Journal
NEUROLOGY
Volume 91, Issue 7, Pages E643-E651Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0000000000006000
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Funding
- Korean Health Technology R&D Project, Ministry of Health and Welfare, Republic of Korea [HI09C1379 [A092077]]
- Alzheimer's Association [IIRG-09-133014]
- National Strategic Reference Framework European Union (NSRF-EU) program: Excellence (ARIS-TEIA) [189 10276/8/9/ 2011]
- European Social Fund
- Greek National resources
- Ministry for Health and Social Solidarity of Greece [DeltaY2beta/omicroniotakappa.51657/14.4.2009]
- National Health and Medical Research Council of Australia Program [568969]
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Objective To investigate the effects of completed pregnancy with childbirth and incomplete pregnancy without childbirth on the late-life cognition and the risk of Alzheimer disease (AD) in women. Methods Using the pooled data of 3,549 women provided by 2 population-based cohort studies, we conducted logistic regression analyses to examine retrospectively the associations of completed and incomplete pregnancy with the risks of mild cognitive impairment and AD. For women without dementia, we also conducted analyses of covariance to examine the associations of completed and incomplete pregnancy with Mini-Mental State Examination (MMSE) score. Results Grand multiparous women who experienced >= 5 completed pregnancies showed an approximate to 1.7-fold higher risk of AD than those who experienced 1 to 4 completed pregnancies (odds ratio [OR] 1.68, 95% confidence interval [CI] 1.04-2.72), while those who had incomplete pregnancies showed half the level of AD risk compared with those who never experienced an incomplete pregnancy (OR 0.43, 95% CI 0.24-0.76 for 1 incomplete pregnancy; OR 0.56, 95% CI 0.34-0.92 for >= 2 incomplete pregnancies). In women without dementia, the grand multiparous had worse MMSE scores than those with 1 to 4 completed pregnancies (p < 0.001), while those who experienced >= 1 incomplete pregnancies had better MMSE scores than those who never experienced an incomplete pregnancy (p = 0.008). Conclusions Grand multiparity was associated with high risk of AD, while incomplete pregnancy was associated with low risk of AD in late life.
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