35 research outputs found

    Identification of HCV protease inhibitor resistance mutations by selection pressure-based method

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    A major challenge to successful antiviral therapy is the emergence of drug-resistant viruses. Recent studies have developed several automated analyses of HIV sequence polymorphism based on calculations of selection pressure (Ka/Ks) to predict drug resistance mutations. Similar resistance analysis programs for HCV inhibitors are not currently available. Taking advantage of the recently available sequence data of patient HCV samples from a Phase II clinical study of protease inhibitor boceprevir, we calculated the selection pressure for all codons in the HCV protease region (amino acid 1–181) to identify potential resistance mutations. The correlation between mutations was also calculated to evaluate linkage between any two mutations. Using this approach, we identified previously known major resistant mutations, including a recently reported mutation V55A. In addition, a novel mutation V158I was identified, and we further confirmed its resistance to boceprevir in protease enzyme and replicon assay. We also extended the approach to analyze potential interactions between individual mutations and identified three pairs of correlated changes. Our data suggests that selection pressure-based analysis and correlation mapping could provide useful tools to analyze large amount of sequencing data from clinical samples and to identify new drug resistance mutations as well as their linkage and correlations

    Endovascular Abdominal Aortic Aneurysm Repair With Ovation Alto Stent Graft: Protocol for the ALTAIR (ALTo endogrAft Italian Registry) Study

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    Background: Since 2010, the Ovation Abdominal Stent Graft System has offered an innovative sealing option for abdominal aortic aneurysm (AAA) by including a sealing ring filled with polymer 13 mm from the renal arteries. In August 2020, the redesigned Ovation Alto, with a sealing ring 6 mm closer to the top of the fabric, received CE Mark approval. Objective: This registry study aims to evaluate intraoperative, perioperative, and postoperative results in patients treated by the Alto stent graft (Endologix Inc.) for elective AAA repair in a multicentric consecutive experience. Methods: All consecutive eligible patients submitted to endovascular aneurysm repair (EVAR) by Alto Endovascular AAA implantation will be included in this analysis. Patients will be submitted to EVAR procedures based on their own preferences, anatomical features, and operators experience. An estimated number of 300 patients submitted to EVAR with Alto stent graft should be enrolled. It is estimated that the inclusion period will be 24 months. The follow-up period is set to be 5 years. Full data sets and cross-sectional images of contrast-enhanced computed tomography scan performed before EVAR, at the first postoperative month, at 24 or 36 months, and at 5-year follow-up interval will be reported in the central database for a centralized core laboratory review of morphological changes. The primary endpoint of the study is to evaluate the technical and clinical success of EVAR with the Alto stent graft in short- (90-day), mid- (1-year), and long-term (5-year) follow-up periods. The following secondary endpoints will be also addressed: operative time; intraoperative radiation exposure; contrast medium usage; AAA sac shrinkage at 12-month and 5-year follow-up; any potential role of patients' baseline characteristics, valuated on preoperative computed tomography angiographic study, and of device configuration (number of component) in the primary endpoint. Results: The study is currently in the recruitment phase and the final patient is expected to be treated by the end of 2023 and then followed up for 5 years. A total of 300 patients will be recruited. Analyses will focus on primary and secondary endpoints. Updated results will be shared at 1- and 3-5-year follow-ups. Conclusions: The results from this registry study could validate the safety and effectiveness of the new design of the Ovation Alto Stent Graft. The technical modifications to the endograft could allow for accommodation of a more comprehensive range of anatomies on-label

    Analysis Of The Core Compaction Phenomenon

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    The compaction of the bundle of core assemblies is an important aspect of the core design particularly for the next generation LMR. The core deformation, caused by dynamic condition like the seismic motion, may determine, at large or small extent, an assembly compaction generally characterized by a radial inward displacement, and subsequently result in a possible insertion of reactivity. The aim of this study is to investigate the deformation of core (and restraint system) geometry of the Advanced Lead Fast Reactor European Demonstrator - ALFRED (300 MWth). Numerical analyses have been carried out by the finite element MSC©Marc code to simulate the mechanical behaviour of the overall reactor system and, specifically, of the main components of the inner vessel, such as the lower and upper grid, the inner vessel, the support skirt, etc.. Suitable boundary and initial conditions, such as that one related to the core sub-assemblies mass, the restrictions imposed to the geometrical in-structures connections, etc. have been assumed to numerically investigate the dynamic response of the structures, since confidence was established by sensitivity analyses of size and type of the adopted elements. The results indicate that the stresses overcome the yielding limit particularly in the upper part of the inner vessel, close to the flange support, in the upper grid and in the annular area neighboring the nozzle penetration. The displacement resulted of course variable along the height of the inner vessel, with a mean value of about 2 cm around the core assemblies. This research activity was developed and financed by the Italian Ministry of Economic Development (MSE) as part of the activities carried out in the framework of the AdP MSE-ENEA-CIRTEN PAR 2013
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