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Published on: January 28, 2020
High-sensitivity C-reactive protein and hypertension: combined effects on coronary severity and cardiovascular
Hui-Hui Liu1, Ye-Xuan Cao1, Di Sun1
1Department and Institution: Cardiology, State Key Laboratory of Cardiovascular Disease, Fu Wai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, 100037, Beijing, China.
Insights
High-sensitivity C-reactive protein (hsCRP) and hypertension significantly increase cardiovascular risk in patients with coronary artery disease (CAD). Combining elevated hsCRP and hypertension identifies high-risk individuals for better stratification.
Area of Science:
- Cardiology
- Inflammation Biomarkers
- Vascular Disease
Background:
- High-sensitivity C-reactive protein (hsCRP) is an inflammation marker linked to atherosclerosis and cardiovascular events.
- The combined impact of hsCRP and hypertension on cardiovascular risk in coronary artery disease (CAD) remains understudied.
Purpose of the Study:
- To investigate the synergistic effects of hsCRP levels and hypertension on coronary lesion severity and cardiovascular event risk.
- To determine if hsCRP can serve as a stratification marker in patients with stable CAD.
Main Methods:
- A cohort of 4291 stable CAD patients was analyzed, categorized by hsCRP levels (<1, 1-3, >3 mg/L) and hypertension status.
- Coronary artery disease severity was assessed using the Gensini score and number of diseased vessels.
- Cardiovascular events were tracked over a median follow-up period.
Main Results:
- Elevated hsCRP correlated with more severe coronary lesions but not significantly increased cardiovascular event risk alone.
- The combination of high hsCRP and hypertension significantly elevated cardiovascular event risk compared to low hsCRP and normotension.
- Both high hsCRP with normal blood pressure and hypertensive patients with any hsCRP level showed more severe coronary lesions.
Conclusions:
- Elevated hsCRP and hypertension act synergistically to increase cardiovascular risk in stable CAD patients.
- The combined presence of high hsCRP and hypertension identifies a high-risk subgroup requiring intensified management.
- hsCRP can be a valuable tool for cardiovascular risk stratification in conjunction with hypertension status.
Abstract:
High-sensitivity C-reactive protein (hsCRP), a marker of inflammation, can promote atherosclerosis and predict cardiovascular events. However, no data are currently available about the combined effects of hsCRP and hypertension on cardiovascular risk. This study sought to elucidate this matter. A total of 7325 consecutive patients with angina-like chest pain undergoing coronary angiography were evaluated, and 4291 patients with stable, newly diagnosed coronary artery disease (CAD) were enrolled. They were subdivided into three groups according to baseline hsCRP levels (<1, 1-3, and >3 mg/L) and further stratified by hypertension status. The severity of CAD was assessed by the Gensini score and number of diseased vessels. All participants were followed for the occurrence of cardiovascular events. The coronary severity and cardiovascular outcomes were compared among these groups. We observed 530 (12.35%) incident cardiovascular events over 14,210 person-years. Elevated hsCRP was associated with more severe coronary lesions (p < 0.05) and an elevated but nonsignificant increased risk of cardiovascular events (p > 0.05). When hypertension was included as a stratifying factor, both patients with high hsCRP and normal blood pressure and hypertensive patients with any level of hsCRP had more severe coronary lesions compared with the reference group with low hsCRP and normotension. However, compared with the reference group, the cardiovascular event risk was only significantly elevated in patients with high hsCRP and hypertension (p < 0.05). The combination of elevated hsCRP and hypertension greatly increased the cardiovascular risk in patients with stable, newly diagnosed CAD, supporting that hsCRP could be treated as a marker for stratification in high-risk patients.
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