Oberdan Parodi

Prof. Oberdan Parodi


Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

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

Representative Publications

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1 January 2015 in BioMed Research International
Verified
Journal Article
Open access
PDF file
PSPanagiotis K. Siogkas
Panagiotis K. Siogkas
Michail PapafaklisMichail Papafaklis
Michail Papafaklis
Antonis SakellariosAntonis Sakellarios
Antonis Sakellarios
KSKostas A. Stefanou
Kostas A. Stefanou
CBChristos V. Bourantas
Christos V. Bourantas
Dimitrios FotiadisDimitrios Fotiadis
Dimitrios Fotiadis
Pressure measurements using finite element computations without the need of a wire could be valuable in clinical practice. Our aim was to compare the computed distal coronary pressure values with the measured values using a pressure wire, while testing the effect of different boundary conditions for the simulation. Eight coronary arteries (lumen and outer vessel wall) from six patients were reconstructed in three-dimensional (3D) space using intravascular ultrasound and biplane angiographic images. Pressure values at the distal and proximal end of the vessel and flow velocity values at the distal end were acquired with the use of a combo pressure-flow wire. The 3D lumen and wall models were discretized into finite elements; fluid structure interaction (FSI) and rigid wall simulations were performed for one cardiac cycle both with pulsatile and steady flow in separate simulations. The results showed a high correlation between the measured and the computed coronary pressure values (coefficient of determination [r2] ranging between 0.8902 and 0.9961), while the less demanding simulations using steady flow and rigid walls resulted in very small relative error. Our study demonstrates that computational assessment of coronary pressure is feasible and seems to be accurate compared to the wire-based measurements.

1 July 2004 in Analytical Biochemistry
Verified
Journal Article
Closed access
RCRaffaele Caruso
Raffaele Caruso
JCJonica Campolo
Jonica Campolo
CDCinzia Dellanoce
Cinzia Dellanoce
RMRosina Mariele
Rosina Mariele
OPOberdan Parodi
Oberdan Parodi
RARoberto Accinni
Roberto Accinni

1 July 2019 in Computer Methods and Programs in Biomedicine
Verified
Journal Article
Closed access
TDTijana Djukic
Tijana Djukic
ISIgor Saveljic
Igor Saveljic
GPGualtiero Pelosi
Gualtiero Pelosi
OPOberdan Parodi
Oberdan Parodi
NFNenad Filipovic
Nenad Filipovic

1 July 1997 in JACC
Verified
Journal Article
Closed access
MTMarco Antonio Rodrigues Torres
Marco Antonio Rodrigues Torres
EPEugenio Picano
Eugenio Picano
GPGuido Parodi
Guido Parodi
RSRosa Sicari
Rosa Sicari
FVFabrizio Veglia
Fabrizio Veglia
OPOberdan Parodi
Oberdan Parodi

1 July 2017
Verified
Conference Paper
Open access
Antonis SakellariosAntonis Sakellarios
Antonis Sakellarios
GRGeorge Rigas
George Rigas
VKVassiliki Kigka
Vassiliki Kigka
PSPanagiotis K. Siogkas
Panagiotis K. Siogkas
PTPanagiota Tsompou
Panagiota Tsompou
DFDimitrios I. Fotiaids
Dimitrios I. Fotiaids
SMARTool aims to the development of a clinical decision support system (CDSS) for the management and stratification of patients with coronary artery disease (CAD). This will be achieved by performing computational modeling of the main processes of atherosclerotic plaque growth. More specifically, computed tomography coronary angiography (CTCA) is acquired and 3-dimensional (3D) reconstruction is performed for the arterial trees. Then, blood flow and plaque growth modeling is employed simulating the major processes of atherosclerosis, such as the estimation of endothelial shear stress (ESS), the lipids transportation, low density lipoprotein (LDL) oxidation, macrophages migration and plaque development. The plaque growth model integrates information from genetic and biological data of the patients. The SMARTool system enables also the calculation of the virtual functional assessment index (vFAI), an index equivalent to the invasively measured fractional flow reserve (FFR), to provide decision support for patients with stenosed arteries. Finally, it integrates modeling of stent deployment. In this work preliminary results are presented. More specifically, the reconstruction methodology has mean value of Dice Coefficient and Hausdorff Distance is 0.749 and 1.746, respectively, while low ESS and high LDL concentration can predict plaque progression.

9 November 2011 in Journal of Neurology, Neurosurgery & Psychiatry
Verified
Journal Article
Closed access
PDF file
JCJonica Campolo
Jonica Campolo
RMRenata De Maria
Renata De Maria
MFMarina Frontali
Marina Frontali
Franco TaroniFranco Taroni
Franco Taroni
DIDomenico Inzitari
Domenico Inzitari
OPOberdan Parodi
Oberdan Parodi
Background and purpose CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) is a rare genetic disease caused by NOTCH3 gene mutations. A dysfunction in vasoreactivity has been proposed as an early event in the pathogenesis of the disease. The aim of this study was to verify whether endothelium dependent and/or independent function is altered in CADASIL patients with respect to controls. Methods Vasoreactivity was studied by a non-invasive pletismographic method in 49 mildly disabled CADASIL patients (30–65 years, 58% male, Rankin scale ≤2) and 25 controls. Endothelium dependent vasodilatation was assessed by reactive hyperaemia (flow mediated dilation–peripheral arterial tone (FMD-PAT)) and endothelium independent vasoreactivity by glyceryl trinitrate (GTN) administration (GTN-PAT). Results Patients and controls showed comparable age, gender and cardiovascular risk factor distribution. GTN-PAT values were significantly lower in CADASIL patients (1.54 (1.01 to 2.25)) than in controls (1.89 (1.61 to 2.59); p=0.041). FMD-PAT scores did not differ between patients and controls (1.88 (1.57 to 2.43) vs 2.08 (1.81 to 2.58); p=0.126) but 17 CADASIL patients (35%) had FMD-PAT scores below the fifth percentile of controls. FMD-PAT and GTN-PAT values correlated both in controls (ρ=0.648, p<0.001) and CADASIL patients (ρ=0.563, p<0.001). By multivariable logistic regression for clinical and laboratory variables, only GTN-PAT (OR 0.39, 95% CI 0.15 to 0.97; p=0.044) was independently associated with FMD-PAT below the fifth percentile in CADASIL patients. Conclusions The impaired vasoreactivity observed in CADASIL patients highlights the fact that both endothelial and smooth muscle functional alterations may already be present in mildly disabled subjects. The improvement in vascular function could be a new target for pharmacological trials in CADASIL patients.