key: cord-1021845-avle90iv
authors: Ishida, Natsuki; Higuchi, Tomohiro; Miyazu, Takahiro; Tamura, Satoshi; Tani, Shinya; Yamade, Mihoko; Iwaizumi, Moriya; Hamaya, Yasushi; Osawa, Satoshi; Furuta, Takahisa; Sugimoto, Ken
title: C-reactive protein is superior to fecal biomarkers for evaluating colon-wide active inflammation in ulcerative colitis
date: 2021-06-14
journal: Sci Rep
DOI: 10.1038/s41598-021-90558-z
sha: c6a14512d7d8a1540ebac92d49b73a0ec6ed1ab3
doc_id: 1021845
cord_uid: avle90iv

We evaluated the association between endoscopic scores of colonic inflammation and fecal calprotectin (FC), fecal immunochemical occult blood test (FIT), and C-reactive protein (CRP) in patients with ulcerative colitis (UC). Endoscopic scores reflecting the most severe lesion [maximum Mayo Endoscopic Subscore (M-MES) and Ulcerative Colitis Endoscopic Index of Severity (UCEIS)] and those reflecting the inflammation of the entire colon [sum of MES (S-MES) and Ulcerative Colitis Colonoscopic Index of Severity (UCCIS)] were evaluated. FC, FIT, and CRP were measured, and their association with the four endoscopic scores was evaluated. Endoscopic scores of 78 complete colonoscopies (66 UC patients) were evaluated using the three biomarkers. FC and CRP tended to correlate more strongly with S-MES and UCCIS than with M-MES and UCEIS. In the M-MES 0, 1 group, compared to CRP, FC and FIT showed stronger correlations with S-MES and UCCIS. Conversely, in the M-MES 2, 3 group, only CRP was significantly correlated with each descriptor. CRP more strongly reflects colon-wide mucosal inflammation than FC and allows reliable assessment of inflammation throughout the colon in active UC.

| (2021) 11:12431 | https://doi.org/10.1038/s41598-021-90558-z www.nature.com/scientificreports/ used in clinical practice because of the complexity of scoring. However, scoring is performed by applying the sum of descriptors to the calculation formula, allowing the objective evaluation of the inflammatory state of the entire colon, which is highly useful in clinical research. Few reports have shown an association between biomarkers and endoscopic scores for evaluating the entire colon, such as the S-MES and UCCIS. In this study, the usefulness of FC, FIT, and CRP as biomarkers for UC was examined using the maximum MES (M-MES) and UCEIS, which show the most severe UC lesions, and the S-MES and UCCIS, which show the degree of inflammation throughout the entire colon. If biomarkers can be confirmed to correlate with colon-wide inflammation in patients with UC, the information may enable the assessment of active disease without the need for colonoscopy, which is associated with an increased risk of perforation in active disease.

Patient population. Patients with UC who were treated at the Hamamatsu University School of Medicine between February 2019 and November 2020 were enrolled in this study. The diagnosis of UC was performed according to established diagnostic criteria, based on clinical, endoscopic, and histological criteria. Patients with IBD who were not diagnosed with UC but were diagnosed with conditions such as indeterminate colitis or unclassified IBD were excluded. UC patients with a history of colorectal surgery were excluded because S-MES and UCCIS require the observation of the total colon. In addition, patients with acute infectious enterocolitis or regular intake of aspirin and/or other nonsteroidal anti-inflammatory drugs were excluded. Seventy-eight patients with UC who met the above criteria were registered.

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. Informed consent was obtained from all individual participants included in the study.

This was a prospective cross-sectional study. The purpose of this study was to assess the usefulness of FC, FIT, and CRP as biomarkers for UC by correlating these biomarkers with four endoscopic scores. The primary endpoint of this study was the identification of markers that show a significant correlation with each endoscopic score. The secondary endpoint was the correlation between the three biomarkers and each endoscopic score, divided into two groups (M-MES of 0, 1 and M-MES of 2, 3).

Endoscopic assessment. Patients with UC underwent bowel preparation consisting of the ingestion of a polyethylene glycol-based electrolyte solution prior to colonoscopy. UC endoscopic scores were assessed using the M-MES, S-MES, UCIES, and UCCIS. M-MES was graded as follows: 0, normal or inactive disease; 1, mild disease with erythema, decreased vascular pattern, and mild friability; 2, moderate disease with marked erythema, absence of vascular patterns, friability, and erosions; and 3, severe disease with spontaneous bleeding and ulceration in the lesion with the most severe inflammation 21 . S-MES was calculated by totaling the MES in five colonic segments (ascending, transverse, descending, sigmoid, and rectum), as described above 23 .

The UCEIS score was calculated as the sum of three descriptors: vascular pattern (score 0-2), erosions and ulcers (score 0-3), and bleeding (score 0-3) 22 . The UCCIS score was assessed using the following descriptors in the fives segments, as in the S-MES: vascular pattern (score 0-2), granularity (score 0-2), erosions and ulcers (score 0-4), and bleeding/friability (score 0-2). These descriptor scores were then applied to the following formula: UCCIS = 3.1 × Sum (vascular pattern across five segments) + 3.6 × Sum (granularity across five segments) + 3.5 × Sum (ulceration across five segments) + 2.5 × Sum (bleeding/friability across five segments) 25, 26 . M-MES 0 or 1 was defined as indicative of mucosal healing.

Clinical activity assessment. Clinical disease activity was evaluated using Lichtiger's clinical activity index (CAI) 27 . CAI was evaluated using the following criteria: the presence of diarrhea (number of stools per day), nocturnal diarrhea, visible blood in stool (percentage of movements), fecal incontinence, abdominal pain or cramping, general well-being, abdominal tenderness, and a need for anti-diarrheal drugs 27 . Clinical remission was defined as a CAI ≤ 3.

Fecal samples were prepared on or before the day of colonoscopic preparation. Samples were collected in plastic tubes for FC measurement and shipped at − 20 °C, as recommended by the laboratory (SRL, Inc., Tokyo, Japan). FC was measured with a Phadia 250 immunoanalyzer (HITACHI Ltd., Tokyo, Japan) using the Elia A Calprotectin 2 reagent (Phadia GmbH, Freiburg, Germany), via fluorescence enzyme immunoassay principles.

FIT measurement. To prevent bleeding due to the endoscopic examination, fecal samples were obtained on or before the day of colonoscopic preparation. A collection kit (Eiken Chemical, Tokyo, Japan) was used to collect stool specimens. Submitted samples were immediately processed and examined using the OC Sensor io (Eiken Chemical). CRP measurement. According to routine clinical practice, serum CRP level was measured to assess the UC activity status of patients. Blood samples were collected within a few days of endoscopic examination. This measurement was performed at the Laboratory Test Department of Hamamatsu University School of Medicine. 

Patient characteristics. Seventy-eight colonoscopies (78 fecal/blood samples) were performed in patients with UC. The baseline characteristics of the patients are shown in Table 1 .

Correlations between each of the three biomarkers and each of the four endoscopic scores were analyzed (Table 2 ). Every endoscopic score showed a significant correlation with all biomarkers. In particular, compared to CRP, FC and FIT showed a stronger correlation with each endoscopic score. FC and CRP levels tended to correlate more strongly with S-MES and UCCIS, which represent the inflammation of the entire colon, than with the M-MES and UCEIS, (Table 2 ). In contrast, FIT tended to correlate more strongly with M-MES and UCEIS (Table 2) .

To find the factors that were responsible for the correlations between the biomarkers and endoscopic scores (Table 2) , we evaluated the correlations between the evaluation items of UCEIS and UCCIS and the three biomarkers (Table 3) . For UCCIS, the correlation between the sum of each descriptor in the five colonic segments and each biomarker was examined. Each biomarker showed a significant correlation with all descriptors (Table 3) . FIT, which reflects bleeding associated with intestinal inflammation, showed a stronger correlation with bleeding items than FC and CRP.

We divided all cases into a group with M-MES 0, 1, which is generally considered to reflect mucosal healing in UC, and a group with M-MES 2, 3, which is associated with endoscopic UC activity. In these two groups, the correlations of S-MES and UCCIS with each biomarker were analyzed (Table 4 (Table 5) . FC and FIT showed significant correlations with each item, except for the sum of bleeding/friability. CRP did not show a significant correlation with any of the UCCIS items. Similarly, the correlations between the sum of the descriptors in UCCIS and the three biomarkers were evaluated in the M-MES 2, 3 group (Table 6 ). FC and FIT did not show a significant correlation with the sum of the UCCIS descriptors. CRP showed a significant correlation with all descriptors, except for the sum of bleeding/friability. In patients with active UC, CRP did not reflect intestinal bleeding but strongly reflected other inflammatory conditions of the colon. 

In this study, we analyzed the usefulness of FC, FIT, and CRP as biomarkers for UC diagnosis using scores representing the most severe lesion (M-MES and UCEIS) and scores representing inflammation throughout the colon (S-MES and UCCIS). FC and CRP tended to correlate more strongly with S-MES and UCCIS than with M-MES and UCEIS. In the M-MES 0, 1 group, compared to CRP, FC and FIT showed stronger correlations with S-MES and UCCIS. Conversely, in the M-MES 2, 3 group, only CRP correlated significantly with each descriptor. To date, several endoscopic scores of UC have been reported, but the MES is the most widely used score in clinical practice and trials. In addition, the UCEIS is often used as an endoscopic score for UC. However, these scores present the lesion with the most severe inflammation and do not indicate inflammation in the entire colon 21, 22 . There are reports of endoscopic scores that evaluate inflammation throughout the colon. In many of these reports, the colon was divided into five to seven segments, the state of the mucosa was evaluated in each segment, and the score of the entire colon was obtained 18, 20, [23] [24] [25] [26] . However, such scoring systems for evaluating the entire colon are rarely used in clinical practice due to the complexity of evaluation. Endoscopic scores, such as the MES and UCEIS, which are widely used in clinical practice, indicate scores in the areas with the most severe inflammation, whereas biomarkers for UC, which have been reported to be useful in recent years, are considered to reflect inflammation throughout the colon. It is considered important to compare inflammation throughout the colon with biomarkers to evaluate the characteristics of UC biomarkers more accurately.

The four endoscopic scores showed a strong significant correlation with the biomarkers, particularly with FC and FIT. Although CRP showed a less strong correlation than FC and FIT, it showed a significant correlation with the four endoscopic scores. FC and CRP showed a stronger correlation with S-MES and UCCIS, which represent the presence of inflammation in the entire colon, than with M-MES and UCEIS, which indicate the most severe lesion. Kawashima et al. reported that the correlation coefficients between FC and M-MES or S-MES were r = 0.79 and r = 0.86, respectively, indicating that FC may more strongly reflect inflammation throughout the colon 23 . In the study by Lobatón et al., the correlation coefficients of FC with MMES, which is synonymous with S-MES, and M-MES, were r = 0.669 and r = 0.725, respectively 24 . The correlations between various markers and cumulative MES (cMES), which is calculated by totaling the MESs of six segments (cecum, ascending colon, transverse colon, descending colon, sigmoid colon, and rectum), were analyzed in a previous study 20 . In that study, the correlation coefficients of FC with M-MES and cMES were r = 0.38 and r = 0.52, respectively, which are similar to our results.

Few studies have evaluated the relationship between the entire colon and various biomarkers. In the present study, FIT tended to have a larger coefficient of correlation with M-MES and UCEIS than with S-MES and UCCIS. Although the cause of these findings is unknown, it may be related to the ability of FIT to reflect the most severely inflamed lesion. Further case accumulation and analysis are therefore required. Furthermore, to www.nature.com/scientificreports/ examine the factors that reflect the inflammation of each marker, the descriptors of UCEIS and UCCIS were compared with each biomarker. The results of this analysis showed that FIT was strongly correlated with bleeding in the UCEIS and the sum of bleeding/friability in the UCCIS. Naganuma et al. reported similar results to those of the present study 28 . In their study, compared to FC, FIT was more strongly correlated with bleeding in the UCEIS and reflected the association of bleeding with inflammation in UC. Next, we examined whether the characteristics of biomarkers differ, depending on the presence or absence of endoscopic activity, using widely used endoscopic scores. In this study, mucosal healing was defined as M-MES 0, 1, and the correlations between endoscopic scores and biomarkers were evaluated. In the M-MES 0, 1 group, although FC, FIT, and CRP showed significant correlations with S-MES and UCCIS, the coefficient of correlation of CRP was lower than those of FC and FIT. Notably, in the M-MES 2, 3 group, only CRP showed a significant correlation with S-MES and UCCIS. In other words, from the viewpoint of the use of biomarkers for the evaluation of the inflammation of the entire colon, although it is desirable to use FC or FIT in the mucosal healing phase, evaluation using CRP may be more useful than using other biomarkers in the endoscopic active phase. Similar findings were also shown in a study by Sonoyama et al. that compared FC and CRP with endoscopic scores 29 . In their report, although there was a significant difference in FC values between groups with MES 0 versus MES 1 versus MES 2 in UC patients with extensive colitis, no significant difference was observed between the MES 2 and MES 3 groups. Contrarily, although no significant difference was shown in CRP value between the MES 0 and MES 1 groups, a significant difference was shown in the MES 1 versus MES 2 versus MES 3 groups. The difference between their study and ours is that they did not evaluate the endoscopic score of the entire colon; however, consistent with our findings, the authors found that CRP was more useful in the endoscopic active phase. In addition, as shown in supplemental Table 1 , the values of FC, FIT, and CRP were significantly higher in the MES 2, 3 group than in the MES 0, 1 group. Furthermore, although there were significant differences in all biomarkers between the mucosal healing phase and the active phase, the correlation coefficient of CRP was higher than those of FC and FIT, as shown in Table 4 , which confirms the lower diagnostic accuracies of FC and FIT compared to that of CRP in the active phase.

Furthermore, to investigate the characteristics of the biomarkers in both the MES 0, 1, and MES 2, 3 groups, the correlation between the sum of descriptors in the UCCIS and each biomarker was analyzed. As expected, FC and FIT showed significant correlations with almost all items in the MES 0, 1 group, whereas these biomarkers did not show correlation with nearly all the descriptors in the MES 2, 3 groups. Conversely, CRP did not show significant correlations with each sum of descriptors in the MES 0, 1 group, whereas a significant correlation of each sum of descriptors was found in the MES 2, 3 group in all items, except for the sum of bleeding/friability. The results of this sub-group analysis reveal that CRP does not reflect the amount of bleeding in the endoscopic active phase but strongly reflects the presence of other factors.

This study had several limitations. First, the sample size was small. In addition, the number of patients with active UC was small. In this study, the entire colon was evaluated in order to sum the MES and UCCIS. However, in clinical practice, the high severity of UC limits the number of cases in which total colonoscopy can be performed, due to the risks of patient distress and complications, such as perforation and bleeding. For this reason, the number of active UC cases was small in this study. However, even with the small number of cases, the significant correlation of CRP with the S-MES and UCCIS in UC patients in the endoscopic active phase indicates that CRP is more strongly correlated with inflammation throughout the colon.

Patients with IBD have a higher risk of perforation than healthy individuals, and colonoscopy, particularly in patients with severe IBD, has the potential of further increasing the risk of perforation 30, 31 . Therefore, we considered that CRP is an adequate marker of active colon inflammation, reducing the requirement of colonoscopy, with the associated risk.

In conclusion, CRP more strongly reflects inflammation throughout the colon than FC and FIT in UC patients with severe endoscopic activity. CRP is useful in situations where endoscopy cannot be performed (for example, when gastrointestinal perforation is suspected or during a pandemic, such as in the current COVID-19 pandemic).

Data available upon request from Ken Sugimoto (sugimken@hama-med.ac.jp).

Received: 26 January 2021; Accepted: 6 May 2021

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This work was supported by a Grant-in-Aid for Scientific Research (C) (No. 18K07908) from the Japanese Ministry of Education, Culture, Sports, Science, and Technology.

N.I. contributed to this work. N.I. and K.S. designed the study. T.H., M.S., S.T., and S.T. collected the data. M.Y., M.I., and Y.H. analyzed the data. N.I. and K.S. wrote the paper. S.O. and T.F. provided critical insights regarding paper preparation.

The authors declare no competing interests.

The online version contains supplementary material available at https:// doi. org/ 10. 1038/ s41598-021-90558-z.Correspondence and requests for materials should be addressed to K.S.Reprints and permissions information is available at www.nature.com/reprints.Publisher's note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.