Laboratory Tests Indicating Inflammation
The core inflammatory laboratory panel consists of C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), complete blood count with differential, and a complete metabolic panel, with CRP being the preferred acute-phase marker due to superior standardization and faster response to disease activity. 1
Tier 1 Screening Tests
Initial inflammatory workup should include:
- Complete blood count (CBC) with manual differential to identify lymphopenia, neutrophilia, thrombocytopenia, leukocytosis, or anemia 2, 1
- C-reactive protein (CRP) is the preferred acute-phase reactant with acceptable precision down to 0.3 mg/L and better correlation with acute disease activity than ESR 1
- Erythrocyte sedimentation rate (ESR) with cutoffs >20 mm/h in men and >30 mm/h in women indicating elevation 1
- Complete metabolic panel including sodium, potassium, glucose, creatinine, liver enzymes (AST, ALT), and albumin to identify hyponatremia, hypoalbuminemia, azotemia, and hepatic involvement 2, 1
Extended Inflammatory Markers
When initial screening suggests inflammation, consider:
- Ferritin typically ranges 500-2,000 ng/dL in inflammatory conditions, though levels <30 μg/L indicate iron deficiency without inflammation 1
- D-dimer is frequently elevated in systemic inflammatory states 1
- Lactate dehydrogenase (LDH) serves as a marker of tissue damage and inflammation 1
- Procalcitonin can be profoundly elevated in inflammatory conditions even without bacterial infection 1
- Fibrinogen is an acute-phase reactant with acceptable precision, though less favored than CRP for routine use 1
- Serum albumin and pre-albumin assess nutritional status and degree of inflammation, particularly in chronic inflammatory conditions 1, 3
Organ-Specific Inflammatory Testing
For cardiac involvement:
- Troponin T and BNP/NT-proBNP are essential when cardiac involvement is suspected, though BNP is an acute-phase reactant and may be elevated in inflammatory conditions without cardiac disease 2, 1
For intestinal inflammation:
- Fecal calprotectin is the most sensitive non-invasive marker for intestinal inflammation 2, 3
- Fecal lactoferrin can also assess intestinal inflammation, though to a lesser degree than calprotectin 2
- Stool cultures and C. difficile toxin testing should be performed to exclude infectious causes 2, 3
Critical Interpretation Caveats
ESR has multiple confounders:
- Anemia, azotemia, elevated immunoglobulins, rheumatoid factor, female sex, and advancing age all increase ESR independent of inflammatory activity 1
- ESR has a longer half-life than CRP, making it more useful for monitoring chronic inflammatory conditions 4
CRP limitations:
- Normal CRP levels do not exclude active inflammation, particularly in ulcerative colitis where some patients have active disease without CRP elevation 1, 3
- CRP is more useful in acute inflammatory conditions and responds more quickly to therapy than ESR 4, 5
CRP/ESR discordance occurs in approximately 12% of patients:
- High CRP/low ESR suggests acute infections (urinary tract, gastrointestinal, pulmonary, bloodstream) or acute thrombotic events 6
- High ESR/low CRP suggests connective tissue diseases (systemic lupus erythematosus), bone/joint infections, or ischemic stroke 6
Monitoring Strategy
For persistent or unexplained elevation:
- Repeat ESR and CRP in 2-4 weeks to determine if elevation is persistent or transitory 1
During active inflammatory disease:
- Monitor ESR every 1-3 months until remission is achieved, then every 3-6 months once low disease activity is maintained 1