METHODS
1. Setting
This was a prospective, observational study assessing the association between the histological remission and long-term clinical course in patients with UC, conducted in the Departments of Gastroenterology and Pathology, Dayanand Medical College and Hospital, Ludhiana, between January 2014 to June 2015 (18 months) and subsequently followed up for 1 year.
2. Patients and Treatment
The diagnosis of UC was based on accepted clinical, endoscopic, and histological criteria. Clinical remission was defined as a Simple Clinical Colitis Activity Index ≤2 for at least 6 months and endoscopic remission (normal with clearly visible vascular pattern or erythema with decreased vascular pattern but no bleeding, i.e., Mayo score ≤1). Patients with active disease on endoscopy (Mayo ≥2) were excluded.
3. Histological Evaluation
Patients who were in clinical remission (n=76) for at least 6 months were subjected to ileocolonoscopy. Patients who were in endoscopic remission (46/76, 60.5%) were subjected to 4 biopsies from the rectosigmoid region to evaluate histological activity. As per Geboes criteria (2000), grade 0/1 was defined as histological remission.
3 All the biopsies were evaluated by 1 gastrointestinal pathologist (N.S.). The patient characteristics (age, gender, endoscopic findings, duration of disease, duration of remission, and histopathology) were recorded (
Fig. 1). Written consent was obtained from the patients and ethical approval from the Institutional Review Board of Dayanand Medical College and Hospital (ECR/715/Inst/PB/2015) was also obtained in April/May 2013.
4. Follow-up
The patients showing endoscopic remission were maintained on a stable dose of mesalamine and azathioprine/6-mercaptoprine and were followed up for 1 year to observe the clinical course. Patients on steroids, biological therapies, rectal mesalamine, or steroid enemas were not included in the present study.
5. Statistical Analysis
The data collected were subjected to statistical analysis. Mean and standard deviation were computed and paired t- and Z-tests were applied to evaluate the association between the 2 variables and to compare the means of the 2 groups. A significance difference was defined at an appropriate degree of freedom at the 1% and 5% levels of significance (P<0.05).
DISCUSSION
Although the concept of “deep remission” has developed in CD, it has not been replicated in those with UC. Most studies on mucosal healing focus on endoscopic scores, and the data from various trials suggests that patients with Mayo score 0 (complete mucosal healing) have longer-lasting remissions. However, patients with UC who are in clinical and endoscopic remission may still have histologically active disease and are at a high risk of having a relapse,
2,4 thus suggesting the need for repeat biopsy and histopathology once mucosal healing has been achieved. Current practice in UC patients is focused on achieving endoscopic mucosal healing and to date there is no consensus about when to include histological remission in the definition of mucosal healing. These observations make this analysis pertinent and are the first from Asia highlighting the discrepancy between endoscopic and histological remission for clinical outcomes of UC patients.
Of the 46 patients who were in endoscopic remission in our study, 67.3% patients (31/46) were in histological remission, but 32.6% (15/46) still had histologically active disease. When the long-term clinical outcomes were assessed after 1 year, the rate of a sustained clinical remission was significantly higher in patients who attained histological remission than among those who showed signs of active inflammation on histopathology (87.1% vs. 46.6%,
P=0.006). A recent study from the United Kingdom also reported moderate concordance between endoscopic and histological remission with 24% of patients with endoscopic remission having persistent mucosal inflammation on biopsy.
4 These findings highlight the fact that histological remission is distinct from endoscopic mucosal healing and it is a better predictor of a sustained clinical remission. Thus, histological remission may be a better endpoint for assessing long-term clinical outcomes including risk of colon cancer, as well as effectiveness of a drug in a clinical trial.
When patients with endoscopically quiescent disease are subjected to biopsy, the histopathology may show features that suggest disease activity. These include the presence of neutrophilic infiltrates in the lamina propria, epithelial cell damage (loss of cells, mucin depletion, cryptitis, crypt abscesses, and erosion), and an increase in lymphocytes and plasma cells. The presence of neutrophils is a reliable indicator of disease activity, with a good inter-observer agreement in various studies. Histology may also predict relapse or dysplasia. Histological findings predictive of ensuing clinical relapse in patients with quiescent disease are the persistence of neutrophils, basal plasmacytosis, mildly active disease, and an elevated number of eosinophils.
2,3,4,5
In our study, more than 70% of patients in endoscopic remission showed mild crypt distortion and mild to moderate increases in chronic inflammatory cells in the lamina propria. The presence of eosinophils and neutrophils in the lamina propria, cryptitis, and crypt abscesses were seen only in the histologically active group. Thus, the presence of acute inflammatory infiltrates and crypt destruction were predictors of activity and relapse. These findings are consistent with other studies.
5,6
In a multivariate analysis of data from 74 patients with inactive UC, relapse was also predicted by the presence of basal plasmacytosis.
7 Although we observed basal plasmacytosis and basal lymphoid aggregates in biopsies of our UC patients, they failed to reach statistical significance to predict relapse. Similar observations were made by our group in a small prospective analysis previously and therefore we believe that some of these changes can be focal and serial step sectioning and better orientation of the specimen might be required.
8 This problem has considerable implications for the precision of scoring. Some index items, such as basal plasmacytosis, require perpendicular sections of well-oriented samples for accurate interpretation. Section thickness may also affect the interpretation of results. Similar observations were made by Riley et al.
5 who in a study of 82 patients with UC in symptomatic and sigmoidoscopic remission found an acute inflammatory cell infiltrate, presence of crypt abscesses, and mucin depletion to be associated with an increased risk of relapse. Most recently, in a retrospective analysis of a cohort of 75 patients with UC, Bessissow et al.
7 showed that despite normal endoscopy, histologic investigation showed inflammatory activity (Geboes score ≥3.1) in 40% of patients, and basal plasmacytosis in 21% of patients.
Factors such as age, gender, extent of disease, and duration of clinical remission were not found to be statistically significant in predicting relapse. We attribute this to the smaller number of patients in the analysis. A limitation of our study is that we did not analyze any of the available biological parameters but during our previous analysis these were not statistically significant.
8 Bessissow et al.
7 showed that on univariate analysis, the only serologic marker that favored clinical remission was CRP ≤5 mg/L, but this effect did not remain significant on multivariate analysis, which was most likely related to the fact that the inflammation was only limited to the mucosa. In addition, Schoepfer et al.
9 demonstrated that CRP is an inadequate biomarker of endoscopic disease activity in UC. It is also not surprising that albumin and hemoglobin were not predictive of relapse, because in patients with prolonged mucosal healing, one would expect them to be normalized.
1
Though achievement of histological healing provides a more accurate picture of recovery and improves the disease outcomes, it seems to be a relatively difficult goal to achieve. In addition to this, there are certain unresolved issues. Most of the scoring systems for endoscopy and histological features are either not validated or only partially validated.
3,4,10 There are no standard guidelines on how often one should perform colonoscopy and biopsy inpatients in clinical remission. Also, the inflammatory process in UC may be discontinuous during the natural course of the disease or after medical treatment, thus suggesting a need for several targeted biopsies, the number and method of acquisition of which is yet not clearly defined. Also, H&E can identify neutrophils and lymphocytes accurately but cannot determine the activation status of lymphocytes, for which immunochemistry is needed.
Thus, in conclusion, histological remission and healing serves as a better marker of treatment efficacy in patients with UC and is a better predictor of sustained remission in patients than endoscopic remission. Histologic remission and healing is an area of increased research focus and has the promise of being an important marker of treatment efficacy in UC, with the potential to guide treatment decisions in the future.
In conclusion, mucosal healing is associated with better clinical outcomes in patients with UC; however, histologic parameters may provide a more accurate picture of the recovery of the mucosa and further improve disease outcomes. This study indicates that histologic healing may be associated with better outcomes in UC thus providing a rationale for making this a treatment goal. The present analysis is small but is a progressive step towards better defining remission in UC.