PVWMH demonstrate larger effects on declining cognitive function than DWMH, particularly for motor and processing speed functions and progress at a faster rate, particularly for motor and processing speed functions and progress at a faster rate.
Abstract
Background: Changes in ischemic white matter hyperintensities volume (WMH) on MRI over time are associated with cognitive decline. We investigated whether changes in WMH volume over time exhibit threshold effects of normalized WMH volume on declining cognitive performance and whether these effects on cognition differ between deep white matter hyperintensities (DWMH) and periventricular white matter hyperintensities (PVWMH). Methods: We followed 339 participants longitudinally from GeneSTAR with brain MRI and neuropsychological testing at baseline (2009–2013) and at 13-year follow-up (2023–present) (62% female, and 33% Black, mean baseline age 49.7±9.6). WMH were classified as PVWMH (within 2 mm of ventricles) or DWMH. Two-segment linear spline regression models using adjusted mixed linear regression identified test-specific thresholds longitudinally beyond which cognitive decline accelerated. Cognitive scores from both timepoints were treated as repeated measures, with WMH included as a time-varying predictor. Results: Declines in motor function and processing speed accelerated beyond thresholds of changing PVWMH and DWMH volumes. For Grooved Pegboard tests, changes in volume were associated with minimal effects below a threshold of changing volume (log-transformed ratio of lesion volume to intracranial volume for: PVWMH −9.42 to −9.29; and DWMH −11.8 to −11.7). Substantial declines in cognitive performance were observed above thresholds of increases in volume (slope differences: PVWMH; 14.5–15.1 seconds per log-unit, p < 0.001; and DWMH; 9.54–10.9, p < 0.001). Digit Symbol Substitution Test demonstrated paradoxical positive associations below changing volume thresholds (PVWMH; β=6.68, p=0.001 and DWMH; β=6.98, p < 0.001), reversing to decline above thresholds of increase in volume for PVWMH (Δβ=−11.2, p < 0.001) and DWMH (Δβ=−9.77, p < 0.001). Conclusion: Changes in WMH volume exhibit nonlinear threshold effects on changes in cognitive performance over time and differ by anatomic region. Minimal cognitive impact occurred below thresholds, with accelerated declines above. PVWMH demonstrate larger effects on declining cognitive function than DWMH, particularly for motor and processing speed functions and progress at a faster rate.
WMH baseline and trajectory changes are key risk factors for CN cognitive decline and WMH trajectory changes are linked to cognitive function and brain Aβ deposition.
W. Ba, Cui-Ping Bao, Ying-Xun Gong et al.· Journal of Alzheimer's Disea...· 0 citations
Introduction: Cerebral small vessel disease (CSVD) lesions, including white matter hyperintensities (WMHs), lacunar infarcts, cerebral microbleeds (CMBs), and enlarged perivascular spaces (PVSs) are associated with increased risk of dementia. In this study, we aimed to examine their associations with risk factors, neur...
Z. Chen, S. Raeesi, A. Metz et al.· medRxiv· 0 citations
White-matter microstructural burden and smaller L_NAcc volume may help characterize LLD patients at higher near-term risk of cognitive decline, and warrant evaluation in larger longitudinal LLD cohorts.
Chaoyue Guo, Yuan Fang, Qi Qiu et al.· International Psychogeriatri...· 0 citations
Lesion composition may offer a more informative framework than global WMH burden for understanding cerebrovascular contributions to aging and neurodegeneration, with potential implications for risk stratification, clinical interpretation, and targeted interventions.
Raúl González-Gómez, Enzo Tagliazuchi, C. G. Campo et al.· Neurology· 0 citations
BackgroundAge-related impairments in cerebrovascular reactivity (CVR) and gray matter volume (GMV) both contribute to cognitive decline, yet their regional interplay and joint impact on cognition remain unclear.ObjectiveTo investigate how CVR and GMV are coupled and interact regionally to influence cognition in normal...
Jia-Jia Zhang, Xue-Jia Jia, Yi-Fei Zhang et al.· Journal of Alzheimer's Disea...· 0 citations
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