Phical test performance


A very useful test for the distinction between organic and functional gastro-intestinal disorders. Consider it when you suspect inflammatory bowel disease.

 

Introduction

PhiCalTest, or the assessment of faecal calprotectin, is a widely used method for detection of organic disease of the gastrointestinal tract. It introduces a new principle for objective determination of the inflammation in IBD (Inflammatory Bowel Disease), i.e. ulcerative colitis (UC) and Crohn´s disease (CD). Traditionally, the disease activity has been evaluated by clinical indices like the Crohn´s disease activity index (CDAI) or by the Harvey-Bradshaw "simple index" (SI). However, the use of more sophisticated methods, for instance the use of isotope labelled white cells, has shown that such indices tend to be inaccurate.   The quantitation of the neutrophil marker protein calprotectin in simple extracts of small (0.1g) stool samples is now available as an attractive alternative to the previous methods. This faecal test is non-invasive, objective and can be used repeatedly for the early detection of IBD. In children with chronic abdominal symptoms where IBD may be suspected, most physicians will hesitate to use isotope labelled leukocytes or endoscopy under general anaesthesia as diagnostic procedures.   The PhiCal Test has such a high negative predictive value that active IBD can be ruled out and invasive procedures avoided. The PhiCal Test is performed by an ELISA kit. 

Sampling

Traditionally, biological markers in stools have been assessed in 24-hour stool collections, but it is rather inconvenient for out-patients to collect and send such materials to the laboratory. Despite some spot variation in stools, one teaspoon full is usually sufficient for analysis. Furthermore, this protein is so stable that stools can be sent by ordinary mail. In fact, samples can be stored at room temperature for up to seven days. The stability of calprotectin is caused by its binding of calcium.  

ELISA

Calprotectin is assessed by a simple ELISA, using antibodies for capture and affinity purified, enzyme (alkaline phosphatase) labelled antibodies for development. The ELISA has between and within assay variations of 14.8% and 1.9% respectively between healthy controls and patiens with IBD.   The new faecal extraction is much more efficient so that both in healthy controls and patients higher values are found. For this reason the cut off value is 50 mg/kg.    

The PhiCal Test versus isotope labelled leukocytes

 

Excretion of isotope labelled leukocytes has been regarded as the "gold standard" of disease activity in IBD. However, this requires three days of hospitalisation for the collection of stools and the determination of the isotope. Furthermore, it also exposes the patient to a potentially hazardous radiation, making this method unsuited for repeated use in children and fertile women.   We have compared this method with the PhiCal Test in nine healthy controls, 10 patients with UC and 19 patients with CD. Although these were all out patients with very low disease activity, a highly significant correlation was found between the three day excretion of 111-indium labelled granulocytes and that of faecal calprotectin (r=0.87, p<0.0001) (figure 2).                              

In a similar study published lately, this close relationship was confirmed. This suggests that the PhiCal Test can replace the use of the isotope method. Its simplicity and low cost makes it an attractive alternative allowing follow-up by repeated testing.    

Calprotectin in patients with Ulcerative Colitis

 

Data from a study of 62 outpatients referred for colonoscopy are shown in Figure 3. The disease activity was determined by endoscopy and histology using accepted criteria. There was a highly significant increased concentration of faecal calprotectin in the group of patients with active disease as determined by histological criteria when compared to patients with no/low disease activity and those with normal colonoscopy. Furthermore, calprotectin levels were better correlated to the degree of inflammation than the extension of the disease.    

PhiCal Test in Crohn´s disease and irritable bowel syndrome It is often difficult to differentiate between patients with IBS and CD by clinical parameters. This results in many unnecessary colonoscopic examinations adding an substantial economical burden on the society.   Calprotectin was determined in 220 patients referred for colonoscopy at King´s College, London. The patients were evaluated by the ROME criteria for possible IBS. The results showed that patients with CD had significantly higher faecal calprotectin levels than those with IBS (p<0.0001) (Fig 4).         A ROC plot analysis revealed that a cut-off level of 150 mg/kg (corresponding to 30 mg/l in the old method) distinguished between CD and IBS with 100% sensitivity and 97% specificity (fig 5).   Among 30 patients with other disorders, elevated calprotectin concentrations were found among 2/2 colorectal cancer, 2/3 adenomas and 6/6 with microscopic colitis. Similar results were reported in a study at Mayo Clinic USA.        

Conclusion

Calprotectin is a non-specific marker of gastrointestinal disease of both inflammatory and neoplastic character. The high sensitivity and negative predictive values can be useful to select patients for colonoscopy. Calprotectin is also an interesting marker of disease in various organs since elevated concentrations are found in plasma/serum, cerebrospinal fluid, synovial fluid or urine during infections or inflammatory conditions and has been used for such purposes in clinical research.  

References

1. Saverumuttu SH. Clinical remission in Crohn´s disease - assessment using faecal 111In granulocyte excretion. Digestion 1986; 33: 74-79.   2. Fagerhol MK, Nomenclature for proteins: is calprotectin a proper name for the elusive myelomonocytic protein ? J Clin Pathol 1996; 49:M74-79   3. Røseth AG, Fagerhol MK, Aadland E, Schjønsby H. Assessment of the neutrophil dominating protein calprotectin in feces. Scand J Gastroentrol 1992; 27:793-98.   4. Røseth AG, Schmidt PN, Fagerhol MK. Correlation between faecal excretion of 111-Indium labelled granulocytes and calprotectin, a granulocyte marker protein in patients with inflammatory bowel disease. Scand J Gastroentrol 1999; 34:50-54.   5. Johne B, Kronborg O, Tøn H, Kristinsson J, Fuglerud P. A new fecal calprotectin test for colorectal neoplasia. Clinical results and comparison with previous method. Scand J Gastroenterol 2001; 36:291-96.   6. Røseth AG, Aadland E, Jahnsen J, Raknerud N. Assessment of disease activity in ulcerative colitis by faecal calprotectin, a novel granulocyte marker protein. Digestion 1997; 58:176-80   7. Tibble J, Teahon K, Tjodleifsson B, Roseth A, Sigthorsson G, Bridger S, Foster R,Sherwood R, Fagerhol M, Bjarnason I. A simple method for assessing intestinal inflammation in Crohn´s disease. Gut 2000; 47:506-13.   8. Limburg PJ, Ahlquist DA, Sandborn WJ, Mahoney DW, Devens ME, Harrington JJ, Zinsmeister AR. Fecal calprotectin levels predict colorectal inflammation among patients with chronic diarrhoea referred for colonoscopy. Am J Gastroenterol 2000; 95:2831-37.   9. Tibble J, Sigthorsson G, Bridger S, Fagerhol M, Bjarnason I. Surrogate markers of intestinal inflammation are predictive of relapse in patients with inflammatory bowel disease. Gastroenterology 2000; 119:15-22.   10. Røseth AG, Kristinsson J, Fagerhol MK, Schjønsby H, Aadland E, Nygaard K, Roald B. Faecal calprotectin: A novel test for the diagnosis of colorectal cancer ? Scand J Gastroentrol 1993; 28:1073-76.   11. Kristinsson J, Røseth A, Fagerhol MK, Aadland E, Schjønsby H, Børmer OP, Raknerud N, Nygaard K. Fecal calprotectin concentration in patients with colorectal carcinoma. Dis Colon Rectum 1998; 41:316-21.  


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General Information

Fecal calprotectin in differential diagnosis of irritable bowel syndrome

Li XG, Lv YM, Gu F, Yang XL., Department of Gastroenterology, Peking University Third May 9, 2015

PhiCal Test FDA approved

The PhiCal Test has now been approved by the FDA for clinical use in the USA October 1, 2014

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