Laboratory of Clinical Investigation, National Institute on Aging, NIH, Baltimore, MD 21224.
Laboratory of Behavioral Neuroscience, National Institute on Aging, NIH, Baltimore, MD 21224.
Proc Natl Acad Sci U S A. 2024 Aug 27;121(35):e2402813121. doi: 10.1073/pnas.2402813121. Epub 2024 Aug 19.
Emerging evidence suggests that altered myelination is an important pathophysiologic correlate of several neurodegenerative diseases, including Alzheimer and Parkinson's diseases. Thus, improving myelin integrity may be an effective intervention to prevent and treat age-associated neurodegenerative pathologies. It has been suggested that cardiorespiratory fitness (CRF) may preserve and enhance cerebral myelination throughout the adult lifespan, but this hypothesis has not been fully tested. Among cognitively normal participants from two well-characterized studies spanning a wide age range, we assessed CRF operationalized as the maximum rate of oxygen consumption (VOmax) and myelin content defined by myelin water fraction (MWF) estimated through our advanced multicomponent relaxometry MRI method. We found significant positive correlations between VOmax and MWF across several white matter regions. Interestingly, the effect size of this association was higher in brain regions susceptible to early degeneration, including the frontal lobes and major white matter fiber tracts. Further, the interaction between age and VOmax exhibited i) a steeper positive slope in the older age group, suggesting that the association of VOmax with MWF is stronger at middle and older ages and ii) a steeper negative slope in the lower VOmax group, indicating that lower VOmax levels are associated with lower myelination with increasing age. Finally, the nonlinear pattern of myelin maturation and decline is VOmax-dependent with the higher VOmax group reaching the MWF peak at later ages. This study provides evidence of an interconnection between CRF and cerebral myelination and suggests therapeutic strategies for promoting brain health and attenuating white matter degeneration.
新出现的证据表明,髓鞘改变是包括阿尔茨海默病和帕金森病在内的几种神经退行性疾病的重要病理生理相关性。因此,改善髓鞘完整性可能是预防和治疗与年龄相关的神经退行性病变的有效干预措施。有人认为,心肺功能(CRF)可以在整个成年期保持和增强大脑的髓鞘形成,但这一假说尚未得到充分验证。在两个具有广泛年龄范围的特征明确的研究中的认知正常参与者中,我们评估了心肺功能,其操作化为最大耗氧量(VOmax),并用我们先进的多分量弛豫度 MRI 方法通过髓鞘水分数(MWF)来定义髓鞘含量。我们发现 VOmax 与多个白质区域的 MWF 之间存在显著的正相关。有趣的是,这种关联的效应大小在易发生早期退化的脑区更高,包括额叶和主要的白质纤维束。此外,年龄与 VOmax 之间的相互作用表现为:i)在年龄较大的组中斜率更为陡峭,表明 VOmax 与 MWF 的关联在中年和老年更强;ii)在 VOmax 较低的组中斜率更为陡峭,表明随着年龄的增长,较低的 VOmax 水平与较低的髓鞘化相关。最后,髓鞘成熟和下降的非线性模式依赖于 VOmax,VOmax 较高的组在较晚的年龄达到 MWF 峰值。这项研究提供了心肺功能与大脑髓鞘之间相互关联的证据,并为促进大脑健康和减轻白质退化提供了治疗策略。