Exploring the Impact of Reproductive History and Hormone Use on Women’s Cognition

Published on January 19, 2023

As women age, they face a higher risk of developing age-related neurocognitive disorders, but there’s still much to learn about how reproductive events and hormone use come into play. In this study, we delved into the relationships between reproductive history, hormone use, a certain genotype, and cognition in over 221,000 middle- to older-aged women from the UK Biobank. We assessed cognitive performance across various tasks and found that factors such as a longer reproductive span, older age at menopause, and the use of hormonal contraceptives were associated with better cognitive performance later in life. However, the number of live births, hysterectomy without oophorectomy, and hormone therapy had mixed findings with both positive and negative associations. Interestingly, the use of hormonal contraceptives showed the strongest positive association with cognition. While the APOE ε4 genotype was linked to reduced processing speed and executive function, it didn’t impact the observed connections between female-specific factors and cognition. These findings support previous research on the complex interplay between reproductive history, hormone use, and women’s cognitive health. Further investigation in this field is necessary for a deeper understanding of women’s brain health and to enhance healthcare for women.

Relative to men, women are at a higher risk of developing age-related neurocognitive disorders including Alzheimer’s disease. While women’s health has historically been understudied, emerging evidence suggests that reproductive life events such as pregnancy and hormone use may influence women’s cognition later in life. We investigated the associations between reproductive history, exogenous hormone use, apolipoprotein (APOE) ε4 genotype and cognition in 221,124 middle- to older-aged (mean age 56.2 ± 8.0 years) women from the UK Biobank. Performance on six cognitive tasks was assessed, covering four cognitive domains: episodic visual memory, numeric working memory, processing speed, and executive function. A longer reproductive span, older age at menopause, older age at first and last birth, and use of hormonal contraceptives were positively associated with cognitive performance later in life. Number of live births, hysterectomy without oophorectomy and use of hormone therapy showed mixed findings, with task-specific positive and negative associations. Effect sizes were generally small (Cohen’s d < 0.1). While APOE ε4 genotype was associated with reduced processing speed and executive functioning, in a dose-dependent manner, it did not influence the observed associations between female-specific factors and cognition. Our findings support previous evidence of associations between a broad range of female-specific factors and cognition. The positive association between a history of hormonal contraceptive use and cognition later in life showed the largest effect sizes (max. d = 0.1). More research targeting the long-term effects of female-specific factors on cognition and age-related neurocognitive disorders including Alzheimer’s disease is crucial for a better understanding of women’s brain health and to support women’s health care.

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