Key result
Elevated arterial stiffness linked to ~65% greater incident CKD risk versus normal stiffness.
Why the study?
The effect of arterial stiffness on incident chronic kidney disease in healthy individuals remains unclear.
Does elevated arterial stiffness, measured by brachial-ankle pulse wave velocity, increase the risk of incident chronic kidney disease in individuals undergoing routine health examinations?
Cohort (n=83,354)
No
Does elevated arterial stiffness, measured by brachial-ankle pulse wave velocity, increase the risk of incident chronic kidney disease in individuals undergoing routine health examinations?
Elevated arterial stiffness is significantly associated with an increased risk of incident chronic kidney disease, a relationship that is potentially mediated by blood pressure and glucose-lipid metabolism dysfunction.
The effect of arterial stiffness (AS) on incident chronic kidney disease (CKD) in healthy individuals remains unclear. In this study, we examined the relationship between AS, measured using brachial-ankle pulse wave velocity (baPWV), and cardiovascular-metabolic comorbidities in predicting CKD development. This two-phase retrospective cohort study used data from the Chinese People’s Liberation Army General Hospital (2009–2021). The cross-sectional phase included 83,354 participants (77,711 without CKD and 5,643 with CKD), whereas the longitudinal phase included 13,738 participants. The association between baPWV and incident CKD was assessed using Cox regression analysis with restricted cubic splines, stratification, and mediation. CKD exhibited a prevalence of 6.77%. Participants with CKD had significantly higher baPWV than those without CKD. Compared to the reference category (< 1,400 cm/s), participants with baPWV ≥ 1,800 cm/s showed markedly increased odds of CKD development. Longitudinal analysis identified 403 incident CKD cases (2.93%) over a mean follow-up of 2.95 ± 2.02 years. A dose–response relationship was observed between baPWV and CKD development (p < 0.001), with the highest baPWV category conferring a 65% greater risk (p < 0.05). Mediation analysis showed significant indirect effects through systolic blood pressure (52.9%), diastolic blood pressure (45.1%), hyperlipidaemia (27.5%), and glycated haemoglobin (15.3%) (all p < 0.05). Elevated baPWV values are associated with greater incident CKD risk, with blood pressure and glucose-lipid metabolism dysfunction potentially mediating this association. Further research is needed to determine whether interventions targeting AS and metabolic parameters reduce CKD incidence.
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Yang et al. (2026) conducted a cohort in Chronic Kidney Disease (n=83,354). Elevated arterial stiffness (baPWV ≥1,800 cm/s) vs. Normal arterial stiffness (baPWV <1,400 cm/s) was evaluated on Incident chronic kidney disease (HR 1.65, p=<0.05). Elevated arterial stiffness (baPWV ≥1,800 cm/s) was associated with a 65% greater risk of incident chronic kidney disease compared to normal arterial stiffness.
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