Key result
Concurrent elevation of hs-CRP and MPV linked to ~123% greater 1-year MACE risk.
Why the study?
Residual cardiovascular risk remains substantial in patients with stable CAD despite guideline-based secondary prevention, prompting investigation into whether systemic inflammation and platelet size jointly influence 1-year MACE.
Does concurrent elevation of hs-CRP and MPV predict an increased 1-year risk of MACE in patients with stable coronary artery disease?
Cohort (n=1,463)
Yes
Does concurrent elevation of hs-CRP and MPV predict an increased 1-year risk of MACE in patients with stable coronary artery disease?
In patients with stable CAD, combined elevation of hs-CRP and MPV identifies a subgroup at higher short-term risk for MACE, highlighting the synergistic impact of inflammation and platelet size on residual risk.
May identify high-risk stable CAD patients for intensified surveillance; extends evidence on synergistic inflammatory-platelet residual risk.
Residual cardiovascular risk remains substantial in patients with stable coronary artery disease (CAD) despite guideline-based secondary prevention. We investigated whether systemic inflammation and platelet size jointly influence 1-year major adverse cardiovascular events (MACE) in 1463 patients with stable CAD. Using high-sensitivity C-reactive protein (hs-CRP) and mean platelet volume (MPV), we defined four joint phenotypes. Multivariable logistic regression was used to examine associations with MACE, with interaction assessed on multiplicative and additive scales. During 1-year follow-up, 71 events occurred. Compared with patients with low hs-CRP and low MPV, those with concurrent elevation of hs-CRP (> 3.0 mg/L) and MPV (≥ 10.1 fL) had a significantly higher risk of MACE (adjusted OR 2.23, 95% CI 1.15–4.25), whereas isolated elevation of either marker alone was not associated with increased risk. Positive interaction was observed on both multiplicative (P = 0.047) and additive scales (Relative Excess Risk due to Interaction 1.49, 95% CI 0.17–3.14). These findings were consistent across sensitivity and subgroup analyses. In stable CAD, combined elevation of hs-CRP and MPV identifies a subgroup at higher short-term risk, suggesting that joint assessment of inflammation and platelet size may improve stratification of residual thrombo-inflammatory risk.
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Hu et al. (2026) conducted a cohort in Stable coronary artery disease (n=1,463). Concurrent elevation of hs-CRP (>3.0 mg/L) and MPV (≥10.1 fL) vs. Low hs-CRP (≤3.0 mg/L) and low MPV (<10.1 fL) was evaluated on 1-year major adverse cardiovascular events (MACE) (OR 2.23, 95% CI 1.15-4.25, p=0.015). Concurrent elevation of hs-CRP (>3.0 mg/L) and MPV (≥10.1 fL) significantly increased the 1-year risk of major adverse cardiovascular events compared to low levels of both markers (OR 2.23).
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