Key inflammation markers compared
| Marker | Normal | Rises within | Best for |
|---|---|---|---|
| CRP (C-reactive protein) | <10 mg/L | 4–8 hours | Acute infection, monitoring treatment response |
| ESR (erythrocyte sedimentation rate) | Men: <15; Women: <20 mm/hr | 24–48 hours | Chronic inflammation, temporal arteritis, myeloma |
| High-sensitivity CRP (hsCRP) | <1.0 mg/L (cardiovascular risk) | 4–8 hours | Cardiovascular risk assessment |
| Procalcitonin (PCT) | <0.25 ng/mL | 2–6 hours | Bacterial infection (vs viral); sepsis severity |
| Ferritin | Men: 24–336 ng/mL; Women: 11–307 ng/mL | Hours to days | Iron stores; extreme rise in haemophagocytic syndrome, Still's disease |
| Fibrinogen | 200–400 mg/dL | Hours | Acute phase reactant; clotting; cardiovascular risk |
CRP vs ESR: which is better?
Different tools for different questions
CRP rises and falls quickly: it's the best marker for monitoring acute infection and treatment response. If CRP falls with antibiotics, the infection is responding. ESR rises more slowly (peaks at 24–48 hours) and falls slowly, it's better for monitoring chronic conditions like rheumatoid arthritis, temporal arteritis, and multiple myeloma. A very high ESR (>100 mm/hr) is characteristic of temporal arteritis, myeloma, severe bacterial infection, and nephrotic syndrome.
What does a very high CRP mean?
| CRP level | Likely cause |
|---|---|
| <10 mg/L | Normal: no significant inflammation |
| 10–50 mg/L | Mild inflammation: viral infection, minor bacterial infection, RA flare |
| 50–200 mg/L | Significant inflammation: active bacterial infection, serious flare |
| >200 mg/L | Severe bacterial infection, sepsis, severe burn, major trauma |
Procalcitonin: the bacterial infection marker
Procalcitonin (PCT) is produced by the body specifically in response to bacterial infection: not viral infections. This makes it useful for distinguishing bacterial pneumonia (high PCT) from viral pneumonia (low/normal PCT), and for deciding whether antibiotics are needed. Rising PCT indicates worsening infection; falling PCT with treatment indicates improvement. PCT is also used to guide antibiotic duration, antibiotics can often be safely stopped when PCT falls below 0.25 ng/mL.
Questions to ask your doctor
- Is my CRP raised: does this suggest active infection or inflammation?
- Is my ESR elevated: could this be temporal arteritis or myeloma?
- Has my procalcitonin been checked to guide antibiotic use?
- Is my inflammation responding to treatment (CRP trending down)?
High-sensitivity CRP and cardiovascular risk
Standard CRP testing detects acute inflammation and infection. High-sensitivity CRP (hsCRP) measures the same protein at much lower concentrations and serves a different purpose: estimating the long-term risk of heart attack and stroke in people with no active illness.
A landmark study of 27,939 women in the Women's Health Study followed participants for eight years and found that hsCRP was a stronger predictor of future cardiovascular events than LDL cholesterol.1 Women with hsCRP above 3.0 mg/L had twice the risk of a first cardiovascular event compared with those in the lowest quartile, even when LDL was within the normal range. This evidence helped establish hsCRP as a recognised cardiovascular risk marker alongside lipids in clinical decision-making.
Interpreting hsCRP for cardiovascular risk: below 1.0 mg/L is low risk; 1.0–3.0 mg/L is intermediate; above 3.0 mg/L is high risk. The test is only meaningful when there is no concurrent infection or inflammatory condition, both of which raise CRP independently of vascular risk. A single high result during an illness tells you about the infection, not your heart.
How quickly do inflammation markers respond to treatment?
CRP falls rapidly once the trigger is removed, making it useful for real-time monitoring. In bacterial pneumonia responding to antibiotics, CRP should fall by roughly 50% within three to four days. A CRP that does not fall – or rises – after starting treatment is a warning sign of treatment failure, a resistant organism, or an undrained focus of infection (abscess, empyema). ESR falls much more slowly; it can take weeks to normalise even after complete recovery, making it unsuitable for monitoring acute treatment response but useful for tracking chronic inflammatory conditions over months.
In polymyalgia rheumatica and giant cell arteritis, both CRP and ESR typically fall dramatically within 48–72 hours of starting prednisolone – so promptly that a failure to respond should prompt a reassessment of the diagnosis. During steroid dose reduction, rising CRP or ESR precedes clinical relapse and provides the earliest laboratory signal to adjust therapy.
References
Sources cited on this page. PubMed links open the original abstract.
- Ridker PM, Hennekens CH, Buring JE, Rifai N. C-reactive protein and other markers of inflammation in the prediction of cardiovascular disease in women. N Engl J Med. 2000;342(12):836–843. PMID 10733371 · doi:10.1056/NEJM200003233421202
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