A comprehensive assessment of age at menopause with well-characterized cognition at 70 years: A population-based British birth cohort

Maturitas. 2023 Apr:170:31-38. doi: 10.1016/j.maturitas.2023.01.009. Epub 2023 Jan 28.

Abstract

Objectives: Associations between age at menopause and cognition post-menopause are examined to determine whether relationships are stronger for certain cognitive domains.

Study design: Women from the Medical Research Council National Survey of Health and Development and its neuroscience sub-study, Insight 46, were included if they had known age at menopause (self-reported via questionnaire) and complete cognitive outcome data at age 69 (n = 746) or at Insight 46 wave I (n = 197). Multivariable linear regression analyses adjusting for life course confounders were run; interactions with menopause type (natural/surgical) and APOE-ε4 status were examined; and the potential contribution of hormone therapy was assessed.

Main outcome measures: Cognitive measures were standardized Addenbrooke's Cognitive Examination - third edition total and sub-domain scores at age 69 (whole cohort) and Preclinical Alzheimer's Cognitive Composite total and sub-test scores at age ~70 (Insight 46).

Results: Older age at menopause was associated with better performance across all outcomes, most strongly for the Addenbrooke's Cognitive Examination memory and visuospatial function sub-domains, and the Preclinical Alzheimer's Cognitive Composite digit-symbol substitution test and face-name associative memory examination sub-tests. Adjusting for early-life factors attenuated all effect estimates, driven by childhood cognition, and accounting for menopause type revealed negative confounding for some outcomes. No significant interactions with menopause type or APOE-ε4 status were detected. Further adjustment for hormone therapy did not meaningfully alter the estimated effects.

Conclusions: Older age at menopause is associated with better later-life cognitive performance, particularly for visual processing and associative learning and memory domains. Childhood cognition was an important contributor.

Keywords: Cognitive domains; Life course; Menopause.

MeSH terms

  • Aged
  • Alzheimer Disease*
  • Apolipoproteins E
  • Birth Cohort*
  • Child
  • Cognition
  • Female
  • Hormones
  • Humans
  • Menopause
  • Neuropsychological Tests

Substances

  • Hormones
  • Apolipoproteins E