C-reactive protein concentration and risk of coronary heart disease, stroke, and mortality: an individual participant meta-analysis
Emerging Risk Factors Collaboration • Lancet
Key Finding
Per 3-fold higher CRP: CHD HR 1.37 (1.27-1.48), ischaemic stroke HR 1.27 (1.15-1.40), vascular mortality HR 1.55 (1.37-1.76) after adjustment
Key Findings
- 1CHD: HR 1.37 (95% CI 1.27-1.48) per 3-fold higher CRP after adjustment
- 2Ischaemic stroke: HR 1.27 (95% CI 1.15-1.40) per 3-fold higher CRP
- 3Vascular mortality: HR 1.55 (95% CI 1.37-1.76) per 3-fold higher CRP
- 4Associations depend on conventional risk factors and inflammation markers
Original title: “C-reactive protein concentration and risk of coronary heart disease, stroke, and mortality: an individual participant meta-analysis”
Plain English Summary
Individual participant meta-analysis of 160,309 participants across 54 prospective studies (1.31 million person-years, 27,769 outcomes) examining CRP associations with vascular and non-vascular mortality.
In-Depth Analysis
Study Details
Authors: Emerging Risk Factors Collaboration (ERFC)
Writing Committee: Kaptoge S, Di Angelantonio E, Lowe G, Pepys MB, Thompson SG, Collins R, Danesh J
Journal: Lancet, 2010 Jan 9; 375(9709):132-140
PMCID: PMC3162187
Study Population
- •Participants: 160,309
- •Studies: 54 prospective studies
- •Person-years: 1.31 million
- •Outcomes: 27,769 disease events
- •Mean age: 60 years (SD 8)
- •Women: 48%
- •Median follow-up: 5.8 years
- •Baseline CRP median: 1.72 mg/L (5th-95th: 0.25-12.4)
Key Results: Hazard Ratios per 3-fold Higher CRP
| Outcome | Age/Sex Adjusted | Fully Adjusted |
|---|---|---|
| Coronary heart disease | 1.63 (1.51-1.76) | 1.37 (1.27-1.48) |
| Ischaemic stroke | 1.44 (1.32-1.57) | 1.27 (1.15-1.40) |
| Vascular mortality | 1.71 (1.53-1.91) | 1.55 (1.37-1.76) |
| Non-vascular mortality | 1.55 (1.41-1.69) | 1.54 (1.40-1.68) |
Authors' Conclusion
"CRP concentration has continuous associations with risk of coronary heart disease, ischaemic stroke, vascular mortality, and death from several cancers and lung disease...Associations with ischaemic vascular disease depend considerably on conventional risk factors and other markers of inflammation."
Source: PMC full text (PMC3162187)
Paradigm Relevance
How this study applies to different clinical perspectives:
Standard Medical
RelevantConventional clinical guidelines used by most doctors
Why it matters:
Foundational evidence for CRP as cardiovascular risk stratification tool in AHA/CDC guidelines
Research Consensus
RelevantCurrent scientific understanding, often ahead of guidelines
Why it matters:
Demonstrates continuous dose-response relationship; even "normal" CRP levels carry gradient of risk
Metabolic Optimization
RelevantProactive targets for optimal health, not just disease absence
Why it matters:
Supports monitoring CRP to assess cardiovascular protection from anti-inflammatory interventions
Study Details
- Type
- Meta-Analysis
- Methodology
- Individual participant meta-analysis. N = 160,309 participants from 54 prospective studies. 1.31 million person-years. 27,769 disease outcomes.
Evidence Quality
Grade A - Large meta-analysis. PMC3162187. Emerging Risk Factors Collaboration.
Related Biomarkers
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Original Source
DOI (Digital Object Identifier) is a permanent link to this publication. Unlike website URLs that can change, a DOI always resolves to the correct source.
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