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Premature Aortic Stiffness in Relation to Cerebral Small-Vessel Disease, Cognitive Decline, Major Cardiovascular
Lin Shi1,2, Ke Zheng3,4, Yujun Qian5
1Department of Nephrology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Insights
Arterial stiffness, measured by pulse wave velocity (PWV), is linked to cerebral small-vessel disease (CSVD) and cognitive decline in dialysis patients. PWV also predicts cardiovascular disease and mortality, offering a valuable early biomarker.
Area of Science:
- Nephrology
- Cardiology
- Neurology
Background:
- Cerebral small-vessel disease (CSVD) poses a significant health burden in dialysis patients.
- Arterial stiffness, assessed by pulse wave velocity (PWV), is a known risk factor for CSVD.
Purpose of the Study:
- To investigate the association between PWV and CSVD in dialysis patients.
- To examine the impact of PWV on cognitive function, cardiovascular disease (CVD), and mortality.
Main Methods:
- A prospective cohort study of maintenance dialysis adults.
- Assessment of CSVD features (cerebral microbleed, lacunae, white matter hyperintensity) and PWV.
- Multivariate regression and Cox proportional hazards models for analysis over 10 years.
Main Results:
- PWV was associated with lacunae and white matter hyperintensity.
- Unadjusted associations were found between PWV and cognitive impairment (global function, verbal memory, executive function).
- PWV independently predicted cardiovascular disease and all-cause mortality.
Conclusions:
- PWV is associated with CSVD and cognitive decline in dialysis patients.
- PWV is a predictor of cardiovascular disease and mortality, independent of age and sex.
- PWV serves as a widely available, early predictive biomarker in this population.
Introduction:
There is a great burden of cerebral small-vessel disease (CSVD) in dialysis population. Arterial stiffness, normally assessed by pulse-wave velocity (PWV), is an important risk factor for CSVD. We aimed to investigate the effect of PWV on CSVD and related consequences, including cognitive function, cardiovascular disease (CVD), and mortality in dialysis.
Methods:
In a prospective cohort of maintenance dialysis adults, 3 features of CSVD including cerebral microbleed (CMB), lacunae, and white matter hyperintensity (WMH) were measured. PWV was assessed by sequential recording of electrocardiogram-gated carotid and femoral artery pressure waves. The effect of PWV on CSVD and cognitive impairment were investigated by multivariate regression analysis. Cox proportional hazards model was used to assess the risk of CVD and mortality up to 10 years follow-up.
Results:
In the 178 study subjects, the frequency of CMB, lacunae, and WMH was 32.6%, 25.3%, and 34.8%. PWV was related to the risk of lacunae in subcortical white matter (odds ratio [OR], 1.11; 95% confidence interval [CI], 1.02-1.20) and WMH (OR, 1.11; 95% CI, 1.02-1.20) in crude analyses. Unadjusted associations between PWV and cognitive impairment, which were reflected in loss of global function, verbal memory, and executive function, were also detected. At follow-up, PWV was associated with CVD (hazard ratio [HR], 1.13; 95% CI, 1.08-1.18) and all-cause mortality (HR, 1.11; 95% CI, 1.06-1.16) after confounder adjustment. Restricted cubic splines depicted a linear relationship between PWV and the outcome events.
Conclusion:
PWV was associated with all-cause mortality and CVD, independent of age and sex. PWV was associated with CVSD and cognitive decline in unadjusted analyses. PWV is a widely available measurement and could be an early biomarker and provide predictive value in this population.
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