Online Submissions: http://www.wjgnet.com/1007-9327ofice wjg@wjgnet.com doi:10.3748/wjg.v18.i15.1773 World J Gastroenterol 2012 April 21; 18(15): 1773-1780 ISSN 1007-9327 (print) ISSN 2219-2840 (online) © 2012 Baishideng. All rights reserved. BRIEF ARTICLE Safety and eficacy of Profermin® to induce remission in ulcerative colitis Aleksander Krag, Hans Israelsen, Bjørn von Ryberg, Klaus K Andersen, Flemming Bendtsen Aleksander Krag, Flemming Bendtsen, Gastrounit, Medical Devision 360, Copenhagen University Hospital Hvidovre, Faculty of Health Sciences, Copenhagen University, DK-2650 Hvidovre, Denmark Hans Israelsen, Bjørn von Ryberg, Nordisk Rebalance A/S, M. D. Madsensvej 14-16, DK-3450 Allerød, Denmark Klaus K Andersen, Statistics Section, Informatics and Mathematical Modelling, Technical University of Denmark, DK-2800 Lyngby, Denmark Author contributions: Israelsen H, von Ryberg B and Andersen KK conceived the study and developed the overall design; Israelsen H and von Ryberg B performed the study; Andersen KK performed the statistical analyses and all authors participated in the interpretation of the overall results; all authors had full access to all data; Krag A drafted the paper and all authors participated in the critical revision for important intellectual content. Supported by Danish Innovation Law Grant, J.nr. 3414-06-01530, from the Danish Food Industry Agency under the Ministry of Food, Agriculture and Fisheries; and Nordisk Rebalance, who developed and manufactured Profermin®, and partly financed the study Correspondence to: Aleksander Krag, MD, PhD, Gastrounit, Medical Devision 360, Copenhagen University Hospital Hvidovre, Faculty of Health Sciences, Copenhagen University, Kettegaard Alle 30, DK-2650 Hvidovre, Denmark. aleksanderkrag@hotmail.com Telephone: +45-3-8623182 Fax: +45-3-8623777 Received: August 15, 2011 Revised: October 23, 2011 Accepted: January 18, 2012 Published online: April 21, 2012 RESULTS: In an intention to treat (ITT) analysis, the mean reduction in SCCAI score was 56.5%. Of the 39 patients, 24 (62%) reached the primary endpoint, which was proportion of patients with ≥ 50% reduction in SCCAI. Our secondary endpoint, the proportion of patients in remission deined as SCCAI ≤ 2.5, was in ITT analysis reached in 18 of the 39 patients (46%). In a repeated-measure regression analysis, the estimated mean reduction in score was 5.0 points (95% CI: 4.1-5.9, P < 0.001) and the estimated mean time taken to obtain half the reduction in score was 28 d (95% CI: 26-30). There were no serious adverse ® events (AEs) or withdrawals due to AEs. Profermin was generally well tolerated. CONCLUSION: Profermin® is safe and may be effective in inducing remission of active UC. © 2012 Baishideng. All rights reserved. Key words: Ulcerative colitis; Diet; Probiotic; Profer® min ; Inlammatory bowel disease; Dietary management; Medical foods Peer reviewer: Alan C Moss, MD, FACG, Assistant Professor of Medicine, Director of Translational Research, Center for Inflammatory Bowel Disease, Beth Israel Deaconess Medical Center, Harvard Medical School, Rose 1 / East, 330 Brookline Ave, Boston, MA 02215, United States Krag A, Israelsen H, von Ryberg B, Andersen KK, Bendtsen F. Safety and eficacy of Profermin® to induce remission in ulcerative colitis. World J Gastroenterol 2012; 18(15): 1773-1780 Available from: URL: http://www.wjgnet.com/1007-9327/full/ v18/i15/1773.htm DOI: http://dx.doi.org/10.3748/wjg.v18. i15.1773 Abstract AIM: To test the eficacy and safety of Profermin® in inducing remission in patients with active ulcerative colitis (UC). METHODS: The study included 39 patients with mild to moderate UC deined as a Simple Clinical Colitis Activity Index (SCCAI) > 4 and < 12 (median: 7.5), who were treat® ed open-label with Profermin twice daily for 24 wk. Daily SCCAI was reported observer blinded via the Internet. WJG|www.wjgnet.com INTRODUCTION Ulcerative colitis (UC) is a chronic relapsing bowel dis- 1773 April 21, 2012|Volume 18|Issue 15| Krag A et al . Profermin® in ulcerative colitis ease characterized by colonic mucosal inflammation. The goal of treatment in UC is to induce and maintain remission of the disease. Failure to induce remission occurs in 20%-30% of patients on current treatments, leaving colectomy as the only alternative in a proportion of patients[1,2]. Furthermore, many patients ind the side effects of treatment with corticosteroids and other drug therapies unacceptable. Accordingly, new treatment alternatives are being sought. The pathogenesis of UC has still not been determined in detail; however, a major hypothesis is suggested to be an aggressive immune response to the intestinal content including, a subset of nonpathogenic enteric bacteria in genetically predisposed individuals. Clinical and experimental studies point towards alterations in the relative balance of aggressive and protective bacterial species in these disorders[3,4]. Interventions to alter the intestinal microlora in order to decrease proinlammatory stimuli and increase antiinlammatory signaling are under investigation[3,5,6]. Some studies have suggested an effect of probiotics in the treatment of UC[5,7-9]. The effects of probiotics on the microlora may only be limited and transient because colonization and survival of the probiotics are dificult to achieve. However, remission from inflammatory bowel diseases may be induced by food for special medical purposes (FSMPs), e.g., elemental diets. In this study we investigated a new dietary product Profermin®, which is intended to be registered as a FSMP for the dietetic management of UC. It consists of fermented oats, Lactobacillus plantarum (L. plantarum) 299v, barley malt, lecithin and water. Our aim was to investigate the safety and possible eficacy of Profermin® in patients with mild to moderate UC. We also assessed the usefulness of a new online daily symptom registration system. Table 1 Simple Clinical Colitis Activity Index Symptom Bowel frequency (d) 1-3 4-6 7-9 >9 Bowel frequency (night) 1-3 4-6 Urgency of defecation Hurry Immediately Incontinence Blood in stool Trace Occasionally frank Usually frank General wellbeing Very well Slightly below par Poor Very poor Terrible Extracolonic features Score 0 1 2 3 1 2 1 2 3 1 2 3 0 1 2 3 4 1 per manifestation interested and had the relevant disease characteristics to contact the trial nurse. The patients had to sign a declaration stating when and where they had been diagnosed with UC and describing the course of their disease including the fulillment of the inclusion criteria. The data were conirmed by cross checking the patients’ medical records. A specialist had diagnosed all patients. Patients were excluded if UC medication was modiied during the study period, however, a dose reduction of ongoing drugs was accepted. The patients were also excluded if new medication that may affect UC symptoms was prescribed for other conditions. MATERIALS AND METHODS Patients The study was conducted between 2008 and 2009. Patients were eligible if they were between 18 and 50 years of age and had an established diagnosis of UC based on clinical, endoscopic and histological features. Active disease was assessed by Simple Clinical Colitis Activity Index (SCCAI) (Table 1) score > 4 and < 12[10]. Patients who initiated treatment with azathioprine, 6-mercaptopurine, cyclosporin or methotrexate within 8 wk prior to inclusion or tumor necrosis factor-α inhibitors within 12 wk before inclusion or had changes in UC treatment within 2 wk before inclusion were ineligible for the study. Concomitant celiac disease, lactose intolerance and irritable bowel syndrome were also exclusion criteria. In addition any malignant or premalignant condition or recent gastroenteritis and irritable bowel syndrome rendered patients ineligible. Patients were recruited through advertisement on the website of the local patients’ association, in local newspapers and through Google ads. The advertisement showed a link to a website that briely described the trial and encouraged patients who were WJG|www.wjgnet.com [10] Outcome measures Our primary endpoint was to estimate the proportion of patients with a ≥ 50% reduction in SCCAI. Our secondary endpoint was to estimate the proportion of patients in remission deined as SCCAI ≤ 2.5[11]. Study design and assessment of outcome measures A prospective open-label study design was used to gain experience with time to response and remission and compliance for the later design of a comprehensive controlled study. After a run-in period of 6-14 d, the patients were followed for 24 wk with daily SCCAI score assessment. The SCCAI was chosen for the following reasons. The SCCAI score has been shown to correlate well with the more complex and invasive scoring systems and it facilitates daily and observer blinded symptoms registration[10,11]. Furthermore, colonoscopy may be experienced as painful and therefore compromise the patients’ willingness to participate in a clinical trial. Internet software was developed by a company specialized in software development for interactive Internet solutions 1774 April 21, 2012|Volume 18|Issue 15| Krag A et al . Profermin® in ulcerative colitis fermin® is packed in 250-mL cartons under sterile conditions. The product is tested for pH and colony forming units (CFU) of Enterobacteriaceae, yeasts/moulds and L. plantarum 299v. The pH must be between 3.6 and 4.2 and the CFU of Enterobacteriaceae, yeasts/moulds must each be < 100/mL. The CFU of L. plantarum must be > 108/mL. After 6-14 d of run in, the Profermin® intervention was initiated by scaling the patient into a daily oral intake of Profermin®. The initial daily Profermin® dose was 125 mL as the irst meal and 125 mL as the last meal of the day. After 2 d, the Profermin® dose was increased to 250 mL as the irst meal and 250 mL as the last meal of the day. However, the protocol was open for periodical changes of the total dose of Profermin® in the interval of 25 mL to 500 mL taken once or twice daily, for example, if a patient experienced AEs during the introduction, the low Profermin® dose was prolonged for up to 2 wk. The median dose was 445 mL/d with an interquartile range of 408-500 mL/d. The patients reported their intake of Profermin® on a daily basis through the trial website and the mean self-reported adherence therapy was > 95%. Patients were recommended to be cautious with consumption of dairy products and concentrated sugar products in accordance with routine dietetic recommendations widely used in Danish IBD clinics[6]. Compliance with this recommendation was not monitored. Patients continued their usual UC medication and clinical followup with gastroenterologists. (Franklyweb, Copenhagen, Denmark). The Internet platform was created according to protocol instructions and used for individual patient registration of SCCAI parameters. Regular access to a computer with Internet access was a criterion for inclusion. Each patient received a username and a password and was instructed to register the SCCAI parameters daily on the trial website. Each SCCAI parameter was formulated as a question e.g. “How many defecations have you experienced during daytime today? Click on the appropriate answer “1-3”, “4-6”, “7-9” or ”> 9”. Each SCCAI question needed to be answered before the patient could continue to the next question. After registration of the last SCCAI question, the patient was shown an overview of the answers to every SCCAI question and was asked to conirm or amend the information. After conirmation, the patient was shown a graph with the daily SCCAI scores from the irst day of the run-in period up to the present date. The patients could communicate on the trial website with the nurse who checked the status of each patient at least twice a week and could send reminders if patients failed to register the daily symptoms. The symptoms were registered on a daily basis. When a patient failed to register a day’s symptoms, the patient was reminded by the nurse about the lacking registration. The registration rate (registered days out of total number of days) was > 95%. The data were transferred from the patients via the Internet in encrypted form (Secure Sockets Layer) and stored on a secure server. The data were instantly copied - in raw and unprocessed form - to a similar server at the Technical University of Denmark, Department of Informatics and Mathematical Modelling, in order to secure the authenticity of the data and to analyze the data statistically. Occasionally some patients did not have access to a computer with an Internet connection. In such cases, these patients received paper SCCAI questionnaires to be completed for each day of the relevant period. When access to the Internet was again established, the patients transferred the SCCAI parameters noted on the questionnaires to the website. During the screening process, 30 of the included patients (77%) had a face-to-face meeting with the trial nurse. There were no other faceto-face contacts with the patients. All other communication was electronic (phone or e-mail). The patients were instructed to report adverse events (AEs) via the trial website. Safety of Profermin® was assessed by analyzing the AE reports. Ethics, approvals and patient consent The trial was approved by the Danish Data Protection Agency (2008-41-2961) and has been cleared with The Ethical Committees of the Copenhagen Region and registered (H-B-2008-FSP-20). As Profermin ® is an FSMP and not a medicinal product, no authorization by the Danish Medicines Agency was required. All patients gave written informed consent according to the Helsinki declaration. The study was registered on www.clinicaltrials.gov (NCT01245465). Statistical analysis In all analyses, we applied the principle of intention-totreat (ITT). Data for patients who dropped out or who were excluded during the study period were included in the analysis by using the principle of last value carried forward. Unadjusted estimates for the primary and secondary endpoints were presented as total numbers and percentages. To gain further insight into the longitudinal effect of Profermin® on the possible decline in SCCAI over time adjusted for the starting value, we applied the following non-linear regression model: Scoreij = b 0 + b 1 × 2-Dayi/q Where the dependent variable Scoreij was the score for person j on Day i. Time was denoted by the independent variable Dayi. In the model, the parameters to be estimated had the following interpretation: b 0 was the ultimate Description of the intervention Profermin® is manufactured as follows. Oat gruel is produced by mixing oats, water and a small amount of barley malt. The mixing process lasts for 1 h at 88 ℃. The gruel is then cooled to 38 ℃, and a L. plantarum 299v starter culture is added. The mixture is kept at 38 ℃ for 15 h with constant gentle stirring. The resulting oat-fermented gruel is cooled to about 8 ℃. Lecithin is then added while the mixture is gently stirred and the resulting Pro- WJG|www.wjgnet.com 1775 April 21, 2012|Volume 18|Issue 15| Krag A et al . Profermin® in ulcerative colitis Patient relection on advertisements in newspapers, the patients’ association website and Google Ads. N = 401 Telephone call N = 360 Patient excluded Inclusion criteria not met Nurse asking for patient’s data. Analysis in relation to inclusion and exclusion criteria N = 41 Criteria met A run-in period of 6-14 d begins The patient enters the SCCAI symptoms daily on the website N=2 Patient excluded A-SCCAI not approved Average-SCCAI (A-SCCAI) for run-in is calculated. Must be 4 < A-SCCAI < 12 Average-SCCAI approved Patient excluded N=0 Consent and relevant data and signatures not provided Consent and relevant data and signatures provided N = 4 excluded due to protocol violation on Days 10, 58, 110, 117. Three were prescribed antibiotics and 1 corticosteroids. N = 8 drop-outs on Days 9, 66, 81, 107, 111, 136, 147, 148 Personal or telephone meeting between patient and nurse. Checking data and obtaining patient’s consent. Profermin is provided N=4 Excluded The 24-wk treatment course begins N=8 End of treatment N = 39 On a daily basis: Intake of Profermin Entering symptoms on the website N = 27 Drop-outs Figure 1 Patient low diagram. SCCAI: Simple Clinical Colitis Activity Index. score (or asymptote), b 1 was the total reduction in score and q was the time taken to obtain half the reduction in score. Besides giving the parameters a marginal interpretation, it was of interest to describe the between-patient variation. Thus, we applied a nonlinear mixed-effects model, assuming that all three parameters in question followed a Gaussian distribution, i.e., each parameter was person-speciic: Scoreij = b 0,j + b 1,j × 2-Dayi/qj Here, we assumed that b 0,j = N(b 0,sb 0), b 1,j = N(b 1,sb 1) and q j = N(q ,sq ). The mixed-effect model led to the following interpretation: the estimated parameter sb 0 was the between-person SD regarding the asymptote. Similarly, sb 1 was the between-person SD related to the total reduction in score, and sq was the between-person SD related to the time taken to obtain half the reduction in score. Before making inference, we examined both standardized residuals and estimated random effects for marginal normality by applying normal probability plots. In all statistical analysis, the software R and the package nlme were used. All tests were done as likelihood ratio tests with a signiicance level of 5%. inclusion criteria were not met (Figure 1). Reasons for exclusions were primarily SCCAI < 5 or recent change in oral corticosteroid treatment. During the run-in period, two additional patients were excluded because the SCCAI criteria were not met. The study comprised 39 patients who were available for ITT analysis: four were excluded and eight dropped out during the 24-wk treatment period (Figure 2 and Table 2). Baseline characteristics and use of concomitant medications are shown in Tables 3 and 4. Safety and tolerability No major AEs were reported and there were no dropouts due to AEs. An increased number of bowel movements were reported by 11 patients (28%), bloating by four (10%) and an increased number of bowel movements and bloating by three (8%). All AEs were selflimiting or managed by dose adjustments. For example, if a patient experienced a presumable AE during the introduction of Profermin®, the period with the low Profermin® dose was prolonged for up to 2 wk. None of the eight dropout or four excluded patients left the trial due to deterioration in UC symptoms. RESULTS Clinical response and remission Of the 39 patients, 27 completed the entire study. For those completing the study, the mean follow-up was The advertisements attracted 401 respondents, of whom 360 were excluded before the run-in period because the WJG|www.wjgnet.com 1776 April 21, 2012|Volume 18|Issue 15| Krag A et al . Profermin® in ulcerative colitis Table 2 Description of four excluded patients and eight dropouts Day SCCAI Reason for run in discontinuation Patient Excluded patients 10 8.9 45 8.0 100 8.2 116 11 Drop-outs 9 8.9 54 4.6 73 5.9 100 5.6 102 9.0 127 6.6 140 6.7 141 8.3 0 50 100 Days since start 150 Reduction Increase 1 1 1 2 6.6 4.1 4.1 3.6 2.3 3.9 4.1 7.4 3 3 3 3 3 3 3 3 6.7 5.1 7.3 8.4 6.7 5.6 5.3 6.3 2.2 0.5 1.4 2.8 2.3 1.0 1.4 2.0 Reasons for discontinuation in the study. 1: Excluded because of new medication prescribed for unrelated diseases; 2: Excluded because of new medication prescribed for colitis; 3: Dropouts main reason: Not satisied with effect of treatment. SCCAI: Simple Clinical Colitis Activity Index. 200 Figure 2 Point indicates that patient has dropped out. Table 3 Demographic and baseline clinical characteristics of patients 176 d (range: 174-179 d). For those not completing the study, the mean follow-up was 94 d (range: 9-141 d). An ITT analysis showed that the mean reduction in SCCAI score was 56.5%. For the primary endpoint, ITT analysis showed that 24 of the 39 patients (62%) achieved a ≥ 50% reduction in SCCAI score (Figure 3A). In per protocol (PP) analysis, 85% reached the primary endpoint. In ITT analysis, four patients (10%) experienced deterioration in SCCAI but 13 (33%) experienced > 75% improvement in SCCAI during the study (Figure 3B). Of the 39 patients, 18 reached the secondary endpoint and obtained remission defined as SCCAI score ≤ 2.5, with an ITT success rate of 46% (Figure 3C). In PP analysis, 67% reached the secondary endpoint remission. Applying only the four defecation scores in the SCCAI (Table 1), four patients (10%) had deterioration and 17 (44%) had > 75% improvement in defecations scores (Figure 3D). When applying the nonlinear model for the ITT decline in SCCAI over time, the estimated ultimate score (or asymptote) was 2.8 points (95% CI: 92.0-3.6), the estimated mean reduction in score was 5.0 points (95% CI: 4.1-5.9, P < 0.0001) and the estimated mean time taken to obtain half of the reduction in score was 28 d (95% CI: 26-30) (Figure 4). Profermin, n = 39 Characteristic Sex, male:female Age, yr, median and range Mean duration of disease, yr, median and range Disease location, n (%) Proctitis Left-sided colitis/procto-sigmoiditis Pancolitis Extraintestinal manifestations, n (%) Initial CRP, mg/L, median and range Initial albumin, g/L, median and range 15/24 35 (19-50) 7 (1-21) 17 (44) 11 (28) 11 (28) 17 (43) 15 (< 1-156) 41 (23-47) CRP: C-reactive protein. Table 4 Concomitant medications n (%) Mesalamine oral Alone Combined with immunosuppressants Mesalamine enema or suppository Azathioprine or 6-mercaptopurine Corticosteroids oral Corticosteroids enema Antibiotics TNF-α inhibitors None Descriptions of exclusions and dropouts Protocol violations accounted for the exclusion of four patients (10%) - days 10, 45, 100 and 116 (Table 4); three were prescribed antibiotics for pneumonia, salmonella infection and gastroenteritis, respectively, and one was prescribed corticosteroids for UC. Among those excluded, the mean SCCAI on inclusion was 9.0 (range: 8.0-11) and at exclusion 4.6 (range: 3.6-6.6). There were eight dropouts (20%) (Table 2). Among these, the mean SCCAI at inclusion was 7.0 (range: 4.6-9.0) and at drop- WJG|www.wjgnet.com SCCAI dropout 21 (54) 8 (21) 6 (15) 3 (8) 0 (0) 1 (3) 0 (0) 3 (8) 3 (8) TNF-α: Tumor necrosis factor alpha. out 6.4 (range: 5.1-8.4). Among the dropouts, three experienced an increase in SCCAI (mean: 1.6) while in the study and ive experienced a decrease (mean: 1.8). The three patients with an increase in their SCCAI score represented treatment failures. 1777 April 21, 2012|Volume 18|Issue 15| Krag A et al . Profermin® in ulcerative colitis A ≥ 50% improvement B 14 Improvement 12 < 50% improvement Aggravation 10 8 6 4 2 Ag gr Ag > 75 gr % 50 % Ag -7 gr 5% 26 % -4 Ag 9% gr 1% -2 5% St at us Im qu pr o 1% Im 2 pr 5% 26 % Im -4 pr 9% 50 % Im 75% pr > 75 % 0 Improvement % 75 5% pr Im Im pr > -7 9% 50 % -4 5% -2 Im pr 26 1% pr Im % qu o 5% us at St 1% gr gr Ag -2 -4 5% -7 75 gr 50 % > gr Ag Ag 9% Aggravation % SCCAI > 2.5 18 16 14 12 10 8 6 4 2 0 Ag D % Remission ≤ 2.5 26 C Figure 3 Intention to treat analysis of the primary (A, B) and secondary (C, D) endpoint. A, B: Proportion of patients with ≥ 50% reduction in Simple Clinical Colitis Activity Index (SCCAI) at week 24 and the relative development in SCCAI score; A: The primary endpoint was in intention to treat (ITT) analysis reached by 24 in 39 patients (62%); B: Illustrates the relative development in SCCAI in the last week of observation compared to the run-in week; C, D: Remission at week 24 and the relative development in the 4 defecation scores; C: The secondary endpoint was in ITT analysis reached by 18 in 39 patients (46%); D: Illustrates the relative development in the 4 defecation scores in the SCCAI (Table 1) in the last week of observation compared to the run-in week. Score = b0 + b12 (-Days/q) 17 for clinical improvement and remission in UC found a relevant clinical improvement to be a decrease of 1.5 SCCAI points and the best cut-off to establish remission as an SCCAI of 2.5[11]. In ITT analysis, the average reduction was > 1.5 SCCAI points 12 d after the intervention was initiated. After 32 d, the average reduction increased to > 3 SCCAI points and after 84 d to > 4.5 (Figure 4). In a repeated measure regression analysis, the mean reduction in SCCAI after 24 wk of Profermin® treatment, adjusted for baseline value, was 5.0 and the estimated ultimate score was calculated to be 2.8 (Figure 4), suggesting a clinically relevant and signiicant effect. A metaanalysis of response rates in the placebo arms of UC trials estimated the placebo rates of remission and response to be 13% (95% CI: 9-18) and 28% (95% CI: 23-33), respectively[12]. The ITT remission and response rates in our study were 33 and 34 percentage points above these standard placebo rates, supporting a possible clinical effect of Profermin® when compared with standard placebo rates of response and remission. The safety proile of Profermin® appears favorable with no major AEs and no withdrawals due to AEs. Mild AEs were observed mainly in the initial days of treatment and ceased within a few days or after dose adjustments. Safety and tolerability of Profermin® are comparable to those of probiotics[7-9]. Profermin® is a complex product and the mode of action is probably complex as well. However, dietary management with Profermin® uses a novel approach and Observed mean Fitted mean Score 10 8 6 4 2 0 0 50 100 Days since start 150 180 Figure 4 Development in Simple Clinical Colitis Activity Index score. DISCUSSION In ITT analysis, 62% of the patients reached the primary endpoint, defined as ≥ 50% reduction in SCCAI, and 46% reached the secondary endpoint of remission, deined as an SCCAI score ≤ 2.5. A study on endpoints WJG|www.wjgnet.com 1778 April 21, 2012|Volume 18|Issue 15| Krag A et al . Profermin® in ulcerative colitis ment in UC is to induce and maintain remission of the disease, however, failure to induce remission occurs in 20%-30% of patients on current treatments. Accordingly, new treatment alternatives and additives are being sought. Dietetic interventions may improve symptoms in UC. cannot be categorized as a probiotic, prebiotic or symbiotic product[13]. The dietary effect may be related to the fermented oats components such as the relatively large amounts of secondary metabolites from the fermentation process and the composition of oats per se. The short chain fatty acids of secondary metabolites have been shown to serve as a major source of energy for colonocytes, and b-glucans have been described as biological response modiiers[14,15]. L. plantarum is a common species in the human gastrointestinal microbiota[16-18]. L. plantarum 299v survives passage through the gastrointestinal tract and has been isolated from feces and rectal and jejunal biopsies 11 d after 10 d administration to healthy volunteers, indicating at least transient colonization of the gut mucosa[19-21]. It has been shown that oat gruel fermented with L. plantarum 299v increases iron absorption by 50%, suggesting an important dietary effect for UC[22]. In addition, the phosphatidylcholine (PC) in lecithin may serve as an important food component because the content of PC in the colonic mucus of patients with UC is signiicantly lower compared with the content in healthy controls[23]. Lastly, the daily intake of relatively large quantities of fermented oats may change the intestinal contents and environment and thereby establish an altered platform for microbial activity. In this study, we introduced a new online self-reporting Internet-based system for assessing daily activity in UC and for monitoring response to treatment. The system allows electronic monitoring of data and enables daily reporting with minimal interruption to the patient’ s daily life. The risk of patients being inluenced in their self-assessment by health personnel is limited. Independent monitoring and statistical analyses can be achieved easily. In Denmark, where most people have Internet access, this system is a very useful research tool in a population of UC patients. Our study had some limitations: (1) it was an uncontrolled study and the results need to be conirmed in a randomized trial; and (2) patients were informed to consider their consumption of dairy products and concentrated sugar products, in particular fresh milk and confectionary. This may have had an effect on UC or may have reinforced the effect of Profermin®. The present study demonstrates that Profermin® is safe and may be effective in inducing remission of active UC. Randomized controlled studies are planned to explore further the clinical eficacy of Profermin®. Research frontiers Clinical and experimental studies point towards alterations in the relative balance of aggressive and protective bacterial species in UC. Interventions to alter the intestinal microlora in order to decrease disease activity are under investigation and prebiotics, probiotics and symbiotics have been investigated in UC but the reported eficacies have varied. Innovations and breakthroughs This is believed to be the first study to assess Profermin® in UC. The study was an open label study that investigated safety and eficacy of Profermin® in patients with moderate active UC. Profermin® is a new developed product for the dietary management of UC. It is a fermented oat gruel with Lactobacillus plantarum 299v, barley malt, lecithin and water. Applications Profermin® is safe and well tolerated and may be effective in reducing symptoms and inducing remission in UC. Larger randomized trials should be performed to investigate further the eficacy of Profermin® in UC. Terminology Simple Clinical Colitis Activity Index (SCCAI) assessed active disease. SCCAI is a clinical scoring system for UC, based on bowel frequency day and night, urgency, fecal blood, general well being and extracolonic manifestations. Peer review The authors have reported a study on the safety of Profermin®, a combination of fermented oats, probiotics and lecithin, in patients with mild to moderate UC. This is primarily an open-label safety study in patients. The agent was welltolerated and may be eficacious. REFERENCES 1 2 3 4 5 6 7 8 ACKNOWLEDGMENTS We thank Jørgen Villumsen for invaluable practical and technical assistance. We also thank Peter Møller and Carsten Toftager Larsen for important advice during the study. 9 COMMENTS COMMENTS 10 Background 11 Ulcerative colitis (UC) is a chronic relapsing bowel disease. The goal of treat- WJG|www.wjgnet.com 1779 Aratari A, Papi C, Clemente V, Moretti A, Luchetti R, Koch M, Capurso L, Caprilli R. Colectomy rate in acute severe ulcerative colitis in the inliximab era. Dig Liver Dis 2008; 40: 821-826 Baumgart DC, Sandborn WJ. Inlammatory bowel disease: clinical aspects and established and evolving therapies. Lancet 2007; 369: 1641-1657 Sartor RB. Therapeutic manipulation of the enteric microlora in inlammatory bowel diseases: antibiotics, probiotics, and prebiotics. Gastroenterology 2004; 126: 1620-1633 Baumgart DC, Carding SR. Inflammatory bowel disease: cause and immunobiology. Lancet 2007; 369: 1627-1640 Prisciandaro L, Geier M, Butler R, Cummins A, Howarth G. Probiotics and their derivatives as treatments for inlammatory bowel disease. Inlamm Bowel Dis 2009; 15: 1906-1914 Yamamoto T, Nakahigashi M, Saniabadi AR. Review article: diet and inflammatory bowel disease--epidemiology and treatment. Aliment Pharmacol Ther 2009; 30: 99-112 Bibiloni R, Fedorak RN, Tannock GW, Madsen KL, Gionchetti P, Campieri M, De Simone C, Sartor RB. VSL#3 probiotic-mixture induces remission in patients with active ulcerative colitis. Am J Gastroenterol 2005; 100: 1539-1546 Huynh HQ, deBruyn J, Guan L, Diaz H, Li M, Girgis S, Turner J, Fedorak R, Madsen K. Probiotic preparation VSL#3 induces remission in children with mild to moderate acute ulcerative colitis: a pilot study. Inlamm Bowel Dis 2009; 15: 760-768 Sood A, Midha V, Makharia GK, Ahuja V, Singal D, Goswami P, Tandon RK. The probiotic preparation, VSL#3 induces remission in patients with mild-to-moderately active ulcerative colitis. Clin Gastroenterol Hepatol 2009; 7: 1202-1209, 1209.e1 Walmsley RS, Ayres RC, Pounder RE, Allan RN. A simple clinical colitis activity index. Gut 1998; 43: 29-32 Higgins PD, Schwartz M, Mapili J, Krokos I, Leung J, Zimmermann EM. Patient deined dichotomous end points for April 21, 2012|Volume 18|Issue 15| Krag A et al . Profermin® in ulcerative colitis 12 13 14 15 16 17 18 19 remission and clinical improvement in ulcerative colitis. Gut 2005; 54: 782-788 Su C, Lewis JD, Goldberg B, Brensinger C, Lichtenstein GR. A meta-analysis of the placebo rates of remission and response in clinical trials of active ulcerative colitis. Gastroenterology 2007; 132: 516-526 Bengmark S, Martindale R. Prebiotics and synbiotics in clinical medicine. Nutr Clin Pract 2005; 20: 244-261 Roy CC, Kien CL, Bouthillier L, Levy E. Short-chain fatty acids: ready for prime time? Nutr Clin Pract 2006; 21: 351-366 Volman JJ, Ramakers JD, Plat J. Dietary modulation of immune function by beta-glucans. Physiol Behav 2008; 94: 276-284 Christensen HR, Frøkiaer H, Pestka JJ. Lactobacilli differentially modulate expression of cytokines and maturation surface markers in murine dendritic cells. J Immunol 2002; 168: 171-178 Ahrné S, Nobaek S, Jeppsson B, Adlerberth I, Wold AE, Molin G. The normal Lactobacillus lora of healthy human rectal and oral mucosa. J Appl Microbiol 1998; 85: 88-94 Lönnermark E, Friman V, Lappas G, Sandberg T, Berggren A, Adlerberth I. Intake of Lactobacillus plantarum reduces certain gastrointestinal symptoms during treatment with antibiotics. J Clin Gastroenterol 2010; 44: 106-112 20 21 22 23 Niedzielin K, Kordecki H, Birkenfeld B. A controlled, double-blind, randomized study on the eficacy of Lactobacillus plantarum 299V in patients with irritable bowel syndrome. Eur J Gastroenterol Hepatol 2001; 13: 1143-1147 Johansson ML, Molin G, Jeppsson B, Nobaek S, Ahrné S, Bengmark S. Administration of different Lactobacillus strains in fermented oatmeal soup: in vivo colonization of human intestinal mucosa and effect on the indigenous lora. Appl Environ Microbiol 1993; 59: 15-20 Adlerberth I, Ahrne S, Johansson ML, Molin G, Hanson LA, Wold AE. A mannose-specific adherence mechanism in Lactobacillus plantarum conferring binding to the human colonic cell line HT-29. Appl Environ Microbiol 1996; 62: 2244-2251 Bering S, Suchdev S, Sjøltov L, Berggren A, Tetens I, Bukhave K. A lactic acid-fermented oat gruel increases nonhaem iron absorption from a phytate-rich meal in healthy women of childbearing age. Br J Nutr 2006; 96: 80-85 Ehehalt R, Wagenblast J, Erben G, Lehmann WD, Hinz U, Merle U, Stremmel W. Phosphatidylcholine and lysophosphatidylcholine in intestinal mucus of ulcerative colitis patients. A quantitative approach by nanoElectrospraytandem mass spectrometry. Scand J Gastroenterol 2004; 39: 737-742 S- Editor Shi ZF WJG|www.wjgnet.com 1780 L- Editor Kerr C E- Editor Li JY April 21, 2012|Volume 18|Issue 15|