regression models were employed: one analyzing cognitive performance at follow-up and another examining changes in cognitive scores over time.

Results: Results indicate that while age, education, HRT use, age at menopause, alcohol consumption, and diet were associated with cognitive function at a single later time point, only age remained a significant predictor when modeling cognition over time.

Discussion: These findings suggest that while HRT, menopausal age and lifestyle factors may support cognitive stability, they do not necessarily predict cognitive decline in post-menopausal older women. A major limitation of the current work is the lack of detail regarding HRT use, such as formulation, timing and duration; caveats that future studies should address. The study underscores the need for longer follow-up periods, consideration of other female-specific risk factors, and more comprehensive lifestyle and health assessments to clarify the complex interplay between HRT use, reproductive history, lifestyle, comorbidities and cognitive aging in women.

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