588 results match your criteria: "Franche-Comte university[Affiliation]"

Refractory invasive pulmonary aspergillosis due to Aspergillus flavus detected with the combination of two in-house Aspergillus qPCR.

J Mycol Med

March 2023

Chrono-Environnement CNRS 6249 Research Team, Franche-Comté University, Besançon 25000, France; Parasitology-Mycology Department, Besançon University Hospital, Besançon 25000, France.

We present a case of probable invasive pulmonary aspergillosis due to Aspergillus flavus, in a female patient treated for an acute myeloid leukemia. Two weeks after an allogenic stem cell transplantation a probable invasive pulmonary aspergillosis was diagnosed based on thoracic imaging combined with positive galactomannan antigen and positive in-house mitochondrial Aspergillus qPCR in serum. Although an antifungal treatment was initiated, Aspergillus qPCR and galactomannan antigen remained positive in serum and worsening of the thoracic lesions was observed.

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Nitric Oxide Metabolic Pathway in Drought-Stressed Nodules of Faba Bean ( L.).

Int J Mol Sci

October 2022

Sophia Agrobiotech Institute, INRAE 1355, CNRS 7254, Côte d'Azur University, 06903 Sophia Antipolis, France.

Drought is an environmental stress that strongly impacts plants. It affects all stages of growth and induces profound disturbances that influence all cellular functions. Legumes can establish a symbiosis with Rhizobium-type bacteria, whose function is to fix atmospheric nitrogen in organs called nodules and to meet plant nitrogen needs.

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Human type I IFN deficiency does not impair B cell response to SARS-CoV-2 mRNA vaccination.

J Exp Med

January 2023

Necker Enfants Malades Institute, INSERM U1151/CNRS UMR 8253, Action thématique incitative sur programme-Avenir Team Auto-Immune and Immune B cell, University Paris Cité, University Paris-Est-Créteil, Créteil, France.

Article Synopsis
  • * Researchers examined SARS-CoV-2 naive patients with specific genetic deficiencies and autoantibodies that affect IFN response to see if this impacted vaccine efficacy.
  • * The study found that despite these deficiencies, the B cell response, including memory B cells and IgG production, remained robust and similar to healthy individuals, indicating type I IFN isn't essential for generating a strong vaccine-induced immune response against SARS-CoV-2.
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  • The study investigates the role of topical antibiotic prophylaxis in preventing acute endophthalmitis after intravitreal injections (IVTs), analyzing data from over 5 million injections in France from 2009 to 2018.
  • Findings reveal a significant decrease in the use of prophylactic antibiotics over time, with 1274 cases of endophthalmitis reported (an incidence rate of 0.0241%).
  • The study concludes that antibiotic prophylaxis does not effectively lower the risk of endophthalmitis, and in fact, using certain combinations of antibiotics with corticosteroids may increase that risk, suggesting that avoiding such prophylaxis could reduce costs and mitigate antibiotic resistance concerns.
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X-ray Microtomography to Assess Determinants of In Vivo N-Butyl Cyanoacrylate Glubran2 Polymerization: A Rabbit-Model Study.

Biomedicines

October 2022

Department of Vascular and Interventional Radiology, Image-Guided Therapy Center, François-Mitterrand University Hospital, 14 Rue Paul Gaffarel, BP 77908, 21079 Dijon, France.

Although introduced decades ago, few cyanoacrylate glues have been approved for endovascular use, despite evidence of their usefulness, notably for complex procedures suchas hemostatic embolization. Indications include massive bleeding requiring emergent hemostasis and prevention of severe bleeding during scheduled surgery to remove a hypervascular tumor. Adding radiopaque Lipiodol Ultra Fluid (LUF) modulates glue polymerization and allows fluoroscopic guidance, but few comparative in vivo studies have assessed the impact of the resulting change in glue concentration or of other factors such as target-vessel blood flow.

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Cordia rothii Roem. & Schult. possesses various beneficial effects and is traditionally used in folk medicine against liver diseases but its molecular mechanism remains unclear.

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An alternative approach-combination of lockdown and open in fighting COVID-19 pandemics.

Environ Sci Pollut Res Int

November 2022

Department of Orthopedic Surgery and BME, College of Medicine, University of Tennessee Health Science Center, 956 Court Ave, Memphis, TN, 38163, USA.

As the COVID-19 pandemic enters its third year and the omicron variant becomes dominant, we propose an alternative strategy for dealing with COVID-19, called hybrid lockdown, that is, the combination of lockdown (the centralized and organized lockdown of the high-risk population) and free mobility (normal mobility) of the low-risk population. Such an approach will enable a country or region, especially with a high population density, to achieve significant prevention and control the effects of the COVID-19 pandemic at the least cost.

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Hypothesis: This review article represents a brief layout of the risk factors and pathophysiology responsible for obesity, customary treatment strategies, and nanotechnology-based nutraceutical for the therapeutics of obesity.

Experiments: An exhaustive search of the literature was done for this purpose, using Google Scholar, PubMed, and ScienceDirect databases. A literature study was conducted using publications published in peer-reviewed journals between 2000 and 2022.

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Osteoporosis (OP) is a serious health problem, and the most popular therapeutic strategy for OP is hormone replacement (estrogen); however, it increases the risk of reproductive cancers. Hydroxyapatite (HA) nanoparticles have a similar chemical structure to the bone mineral component and can be used as a new remedy for OP. This study was designed to investigate the osteoporosis-protective potential of nano zinc hydroxyapatite (ZnHA-NPs) and/or estradiol (E2) combined therapy.

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Article Synopsis
  • Molecular profiling of stage I-II non-small cell lung cancer (NSCLC) can enhance prognosis and tailor treatment approaches, focusing on the role of EGFR mutations.
  • In a study of surgical NSCLC patients, a higher rate of EGFR mutations (12.9%) was observed compared to non-surgical cases, with rates reaching 27% among women.
  • Despite the presence of EGFR mutations, there were no significant differences in disease recurrence or survival rates between EGFR-mutant and wild-type tumors, with a notable 5-year overall survival of 75% for resected EGFR-mutated tumors.
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  • Young breast cancer survivors often struggle with issues related to fertility and sexuality due to treatment side effects, highlighting the importance of incorporating their perspectives into medical care.
  • The study aims to assess the clinical, social, and economic factors affecting these survivors in France, while also examining their experiences and information needs around fertility preservation and sexual health.
  • A mixed-methods approach will be used, combining quantitative surveys and qualitative interviews to gather comprehensive data from young women diagnosed with non-metastatic breast cancer.
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Insights into the pivotal role of statins and its nanoformulations in hyperlipidemia.

Environ Sci Pollut Res Int

November 2022

Department of Pharmacy, Faculty of Medicine and Pharmacy, University of Oradea, Oradea, Romania.

Hyperlipidemia is the primary cause of heart disorders and has been manifested as the condition with remarkable higher levels of very-low-density lipoproteins, low-density lipoproteins, intermediate-density lipoprotein, triglycerides, and cholesterol in blood circulation. Genetic causes or systemic metabolic illnesses like diabetes mellitus, increased alcohol consumption, hypothyroidism, and primary biliary cirrhosis are several reasons behind development of hyperlipidemia. Higher levels of lipids and lipoproteins in plasma are responsible for various health disorders in human body like occlusion of blood vessels, acute pancreatitis, and reduced artery lumen elasticity.

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Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder resulting from biallelic alterations of the SMN1 gene: deletion, gene conversion or, in rare cases, intragenic variants. The disease severity is mainly influenced by the copy number of SMN2, a nearly identical gene, which produces only low amounts of full-length (FL) mRNA. Here we describe the first example of retrotransposon insertion as a pathogenic SMN1 mutational event.

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Article Synopsis
  • This study investigated the effectiveness of tocilizumab, an IL-6 antagonist, for treating glucocorticoid-dependent polymyalgia rheumatica, a condition with limited treatment options.
  • Conducted as a double-blind, placebo-controlled trial, 101 patients participated over roughly three years, comparing the effects of tocilizumab and placebo alongside a standardized reduction of prednisone.
  • Results showed that 67.3% of participants receiving tocilizumab met the primary efficacy goal, compared to 31.4% in the placebo group, indicating a significant difference in disease activity reduction.
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Neurodegeneration is the loss of neuronal capacity and structure over time which causes neurodegenerative disorders like Alzheimer, amyotrophic lateral sclerosis, Parkinson, and Huntington's disease (HD). This review is primarily concerned with HD, which was fully described by George Huntington in 1872. In developed countries, HD has become another common single-gene neurological disorder.

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Guadeloupe (French West Indies), a Caribbean island, is an ideal place to study the reservoirs of the Klebsiella pneumoniae species complex (KpSC) and identify the routes of transmission between human and nonhuman sources due to its insularity, small population size, and small area. Here, we report an analysis of 590 biological samples, 546 KpSC isolates, and 331 genome sequences collected between January 2018 and May 2019. The KpSC appears to be common whatever the source.

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Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants.

Genet Med

November 2022

Adelaide Medical School, The University of Adelaide, Adelaide, South Australia, Australia; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia. Electronic address:

Article Synopsis
  • Germline loss-of-function variants in the CTNNB1 gene are linked to neurodevelopmental disorders that include spastic diplegia and visual issues, making them a common genetic cause of cerebral palsy (CP).
  • A study analyzed genetic data from 404 individuals with pathogenic CTNNB1 variants, including newly detailed phenotypes for 52 cases, to explore how these variants relate to CP and other traits.
  • Findings showed that individuals with CTNNB1 variants exhibited similar clinical features, suggesting that CP is part of the neurodevelopmental disorder spectrum rather than a separate condition; two specific variants were found to disrupt WNT signaling processes.
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Background: Lesions detected by magnetic resonance imaging (MRI) of the sacroiliac joints are critical to the diagnosis of non-radiographic axial spondyloarthritis. However, inflammatory and structural lesions may be encountered in other conditions.

Objectives: The objective of this study was to evaluate and compare the frequency and localization of inflammatory and structural lesions on MRIs of the sacroiliac joint of spondyloarthritis (SpA) and non-spondyloarthritis (non-SpA) patients.

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Pollution is a significant and growing concern for any population regardless of age because these environmental contaminants exhibit different neurodegenerative effects on persons of different ages. These environmental contaminants are the products of human welfare projects like industry, automobile exhaust, clinical and research laboratory extrudes, and agricultural chemicals. These contaminants are found in various forms in environmental matrices like nanoparticles, particulate matter, lipophilic vaporized toxicants, and ultrafine particulate matter.

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Article Synopsis
  • The study focused on assessing the cancer risk associated with pathogenic variants (PV) in families meeting the hereditary diffuse gastric cancer (HDGC) criteria.
  • Researchers gathered data from existing families and collaborated internationally to analyze the cumulative risk of diffuse gastric cancer (DGC) for PV carriers using advanced statistical methods.
  • Findings revealed that PV carriers face a cumulative DGC risk of 49% to 57% by age 80, with significantly heightened risk ratios at earlier ages, marking this as a critical insight for improving patient management and genetic testing.
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International Recommendations to Manage Poststroke Equinovarus Foot Deformity Validated by a Panel of Experts Using Delphi.

Arch Phys Med Rehabil

March 2023

UPOH (Unité Péri Opératoire du Handicap, Perioperative Disability Unit), Physical and Rehabilitation Medicine Department, Raymond-Poincaré Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Garches, France; Versailles Saint-Quentin-en-Yvelines University (UVSQ), UFR Simone Veil - Santé, Montigny-le-Bretonneux, France; Garches Neuro-Orthopaedics Research Group (GRENOG), Garches, France. Electronic address:

Objective: To establish international recommendations for the management of spastic equinovarus foot deformity.

Design: Delphi method.

Setting: International study.

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Exploring the pivotal role of endothelin in rheumatoid arthritis.

Inflammopharmacology

October 2022

Department of Pharmacy, Faculty of Medicine and Pharmacy, University of Oradea, Oradea, Romania.

A chronic inflammatory disorder, rheumatoid arthritis (RA) is an autoimmune and systemic disease characterized by progressive and prolonged destruction of joints. This results in increased mortality, physical disability and destruction. Cardiovascular disorders are one of the primary causes of mortality in patients with RA.

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Evaluation of Next-Generation Sequencing Applied to and Epidemiological Study.

Pathogens

August 2022

Parasitology-Mycology Laboratory, University Hospital Biology Platform, Dijon University Hospital Center, 21000 Dijon, France.

. Nowadays, most of the and epidemiological studies are based on gp60 gene subtyping using the Sanger sequencing (SgS) method. Unfortunately, SgS presents the limitation of being unable to detect mixed infections.

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Could 18-FDG PET-CT Radiomic Features Predict the Locoregional Progression-Free Survival in Inoperable or Unresectable Oesophageal Cancer?

Cancers (Basel)

August 2022

INSERM, Établissement Français du Sang Bourgogne Franche-Comté, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, Bourgogne Franche-Comté University, F-25000 Besancon, France.

Background: We evaluated the value of pre-treatment positron-emission tomography−computed tomography (PET-CT)-based radiomic features in predicting the locoregional progression-free survival (LR-PFS) of patients with inoperable or unresectable oesophageal cancer. Material and Methods: Forty-six patients were included and 230 radiomic parameters were extracted. After a principal component analysis (PCA), we identified the more robust radiomic parameters, and we used them to develop a heatmap.

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