Rongxiang Tang, Jeremy A Elman, Anders M Dale, Stephen M Dorros, Lisa T Eyler, Christine Fennema-Notestine, Daniel E Gustavson, Donald J Hagler, Michael J Lyons, Matthew S Panizzon, Olivia K Puckett, Chandra A Reynolds, Carol E Franz, William S Kremen
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Here, within the DMN, we examined whether its cortical microstructural integrity-an early marker of structural vulnerability that increases the risk for future cognitive decline and neurodegeneration-is associated with episodic memory in adults at ages 56-66, and whether childhood disadvantage moderates this association.</p><p><strong>Methods: </strong>Cortical mean diffusivity (MD) obtained from diffusion magnetic resonance imaging was used to measure microstructural integrity in 350 community-dwelling men. We examined both visual and verbal episodic memory in relation to DMN MD and divided participants into disadvantaged and nondisadvantaged groups based on parental education and occupation.</p><p><strong>Results: </strong>Higher DMN MD was associated with poorer visual memory but not verbal memory (β = -0.11, p = .040 vs β = -0.04, p = .535). 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引用次数: 0
摘要
背景:童年时期的不利处境是认知和大脑老化的一个突出风险因素。童年时期的不利处境与中年后期较差的外显记忆以及默认模式网络(DMN)的大脑功能和结构异常有关。虽然默认模式网络中与年龄相关的变化与老年人的外显记忆衰退有关,但目前仍不清楚童年时期的不利条件是否会在衰老过程的早期对晚年大脑与认知之间的关系产生持久影响。在此,我们研究了DMN内部的皮质微结构完整性--一种结构脆弱性的早期标志物,会增加未来认知能力下降和神经退行性变的风险--是否与56-66岁成年人的外显记忆有关,以及童年的不利条件是否会缓和这种关联:方法:我们利用扩散磁共振成像获得的皮层平均扩散率(MD)来测量 350 名社区男性的微观结构完整性。我们研究了视觉和言语外显记忆与DMN MD的关系,并根据父母的教育程度和职业将参与者分为弱势组和非弱势组:较高的DMN MD与较差的视觉记忆有关,但与言语记忆无关(β=-.11,p=.040 vs. β=-.04,p=.535)。这种关联受童年劣势的调节,仅在劣势组中显著(β=-.26,p=.002 vs. β=-.00,p=.957):较低的DMN皮质微结构完整性可能反映了认知正常的成年人在衰老过程早期视觉记忆的脆弱性。童年时期处于不利地位的个体与非处于不利地位的同龄人相比,更容易出现与皮质微结构相关的视觉记忆功能障碍,而后者在皮质微结构完整性较低的情况下表现出了恢复能力。
Childhood Disadvantage Moderates Late Midlife Default Mode Network Cortical Microstructure and Visual Memory Association.
Background: Childhood disadvantage is a prominent risk factor for cognitive and brain aging. Childhood disadvantage is associated with poorer episodic memory in late midlife and functional and structural brain abnormalities in the default mode network (DMN). Although age-related changes in DMN are associated with episodic memory declines in older adults, it remains unclear if childhood disadvantage has an enduring impact on this later-life brain-cognition relationship earlier in the aging process. Here, within the DMN, we examined whether its cortical microstructural integrity-an early marker of structural vulnerability that increases the risk for future cognitive decline and neurodegeneration-is associated with episodic memory in adults at ages 56-66, and whether childhood disadvantage moderates this association.
Methods: Cortical mean diffusivity (MD) obtained from diffusion magnetic resonance imaging was used to measure microstructural integrity in 350 community-dwelling men. We examined both visual and verbal episodic memory in relation to DMN MD and divided participants into disadvantaged and nondisadvantaged groups based on parental education and occupation.
Results: Higher DMN MD was associated with poorer visual memory but not verbal memory (β = -0.11, p = .040 vs β = -0.04, p = .535). This association was moderated by childhood disadvantage and was significant only in the disadvantaged group (β = -0.26, p = .002 vs β = -0.00, p = .957).
Conclusions: Lower DMN cortical microstructural integrity may reflect visual memory vulnerability in cognitively normal adults earlier in the aging process. Individuals who experienced childhood disadvantage manifested greater vulnerability to cortical microstructure-related visual memory dysfunction than their nondisadvantaged counterparts who exhibited resilience in the face of low cortical microstructural integrity.
期刊介绍:
Publishes articles representing the full range of medical sciences pertaining to aging. Appropriate areas include, but are not limited to, basic medical science, clinical epidemiology, clinical research, and health services research for professions such as medicine, dentistry, allied health sciences, and nursing. It publishes articles on research pertinent to human biology and disease.