The flexibility of cognitive reserve in regulating the frontoparietal control network and cognitive function in subjects with white matter hyperintensities

• Published in: Behavioural brain research 2022-05, Vol.425, p.113831-113831, Article 113831
• Main Authors: Chen, Huiping, Zhu, Huahong, Huang, Lili, Chen, Haifeng, Liu, Renyuan, Qin, Ruomeng, Shao, Pengfei, Xu, Hengheng, Ma, Junyi, Cheng, Yue, Xu, Yun, Ye, Qing
• Format: Article
• Language: English
• Subjects: Brain; Cognition - physiology; Cognitive Dysfunction - diagnostic imaging; Cognitive function; Cognitive Reserve; Frontoparietal control network; Humans; Magnetic Resonance Imaging - methods; Neuropsychological Tests; White Matter - diagnostic imaging; White matter hyperintensities
• ISSN: 0166-4328; 1872-7549
• DOI: 10.1016/j.bbr.2022.113831

High cognitive reserve (CR) protects against cognitive decline in individuals with white matter hyperintensities (WMH). However, the functional mechanisms remain relatively unknown. This work aimed to explore the effects of CR on the frontoparietal control network (FPCN) and cognitive function in subjects with WMH. One hundred and thirty-seven subjects with WMH and 95 control subjects without WMH underwent neuropsychological testing, CR assessments, and multimodal magnetic resonance imaging (MRI) scanning. A mixed analysis of covariance with CR level (high CR vs. low CR) and WMH status (with WMH vs. without WMH) as fixed factors was performed on the FPCN. WMH volume was negatively correlated with global cognitive function in subjects with low CR not in those with high CR, suggesting a buffering effect of high CR. An interaction between CR and WMH was detected on the right FPCN in frontal regions. Specifically, control subjects with high CR had significantly higher functional connectivity (FC) in frontal regions than control subjects with low CR, whereas this relation was inverted in WMH subjects. Correlative analyses showed positive associations of the FC with cognitive performance in both WMH subjects and control subjects, although the associations were not significant after correction for multiple comparisons. In conclusion, CR differentially regulated the FPCN in frontal regions between subjects with WMH and those without WMH. This regulation supports the flexibility of CR in regulating brain function and may underlie the effects of CR on cognitive function in WMH subjects. •CR buffers the damaging effect of WMH on cognitive function.•CR interacts with WMH to regulate the frontoparietal control network (FPCN).•CR differentially regulates the FPCN between WMH subjects and control subjects.