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The esophageal mucosal integrity is impaired in eosinophilic esophagitis (EoE) and it has been suggested that the duodenal permeability is increased. The absence of food allergens may restore the integrity. The aims of this study were to assess duodenal permeability in EoE and to evaluate the effect of an elemental diet on the esophageal and duodenal integrity.
In this prospective study 17 adult EoE patients and 8 healthy controls (HC) were included. Esophageal biopsy specimens were sampled before and after 4 weeks of elemental diet to measure eosinophil counts and gene expression of tight junction and barrier integrity proteins. Esophageal and duodenal impedance were measured by electrical tissue impedance spectroscopy and Ussing chambers were used to measure transepithelial resistance (TER) and transepithelial molecule flux. Small intestinal permeability was measured using a test, measuring lactulose/mannitol (L/M) ratios.
In EoE patients, the esophageal but not the duodenal integrity was impaired, compared with HC. We observed no significant difference between L/M ratios of HC and EoE patients. After diet, eosinophil counts decreased significantly, which was paralleled by normalization of esophageal impedance and transepithelial molecule flux. The esophageal TER improved significantly, but did not reach values seen in HC. Esophageal expression of genes encoding for barrier integrity proteins filaggrin and desmoglein-1 was impaired at baseline and restored after diet.
An elemental diet restores esophageal integrity, suggesting that it is at least partly secondary to allergen exposure. Duodenal integrity seems not to be affected in EoE, and possibly plays a minor role in its pathophysiology.
Eosinophilic esophagitis (EoE) is an allergic inflammatory disease of the esophagus, characterized histologically by a mucosal infiltration of eosinophils and symptomatically by dysphagia and food impaction (1). Since EoE was first described as a distinct entity in 1993, the incidence of the disease has increased tremendously and EoE has become the most common cause of dysphagia in adolescents and young adults. Without adequate treatment, continuous inflammation leads to progressive narrowing of the esophagus (2).
Although the pathophysiology of EoE has not been completely elucidated, it seems to align with other atopic diseases such as atopic dermatitis and asthma (3). Ingested food allergens are thought to be the driver of the inflammation and studies have shown that elimination of food allergens can induce disease remission, providing further evidence for the allergic component of the disease (4, 5). However, the exact mechanism of how exposure to food allergens results in EoE is unknown. In patients with active EoE, the esophageal mucosal integrity is impaired and intercellular spaces are dilated (6). The relationship between an impaired epithelial barrier function and allergy has been studied extensively in atopic dermatitis, in which an increased skin permeability is primarily responsible for permeation of allergens and subsequent activation of immune system (7). This increased permeability is thought to be induced by a dysregulation of tight junction proteins: claudin 1 (CLDN1) and zonula occludes 1 (ZO-1) (8). However, it is also possible that the impaired mucosal integrity found in EoE is only secondary to products produced by the inflammatory infiltrate, and thus merely the result of the inflammation and not its cause. Previous studies have shown that the EoE-associated inflammatory cytokine interleukin (IL)-13 and IL-5 have indeed the ability to downregulate desmoglein (DSG1) and filaggrin (FLG), two barrier integrity proteins (9, 10). Interestingly, in atopic dermatitis, barrier dysfunction was not only observed in the skin but also in the small intestine (11). This raises the question whether the esophagus is the sole site of allergen uptake in EoE, or whether allergens also permeate through the small intestine and initiate or aggravate an inflammation in a distant organ—the esophagus. The current literature on duodenal involvement in EoE is contradictory, with indications for increased small intestinal permeability found in one study in adults but not in another study in children (12, 13). Either way, esophageal and/or small intestinal mucosal integrity may be of pathophysiological relevance, and restoration of the mucosal integrity may be essential to accomplish complete histological remission.
Studies with elemental diets, lacking food allergens, showed impressive clinical and pathologic response in EoE (14, 15). However, the effect of absence of food allergens, through an elemental diet, on the mucosal integrity has never been investigated in these patients.
We aimed to investigate the effect of an elemental diet on the esophageal and small intestinal mucosal integrity in adult EoE patients. We hypothesized that in adult EoE patients complete avoidance of food allergens by an elemental (amino acid-based) diet restores the impaired esophageal mucosal integrity and decreases the esophageal inflammation. In addition, we hypothesized that the duodenal mucosal integrity is impaired in patients with active EoE.
In this prospective cohort study patients were included from the outpatient clinic of the Academic Medical Centrum Amsterdam between December 2014 and October 2015. Healthy controls were recruited through advertisement. Adults were eligible for enrolment if EoE was diagnosed according to current guidelines, defined as typical symptoms of EoE (dysphagia and/or food impaction) and the presence of more than 15 eosinophils per high-power field (HPF) during a high dosage of proton pump inhibition or H2 blockers (1). Exclusion criteria were: other esophageal or gastrointestinal diseases, previous surgery of the digestive tract, severe comorbidity scored as ASA class III or higher, and the inability to stop anti-inflammatory drugs (i.e., topical or systemic steroids and leukotriene inhibitors). Healthy controls were recruited exclusively for participation in this trial and underwent endoscopy solely for study purpose. They were pre-screened to ensure they had no atopic predisposition or other severe comorbidities classified as ASA II or higher. Each study subject gave written informed consent, and the study protocol was approved by the Medical Ethics Committee of our institution and prospectively registered in the Dutch trial registry (Trialregister.nl NTR4892).
In this trial, patients were treated with a newly developed amino acid-based formula (Neocate Nutricia, Utrecht, The Netherlands). The clinical results of the dietary trial have been published before (16), the focus of the current study is on the effects on esophageal and duodenal barrier function. In order for patients to meet their nutritional requirements during the elemental diet, patients visited a dietician with expertise in EoE, who calculated the minimal required daily formula consumption based on a patient’s body mass index (BMI) and weekly physical activity. After a washout period of four weeks during which patients were not allowed to use any immunosuppressive drugs, a baseline endoscopy was performed. After four weeks of elemental diet patients underwent a second endoscopy. Healthy controls were not treated with an elemental diet and only underwent the baseline endoscopy. Before each endoscopy, patients and healthy controls were instructed to consume a dual sugar solution and to collect their urine over 5h. Details regarding this lactulose/mannitol test will be provided below.
The endoscopies were performed by a single gastroenterologist per standardized protocol. After routine inspection of the esophagus and stomach, electrical tissue impedance spectroscopy (ETIS) measurements were performed in the esophagus and proximal duodenum, as described below. Subsequently four biopsy specimens were taken in the duodenum for histopathology and two for gene expression profiling. In the same region, another four biopsy specimens were obtained with a larger biopsy forceps (diameter, 3.7mm) for in vitro analysis of mucosal integrity in Ussing chambers. These measurements were also performed in the mid esophagus. In total, 10 biopsy specimens were taken in the duodenum and 10 in the esophagus.
Duodenal and esophageal biopsy specimens were directly fixed in formalin and subsequently embedded in paraffin. The biopsy specimens were sectioned at 5 microns and stained with hematoxylin and eosin (H&E) and tryptase. In a low-power view setting the area of most densely populated eosinophilia in the esophageal biopsy specimen was determined. Subsequently a × 400 magnification was used in order to determine the peak eosinophil count per HPF (an area of 0.24mm2). According to previous literature, complete histologic response was defined as <15 eosinophils/HPF with a decline of more than 50% of pre-diet eosinophil count (17). Partial response was defined as a decline of more than 50% of pre-diet peak eosinophil count but with ≥15 eosinophils/HPF after diet. A gastrointestinal pathologist with extensive expertise in EoE, who was blinded to the patients’ treatment status, scored the biopsy specimens. Other analyzed histologic features included: (i) basal hyperplasia, graded on a scale of 0–3 (absent to severe hyperplasia in two upper third of total epithelial thickness) and (ii) spongiosis, which was scored analogous to basal hyperplasia (18). Duodenal biopsy specimens were evaluated according to the modified Marsh-Oberhuber classification, which describes mucosal architectural and inflammatory changes, villous atrophy, crypt hyperplasia and increased intraepithelial lymphocytes (IELs) (19). All analyses were performed using an Olympus BX41 microscope (Olympus Europe, Hamburg, Germany).
ETIS measurements were performed as previously described (20). In brief, impedance is the measure of the degree to which an electric circuit resists to an alternating electric current when impressed through tissue (21). Mucosal impedance reflects how electricity travels through intestinal tissue (22). During endoscopy a flexible ETIS probe with a diameter of 3.2mm was advanced through the working channel of the endoscope and placed against the esophageal and duodenal mucosa. The probe consists of four electrodes, two inject an alternating current and the other two electrodes measure the potential difference between them. In each patient, measurements were performed mid esophageal and in the proximal duodenum, in four quadrants, and since the impedance measurements were directly visualized on the data acquisition unit only stable measurements were obtained. All measurements were performed by the same gastroenterologist with expertise in ETIS.
In vitro analysis of mucosal integrity was performed according to previously described methods (20). Briefly, biopsy specimens were directly transferred to Ussing chambers, consisting of two baths filled with Meyler solution and gassed with oxygen. The biopsy specimens were mounted in between the baths, separating the two solutions. A voltage electrode measured the ion transport across the membrane, and two electrodes were injecting a constant current. According to Ohm’s law, the transepithelial resistance (TER) was calculated. Simultaneously, transepithelial flux of two fluorescent molecules, fluorescein (molecular weight 0.3kDa) and rhodamine (40kDa; size similar to that of common food allergens), was measured. On the luminal side, the Meyler solution was replaced for the same solution with addition of the fluorescing molecules. A sample of the solution was taken from the opposite side, and the concentration of the two molecules was measured, which reflects the permeability of the mucosa in vitro.
The dual sugar test measuring the L/M ratio is one of the most commonly used test for the analysis of small intestinal permeability (23). It consists of a simultaneous oral administration of the disaccharide lactulose and the monosaccharide mannitol and their urinary excretion over period of time. Lactulose is a large non-metabolizable molecule; of which only a small proportion permeates through the small intestinal mucosa, and is excreted in the urine. If the mucosal integrity is impaired the urinary excretion of lactulose will increase. In contrast, mannitol, the smaller molecule, can always pass through the membrane freely, and the percentage that is excreted in the urine is higher. Intestinal permeability is expressed as the ratio of urinary excretion of lactulose vs. mannitol; the higher the ratio the higher the permeability of the small intestine. Patients and healthy controls drank 100ml of water with 2g of lactulose and 5g of mannitol. The subjects consumed the solution within the period of fasting that preceded the endoscopic procedure. Subsequently, urine was collected for 5h after ingestion, which is a validated timeframe for small intestinal permeability (24). An aliquot of the total urine volume was preserved in a −20° freezer until analysis. L/M ratios were calculated by high-performance liquid chromatography (HPLC). The upper limit of a normal L/M ratio was defined as 0.03, as previously described (25).
Expression of genes encoding for barrier integrity and tight junction proteins was measured by qPCR as previously described (16). Briefly, esophageal and duodenal biopsy specimens were immediately immersed in RNA stabilization reagent (RNAlater, Qiagen, Hilden, Germany). RNA was extracted from homogenized biopsy specimens according to the manufacturer’s instructions of RNeasy Micro Kit (Qiagen). A Nanodrop Spectrophotometer (Nanodrop Technologies, Wilmington, DE) calculated the concentration of RNA, and subsequently cDNA was synthesized by making use of a reverse transcriptase reaction which was performed according to the MBI Fermentas cDNA synthesis kit (Fermentas, Vilnius, Lithuania), using both the Oligo (dT) 18 and the D (N) 6 primers. Quantitative real-time RTPCR was performed on a LightCycler 480 (Roche Diagnostic, Almere, The Netherlands) using SYBR Green PCR Master Mix (Roche Diagnostic) and primers from Invitrogen. For quantitative real-time PCR, samples were normalized for the mean of the two most stable housekeeping genes Cyclophilin and Hypoxanthine-Guanine Phosphoribosyl Transferase (HGPRT). Transcript values of zonula occludes 1(ZO-1), desmoglein-1 (DSG1), claudin-1 (CLDN1), and filaggrin (FLG) were determined in duplicate. Primer sequences are applied as Supplementary Table 1 online.
Statistical analysis was performed using IBM SPSS Statistics (version 22.0) (SPSS, Chicago, USA). Descriptive statistics were used to summarize findings. Categorical variables were described as percentages and continuous variables were expressed as median with interquartile ranges. Before and after treatment, binary data were compared using McNemar’s test and ordinal data were compared using the Wilcoxon’s signed rank test for non-parametric variables. Unpaired non-parametric data were compared using the Mann–Whitney U-test for ordinal data and a χ2-test for categorical data. Correlations were calculated using the Spearman correlation coefficient. A P-value <0.05 was considered significant.
Twenty-five patients were eligible for participation. After baseline endoscopy, four patients were excluded because of spontaneous remission with a peak eosinophil counts <15 eos/HPF. Seventeen of the 21 patients, who started the elemental diet, completed the trial according to the protocol guidelines. Eight age-matched healthy controls were included and underwent the baseline endoscopy. Baseline characteristics of the included EoE patients and healthy controls are listed in Table 1.
After four weeks of elemental diet the peak eosinophil count in the esophageal mucosa had decreased significantly, from 43 (29–80) per HPF to 9 (2–18) per HPF (median, interquartile range) (P<0.001; Figure 1). Twelve of the 17 (71%) patients achieved complete histological response and 4 (24%) patients achieved partial response. One patient was classified as a non-responder.
The proportion of patients with moderate to severe spongiosis in their esophageal biopsies was significantly higher before the diet, and decreased from 13 (76%) to 5 (30%) after the diet (P=0.015). In a minority of patients spongiosis had completely disappeared after the diet (6%). Likewise, the diet had an effect on basal cell hyperplasia: 13 (76%) patients had moderate to severe basal cell hyperplasia before the diet, compared with 2 (12%) patients after the diet (P=0.006).
In the duodenal biopsy specimens of EoE patients no abnormalities were observed before or after elemental diet and all biopsy specimens were classified as Marsh 0. In the healthy controls, no abnormalities were observed in the esophageal and duodenal biopsy specimens.
At baseline, patients had a significantly lower esophageal mucosal impedance (ETIS) than after the diet and as compared with healthy controls. After the diet, esophageal mucosal impedance values in both groups were no longer significantly different. Accordingly, the esophageal TER had significantly improved in patients after diet when compared with baseline TER. However, despite this improvement, the esophageal TER in EoE patients after diet remained significantly lower than the TER in healthy controls (Table 2 and Figure 2). Although not statistically significantly different, after treatment the TER in the complete responders was considerably higher than the TER in the partial/non-responder (124Ωcm2 vs. 80Ωcm2 (MEDIANS)). Subsequently, the esophageal mucosal permeability, measured by the transepithelial flux of 0.3kDa fluorescein molecules and 40kDa rhodamine molecules, had decreased significantly after the diet. After the diet, esophageal fluorescein and rhodamine flux in patients were reduced to healthy control levels (Table 2 and Figure 2). In the compete responders the mean transepithelial fluorescein and rhodamine flux were lower (MEDIAN 43μmol/cm2/h and 15μmol/cm2/h) compared with the mean flux in partial/non-responders (MEDIAN 768μmol/cm2/h and 162μmol/cm2/h), although statistical significance was not reached.
The duodenal mucosal impedance and TER values in EoE patients were similar to those found in healthy controls and were not affected by the diet (Table 2 and Figure 3). Accordingly, the duodenal mucosa in patients before and after diet and in healthy controls was completely impermeable for fluorescein and rhodamine molecules (Table 2).
The L/M ratios of patients before the diet (median (interquartile range) 0.018 (0.007–0.047)), after the diet (median (interquartile range) 0.022 (0.012–0.061)) and in healthy controls (median (interquartile range) 0.020 (0.013–0.024) were all within the reference range and fell below the upper limit of normal permeability values (0.03). There was no statistically significant difference between groups (P>0.05).
The expression of the transcripts for tight junction and barrier integrity proteins FLG and DSG1, measured in the esophageal biopsy specimens of EoE patients at the onset of the diet, were significantly lower when compared with healthy controls. The expression of the transcripts for both proteins was increased significantly after the diet. The gene expression of the transcripts for FLG reached values similar to those in healthy controls. Despite the increased expression of the transcripts for DSG1 after the diet, expression levels were still lower than in healthy controls (Figure 4). Comparison of the baseline DSG1 and FLG expression in partial/non-responders to complete responders showed that the expression in partial/non-responders seems to be below those of responders, although it did not reach statistical significance (FLG 4 × 10−2(1 × 10−2–2 × 10−2) vs. 19 × 10−2(10 × 10−2–32 × 10−2), P=0.06 and DSG1 8 × 10−3(.6 × 10−3–22 × 10−3) vs. 30 × 10−3(10 × 10−3–140 × 10−3) P=0.08). This potential difference in FLG and DSG1 gene expression between responders and partial/non-responders persisted after the elemental diet.
The baseline gene expression levels of the tight junction proteins ZO-1 and CLDN1 were not significantly different compared with those found after the diet. In addition, the expression of ZO-1 and CLDN1 after diet did not significantly differ from values seen in healthy controls. Interestingly, the baseline expression of CLDN1 was significantly higher in EoE patients compared with healthy controls (Figure 4).
The expression of genes encoding FLG, ZO-1 and CLDN1 in the duodenal biopsy specimens was not affected by the diet and values before and after the diet were not significantly different. Notably, the baseline gene expression of DSG1 was significantly higher compared with the expression values after diet. Comparison of the gene expression of FLG, DSG1, and ZO-1 in patients at baseline and after the diet to the gene expression in healthy controls showed no significant differences. However, the baseline CLDN1 expression in EoE patients was significantly higher than that in healthy controls (Figure 5).
Spearman’s correlation analysis demonstrated a negative correlation between peak eosinophil counts and esophageal mucosal impedance and TER (r=−0.48 and r=−0.68 both <0.05). A positive correlation was found between peak eosinophil counts and esophageal mucosa permeability, expressed as the transepithelial flux of fluorescein and rhodamine (r=0.43 and r=0.49, both P<0.05). Consequently, a negative correlation was found between peak eosinophil counts and the esophageal gene expression of the transcripts for the barrier integrity proteins FLG and DSG1 (r=−0.56 and r=−0.57, both P<0.05).
Esophageal TER was positively correlated to the gene expression of FLG (r=0.44, P<0.05) and DSG1 (r=0.61, P<0.05). In addition, esophageal mucosal impedance correlated positively with the gene expression of the transcripts for the barrier integrity proteins FLG (r=0.46, P<0.05) and DSG1 (r=0.54, P<0.05).
This prospective study was the first study to demonstrate that, in EoE, induction of remission, by excluding dietary allergen with use of an elemental diet, leads to recovery of the esophageal mucosal integrity. To our knowledge, the small intestinal permeability of EoE patients has never been investigated prospectively before and after treatment in the same cohort. Our study gives a comprehensive overview of the esophageal and duodenal mucosal integrity in EoE by studying five different measures.
We demonstrate that complete avoidance of dietary allergens, achieved by an elemental diet, leads to restoration of the mucosal impedance and disturbed permeability of the esophageal mucosa. After 4 weeks of elemental diet, the esophageal mucosal impedance and permeability corresponded with the values observed in healthy controls. Although the elemental diet significantly improved the esophageal TER, values did not completely normalize when compared with healthy controls. Besides restoration of the esophageal mucosal integrity, the reduced baseline gene expression of the transcripts for barrier integrity protein FLG and DSG1 in the esophageal biopsy specimens is increased significantly by an elemental diet. Comparison of esophageal TER and FLG and DSG1 expression of complete responders to partial/non-responders showed that responders had a greater improvement after diet, suggesting that improvement paralleled histologic response. In contrast to the convincing effects of the elemental diet on the esophageal mucosal integrity, the duodenal mucosal integrity seemed not be affected and the duodenal mucosal integrity was not impaired compared with healthy controls.
The small intestinal permeability of EoE patients has been investigated twice before. Our results are in keeping with the conclusion of Leung et al., that an alteration in small intestinal permeability does not play a role in EoE (26). In contrast, the group of Katzka et al. demonstrated an increased small intestinal permeability in patients with active EoE (12). Intestinal permeability depends on numerous factors, and potentially plays a role in atopic dermatitis, food allergy and asthma (27). EoE patients often present with concurrent allergic diatheses, and although Katzka et al. found an equal distribution of concurrent allergic diatheses among groups, the disease severity and activity could have differed between groups. This may have been an explanation for the observed increased intestinal permeability. Additionally, the measurements were not performed in the same patients before and after treatment. Furthermore, in a majority of Katzka’s patients disease remission was achieved upon topical steroid treatment, which could have had a beneficial effect on other atopic diatheses, which are associated with increased intestinal permeability.
The present study indicates that in EoE patients the inflammation and mucosal integrity disruption seem to be restricted to the esophagus. A possible explanation is that EoE is initiated and regulated by a local immune response. Indeed, several studies suggested local esophageal B and T cell activation, including class cell recombination to IgE in the esophagus, local IgE production and IgE-bearing mast cells in the esophageal mucosa (28, 29). Moreover, it has been shown that esophageal epithelial cells are able to process and present antigens, possibly stimulating a Th-2 immune response (30).
Given the paucity of data in the literature on the effect of dietary treatment on the esophageal mucosal integrity, a direct comparison between previous studies is difficult. However, we previously demonstrated that, in PPI-REE patients, histological response to PPI treatment was associated with improvement of the esophageal integrity (31). Subsequently, it was shown that successful topical steroid treatment restored the esophageal integrity in EoE patients (6). An elemental diet counteracts the esophageal inflammation in EoE by elimination of food allergens in sensitized patients, whereas topical steroids attack the inflammatory cells or modify signaling pathways (32). Despite different approaches, the esophageal mucosal integrity values of patients who responded successfully to topical steroid treatment were also comparable with values in healthy controls (6). These findings imply that histologic response to dietary or immunosuppressant approaches result in a comparable complete restoration of the esophageal mucosal integrity, suggesting that the disruption is at least partly secondary to esophageal inflammatory damage. Nevertheless our study was not specifically designed to answer this question and further mechanistic research is warranted to confirm that the barrier function defect is indeed secondary to inflammatory injury.
A major question relevant for EoE is how food allergens initiate the esophageal inflammation and disrupt the esophageal mucosal integrity. We have previously shown that Thymic Stromal Lymphopoietin (TSLP), a cytokine which drives the inflammatory response in multiple Th2-type associated allergic diatheses, was overexpressed in esophageal biopsy specimens of patients with active EoE, and normalized by complete absence of food allergens (16, 33). Recently, in an experimental study, it was shown that in vitro food allergen stimulation of esophageal epithelial cells induced TSLP secretion, which in turn may activate esophageal dendritic cells leading to a Th-2 immune response (33). In addition, in vitro incubation of monocytes with specific allergens led to elevations of the EoE-associated inflammatory cytokines IL-5 and IL-13, showing that food allergens can directly activate the immune system. Our current study follows previous work in which we have demonstrated that the overexpression of the transcripts for IL-5 and IL-13 in active EoE was reversed by absence of food allergens through an elemental diet (16). Considering the ability of IL-13 to downregulate DSG1 and FLG, we assume that in our study the upregulation of IL-13 is at least partly responsible for the impaired gene expression of the transcripts for FLG and DSG1 (9, 10). Although the gene expression of FLG was normalized, gene expression of DSG1 was only partly restored upon elemental dietary treatment. DSG1 dysfunction induces segregation of epithelial cells which is histologically described as diluted intercellular spacing (DIS) or spongiosis (10). Remarkably, spongiosis could not completely be resolved by elemental dietary treatment or by topical steroid treatment (6); these findings may support the hypothesis that the expression of DSG1 recovers slower than the 4-week follow-up of our study (6, 14).
An alternative explanation is that this resultant impairment of the mucosal barrier in the absence of food allergens is preexisting and may facilitate initial transepithelial allergen passage and thus initiate inflammation. It has recently been shown that antigen penetration in active EoE might indeed be facilitated by impairment of epithelial integrity (34). These findings would argue against impaired mucosal integrity as a pure consequence of the inflammation, and suggest it is a primary defect predisposing to EoE. Given that the relationship between an impaired epithelial barrier function and allergy has been studied extensively in atopic dermatitis, and since the pathophysiological mechanisms seem to align, we hypothesized that tight junction proteins CLDN1 and ZO-1, both dysregulated in atopic dermatitis, would play a role in the pathogenesis of EoE (8). However, in this study we found no decreased expression of genes encoding CLDN1 and ZO-1. These results are in keeping with the conclusion for previous studies (10). Altogether, these data suggest that the impaired mucosal integrity in EoE is not affected by an alteration of tight junctions.
The limitations of this study must be pointed out. The first of these is the relatively small sample size, which is, however, comparable with that of other prospective mechanistic EoE trials. The sample size was large enough to find strong significant differences. Second, the ETIS has not been validated for duodenal tissue. However, the values of healthy controls served as a valuable reference standard and ETIS has successfully been used to detect the electrical characteristics of many different tissues, and ETIS measurements correlated with the other parameters of duodenal mucosal integrity (35). Third, we have evaluated gene expressions, which is a prediction of protein expression. It would have provided additional information if we would have measured the actual changes in the encoded proteins.
In conclusion, complete dietary allergen avoidance, using an elemental diet, restores the impaired esophageal mucosal integrity. This study confirms that dysregulation of filaggrin and desmoglein-1 plays a role in the impaired esophageal barrier function rather than alterations in tight junction proteins. Finally, our study provides further evidence that impaired duodenal mucosal integrity is not involved in the pathogenesis of EoE.
SUPPLEMENTARY MATERIAL is linked to the online version of the paper at http://www.nature.com/ajg
Guarantor of the article: Marijn J. Warners, MD.
Specific author contributions: Conception and design; M.J.W., B.J.V.-B., B.D.v.R., M.T.J.V.A., L.F.H. and A.J.B. Analysis and interpretation of the data; M.J.W., P.H.P.v.H., B.J.V.-B., J.V., W.J.J. and A.J.B. Drafting of the article: M.J.W. Critical revision of the article for important intellectual content; M.J.W., B.J.V.-B., J.V., B.D.v.R., M.T.J.V.A., L.F.H., W.J.J., A.J.P.M.S. and A.J.B. Final approval of the article; M.J.W., B.J.V.-B., P.H.P.v.H., J.V., B.D.v.R., M.T.A., L.F.H., W.J.J., A.J.P.M.S. and A.J.B.
Financial support: A.J.B. received research funding from Endostim and Danone and received speaker and/or consulting fees from MMS, Astellas, AstraZeneca, Almirall and Allergan. W.J.J. (VIDI grant) is supported by the Netherlands Organization for Scientific Research (NWO). W.J.J. received research funding from Glaxo Smith Kline Research, and Mead Johnson Nutrition. M.T.A. and L.F.H. are employees of Nutricia Research—results of the current study do not affect salary. This study was an investigator-initiated study, partly funded by Nutricia Research.
Potential competing interests: None.