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英国年轻人早期心血管危险因素与灰质结构的关联:阿冯纵向父母与儿童研究(ALSPAC)

Association of early life cardiovascular risk factors with grey matter structure in young adults in the United Kingdom: the ALSPAC study.

作者信息

Haines Holly T, Suri Sana, Patel Raihaan, Chiesa Scott T

机构信息

Department of Experimental Psychology, University of Oxford, United Kingdom; Wellcome Centre for Integrative Neuroimaging, Oxford Centre for Human Brain Activity, University of Oxford, United Kingdom; Department of Psychiatry, Warneford Hospital, University of Oxford, United Kingdom.

Wellcome Centre for Integrative Neuroimaging, Oxford Centre for Human Brain Activity, University of Oxford, United Kingdom; Department of Psychiatry, Warneford Hospital, University of Oxford, United Kingdom.

出版信息

EBioMedicine. 2024 Dec;110:105490. doi: 10.1016/j.ebiom.2024.105490. Epub 2024 Dec 3.

Abstract

BACKGROUND

Cumulative exposures to obesity, hypertension, and physical inactivity from midlife (40-65 years) onwards are three known cardiovascular risk factors for dementia and associated cerebral structural damage. Exactly how early in the lifespan sensitive periods for exposure to these risk factors begin is yet to be established, specifically with respect to onset of cerebral structural changes. We aimed to investigate whether cardiovascular risk across childhood and adolescence is already associated with cerebral structure in regions previously linked with dementia, during young adulthood.

METHODS

Participants were selected from the Avon Longitudinal Study of Parents and Children (ALSPAC), a UK-based prospective cohort of young people, if they had participated in a neuroimaging sub-study (N = 862). We entered data from repeated clinical assessments into mixed-effects models to estimate baseline and rate of change in body mass index (BMI) and mean arterial pressure (MAP) between ages 7-17 years, and physical activity (PA) between 11-15 years. Linear models assessed whether cardiovascular risk factors were associated with grey matter macrostructural indices (cortical thickness, surface area, volume) in young adulthood (∼20 years).

FINDINGS

BMI was found to be associated with grey matter macrostructure in nodes of Default Mode Network previously found to show atrophy in dementia. Baseline BMI was associated with thickness of precuneus cortex and entorhinal surface area, whilst rate of change in BMI across childhood and adolescence was associated with thickness of parahippocampal and middle temporal gyri and inferior parietal cortex in addition to entorhinal and parahippocampal surface area. Further, we identified associations between baseline MAP and PA and entorhinal surface area. Exploratory whole-brain analyses revealed associations between baseline and rate of change in these cardiovascular risk factors and the cortical thickness, surface area, and volume of broader groups of cortical and subcortical regions.

INTERPRETATION

Findings provide preliminary evidence that cerebral structural differences in regions linked to dementia in old age may be legacy of developmental differences associated with cardiovascular risk exposure during early life. This has relevance for lifespan models of dementia risk and timing of preventative interventions. Further work is required to generalise findings beyond this predominantly white, male, and middle-class sample to more diverse cohorts.

FUNDING

NIHR Oxford Health BRC (NIHR203316), Wellcome Trust (203139/Z/16/Z).

摘要

背景

从中年(40 - 65岁)起,肥胖、高血压和缺乏身体活动的累积暴露是已知的痴呆症及相关脑结构损伤的三种心血管危险因素。这些危险因素暴露的敏感时期在生命早期究竟何时开始,特别是与脑结构变化的发生相关的时间,尚未确定。我们旨在研究儿童期和青少年期的心血管风险是否已经与成年早期与痴呆症相关区域的脑结构有关。

方法

如果参与者参加了神经影像学子研究(N = 862),则从英国基于年轻人的前瞻性队列阿冯父母与儿童纵向研究(ALSPAC)中进行选择。我们将重复临床评估的数据输入混合效应模型,以估计7 - 17岁之间体重指数(BMI)和平均动脉压(MAP)的基线和变化率,以及11 - 15岁之间的身体活动(PA)。线性模型评估心血管危险因素是否与成年早期(约20岁)的灰质宏观结构指标(皮质厚度、表面积、体积)相关。

研究结果

发现BMI与默认模式网络节点中的灰质宏观结构相关,该网络先前被发现存在痴呆症萎缩。基线BMI与楔前叶皮质厚度和内嗅区表面积相关,而儿童期和青少年期BMI的变化率除了与内嗅区和海马旁回表面积相关外,还与海马旁回和颞中回以及顶下小叶皮质厚度相关。此外,我们确定了基线MAP和PA与内嗅区表面积之间的关联。探索性全脑分析揭示了这些心血管危险因素的基线和变化率与更广泛的皮质和皮质下区域组的皮质厚度、表面积和体积之间的关联。

解读

研究结果提供了初步证据,表明老年期与痴呆症相关区域的脑结构差异可能是早期生命中与心血管风险暴露相关的发育差异的遗留影响。这与痴呆症风险的寿命模型和预防性干预的时机相关。需要进一步开展工作,将这些发现推广到除这个主要为白人、男性和中产阶级的样本之外的更多样化队列。

资金来源

NIHR牛津健康生物医学研究中心(NIHR203316),惠康信托基金会(203139/Z/16/Z)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d4c/11652839/339baed0f360/gr1.jpg

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