Carlo Sguazzini
University of Turin
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Featured researches published by Carlo Sguazzini.
Inflammatory Bowel Diseases | 2008
Daniele Simondi; Giulio Mengozzi; Silvia Betteto; Renato Bonardi; Roberta Patrizia Ghignone; Sharmila Fagoonee; Rinaldo Pellicano; Carlo Sguazzini; Roberto Pagni; Mario Rizzetto; Marco Astegiano
Background: The objective of the study was to evaluate the diagnostic accuracy of recently developed antiglycan serological tests in clinical practice for the diagnosis of Crohns disease. Methods: This study was a cohort analysis of both clinical and biochemical parameters of patients with diagnosed inflammatory bowel disease compared with those in a control population. Antiglycan antibodies were determined using commercially available enzyme immunoassays. The setting was the outpatient unit of the gastroenterology department of a large, tertiary‐care referral academic hospital. Participants were 214 consecutive patients, enrolled over a 5‐month period, including 116 with Crohns disease and 53 with ulcerative colitis, as well as 45 with other gastrointestinal diseases and 51 healthy controls. Results: Anti–Saccharomyces cerevisiae antibodies showed the best performance (54% sensitivity and 88%–95% specificity for Crohns disease). Among patients with negative anti‐Saccharomyces antibodies, 19 (34%) had high titers of at least another tested antiglycan antibody. Anti‐Saccharomyces and anti‐laminaribioside antibodies were associated with disease involving the small bowel and with penetrating or stricturing phenotype. Anti‐laminaribioside was significantly higher in patients with a familial history of inflammatory bowel disease. Conclusions: The new proposed serological markers are significantly associated with Crohns disease, with low sensitivity but good specificity. About one third of anti‐Saccharomyces‐negative patients may be positive for at least 1 of those markers. Antiglycan antibodies appear to be associated with characteristic localization and phenotype of the disease.
Scandinavian Journal of Gastroenterology | 2015
Anna Greco; Gian Paolo Caviglia; Paola Brignolo; Davide Giuseppe Ribaldone; S. Reggiani; Carlo Sguazzini; Antonina Smedile; Rinaldo Pellicano; Andrea Resegotti; Marco Astegiano; Francesca Bresso
Abstract Objective. Small intestinal bacterial overgrowth (SIBO) is characterized by an abnormal proliferation of bacterial species in the small bowel. It has been shown that patients with Crohn’s disease (CD) have a higher risk of SIBO development. The aim of the present study was to investigate SIBO prevalence in CD patients, possible clinical predictors of SIBO development and response to antibiotic therapy. Material and methods. Sixty-eight patients (42 male, 26 female; mean age 49.3 ± 12.8 years) with CD reporting abdominal complaints were prospectively evaluated for SIBO with H2/CH4 glucose breath test (GBT). Results. Of the 68 patients enrolled, 18 (26.5%) tested positive for SIBO. Patients with SIBO exhibited increased stool frequency and significant reduction of stool solidity (p = 0.014), were older than patients tested negative to GBT (54.3 ± 13.0 years vs. 47.5 ± 12.3 years, p = 0.049), reported a longer history of CD (21.2 ± 10.3 years vs. 15.7 ± 10.2 years, p = 0.031) and showed a significant higher frequency of prior surgery (p = 0.001), revealing an association of number of surgical procedures (OR = 2.8315, 95% CI = 1.1525–6.9569, p = 0.023) with SIBO. Breath test normalization occurred in 13/15 patients evaluated after antibiotic and probiotic therapy. Although vitamin B12 levels were lower in patients with SIBO (p = 0.045) and a significant improvement was found after treatment (p = 0.011), this could be due to the heterogeneity, regarding vitamin B12 treatment, in our cohort. Conclusion. SIBO is a frequent but underestimated condition in CD, which often mimics acute flare, effectively identified with GBT and could be treated with a combined antibiotic and probiotic therapy.
Minerva Medica | 2017
Gian Paolo Caviglia; Carlo Sguazzini; Fabio Cisarò; Davide Giuseppe Ribaldone; Chiara Rosso; Sharmila Fagoonee; Antonina Smedile; Giorgio Saracco; Marco Astegiano; Rinaldo Pellicano
BACKGROUND Gastric motility is a key-factor in the pathogenesis of functional dyspepsia (FD). 13C-octanoic Acid Breath Test (OBT) is a tool used for measuring gastric emptying time in clinical setting. We aimed to investigate the variation in FD symptoms and OBT parameters after treatment with buspirone, amitriptyline or clebopride. METHODS Between Jan-2007 and Dec-2014, we enrolled 59 patients with FD unresponsive to first-line therapy with proton pump inhibitors and/or domperidone that underwent OBT before and after 3 months of buspirone (N.=32), amitriptyline (N.=16) or clebopride (N.=11) treatment. RESULTS Early satiation severity was positively correlated with gastric half emptying time (t1/2) (r=0.3789, P=0.003) and gastric lag phase (r=0.3371, P=0.011), and negatively correlated with gastric emptying coefficient (r=-0.3231, P=0.015). A reduction in t1/2 measurement in association to postprandial fullness, and early satiation severity improvement was observed (P=0.009, P=0.005 and P<0.001, respectively). Patients treated with buspirone obtained both a decrease in t1/2 (P=0.005) and an amelioration in early satiation (P=0.001). Patients under amitriptyline treatment experienced an improvement in postprandial fullness (P=0.046), whereas no variation was reported in patients treated with clebopride. CONCLUSIONS Patients with FD, non-responders to first-line therapy and reporting meal-related discomfort, may benefit from buspirone or amitriptyline-based therapies.
Minerva Medica | 2008
Sapone N; Rinaldo Pellicano; Daniele Simondi; Carlo Sguazzini; Reggiani S; Terzi E; Mario Rizzetto; Marco Astegiano
Journal of Ultrasound | 2015
Davide Giuseppe Ribaldone; Teresa Cammarota; Andrea Resegotti; Antonino Sarno; Daniela Robotti; Paola Debani; Giovanni Bonenti; Francesca Bresso; Rinaldo Pellicano; Alessandro Adriani; Carlo Sguazzini; S. Reggiani; Marco Astegiano
Digestive and Liver Disease | 2015
M. Bruno; Andrea Marengo; C. Elia; S. Caronna; W. Debernardi-Venon; Selene F. Manfrè; A. Musso; Flavia Puglisi; Carlo Sguazzini; Mario Rizzetto; Claudio De Angelis
Digestive and Liver Disease | 2014
Marco Astegiano; P Brignolo; Alessandro Adriani; S. Reggiani; Carlo Sguazzini; Davide Giuseppe Ribaldone; Nicoletta Sapone; I Dileo; Andrea Resegotti; Rinaldo Pellicano
Digestive and Liver Disease | 2013
Stefano Pantaleoni; Giovanni Antonio Touscoz; Gian Paolo Caviglia; Alessandro Adriani; Carlo Sguazzini; Nicoletta Sapone; S. Reggiani; Mario Rizzetto; Marco Astegiano
Digestive and Liver Disease | 2012
Alida Andrealli; M. Luchino; Davide Giuseppe Ribaldone; N. Sapone; L. Cosso; Carlo Sguazzini; F. Cisarò; Marco Astegiano
Digestive and Liver Disease | 2011
G. Bonagura; Carlo Sguazzini; L. Bertolusso; M. Luchino; D. Simondi; Rinaldo Pellicano; N. Sapone; Mario Rizzetto; Marco Astegiano