Francesco Vasuri

Prof. Francesco Vasuri

Pathology Unit, S.Orsola-Malpighi Hospital, Bologna University, Bologna, Italy
orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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7 June 2022 in American Journal of Transplantation
Verified
Journal Article
Open access
Matteo RavaioliMatteo Ravaioli
Matteo Ravaioli
GGGiuliana Germinario
Giuliana Germinario
GDGerti Dajti
Gerti Dajti
MSMaurizio Sessa
Maurizio Sessa
FVFrancesco Vasuri
Francesco Vasuri
Matteo CesconMatteo Cescon
Matteo Cescon
Hypothermic Oxygenated Perfusion (HOPE) of the liver can reduce the incidence of early allograft dysfunction (EAD) and failure in extended criteria donors (ECD) grafts, although data from prospective studies are very limited. In this monocentric, open‐label study, from December 2018 to January 2021, 110 patients undergoing transplantation of an ECD liver graft were randomized to receive a liver after HOPE or after static cold storage (SCS) alone. The primary endpoint was the incidence of EAD. The secondary endpoints included graft and patient survival, the EASE risk score, and the rate of graft or other graft‐related complications. Patients in the HOPE group had a significantly lower rate of EAD (13% vs. 35%, p = .007) and were more frequently allocated to the intermediate or higher risk group according to the EASE score (2% vs. 11%, p = .05). The survival analysis confirmed that patients in the HOPE group were associated with higher graft survival one year after LT (p = .03, log‐rank test). In addition, patients in the SCS group had a higher re‐admission and overall complication rate at six months, in particular cardio‐vascular adverse events (p = .04 and p = .03, respectively). HOPE of ECD grafts compared to the traditional SCS preservation method is associated with lower dysfunction rates and better graft survival.

15 August 2013 in PLOS ONE
Verified
Journal Article
Open access
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MCMaria Conte
Maria Conte
FVFrancesco Vasuri
Francesco Vasuri
Giovanni TrisolinoGiovanni Trisolino
Giovanni Trisolino
EBElena Bellavista
Elena Bellavista
ASAurelia Santoro
Aurelia Santoro
SSStefano Salvioli
Stefano Salvioli
Though traditionally perceived as weapons, antibiotics are also hypothesized to act as microbial signals in natural habitats. However, while subinhibitory concentrations of antibiotics (SICA) are known to shift bacterial gene expression, specific hypotheses as to how SICA influence the ecology of natural populations are scarce. We explored whether antibiotic ‘signals’, or SICA, have the potential to alter nutrient utilization, niche overlap, and competitive species interactions among Streptomyces populations in soil. For nine diverse Streptomyces isolates, we evaluated nutrient utilization patterns on 95 different nutrient sources in the presence and absence of subinhibitory concentrations of five antibiotics. There were significant changes in nutrient use among Streptomyces isolates, including both increases and decreases in the capacity to use individual nutrients in the presence vs. in the absence of SICA. Isolates varied in their responses to SICA and antibiotics varied in their effects on isolates. Furthermore, for some isolate-isolate-antibiotic combinations, competition-free growth (growth for an isolate on all nutrients that were not utilized by a competing isolate), was increased in the presence of SICA, reducing the potential fitness cost of nutrient competition among those competitors. This suggests that antibiotics may provide a mechanism for bacteria to actively minimize niche overlap among competitors in soil. Thus, in contrast to antagonistic coevolutionary dynamics, antibiotics as signals may mediate coevolutionary displacement among coexisting Streptomyces, thereby hindering the emergence of antibiotic resistant phenotypes. These results contribute to our broad understanding of the ecology and evolutionary biology of antibiotics and microbial signals in nature.

1 March 2009 in Digestive and Liver Disease
Verified
Journal Article
Closed access
Francesco CorradiFrancesco Corradi
Francesco Corradi
FPFabio Piscaglia
Fabio Piscaglia
SFS. Flori
S. Flori
ADA. D’eRrico-Grigioni
A. D’eRrico-Grigioni
FVFrancesco Vasuri
Francesco Vasuri
LBL. Bolondi
L. Bolondi

24 November 2009 in Liver Transplantation
Verified
Journal Article
Open access
PDF file
MFMichelangelo Fiorentino
Michelangelo Fiorentino
FVFrancesco Vasuri
Francesco Vasuri
Matteo RavaioliMatteo Ravaioli
Matteo Ravaioli
LRLorenza Ridolfi
Lorenza Ridolfi
WGWalter Franco Grigioni
Walter Franco Grigioni
ADAntonia D'ERrico-Grigioni
Antonia D'ERrico-Grigioni
Histological quality assessment of donated livers is a key factor for extending the cadaveric donor pool for liver transplantation. We retrospectively compared frozen-section analysis with routine histological permanent slides and the outcomes of grafts in liver biopsies from 294 candidate donors. The κ concordance coefficient of agreement between frozen-section analysis and routine histological analysis was very good for macrosteatosis (κ = 0.934), microsteatosis (κ = 0.828), and total steatosis (κ = 0.814). The correlation between the mean amounts of macrosteatosis, microsteatosis, and total steatosis in frozen and permanent sections was also significant ( P < 0.001, Spearman's test). Macrosteatosis and microsteatosis were overestimated to >30% in 4 of 32 cases (12.5%) and in 23 of 62 cases (37.1%), respectively. The only 2 histological parameters of frozen sections able to predict graft dysfunction within 7 days of transplantation were macrosteatosis and total steatosis ( P = 0.018 and P = 0.015, respectively, Mann-Whitney test). None of the other histopathological features evaluated in frozen sections, including portal inflammation, lobular necrosis, myointimal thickening, biliocyte regression, cholestasis, hepatocellular polymorphism, lipofuscin storage, and fibrous septa, were significantly correlated with the graft outcome. The frozen-section histological evaluation of biopsies from cadaveric liver donors is an accurate, time-effective, and predictive method for the assessment of graft suitability. Liver Transpl 15:1821-1825, 2009. © 2010 AASLD.

29 October 2020 in Cancers
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Journal Article
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SLStefania De Lorenzo
Stefania De Lorenzo
Francesco TovoliFrancesco Tovoli
Francesco Tovoli
Alessandro MazzottaAlessandro Mazzotta
Alessandro Mazzotta
FVFrancesco Vasuri
Francesco Vasuri
JEJulien Edeline
Julien Edeline
GBGiovanni Brandi
Giovanni Brandi
Non-alcoholic fatty liver disease (NAFLD) and its most aggressive form, non-alcoholic steatohepatitis (NASH), are causing a rise in the prevalence of hepatocellular carcinoma. Data about NAFLD/NASH and intrahepatic cholangiocarcinoma (iCCA) are few and contradictory, coming from population registries that do not correctly distinguish between NAFLD and NASH. We evaluated the prevalence of NAFLD and NASH in peritumoral tissue of resected iCCA (n = 180) and in needle biopsies of matched liver donors. Data of iCCA patients were subsequently analysed to compare NASH-related iCCA (Group A), iCCA arisen in a healthy liver (Group B) or in patients with classical iCCA risk factors (Group C). NASH was found in 22.5% of 129 iCCA patients without known risk factors and in 6.2% of matched controls (risk ratio 3.625, 95% confidence interval 1.723–7.626, p < 0.001), while NAFLD was equally represented in both groups. The overall survival of NASH-related iCCA was inferior to that of patients with healthy liver (38.5 vs. 48.1 months, p = 0.003) and similar to that of patients with known risk factors (31.9 months, p = 0.948), regardless of liver fibrosis. The multivariable Cox regression confirmed NASH as a prognostic factor (hazard ratio 1.773, 95% confidence interval 1.156–2.718, p = 0.009). We concluded that NASH (but not NAFLD) is a risk factor for iCCA and might affect its prognosis. Dissecting NASH from NAFLD by histology is necessary to correctly assess the actual role of these conditions. Prevention protocols for NASH patients should also consider the risk for iCCA and not only HCC. Mechanistic studies aimed to find a direct pathogenic link between NASH and iCCA could add further relevant information.

21 June 2011 in Virchows Archiv
Verified
Journal Article
Closed access
PDF file
FVFrancesco Vasuri
Francesco Vasuri
Rita GolfieriRita Golfieri
Rita Golfieri
MFMichelangelo Fiorentino
Michelangelo Fiorentino
ECElisa Capizzi
Elisa Capizzi
Matteo RenzulliMatteo Renzulli
Matteo Renzulli
ADAntonia D’errico-Grigioni
Antonia D’errico-Grigioni