ISRN GastroenterologyVolume 2013 (2013), Article ID 179024, 5 pageshttp://dx.doi.org/10.1155/2013/179024

Clinical Study

Fecal Calprotectin and Clinical Disease Activity in Pediatric Ulcerative Colitis

Kaija-Leena Kolho¹ and Dan Turner²

¹Children's Hospital, Helsinki University Central Hospital, P.O. Box 281, 00029 Helsinki, Finland²Pediatric Gastroenterology Unit, Shaare Zedek Medical Center, The Hebrew University of Jerusalem, P.O. Box 3235, Jerusalem 91031, Israel

Received 5 January 2013; Accepted 29 January 2013

Academic Editors: A. Amedei, A. W. Mangel, J. M. Pajares, L. Rodrigo, A. A. te Velde, and A. Weimann

Copyright © 2013 Kaija-Leena Kolho and Dan Turner. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Objective. To explore fecal calprotectin levels in pediatric ulcerative colitis (UC) in relation with the validated clinical activity index PUCAI. Methods. This study included all 37 children (median age 14 years) with UC who had calprotectin measured (PhiCal ELISA Test) by the time of PUCAI assessment at the Children's Hospital of Helsinki in a total of 62 visits. Calprotectin values <100 μg/g of stool were considered as normal. The best cut-off value of each measure to predict 3-month clinical outcome was derived by maximizing sensitivity and specificity. Results. In clinically active disease (PUCAI ≥ 10), calprotectin was elevated in 29/32 patients (91% sensitivity). When in clinical remission, 26% (8/30) of the children had normal calprotectin but 7 (23%) had an exceedingly high level (>1000 μg/g). The best cut-off value for calprotectin for predicting poor outcome was 800 μg/g (sensitivity 73%, specificity 72%; area under the ROC curve being 0.71 (95%CI 0.57–0.85)) and for the PUCAI best cut-off values >10 (sensitivity 62%, specificity 64%; area under the ROC curve 0.714 (95%CI 0.58–0.85)). Conclusion. The clinical relevance of somewhat elevated calprotectin during clinical remission in pediatric UC is not known and, until further evidence accumulates, does not indicate therapy escalation.

1. Introduction

Neutrophil-derived markers, such as fecal calprotectin or lactoferrin, have proven to correlate well with mucosal inflammation of ulcerative colitis (UC) at a rho range of 0.6–0.8 [1–4]. Fecal level of these markers reflects the mucosal influx of inflammatory cells in the gut. When the level of these markers is low, the presence of active inflammation in the colon is unlikely [3, 5–8]. The probability of 1-year remission in UC children with normal calprotectin may be as high as 75% [9]. On the other hand, in UC (and unlike in Crohn’s disease), clinical judgment of symptoms also correlates well with endoscopic appearance, at a range of rho 0.7–0.8 [10], and clinical assessment also predicts well clinical outcomes in both adult [11] and pediatric severe UC [12]. Recently, we showed that calprotectin levels rarely decline completely during therapy with glucocorticoids or TNF-α-antagonist agents suggesting ongoing inflammation in the majority [13, 14].

The PUCAI is the validated pediatric ulcerative colitis activity index showing good correlation with endoscopic disease activity [15–17]. The index is based on item scores reflecting the clinical situation within the last two days and may thus be used in the acute setting [15]. In acute severe colitis, PUCAI reflects therapeutic response better than calprotectin, the levels of which do not change as rapidly along improvement as the PUCAI scores [18, 19]. There are, however, limited data on the performance of fecal markers related to simple clinical assessment of pediatric UC in clinical practice. We aimed to explore calprotectin levels in relation to clinical disease activity assessed with the validated activity index PUCAI in pediatric UC.

2. Subjects and Methods

This retrospective study included all children with UC who had calprotectin measured and clinical data recorded for the assessment of the PUCAI at the Children’s Hospital of Helsinki from December 2005 to January 2012, most samples being from the three recent years. Diagnosis of UC was based on typical clinical presentation as well as upper and lower endoscopy [20].

Clinical disease activity was scored using the PUCAI consisted that of six clinical items scored from 0 to 85 points ( abdominal pain 0–10; rectal bleeding 0–30; stool consistency 0–10; number of stools per 24 hours (0–15); nocturnal stools (0–10), and activity level (0–10)). Cut-off scores for remission (PUCAI < 10 points), mild (10–34), moderate (35–64)) and severe (≥65) disease activity have been validated on three different cohorts with sensitivity and specificity of >90% [10, 15, 16].

Three-month clinical outcome was assessed using a physicians global assessment (PGA) from 0 (remission) to 3 (severe disease). Good outcome was defined as no need to change maintenance medication, successful weaning of steroids when applicable, and disease activity of no more than 1 according to PGA.

Children provided a stool sample within two days of the time of PUCAI assessment. The samples in children undergoing endoscopy were taken prior to bowel cleansing [21]. Fecal calprotectin was measured using the PhiCal ELISA Test (Nova Tec Immunodiagnostica, Dietzenbach, GmBH, Germany). Calprotectin value <100 μg/g of stool was considered as normal whereas values >1000 μg/g were considered as exceedingly high [9, 13, 14].

2.1. Ethics

The patients involved in this study participated in a study on pediatric inflammatory bowel disease approved by the Ethics Committee of the Helsinki University Central Hospital. The patients/their guardians signed an informed consent form when entering the study.

2.2. Statistical Analyses

Data are presented as means (±standard deviation) or medians (interquartile range) as appropriate for the distribution normality. Correlations between individual parameters were sought using Spearman correlation. To compare the predictive utility of the PUCAI as compared with calprotectin, area under the receiver operating characteristics (ROC) curve (±95% CI) was used. The best cut-off values of each measure to predict 3-month clinical outcome were derived by maximizing sensitivity and specificity. All analyses were performed using SPSS V16.

3. Results

A total of 62 visits were included from 37 different children with fecal calprotectin values available by the time of the assessment of the PUCAI ( 18 (49%) males, median age 14.3 years (IQR 13.0–15.8, 33 (89%) with extensive disease and the others with left-sided disease; Table 1). Fourteen (38%) children were at disease onset and the others with median disease duration of 1.5 (IQR 0.7–3.0) years. Sixteen of the visits were during clinical remission (judged by PGA), 16 (26%) during mild disease activity, 12 (19%) during moderate disease activity, and 18 (29%) during severe disease activity. Median number of samples per patient was 1 (IQR: 1-2, range 1–5).

Table 1: Background data of the 37 pediatric patients with ulcerative colitis.

Age (years)
14 (median, range 4.5–17)

Gender
Male

Disease duration (years)
1.5 (median, range 0–5)

Disease extension
Pancolitis

Left-sided colitis

Medication
5-ASA

5-ASA and/or azathioprine

Infliximab

Glucocorticoids

None

In the total sample set, the correlation of calprotectin and the PUCAI was good (, , ). The correlation between PUCAI and calprotectin among the 14 children at diagnosis (all with clinically active disease) was higher (, ; Figure 1).

Figure 1: The Spearman correlation of the pediatric ulcerative activity index (PUCAI) and fecal calprotectin in pediatric patients with ulcerative colitis undergoing diagnostic endoscopy.

The best calprotectin cutoff to identify the 30/62 visits in clinical remission was <800 μg/g (sensitivity 73% and specificity 72%; area under the ROC curve of 0.76 (95% CI 0.63–0.88); Figure 2). The values were not different when considering only one observation per patient to avoid possible repeated measures bias (the first visit per patient; ) with an area under the ROC curve of 0.71 (0.53–0.89) and similar cut-off value.

Figure 2: The relation of the pediatric ulcerative activity index (PUCAI) and fecal calprotectin in pediatric patients with ulcerative colitis. The arrow shows the best fecal calprotectin cutoff (by maximizing sensitivity and specificity) to identify patients in clinical remission according the PUCAI.

Calprotectin was exceedingly high in all 13 samples collected during a severe attack (i.e., PUCAI ≥ 65) (median 2179 μg/g range 1190–9504 (IQR 1682–5310)). All those with PUCAI scores reflecting moderate-severe disease (40–85) had elevated calprotectin values. In mild-to-moderate disease (PUCAI 10–64, ) calprotectin was elevated in all except two patients (median 829 μg/g, range 7–7287 (IQR 416–1599)). Calprotectin was completely normal in 8 of 30 assessments performed during clinical remission (26%). In seven (23%), calprotectin level was exceedingly high (>1000 μg/g). In four of these, the assessments were done on the day of maintenance infusion of infliximab, in two cases steroids had been tapered within one-to-two weeks earlier and, one was on only 5-ASA. Three of these seven (two on infliximab, one in whom steroids were tapered off) remained in sustained-steroid-free clinical remission 3-months after the sample date, despite the very high calprotectin level.

The PUCAI performed just as well as calprotectin in predicting 3-month clinical outcome (poor versus good outcome), area under the ROC curve being 0.71 (95% CI 0.57–0.85) versus 0.714 (95% CI 0.58–0.85), respectively. The best cutoff for calprotectin for predicting poor outcome was 800 μg/g (sensitivity 73%, specificity 72%) and for the PUCAI best cut-off >10 (sensitivity 62%, specificity 64%).

Of the 30 assessments in clinical remission, 20 (66%) remained in steroid-free clinical remission for the forthcoming three months. All 10 assessments of both clinical remission or mild clinical disease (i.e., PUCAI < 35), and normal calprotectin <100, remained in steroid-free remission in 3 months. The calprotectin values and outcome of the patients in remission or having mild-to-moderate disease activity according to the PUCAI during the following three months ara shown in Table 2.

Table 2: Three-month outcome of pediatric patients with mild-to-moderate ulcerative colitis according to the clinical disease activity index PUCAI and fecal calprotectin at baseline. The outcome was determined according to physicians global assessment.

No.
Disease activity according to the PUCAI (total score)
Calprotectin µg/g of stool
Outcome within 3 months

1
Remission (<10)
14
Remission

2

14
Remission

3

16
Remission*

4

30
Remission

5

45
Remission

6

69
Remission

7

69
Remission

8

90
Remission

9

131
Remission

10

155
Flare (within two months)

11

189
Flare (when tapering corticoid)

12

333
Remission*

13

345
Flare

14

372
Remission

15

411
Remission

16

441
Remission

17

521
Remission

18

532
Flare (when tapering corticoid)

19

581
Remission

20

628
Remission

21

663
Flare (within a month)

22

796
Remission

23

902
Flare*

24

1052
Remission*

25

1173
Flare*

26

1233
Remission

27

1976
Flare (when tapering corticoid)

28

2295
Flare*

29

4518
Flare (within two weeks)

30

9625
Remission

31
Mild-to-moderate disease (10–64)
7
Remission

32

55
Remission

33

87
Remission

34

327
Flare (when tapering corticoid)

35

416
Remission

36

611
Lost from followup

37

653
Flare

38

751
Flare

39

766
Flare

40

829
Flare (ongoing)

41

856
Remission

42
Mild-to-moderate disease (10–34)
1067
Flare

43
1110
Remission

44

1127
Remission

45

1599
Flare (when tapering corticoid)

46

1667
Flare (within two weeks)

47

1911
Flare (ongoing)

48

2604
Flare

49

7287
Flare (when tapering corticoid)

 *Sample taken on the day of infliximab administration.

4. Discussion

The use of calprotectin as a surrogate marker for intestinal inflammation is emerging. However, the data on calprotectin related to clinical disease activity in children with UC are sparse. We show good correlation between the PUCAI and fecal calprotectin. In the clinically severe disease (PUCAI > 65), calprotectin was exceedingly high (>1000 μg/g) in all cases and did not bring any additional information to clinical assessment. It is worthwhile noting that the PUCAI is much more responsive to a rapid change than calprotectin in severe disease; that is, the PUCAI shows a sharp decrease within only a few days of starting effective medication [18] reflecting the well-known notion that mucosal healing lags after clinical remission. On the other hand, some of those in clinical remission according to PUCAI still had elevated calprotectin levels, but in the majority the levels were only moderately elevated. Our data suggests, however, that closer monitoring should be offered to the patients in clinical remission but with exceedingly high calprotectin level since many of them may show deterioration within the forthcoming weeks. It may also suggest that the current therapies are unable to induce complete attenuation of mucosal inflammation in a large proportion of the pediatric patients. Recently, we showed that only one-third of 41 children with UC had normal calprotectin levels while 13% had exceedingly high levels despite all being in longstanding clinical remission defined using the PGA (i.e., 80% with at least 6-month duration followup) [9].

Although mucosal healing has been shown in adults, to predict favourable clinical outcome in UC [11, 22, 23] is yet to be proven that this is superior to clinical assessment of remission. Indeed, in the combined ACT cohorts (466 adults with UC treated with either infliximab or placebo) endoscopic healing after 8 weeks of therapy predicted 1-year colectomy overall but not among the subset of patients with clinical remission [22]. Moreover, clinical judgment of response to steroid treatment in acute severe UC has been shown to predict long-term, clinically important, outcomes, both in adults [11] and in children [12, 24], irrespective of endoscopic healing. Similarly here, we could not find any major difference between clinical (PUCAI) and endoscopic (calprotectin) assessment of disease activity with regards to predicting 3-month steroid free remission although the sensitivity and specificity of calprotectin were somewhat higher than the PUCAI. This should be interpreted with caution given the small sample size, the retrospective design, and the relatively short follow-up duration.

Notably, it remains an unanswered question whether immunosuppressive therapy should be escalated during clinical remission solely based on the presence of elevated calprotectin. The question is not merely if calprotectin levels during remission are independently predictive, but if the predictive power is large enough to justify the associated adverse events. In other words, how many children in remission will be required to step up from 5-ASA to thiopurines or even anti-TNF in order to obtain one favourable outcome (i.e., number needed to treat). Currently, this cannot be recommended until evidence is available to show that this aggressive approach indeed leads to better outcomes.

Furthermore, the target level of fecal surrogate markers to define acceptable therapeutic response is not known. In a previous study, 89% of 25 young patients with Crohn’s disease in clinical remission remained in remission for nine months if their fecal calprotectin level was lower than 400 μg/g [25]. Here, the best cutoff for calprotectin for predicting 3-month poor outcome was as high as >800 μg/g and for the PUCAI scores ≥10 (which is the PUCAI definition for active disease) with no major difference in sensitivity and specificity.

In conclusion, in pediatric UC, clinical disease activity assessed with the validated index PUCAI shows good correlation with the levels of calprotectin. At present, the clinical relevance of elevated calprotectin level when in sustained clinical remission is not known and, until known otherwise, does not indicate escalating therapy based on this isolated finding only. However, it may indicate closer monitoring, especially in those with values >800 μg/g.

Acknowledgments

The authors thank Ms. Anne Nikkonen for her excellent assistance in gathering the patient data. The study was supported by the Finnish Pediatric Research Foundation and the Helsinki University Central Hospital Research Fund. D. Turner declares receiving royalties from the Hospital for Sick Children. There is no conflict of financial interests.

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