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Changes in C-reactive protein in response to anti-inflammatory therapy as a predictor of cardiovascular outcomes: A
1British Heart Foundation Centre of Research Excellence, School of Cardiovascular Medicine and Sciences, King's College London, UK.
Insights
Targeting C-reactive protein (CRP) does not improve cardiovascular outcomes beyond lipid-lowering therapy for most patients. However, CRP reduction is beneficial for those with high residual inflammatory risk despite normal lipid levels.
Area of Science:
- Cardiology
- Inflammation Biology
- Clinical Risk Assessment
Background:
- Aggressive lipid-lowering therapies do not fully mitigate cardiovascular event risk in many patients.
- C-reactive protein (CRP) is an inflammation marker linked to high cardiovascular risk.
- The clinical benefit of targeting CRP for cardiovascular outcomes remains uncertain.
Purpose of the Study:
- To characterize the relationship between CRP and cardiovascular outcomes.
- To evaluate if CRP reduction correlates with cardiovascular risk reduction.
- To assess the influence of lipid levels on CRP-targeted therapy efficacy.
Main Methods:
- Systematic review of randomized controlled trials measuring CRP and cardiovascular events.
- Meta-analysis of placebo-controlled studies on CRP reduction and cardiovascular risk.
- Meta-regression to analyze the impact of low-density lipoprotein and triglycerides.
Main Results:
- Fifteen studies were included; nine were placebo-controlled.
- No correlation found between CRP reduction magnitude and cardiovascular risk reduction.
- A strong correlation exists between CRP and low-density lipoprotein reduction (adjusted r²=0.8).
- Lipid changes explained event reduction in 8 studies; 5 suggested other factors.
Conclusions:
- Targeting CRP offers no additional cardiovascular risk reduction benefit over targeting low-density lipoprotein in the general population.
- Targeting CRP is valuable for patients with high residual inflammatory risk despite optimal lipid management.
Background:
Despite the availability of aggressive lipid-lowering strategies, many patients remain at risk of cardiovascular events. C-reactive protein is a marker of inflammation elevated in patients at high risk of cardiovascular events. C-reactive protein has demonstrated value as a predictor of cardiovascular risk; however, it is unclear whether targeting C-reactive protein levels improves outcomes. This systematic review aimed to characterise the relationship between C-reactive protein and cardiovascular outcomes and to assess whether the magnitude of C-reactive protein reduction correlates to the extent of cardiovascular risk reduction.
Methods:
A systematic review was conducted to identify randomised controlled trials that measured C-reactive protein before and after administration of therapies for cardiovascular disease and measured incidence of cardiovascular events. A meta-analysis of placebo-controlled studies assessed the relationship between extent of C-reactive protein reduction and cardiovascular risk reduction. Placebo-controlled studies where low-density lipoprotein and triglyceride data were available were also included in a meta-regression to assess the influence of these established risk factors on the efficacy of treatment when compared to C-reactive protein.
Results:
Fifteen studies met the criteria for inclusion in this review, of which six were active comparator studies and nine were placebo controlled. Six placebo-controlled studies had data available for meta-regression. Eight studies demonstrated a reduction in events that could be explained by changes in lipid levels, whereas the results of five studies suggested that the association between C-reactive protein reduction and event rates cannot be explained by changes in lipid levels alone. No correlation was found between magnitude of C-reactive protein reduction and cardiovascular risk reduction. A strong correlation was found between C-reactive protein and low-density lipoprotein reduction (adjusted r 2 = 0.8).
Conclusions:
Targeting C-reactive protein does not offer additional benefit over targeting low-density lipoprotein across the general population in terms of cardiovascular risk reduction. However, there is value in targeting C-reactive protein in patients at high residual inflammatory risk despite non-elevated lipid levels or use of lipid-lowering therapy.
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