C-Reactive Protein (CRP) Detection of Inflammation
C-Reactive Protein (CRP) can detect inflammation for approximately 7-10 days after the inflammatory stimulus has resolved, with its levels peaking at 36-50 hours after the initial inflammatory trigger and gradually declining thereafter.
CRP Production Timeline
CRP is an acute-phase protein synthesized exclusively by the liver in response to inflammatory cytokines, particularly interleukin-6. The timeline of CRP response follows a predictable pattern:
- Initial response: CRP secretion begins 4-6 hours after an inflammatory stimulus 1
- Doubling rate: CRP concentration doubles approximately every 8 hours 1, 2
- Peak levels: CRP reaches maximum concentration at 36-50 hours (approximately 2 days) after the initial inflammatory trigger 1, 2, 3
- Decline phase: CRP levels decrease rapidly with the resolution of inflammation 3
Factors Affecting CRP Detection
The detection of inflammation via CRP is influenced by several factors:
- Synthesis rate: The sole determinant of CRP plasma levels is its synthesis rate, which is proportional to the intensity of the inflammatory insult 1
- Half-life: CRP has a relatively short half-life compared to other inflammatory markers
- Sensitivity and specificity: CRP has a sensitivity of 68-92% and a specificity of 40-67% as a marker of bacterial infection 1
Clinical Applications
CRP is widely used in clinical practice for detecting and monitoring inflammation:
- Surgical infections: CRP and procalcitonin (PCT) help clinicians diagnose surgical infections 1, 2
- Appendicitis: CRP has a reported sensitivity of 93-96% in diagnosing appendicitis 1, 2
- Post-surgical monitoring: CRP levels peak on day 2 following soft-tissue coverage and fall thereafter; peaks after day 4 indicate infective complications 4
- Bacterial infection: In ICU patients with fever but no clear focus of infection, measuring CRP can help rule out bacterial infection 1
Interpretation of Serial CRP Measurements
Serial CRP measurements provide more valuable information than single measurements:
- Treatment response: CRP levels that fail to decrease or continue to rise after 48 hours of antibiotic therapy suggest treatment failure 3
- Infection exclusion: Two CRP measurements 24 hours apart that are <10 mg/L are useful in excluding sepsis in infants 3, 5
- Persistent elevation: Persistently elevated CRP following surgery is associated with infection and nonunion 4
Pitfalls and Limitations
Important caveats when using CRP to detect inflammation:
- Non-specificity: CRP is a non-specific marker of inflammation and cannot differentiate between bacterial infections and non-infectious causes of inflammation 1
- Confounding factors: CRP concentrations can be affected by neutropenia, immunodeficiency, and the use of nonsteroidal anti-inflammatory drugs 1, 2
- Single measurement limitations: A single CRP level is neither sensitive nor specific enough to identify all patients with serious bacterial infection 3
- Disease-specific variations: Some conditions like ulcerative colitis have only a modest to absent CRP response despite active inflammation 6
In conclusion, while CRP is a valuable marker for detecting inflammation, its interpretation must consider the timeline of production, peak, and decline, as well as the clinical context and potential confounding factors. Serial measurements provide more reliable information than single measurements for monitoring the course of inflammation.