Key result
Combined high brachial-ankle pulse wave velocity and hs-CRP increased the risk of major adverse cardiovascular events compared to low levels of both (HR 7.08; 95% CI 3.76-13.30; P<0.001).
Why the study?
Both CRP and arterial stiffness are associated with CVD, but whether combining hs-CRP and baPWV improves cardiovascular risk stratification remained to be investigated.
Does the combination of high-sensitivity C-reactive protein and brachial-ankle pulse wave velocity improve prediction of long-term cardiovascular events compared to either measurement alone?
Cohort (n=6,572)
Does the combination of high-sensitivity C-reactive protein and brachial-ankle pulse wave velocity improve prediction of long-term cardiovascular events compared to either measurement alone?
Hazard Ratio: 7.08 (95% CI 3.76–13.3)
p-value: p=<0.001
The combination of hs-CRP and baPWV provides incremental prognostic value over clinical factors and individual measurements for predicting long-term cardiovascular events.
Supports incremental prognostic value of combined baPWV and hs-CRP; hypothesis-generating pending prospective validation.
Background: Both C-reactive protein (CRP) and arterial stiffness are associated with the development of cardiovascular disease (CVD). This study was performed to investigate whether a combination of these two measurements could improve cardiovascular risk stratification. Methods: A total of 6572 consecutive subjects (mean age, 60.8 ± 11.8 years; female, 44.2%) who underwent both high-sensitivity CRP (hs-CRP) and brachial–ankle pulse wave velocity (baPWV) measurement within 1 week were retrospectively analyzed. Major adverse cardiovascular events (MACE), including cardiovascular death, acute myocardial infarction, coronary revascularization, and stroke were assessed during the clinical follow-up. Results: During a mean follow-up period of 3.75 years (interquartile range, 1.78–5.31 years), there were 182 cases of MACE (2.8%). The elevated baPWV (≥1505 cm/s) (hazard ratio (HR), 4.21; 95% confidence interval (CI), 2.73–6.48; p < 0.001) and hs-CRP (≥3 mg/L) (HR, 1.57; 95% CI, 1.12–2.21; p < 0.001) levels were associated with MACE even after controlling for potential confounders. The combination of baPWV and hs-CRP further stratified the subjects’ risk (subjects with low baPWV and hs-CRP vs. subjects with high baPWV and hs-CRP; HR, 7.08; 95% CI, 3.76−13.30; p < 0.001). Adding baPWV information to clinical factors and hs-CRP had an incremental prognostic value (global Chi-square score, from 126 to 167, p < 0.001). Conclusions: The combination of hs-CRP and baPWV provided a better prediction of future CVD than either one by itself. Taking these two simple measurements simultaneously is clinically useful in cardiovascular risk stratification.
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Kim et al. (2021) conducted a cohort in Cardiovascular disease risk (n=6,572). High baPWV (≥1505 cm/s) and high hs-CRP (≥3 mg/L) vs. Low baPWV and low hs-CRP was evaluated on Major adverse cardiovascular events (MACE), including cardiovascular death, acute myocardial infarction, coronary revascularization, and stroke (HR 7.08, 95% CI 3.76-13.30, p=<0.001). Combined high brachial-ankle pulse wave velocity and hs-CRP increased the risk of major adverse cardiovascular events compared to low levels of both (HR 7.08; 95% CI 3.76-13.30; P<0.001).
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