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Dive into the research topics where Rosa Rosania is active.

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Featured researches published by Rosa Rosania.


World Journal of Gastrointestinal Pathophysiology | 2011

Mechanisms of Helicobacter pylori antibiotic resistance: An updated appraisal

Vincenzo De Francesco; Angelo Zullo; Cesare Hassan; Floriana Giorgio; Rosa Rosania; Enzo Ierardi

Helicobacter pylori (H. pylori) antibiotic resistance is the main factor affecting the efficacy of the current eradicating therapies. The aim of this editorial is to report on the recent information about the mechanisms accounting for the resistance to the different antibiotics currently utilized in H. pylori eradicating treatments. Different mechanisms of resistance to clarithromycin, metronidazole, quinolones, amoxicillin and tetracycline are accurately detailed (point mutations, redox intracellular potential, pump efflux systems, membrane permeability) on the basis of the most recent data available from the literature. The next hope for the future is that by improving the knowledge of resistance mechanisms, the elaboration of rational and efficacious associations for the treatment of the infection will be possible. Another auspicious progress might be the possibility of a cheap, feasible and reliable laboratory test to predict the outcome of a therapeutic scheme.


Current Clinical Pharmacology | 2013

Effect of probiotic or prebiotic supplementation on antibiotic therapy in the small intestinal bacterial overgrowth: A comparative evaluation

Rosa Rosania; Floriana Giorgio; Mariabeatrice Principi; Annacinzia Amoruso; Rosa Monno; Alfredo Di Leo; Enzo Ierardi

UNLABELLED Bacterial intestinal overgrowth syndrome (SIBO) treatment is based on antibiotics. Probiotics have been shown to give similar results, whilst no study is available about prebiotics. This study evaluated the addition of probiotics or prebiotics to antibiotics on SIBO symptoms in a 6-month follow-up. We enrolled 40 patients (14 males and 26 females) reporting abdominal compliant without gastrointestinal diseases/alarm symptoms. SIBO was diagnosed by the agreement of lactulose and glucose breath tests. Patients were randomly divided into two groups homogeneous for sex and age: group 1 received Rifaximin 400 mg/day for 7 days/month followed by Lactobacillus casei for 7 days more and group 2 antibiotic followed by short chain fructo-oligosaccharides. All patients recorded a questionnaire for subjective symptom evaluation according to Rome III criteria and Bristol scale for stool characters before the study and after 6 months. STATISTICS Students t and Fishers exact tests. In group 1, a significant improvement was obtained in 5 out of 6 symptoms, whilst in group 2 in 4 out of 6 symptoms (nausea and number of bowel movements failed to improve). Despite we observed a trend of probiotics to be more effective than prebiotics, the difference in the percentage of improved symptoms was not significant (83,3% vs 66.6%; p= 0.57). Our preliminary data show a good outcome with sequential antibioticprobiotic/ prebiotic administration in patients with SIBO.


Digestive and Liver Disease | 2009

Segmental colitis associated with diverticula: a rare clinical entity and a new challenge for the gastroenterologist

Enzo Ierardi; Cesare Hassan; Angelo Zullo; V. De Francesco; N. Della Valle; S. Prencipe; Rosa Rosania; Sergio Morini; C. Panella

BACKGROUND AND AIM Segmental colitis associated with diverticula (SCAD) has recently drawn a particular attention in the field of rare forms of colitis because of some peculiarities suggesting both its autonomy as a clinical entity and a resemblance with the most relevant forms of inflammatory bowel diseases (IBD). Aim of this review was to report the state of art on this topic. METHODS Epidemiological, clinical, endoscopic/histological and diagnostic features are described. Moreover, from both the pathogenetic and therapeutic point of view, new relevant information is highlighted regarding the possible role of tumour necrosis factor alpha (TNF-alpha) in mucosal inflammation. RESULTS SCAD would appear as a rare autonomous clinical entity distinctive of old age, although it is still not well defined. It is likely that prevalence of SCAD could have been underestimated in the past since its main clinical presentation (namely bleeding without pain) is often found in elderly patients with diverticula. Endoscopy and histology could be helpful to discriminate it from infectious diverticulitis. Increasing evidence encourages the concept that SCAD includes pathogenetic and therapeutic aspects peculiar of IBD. This could be relevant for clinical management of SCAD. Indeed, the resolution of a severe, refractory case of SCAD has been recently reported with biological drugs used for IBD therapy. This observation could encourage, in the near future, the use of biological therapy in severe forms of SCAD as an alternative to surgery.


European Journal of Clinical Nutrition | 2016

A comparison of the nutritional status between adult celiac patients on a long-term, strictly gluten-free diet and healthy subjects

Michele Barone; N Della Valle; Rosa Rosania; Antonio Facciorusso; A. Trotta; F. Cantatore; S. Falco; S. Pignatiello; Maria Teresa Viggiani; Annacinzia Amoruso; R De Filippis; A. Di Leo; Ruggiero Francavilla

Background/Objectives:There are conflicting data on the effect of a gluten-free diet (GFD) on the nutritional status of celiac patients. In the present study, we evaluated, in adult celiac patients, the influence of a long-term, strictly GFD on their nutritional status and compared it with matched healthy volunteers.Subjects/Methods:Our study included 39 celiac patients and 39 healthy volunteers. The body mass index (BMI) of patients and controls was evaluated at enrollment, while the patients’ BMI before the GFD was retrieved from clinical records. In addition, at enrollment, in both groups, we compared BMI, fat mass (FM), bone mineral density (BMD), as well as their dietary intake, recorded on a 7-day diary.Results:At the time of diagnosis, the majority of celiac patients (82.0%) had a normal BMI or were overweight, while 10.3% were malnourished. After the GFD, patients with a normal BMI showed a significant weight increase (P=0.002), but none of them switched in the overweight or obese category. Two (50%) of the four malnourished patients achieved a normal BMI. Controls and patients on a GFD had a similar BMI, FM, BMD and total calorie intake, but the amount of lipids and fiber intake was significantly different in the two groups (P=0.003 and P<0.0001, respectively).Conclusions:Our study demonstrates that a GFD is able to improve the nutritional status of celiac patients without inducing overweight or obesity. Our findings are related to a celiac population adopting a GFD based on a Mediterranean-type diet.


Scandinavian Journal of Gastroenterology | 2010

Mucosal assessment of tumor necrosis factor alpha levels on paraffined samples: a comparison between immunohistochemistry and real time polymerase chain reaction

Enzo Ierardi; Floriana Giorgio; Rosa Rosania; M. Zotti; S. Prencipe; Nicola Della Valle; Vincenzo De Francesco; C. Panella

Author(s) : Enzo IerardiArticle title : Mucosal assessment of tumor necrosis factor alpha levels on paraffined samples:a comparison between immunohistochemistry and real time polymerase chainreactionArticle no : 483739Dear Author,Please check these proofs carefully. It is the responsibility of the corresponding author to checkagainst the original manuscript and approve or amend these proofs. A second proof is notnormally provided. Informa Healthcare cannot be held responsible for uncorrected errors, even ifintroduced during the composition process. The journal reserves the right to charge for excessiveauthor alterations, or for changes requested after the proofing stage has concluded.The following queries have arisen during the editing of your manuscript and are marked in themargins of the proofs. Unless advised otherwise, submit all corrections using the CATS onlinecorrection form. Once you have added all your corrections, please ensure you press the “SubmitAll Corrections” button.


World Journal of Gastrointestinal Pathophysiology | 2010

Metabolic syndrome and gastro-esophageal reflux: A link towards a growing interest in developed countries

Enzo Ierardi; Rosa Rosania; M. Zotti; Simonetta Principe; G. Laonigro; Floriana Giorgio; Vincenzo De Francesco; C. Panella

The aim of this Editorial is to describe the growing possibility of a link between gastro-esophageal reflux disease (GERD) and metabolic syndrome on the light of recent epidemiological and pathophysiological evidence. The state of the art of GERD is described, based on recent definitions, pathophysiological evidence, epidemiology in developed countries, clinical subtypes together with a diagnostic approach specifically focussed on the appropriateness of endoscopy. Metabolic syndrome is accurately defined and the pivotal role of insulin resistance is emphasized. The strong relationship between GERD and metabolic syndrome has been pathophysiologically analyzed, taking into account the role of obesity, mechanical factors and metabolic changes. Data collected by our group regarding eating habits and GERD are briefly summarized at the end of a pathophysiological analysis. The literature on the subject strongly supports the possibility that lifestyle and eating habits may be involved in both GERD and metabolic syndrome in developed countries.


Journal of Clinical Pathology | 2011

Infliximab therapy downregulation of basic fibroblast growth factor/syndecan 1 link: a possible molecular pathway of mucosal healing in ulcerative colitis

Enzo Ierardi; Floriana Giorgio; M. Zotti; Rosa Rosania; Mariabeatrice Principi; S. Marangi; Nicola Della Valle; Vincenzo De Francesco; Alfredo Di Leo; Marcello Ingrosso; C. Panella

Background It is known that syndecan 1 in inflammatory bowel diseases is able to migrate from epithelial basolateral site to the stromal area and apical surface of epithelium with a consequent activation and modulation of basic fibroblast growth factor (bFGF), and this process sustains mucosal healing of ulcers. On the other hand, tumour necrosis factor (TNF) α mucosal levels are directly related to the entity of the damage in these disorders. Aim of the study A ‘post-hoc’ retrospective study was performed to estimate mucosal TNF α in rectal biopsies of subjects with ulcerative colitis (UC) before and after effective infliximab therapy and its relationship with syndecan 1, bFGF and endoscopic mucosal healing. Material and methods Paraffin-embedded rectal samples from 12 patients with UC responders to infliximab were analysed for TNF α, syndecan 1 and bFGF before and 6 months after therapy using a real-time reverse transcriptase polymersase chain reaction. Additionally, syndecan 1 location was evaluated by immunohistochemistry. Samples from 12 subjects with irritable bowel symptoms without endoscopic/histological abnormalities represented the control group. Mucosal healing induced by the treatment was defined by an endoscopic Mayo subscore changing from 2–3 to 0. ANOVA plus Student–Newman–Keuls was used for statistical analysis. Results The authors found that in the active disease, an increase in TNF α (p<0.001) is accompanied by raised levels of both syndecan 1 (p<0.005) and bFGF (p<0.005) compared with the control group. Infliximab-induced TNF α decrease to levels similar to controls is associated with both endoscopic mucosal healing and adhesion molecule/growth factor significant reduction. Additionally, syndecan 1 location, which is predominant in the stromal cells and apical epithelium in the active disorder, is quite exclusively located at the basolateral epithelial area in both healed mucosa and controls. Conclusions Balanced interaction among TNF α inhibition by infliximab, syndecan 1 migration, bFGF repair modulation and final adhesion molecule reversal to its normal location might represent a suitable molecular pathway of endoscopic mucosal healing in UC.


World Journal of Gastrointestinal Oncology | 2010

From chronic liver disorders to hepatocellular carcinoma: Molecular and genetic pathways

Enzo Ierardi; Rosa Rosania; M. Zotti; Floriana Giorgio; S. Prencipe; Nicola Della Valle; Vincenzo De Francesco; C. Panella

Hepatocarcinogenesis is a process attributed to progressive genomic changes that alter the hepatocellular phenotype producing cellular intermediates that evolve into hepatocellular carcinoma (HCC). During the preneoplastic phase, the liver is often the site of chronic hepatitis and/or cirrhosis, and these conditions induce liver regeneration with accelerated hepatocyte cycling in an organ that is otherwise proliferatively at rest. Hepatocyte regeneration is accelerated by upregulation of mitogenic pathways involving molecular and genetic mechanisms. Hepatic growth factors, inhibitors and triggers may also play a role. This process leads to the production of monoclonal populations of aberrant and dysplastic hepatocytes that have telomerase re-expression, microsatellite instability, and occasionally structural aberrations in genes and chromosomes. Development of dysplastic hepatocytes in foci and nodules and the emergence of HCC are associated with the accumulation of irreversible structural alterations in genes and chromosomes even if the genomic basis of the malignant phenotype is largely heterogeneous. Therefore, a malignant hepatocyte phenotype may be produced by changes in genes acting through different regulatory pathways, thus producing several molecular variants of HCC. On these bases, a key point for future research will be to determine whether the deletions are specific, due to particular loci in the minimally deleted regions of affected chromosome arms, or whether they are non-specific with loss of large portions of chromosomes or entire chromosome arms leading to passive deletion of loci. The final aim is the possibility of identifying a step where carcinogenetic processes could be terminated.


Current Drug Safety | 2011

The Use of Human Albumin for the Treatment of Ascites in Patients with Liver Cirrhosis: Item of Safety, Facts, Controversies and Perspectives

Antonio Facciorusso; Maurizio Cosimo Nacchiero; Rosa Rosania; G. Laonigro; Nunzio Longo; C. Panella; Enzo Ierardi

Albumin constitutes approximately one half of the proteins in the plasma and plays a pivotal role in modulating the distribution of fluid between body compartments. Hence it is commonly employed in cirrhotic patients in association with diuretics for the treatment of ascites. Nevertheless, its usefulness is controversial in this condition and well-stated only in some circumstances. The item of safety of the drug appears to be convincing due to the accurate cautions in the course of its preparation. Side effects are described in literature only as sporadic events. Indeed, albumin administration is effective to prevent the circulatory dysfunctions after large-volume paracentesis and renal failure and after Spontaneous Bacterial Peritonitis (SBP). Finally albumin represents, associated with vasoconstrictors, the therapeutic gold standard for the hepatorenal-syndrome (HRS). Physiopathological bases of the therapeutic use of albumin in hepatic cirrhosis consist in both hypoalbuminemia and portal hypertension consequences. In fact, cirrhotic patient with ascites, in spite of hydrosaline retention, shows an effective hypovolemia with peripheral arterial vasodilatation and increase in heart rate. Therefore the effectiveness of albumin administration in the treatment of ascites is due to its plasma volume expander property as well as its efficacy in restoring plasmatic oncotic pressure. Trials are in progress in order to define the effectiveness of the prolonged home-administration of human albumin in the treatment and prevention of ascites. Finally, it has been recently demonstrated that the binding, transport and detoxification capacities of human albumin are severely reduced in cirrhotics and this impairment correlates with the degree of liver failure. Therefore, the next challenge will be to determine whether the alterations of non-oncotic properties of albumin are able to forecast mortality in cirrhotics with ascites and exogenous albumin chronic administration will be effective in predicting and preventing such alterations.


Gastroenterology | 2013

Su1986 Epithelial Proliferation/Apoptosis Balance in Atrophic Gastritis in Presence and Absence of Gastric Cancer: A Molecular/ Immunohistochemical Evaluation

Rosa Rosania; Mariya Varbanova; Cosima Langner; Jan Bornschein; Eloriana Giorgio; Enzo Ierardi; Peter Malfertheiner

Background/Aims: According to Correas hypothesis, adenoma at stomach plays a role in gastric carcinogenesis as a precursor. Since endoscopic resection including endoscopic submucosal dissection for premaligant or cancerous lesion has been generally accepted as one of treatment options, endoscopist may have a chance to get the pathologic results showing early gastric cancer arising from adenoma (EGC-AFA). However there have been few reports about clinicopathologic characteristics of EGC-AFA. The aim of this study was to evaluate characteristics of EGC-AFA compared to de novo EGC treated by endoscopic resection. Methods: Between January 2008 and December 2011, 1005 EGCs form 981 S-524 AGA Abstracts patients by endoscopic resectionwere enrolled.We retrospectively reviewed clinicopathologic data of 1005 EGC lesions. Among them 161 lesions (16%) were EGC-AFA and 844 (84%) were de novo EGC. Results: There was no significant difference of age, sex, location of tumor, and gross morphology on EGD between two groups. Synchronous cancer was significantly more frequent in EGC-AFA than in de novo EGC (19.3% vs 10.3%, p=0.001). The tumor size of EGC-AFA measured on EGD was significantly larger than that of de novo EGC (16.6±9.9mm vs 14.5±7.3mm, p=0.004). However, there was no significant difference of actual tumor size on pathologic specimen. The frequency of pathologic discrepancy between biopsy specimen and resected one was higher in EGC-AFA than in de novo EGC (36.6% vs 24.2%, p=0.01). In pathologic characteristics, the differentiated type adenocarcinoma has been shown more frequent in EGC-AFA than de novo EGC (95% vs 88%, p= 0.009), and the submucosal invasion according to T stage (T1b) was significantly less frequent in EGC-AFA than in de novo EGC (12.4% vs 18.0%, p=0.001). Conclusion: The observation of co-existence of adenoma and carcinoma in one specimen is not uncommon. Due to association of adenomatous changes around cancerous lesion, misdiagnosis rate at biopy specimen higher in EGC-AFA and the size measurement of EGC-AFA might be exaggerated on EGD examination. The features of more differentiation and less invasiveness would give more favorable prognosis to EGC-AFA. The endoscopist should pay attention on synchronous ormetachronous lesions on follow up endoscopic examinationwhen encountered EGC-AFA.

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M. Zotti

University of Foggia

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N. Della Valle

University of Naples Federico II

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