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Dive into the research topics where S. Moscarella is active.

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Featured researches published by S. Moscarella.


Hepatology | 2007

Acute viral hepatitis increases liver stiffness values measured by transient elastography

Umberto Arena; Francesco Vizzutti; Giampaolo Corti; Silvia Ambu; Cristina Stasi; Silvia Bresci; S. Moscarella; Vieri Boddi; Antonio Petrarca; Giacomo Laffi; Fabio Marra; Massimo Pinzani

Liver tissue alterations other than fibrosis may have an impact on liver stiffness measurement. In this study we evaluated 18 patients without a previous clinical history of liver disease, consecutively admitted for acute viral hepatitis. In each patient, aminotransferase determination and liver stiffness measurement were performed on the same study day, at 3 different points: (1) peak increase in aminotransferase; (2) aminotransferase 50% or less of the peak; (3) aminotransferase levels ≤2× the upper limit of normal. In all patients, the degree of liver stiffness at the time of the peak increase in aminotransferases exceeded the cutoff values proposed for the prediction of significant fibrosis or cirrhosis. A progressive significant reduction in liver stiffness values was observed (P < 0.0001) in the follow‐up period in parallel with the reduction of aminotransferase levels (P < 0.0001). Moreover, a statistically significant, positive correlation between aminotransferases and liver stiffness measurement (LSM) at the onset of acute viral hepatitis was found (r = 0.53, P = 0.02 and r = 0.51, P = 0.03 for alanine aminotransferase and aspartate aminotransferase, respectively). In conclusion, the extent of necroinflammatory activity needs to be carefully considered in future studies aimed at further validating transient elastography, particularly in patients with absent or low‐stage liver fibrosis (in other words, F0‐F2 METAVIR). LSM does not represent a reliable instrument to detect the presence of advanced fibrosis and cirrhosis in patients presenting with a clinical picture of acute hepatitis. (HEPATOLOGY 2007.)


Hepatology | 2007

Liver stiffness measurement predicts severe portal hypertension in patients with HCV‐related cirrhosis

Francesco Vizzutti; Umberto Arena; Roberto Giulio Romanelli; Luigi Rega; Marco Foschi; Stefano Colagrande; Antonio Petrarca; S. Moscarella; Giacomo Belli; Anna Linda Zignego; Fabio Marra; Giacomo Laffi; Massimo Pinzani

Measurement of hepatic venous pressure gradient (HVPG) is a standard method for the assessment of portal pressure and correlates with the occurrence of its complications. Liver stiffness measurement (LSM) has been proposed as a noninvasive technique for the prediction of the complications of cirrhosis. In this study, we evaluated the ability of LSM to predict severe portal hypertension compared with that of HVPG in 61 consecutive patients with HCV‐related chronic liver disease. A strong relationship between LSM and HVPG measurements was found in the overall population (r = 0.81, P < 0.0001). However, although the correlation was excellent for HVPG values less than 10 or 12 mm Hg (r = 0.81, P = 0.0003 and r = 0.91, P < 0.0001, respectively), linear regression analysis was not optimal for HVPG values ≥10 mm Hg (r2 = 0.35, P < 0.0001) or ≥12 mm Hg (r2 = 0.17, P = 0.02). The AUROC for the prediction of HVPG ≥10 and ≥12 mm Hg were 0.99 and 0.92, respectively and at LSM cutoff values of 13.6 kPa and 17.6 kPa, sensitivity was 97% and 94%, respectively. In patients with cirrhosis, LSM positively correlated with the presence of esophageal varices (P = 0.002), although no correlation between LSM and esophageal varices size was detected. The area under the ROC for the prediction of EV was 0.76 and at a LSM cutoff value of 17.6 kPa sensitivity was 90%. Conclusion: LSM represents a non‐invasive tool for the identification of chronic liver disease patients with clinically significant or severe portal hypertension and could be employed for screening patients to be subjected to standard investigations including upper GI endoscopy and hemodynamic studies. (HEPATOLOGY 2007;45:1290–1297.)


Gut | 2008

Reliability of transient elastography for the diagnosis of advanced fibrosis in chronic hepatitis C

Umberto Arena; Francesco Vizzutti; Juan G. Abraldes; Giampaolo Corti; Cristina Stasi; S. Moscarella; Stefano Milani; E. Lorefice; Antonio Petrarca; Roberto Giulio Romanelli; Giacomo Laffi; Jaume Bosch; Fabio Marra; Massimo Pinzani

Background: Transient elastography (TE) has received increasing attention as a means to evaluate disease progression in patients with chronic liver disease. Aim: To assess the value of TE for predicting the stage of fibrosis. Methods: Liver biopsy and TE were performed in 150 consecutive patients with chronic hepatitis C-related hepatitis (92 men and 58 women, age 50.6 (SD 12.5) years on the same day. Necro-inflammatory activity and the degree of steatosis at biopsy were also evaluated. Results: The areas under the curve for the prediction of significant fibrosis (⩾F2), advanced fibrosis (⩾F3) or cirrhosis were 0.91, 0.99 and 0.98, respectively. Calculation of multilevel likelihood ratios showed that values of TE <6 or ⩾12, <9 or ⩾12, and <12 or ⩾18, clearly indicated the absence or presence of significant fibrosis, advanced fibrosis, and cirrhosis, respectively. Intermediate values could not be reliably associated with the absence or presence of the target condition. The presence of inflammation significantly affected TE measurements in patients who did not have cirrhosis (p<0.0001), even after adjusting for the stage of fibrosis. Importantly, TE measurements were not influenced by the degree of steatosis. Conclusions: TE is more suitable for the identification of patients with advanced fibrosis than of those with cirrhosis or significant fibrosis. In patients in whom likelihood ratios are not optimal and do not provide a reliable indication of the disease stage, liver biopsy should be considered when clinically indicated. Necro-inflammatory activity, but not steatosis, strongly and independently influences TE measurement in patients who do not have cirrhosis.


Hepatology | 2013

Liver stiffness is influenced by a standardized meal in patients with chronic hepatitis C virus at different stages of fibrotic evolution

Umberto Arena; Monica Lupsor Platon; Cristina Stasi; S. Moscarella; Alı̀ Assarat; Giorgio Bedogni; Valeria Piazzolla; Radu Badea; Giacomo Laffi; Fabio Marra; Alessandra Mangia; Massimo Pinzani

Transient elastography (TE) is increasingly employed in clinical practice for the noninvasive detection of tissue fibrosis in patients with chronic liver disease (CLD), and particularly chronic hepatitis C virus (HCV)‐related hepatitis. The present study was designed to provide a definitive characterization of the “confounding” increase in liver stiffness (LS) following a standardized meal in a consecutive population of 125 patients with chronic HCV infection at different stages of fibrotic evolution. LS values were obtained after overnight fasting and 15, 30, 45, 60, and 120 minutes following the onset of a standardized liquid meal (400 mL, 600 Kcal, 16.7% protein, 53.8% carbohydrates, 29.5% fat). An evident increase in LS values was observed 15 to 45 minutes after the onset of the meal with return to baseline premeal levels within 120 minutes in all patients. The peak postmeal delta increase in LS was progressively more marked with increasing stages of fibrosis (P < 0.001), becoming maximal in patients with cirrhosis. However, the probability of identifying the Metavir stage of fibrosis, the Child‐Pugh class, or the presence/absence of esophageal varices with the postmeal delta increase in LS was inferior to that obtained with baseline LS values. Conclusion: The results of the present study provide definitive evidence of the confounding effect of a meal on the accuracy of LS measurements for the prediction of fibrosis stage in patients with chronic HCV hepatitis and suggest that a fasting period of 120 minutes should be observed before the performance of TE. (HEPATOLOGY 2013;)


Current Therapeutic Research-clinical and Experimental | 1993

THERAPEUTIC AND ANTILIPOPEROXIDANT EFFECTS OF SILYBIN-PHOSPHATIDYLCHOLINE COMPLEX IN CHRONIC LIVER DISEASE: PRELIMINARY RESULTS

S. Moscarella; A. Giusti; Fabio Marra; C. Marena; M. Lampertico; P. Relli; Paolo Gentilini; G. Buzzelli

Abstract Eight patients (two men and six women; mean age, 54.6 + 5 years) with viral chronic active hepatitis were treated with silipide (IdB1016), a new silybin-phosphatidylcholine complex, for 2 months. After treatment with IdB1016, serum malondialdehyde levels decreased by 36%, and the quantitative liver function evaluation, as expressed by galactose elimination capacity, increased by 15%. A statistically significant reduction ( P


Liver International | 2007

Performance of Doppler ultrasound in the prediction of severe portal hypertension in hepatitis C virus‐related chronic liver disease

Francesco Vizzutti; Umberto Arena; Luigi Rega; Roberto Giulio Romanelli; Stefano Colagrande; Stefania Cuofano; S. Moscarella; Giacomo Belli; Fabio Marra; Giacomo Laffi; Massimo Pinzani

Purpose: To evaluate the correlation between hepatic vein pressure gradient measurement and Doppler ultrasonography (DUS) in patients with chronic liver disease (CLD).


Blood | 2003

Effect of antiviral treatment in patients with chronic HCV infection and t(14;18) translocation

Francesca Giannelli; S. Moscarella; Carlo Giannini; Patrizio Caini; Monica Monti; Laura Gragnani; Roberto Giulio Romanelli; Vera Solazzo; Giacomo Laffi; Giorgio La Villa; Paolo Gentilini; Anna Linda Zignego


Liver | 2008

Interferon and thymosin combination therapy in naive patients with chronic hepatitis C : preliminary results

S. Moscarella; G. Buzzelli; Roberto Giulio Romanelli; Monica Monti; Carlo Giannini; Grazia Careccia; E. M. Marrocchi; A. L. Zignegoy


Alcohol and Alcoholism | 1989

HEPATIC LIPID PEROXIDATION AND ALDEHYDE DEHYDROGENASE ACTIVITY IN ALCOHOLIC AND NON ALCOHOLIC LIVER DISEASE

Roberto Mazzanti; S. Moscarella; Giuliano Bensi; Enrica Altavilla; Paolo Gentilini


Hepato-gastroenterology | 1984

Expired hydrocarbons in patients with chronic liver disease.

S. Moscarella; Giacomo Laffi; G. Buzzelli; Roberto Mazzanti; Caramelli L; Paolo Gentilini

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Fabio Marra

University of Florence

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Massimo Pinzani

University College London

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G. Buzzelli

University of Florence

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