Early-Life Adversity Predicts Markers of Aging-Related Neuroinflammation, Neurodegeneration, and Cognitive Impairment in Women

IF 7.7 1区 医学 Q1 CLINICAL NEUROLOGY Annals of Neurology Pub Date : 2025-01-09 DOI:10.1002/ana.27161
Lara Fleck MSc, Claudia Buss PhD, Martin Bauer MSc, Maike Stein MD, Ralf Mekle PhD, Lena Kock MSc, Heiko Klawitter MSc, Malvika Godara PhD, Judith Ramler MSc, Sonja Entringer PhD, Matthias Endres MD, Christine Heim PhD
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Abstract

Objective

Despite the overwhelming evidence for profound and longstanding effects of early-life stress (ELS) on inflammation, brain structure, and molecular aging, its impact on human brain aging and risk for neurodegenerative disease is poorly understood. We examined the impact of ELS severity in interaction with age on blood-based markers of neuroinflammation and neurodegeneration, brain volumes, and cognitive function in middle-aged women.

Methods

We recruited 179 women (aged 30–60 years) with and without ELS exposure before the onset of puberty. Using Simoa technology, we assessed blood-based markers of neuroinflammation and neurodegeneration, including serum concentrations of glial fibrillary acidic protein (GFAP) and neurofilament light chain (NfL). We further obtained T1-weighted and T2-weighted magnetic resonance images to assess brain volumes and we assessed cognitive performance sensitive to early impairments associated with the development of dementia, using the Cambridge Neuropsychological Automated Test Battery. We used generalized additive models to examine nonlinear interaction effects of ELS severity and age on these outcomes.

Results

Analyses revealed significant nonlinear interaction effects of ELS severity and age on NfL and GFAP serum concentrations, total and subcortical gray matter volume loss, increased third ventricular volume, and cognitive impairment.

Interpretation

These findings suggest that ELS profoundly exacerbates peripheral, neurostructural, and cognitive markers of brain aging. Our results are critical for the development of novel early prevention strategies that target the impact of developmental stress on the brain to mitigate aging-related neurological diseases. ANN NEUROL 2025;97:642–656

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早期生活逆境可预测女性衰老相关神经炎症、神经变性和认知障碍的标志物。
目的:尽管有大量证据表明,早期生活压力(ELS)对炎症、大脑结构和分子衰老有深远而长期的影响,但其对人类大脑衰老和神经退行性疾病风险的影响尚不清楚。我们研究了ELS严重程度与年龄的相互作用对中年女性神经炎症和神经退行性变、脑容量和认知功能的血液标志物的影响。方法:我们招募了179名女性(年龄30-60岁),在青春期开始前有或没有接触过ELS。使用Simoa技术,我们评估了基于血液的神经炎症和神经变性标志物,包括血清胶质纤维酸性蛋白(GFAP)和神经丝轻链(NfL)的浓度。我们进一步获得了t1加权和t2加权磁共振图像来评估脑容量,我们使用剑桥神经心理学自动测试电池评估了与痴呆发展相关的早期损伤的认知能力。我们使用广义加性模型来检验ELS严重程度和年龄对这些结果的非线性相互作用效应。结果:分析显示,ELS严重程度和年龄对NfL和GFAP血清浓度、总灰质和皮层下灰质体积损失、第三心室体积增加和认知功能障碍有显著的非线性相互作用。解释:这些发现表明,ELS严重加剧了大脑衰老的周围、神经结构和认知标志物。我们的研究结果对于开发新的早期预防策略至关重要,这些策略针对大脑发育压力的影响,以减轻与衰老相关的神经系统疾病。Ann neurol 2025。
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来源期刊
Annals of Neurology
Annals of Neurology 医学-临床神经学
CiteScore
18.00
自引率
1.80%
发文量
270
审稿时长
3-8 weeks
期刊介绍: Annals of Neurology publishes original articles with potential for high impact in understanding the pathogenesis, clinical and laboratory features, diagnosis, treatment, outcomes and science underlying diseases of the human nervous system. Articles should ideally be of broad interest to the academic neurological community rather than solely to subspecialists in a particular field. Studies involving experimental model system, including those in cell and organ cultures and animals, of direct translational relevance to the understanding of neurological disease are also encouraged.
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