Boots A, Wiegersma A M, Vali Y, van den Hof M, Langendam M W, Limpens J, Backhouse E V, Shenkin S D, Wardlaw J M, Roseboom T J, de Rooij S R
Amsterdam UMC location University of Amsterdam, Department of Epidemiology and Data Science, Meibergdreef 9, Amsterdam, the Netherlands; Aging and later life, Amsterdam Public Health, Amsterdam, the Netherlands; Amsterdam Reproduction and Development, Amsterdam, the Netherlands.
Amsterdam UMC location University of Amsterdam, Department of Epidemiology and Data Science, Meibergdreef 9, Amsterdam, the Netherlands; Aging and later life, Amsterdam Public Health, Amsterdam, the Netherlands; Amsterdam Reproduction and Development, Amsterdam, the Netherlands.
Neurosci Biobehav Rev. 2023 Mar;146:105019. doi: 10.1016/j.neubiorev.2022.105019. Epub 2023 Jan 3.
Environmental exposures including toxins and nutrition may hamper the developing brain in utero, limiting the brain's reserve capacity and increasing the risk for Alzheimer's disease (AD). The purpose of this systematic review is to summarize all currently available evidence for the association between prenatal exposures and AD-related volumetric brain biomarkers. We systematically searched MEDLINE and Embase for studies in humans reporting on associations between prenatal exposure(s) and AD-related volumetric brain biomarkers, including whole brain volume (WBV), hippocampal volume (HV) and/or temporal lobe volume (TLV) measured with structural magnetic resonance imaging (PROSPERO; CRD42020169317). Risk of bias was assessed using the Newcastle Ottawa Scale. We identified 79 eligible studies (search date: August 30th, 2020; Ntotal=24,784; median age 10.7 years) reporting on WBV (N = 38), HV (N = 63) and/or TLV (N = 5) in exposure categories alcohol (N = 30), smoking (N = 7), illicit drugs (N = 14), mental health problems (N = 7), diet (N = 8), disease, treatment and physiology (N = 10), infections (N = 6) and environmental exposures (N = 3). Overall risk of bias was low. Prenatal exposure to alcohol, opioids, cocaine, nutrient shortage, placental dysfunction and maternal anemia was associated with smaller brain volumes. We conclude that the prenatal environment is important in shaping the risk for late-life neurodegenerative disease.
包括毒素和营养在内的环境暴露可能会在子宫内影响发育中的大脑,限制大脑的储备能力,并增加患阿尔茨海默病(AD)的风险。本系统评价的目的是总结目前所有关于产前暴露与AD相关脑容量生物标志物之间关联的现有证据。我们系统检索了MEDLINE和Embase数据库,查找关于人类产前暴露与AD相关脑容量生物标志物之间关联的研究,这些生物标志物包括通过结构磁共振成像测量的全脑体积(WBV)、海马体积(HV)和/或颞叶体积(TLV)(国际前瞻性系统评价注册库;CRD42020169317)。使用纽卡斯尔渥太华量表评估偏倚风险。我们确定了79项符合条件的研究(检索日期:2020年8月30日;总样本量=24784;中位年龄10.7岁),这些研究报告了暴露类别为酒精(n = 30)、吸烟(n = 7)、非法药物(n = 14)、心理健康问题(n = 7)、饮食(n = 8)、疾病、治疗和生理状况(n = 10)、感染(n = 6)和环境暴露(n = 3)的WBV(n = 38)、HV(n = 63)和/或TLV(n = 5)。总体偏倚风险较低。产前暴露于酒精、阿片类药物、可卡因、营养缺乏、胎盘功能障碍和母体贫血与较小的脑容量有关。我们得出结论,产前环境对塑造晚年神经退行性疾病的风险很重要。