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脑血管健康通过前脑白质改变影响处理速度:一项英国生物银行研究。

Cerebrovascular health impacts processing speed through anterior white matter alterations: a UK biobank study.

作者信息

Moran Katie L, Smith Craig J, McManus Elizabeth, Allan Stuart M, Montaldi Daniela, Muhlert Nils

机构信息

Division of Psychology, Communication and Human Neurosciences, School of Health Sciences, University of Manchester, Manchester, UK.

Geoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Foundation Trust, University of Manchester, ManchesterManchester, UK.

出版信息

Sci Rep. 2025 Mar 21;15(1):9860. doi: 10.1038/s41598-025-93399-2.

Abstract

Cerebrovascular disease is associated with an increased likelihood of developing dementia. Cerebrovascular risk factors are modifiable and may reduce the risk of later-life cognitive dysfunction, however, the relationship between cerebrovascular risk factors, brain integrity and cognition remains poorly characterised. Using a UK Biobank sample of mid-to-old aged adults, without neurological disease, our structural equation mediation models showed that poor cerebrovascular health, indicated by the presence of cerebrovascular risk factors, was associated with slowed processing speed. This effect was best explained by anterior white matter microstructure (e.g. genu, anterior corona radiata), rather than posterior (e.g. splenium, posterior corona radiata)-the mediatory effect of anterior white matter strengthened further with age. Effects were also significantly reduced when considering other forms of cognition, demonstrating both regional- and cognitive-specificity. Our findings also illustrate that cerebrovascular risk factors cross-sectionally predict cognitive processing speed performance, which can be further strengthened by accounting for risk factor duration, particularly hypertensive duration. In summary, our study highlights the vulnerability of anterior regions and sensitivity of processing speed performance to cerebrovascular burden, and show this effect is amplified with age. We also highlight an improved method of cerebrovascular burden quantification, which accounts for factor duration, as well as risk factor presence and degree. Future work will aim to establish the role of medication and effective risk factor control in alleviating or preventing white matter pathology and cognitive dysfunction.

摘要

脑血管疾病与患痴呆症的可能性增加有关。脑血管危险因素是可改变的,可能会降低晚年认知功能障碍的风险,然而,脑血管危险因素、脑完整性和认知之间的关系仍未得到充分描述。利用英国生物银行中老年人样本(无神经疾病),我们的结构方程中介模型表明,存在脑血管危险因素所表明的不良脑血管健康与处理速度减慢有关。这种效应最好由前白质微观结构(如膝部、放射冠前部)来解释,而不是后部(如压部、放射冠后部)——前白质的中介效应随着年龄的增长而进一步增强。在考虑其他认知形式时,效应也显著降低,显示出区域特异性和认知特异性。我们的研究结果还表明,脑血管危险因素可横断面预测认知处理速度表现,通过考虑危险因素持续时间,尤其是高血压持续时间,这种预测能力可进一步增强。总之,我们的研究强调了前部区域的脆弱性以及处理速度表现对脑血管负担的敏感性,并表明这种效应会随着年龄的增长而放大。我们还强调了一种改进的脑血管负担量化方法,该方法考虑了因素持续时间以及危险因素的存在和程度。未来的工作将旨在确定药物治疗和有效控制危险因素在减轻或预防白质病变和认知功能障碍中的作用。

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