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H1N1 influenza vaccination and IBD
The global pandemic of novel influenza A (H1N1) affected 70 countries in 2009. There was particular concern for infection in immunocompromised patients, including those with IBD. The 2009 H1N1 influenza vaccine produced seroprotection rates of >85% in the general population but there are no data on the immunogenicity of the vaccine in patients with IBD. In this issue of Gut, Cullen et al report their observational prospective open-label study which examined the immunogenicity of the 2009 H1N1 influenza vaccine in IBD patients. Patients with IBD vaccinated with the 2009 H1N1 influenza vaccine had a low rate of seroprotection, particularly those who were immunosuppressed or received combination immunosuppression (see table 1). An assay of T lymphocyte function may indicate those at risk of low rates of vaccine response. The work highlights the need for studies of the clinical benefit of vaccines in this population and patients with IBD need to be aware of this reduced immunogenicity (see page 385).
Visceral hypersensitivity in endometriosis
Patients with minimal to mild endometriosis often have symptoms that are out of proportion to the laparoscopic findings. The reason for this observation is unknown. IBS is also common in this setting and it feasible that the visceral hypersensitivity associated with this condition might be amplifying the symptoms of endometriosis. In this issue of Gut, Issa et al assessed visceral sensitivity to balloon distension, symptoms and psychological status following laparoscopy in women with minimal to mild endometriosis, moderate to severe endometriosis, laparoscopy negative abdominal pain and asymptomatic women undergoing laparoscopic sterilisation who acted as controls, and compared with women with IBS. They show that visceral hypersensitivity is common in patients with endometriosis and especially those with minimal to mild disease (see figure 1). They speculate that this might be the underlying mechanism that explains the paradoxical discrepancy between symptoms and extent of disease. This study has introduced a completely new concept into the understanding of pain in endometriosis and could open up new opportunities for treatment (see page 367).
A better way to do colonoscopy?
It is well known that standard colonoscopy misses adenomas, especially those located on the proximal aspects of haustral folds. So, there has been a lot effort put into developing more accurate endoscopic methods for polyp detection. Cap assisted colonoscopy is one of these methods. It uses a transparent plastic cap attached to the tip of the colonoscope that can help flatten and depress the colonic folds, thereby decreasing the blind mucosal areas. Although conceptually appealing and technically straight-forward, the results from prior studies have shown variable success rates with this method. In this issue, Amit and colleagues report on a randomised controlled trial on cap assisted colonoscopy in a western cohort. In this well-designed study, they found cap assisted colonoscopy detected a significantly higher proportion of subjects with at least one adenoma as well as higher number of adenomas per subject compared to standard colonoscopy. Perhaps most importantly, they found cap assisted colonoscopy also detected significantly more right sided adenomas and flat adenomas compared to standard colonoscopy (see page 402).
New molecular markers for high-risk GISTs
Gastrointestinal stromal tumours (GIST's) are the most common mesenchymal tumours of the gastrointestinal tract. They are often cured by surgical resection alone, but a subset of these tumours will metastasize. There are two predominant prognostic features (tumour size and mitotic index) of primary GISTs that are currently used for risk stratification. Although clinically of some value, these features misclassify a subset of cases as low risk that nonetheless metastasize. Okamoto and colleagues have now used state of the art genome-wide DNA methylation analysis to find more accurate molecular markers for determining the prognosis of GISTs. They found more genes were methylated in advanced GIST than small GIST, suggesting a link between the accumulation of DNA methylation and disease progression. In one of the largest series of GISTs published to date, they found three methylated genes, REC8, PAX3 and p16/CDKN2A, significantly correlated with a worse prognosis, suggesting that these may be used in the clinic in the near future to identify those patients who may be candidates for adjuvant therapy (see page 392).
MR spectroscopy for detection of NAFLD in a Chinese population
This interesting paper describes a prospective, cross-sectional study on the prevalence of non-alcoholic fatty liver disease (NAFLD) in a large cohort randomly selected from the Hong Kong population. Just recently Clavien's group suggested MR imaging as new reference standard for quantifying hepatic steatosis (Gut 2012;61:117–27). Interestingly, by use of proton MR spectroscopy the present study found a 27% prevalence of NAFLD which was clearly age dependent and to some extent also gender dependent (see figure 3). Advanced fibrosis as determined by elastography was found in only 4%. Modest alcohol consumption was not associated with neither fatty liver nor with fibrosis. These results indicate that MR spectroscopy might be a useful tool to screen for NAFLD (see page 409).
An intra-tumoral gene signature focusing on inflammation predicts survival in patients with early HCC
This intriguing study investigated the importance of inflammation in the tumour microenvironment for progression of hepatocellular carcinoma (HCC). The authors identified a signature of 14 immune genes expressed in resected HCC tissue as predictor of survival in training and independent validation cohorts, respectively. This was striking for patients with early stages of HCC. The thorough and comprehensive work also demonstrates a functional correlation between the expression of some of these genes coding for chemokines and the infiltration by lymphocytes or NK cells. The authors propose a model (lure 6F) to explain the immune mechanism underlying survival probability in early HCC (see figure 4) (see page 427).
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