Laboratory Tests for Crohn's Disease and Ulcerative Colitis
No single laboratory test can diagnose Crohn's disease or ulcerative colitis—diagnosis requires a combination of clinical, biochemical, endoscopic, imaging, and histological investigations. 1
Essential Laboratory Tests at Initial Evaluation
Blood Tests
- Complete blood count (CBC) to detect anemia (hemoglobin <13 g/dL for men, <12 g/dL for women), which affects quality of life and occurs frequently in IBD 1, 2
- C-reactive protein (CRP) or erythrocyte sedimentation rate (ESR) as inflammatory markers, though approximately 20% of patients with active Crohn's disease may have normal CRP levels 2, 3
- Serum albumin to assess nutritional status and disease severity 4
- Liver function tests as part of baseline assessment 2
- Renal function tests for baseline evaluation 4
- Vitamin B12 levels, particularly important in Crohn's disease with ileal involvement 4
Iron Status Assessment
The interpretation of iron studies depends critically on inflammation status:
- Without active inflammation: Serum ferritin <30 μg/L indicates iron deficiency 1
- With active inflammation: Serum ferritin up to 100 μg/L may still indicate iron deficiency 1
- Anemia of chronic disease: Serum ferritin >100 μg/L with transferrin saturation <20% in the presence of inflammation 1, 2
- Mixed picture: Ferritin 30-100 μg/L suggests combined iron deficiency and anemia of chronic disease 1
Stool Tests
- Fecal calprotectin is highly accurate with 93% sensitivity and 96% specificity for diagnosing IBD in adults, with optimal threshold of 100 μg/g 4, 2
- Stool cultures and C. difficile toxin testing are mandatory to exclude infectious causes before confirming IBD diagnosis—loose stools for more than 6 weeks usually discriminate IBD from infectious diarrhea 1, 4, 2
- Ova, cysts, and parasites if travel history or other risk factors are present 1
Serological Markers: Limited Utility
Serological markers have limited accuracy and should not be used as primary diagnostic tools:
- pANCA and ASCA antibodies may support diagnosis but are ineffective at differentiating colonic Crohn's disease from ulcerative colitis 1, 2
- Antiglycan and antimicrobial antibodies (anti-OmpC, CBir1) provide minimal additional diagnostic value 1, 2
- Genetic testing for IBD-associated SNPs is not recommended for diagnosis despite identification of over 250 variants 1, 2
Critical Diagnostic Pitfalls to Avoid
- Never rely on laboratory tests alone—they must be interpreted alongside endoscopic findings, imaging, and histology 2, 5
- Normal CRP does not exclude active disease—up to 20% of patients with active Crohn's disease have normal CRP 2
- Always exclude infectious causes first before making an IBD diagnosis to avoid inappropriate treatment 1, 2
- Interpret iron studies in the context of inflammation—failure to do so leads to missed iron deficiency diagnosis 1, 2
- Do not use serological markers alone to differentiate between Crohn's disease and ulcerative colitis 1, 2
The Diagnostic Algorithm
Laboratory tests serve as supportive evidence within a comprehensive diagnostic pathway:
- Initial blood work (CBC, CRP/ESR, albumin, liver/renal function, iron studies, B12) establishes baseline and identifies complications 4, 2
- Stool testing excludes infectious causes and provides fecal calprotectin for IBD likelihood 1, 2
- Ileocolonoscopy with biopsies from inflamed and uninflamed segments remains the gold standard for diagnosis 1, 4
- Cross-sectional imaging (MR enterography preferred) evaluates extent and complications beyond endoscopic reach 4, 3
- Histology confirms diagnosis, though it is often "compatible with" rather than "diagnostic of" IBD 5
Laboratory tests cannot establish or rule out IBD independently—they function as one component of a multimodal diagnostic approach that prioritizes endoscopic visualization and histological confirmation. 1, 2, 5