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Differential effects of completed and incomplete pregnancies on the risk of Alzheimer disease
Year of publication 2018
Title of paper Differential effects of completed and incomplete pregnancies on the risk of Alzheimer disease
Author Hyesue Jang, Jong Bin Bae, Efthimios Dardiotis, Nikolaos Scarmeas, Perminder S. Sachdev, Darren M. Lipnicki, Ji Won Han, Tae Hui Kim, Kyung Phil Kwak, Bong Jo Kim, Shin Gyeom Kim, Jeong Lan Kim, Seok Woo Moon, Joon Hyuk Park, Seung-Ho Ryu, Jong Chul Youn, Dong Young Lee, Dong Woo Lee, Seok Bum Lee, Jung Jae Lee, Jin Hyeong Jhoo, Mary Yannakoulia, Mary H. Kosmidis, Giorgos M. Hadjigeorgiou, Paraskevi Sakka, Ki Woong Kim
Publication in journal Neurology
Status of publication accepted
Vol 91(7), 14(7):e643-e651
Link https://n.neurology.org/content/91/7/e643 177회 연결

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 ≈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.