Showing papers by "Université catholique de Louvain published in 2022"

A comprehensive survey on ‘circular polarized antennas’ for existing and emerging wireless communication technologies

Abstract: Circular polarized (CP) antennas are well suited for long-distance transmission attainment. In order to be adaptable for beyond 5G communication, a detailed and systematic investigation of their important conventional features is required for expected enhancements. The existing designs employing millimeter wave, microwave, and ultra-wideband frequencies form the elementary platform for future studies. The 3.4 to 3.8 GHz frequency band has been identified as a worthy candidate for 5G communications because of spectrum availability. This band comes under ultra-wideband frequencies (3.1 to 10.6 GHz). In this survey, a review of CP antennas in the selected areas to improve the understanding of early-stage researchers specially experienced antenna designers has presented for the first time as best of our knowledge. Design implementations involving size, axial ratio, efficiency, and gain improvements are covered in detail. Besides that, various design approaches to realize CP antennas including (i) printed CP antennas based on parasitic or slotted elements, (ii) dielectric resonator CP antennas, (iii) reconfigurable CP antennas, (iv) substrate integrated waveguide (SIW) CP antennas, (v) fractal CP antennas, (vi) hybrid techniques CP antennas, and (vii) 3-D printing CP antennas with single and multiple feeding structures have investigated and analyzed. The aim of this work is to provide necessary guidance for the selection of CP antenna geometries in terms of the required dimensions, available bandwidth, gain, and useful materials for the integration and realization in future communication systems.

Bile acids contribute to the development of non-alcoholic steatohepatitis in mice.

Abstract: Background & Aims Through FXR and TGR5 signaling, bile acids (BAs) modulate lipid and glucose metabolism, inflammation and fibrosis. Hence, BAs returning to the liver after enteric secretion, modification and reabsorption may contribute to the pathogenesis of non-alcoholic steatohepatitis (NASH). Herein, we characterized the enterohepatic profile and signaling of BAs in preclinical models of NASH, and explored the consequences of experimental manipulation of BA composition. Methods We used high-fat diet (HFD)-fed foz/foz and high-fructose western diet-fed C57BL/6J mice, and compared them to their respective controls. Mice received a diet supplemented with deoxycholic acid (DCA) to modulate BA composition. Results Compared to controls, mice with NASH had lower concentrations of BAs in their portal blood and bile, while systemic BA concentrations were not significantly altered. Notably, the concentrations of secondary BAs, and especially of DCA, and the ratio of secondary to primary BAs were strikingly lower in bile and portal blood of mice with NASH. Hence, portal blood was poor in FXR and TGR5 ligands, and conferred poor anti-inflammatory protection in mice with NASH. Enhanced primary BAs synthesis and conversion of secondary to primary BAs in NASH livers contributed to the depletion in secondary BAs. Dietary DCA supplementation in HFD-fed foz/foz mice restored the BA concentrations in portal blood, increased TGR5 and FXR signaling, improved the dysmetabolic status, protected from steatosis and hepatocellular ballooning, and reduced macrophage infiltration. Conclusions BA composition in the enterohepatic cycle, but not in systemic circulation, is profoundly altered in preclinical models of NASH, with specific depletion in secondary BAs. Dietary correction of the BA profile protected from NASH, supporting a role for enterohepatic BAs in the pathogenesis of NASH. Lay summary This study clearly demonstrates that the alterations of enterohepatic bile acids significantly contribute to the development of non-alcoholic steatohepatitis in relevant preclinical models. Indeed, experimental modulation of bile acid composition restored perturbed FXR and TGR5 signaling and prevented non-alcoholic steatohepatitis and associated metabolic disorders.

Parkinson's disease protein PARK7 prevents metabolite and protein damage caused by a glycolytic metabolite

Abstract: Cells are continuously exposed to potentially dangerous compounds. Progressive accumulation of damage is suspected to contribute to neurodegenerative diseases and aging, but the molecular identity of the damage remains largely unknown. Here we report that PARK7, an enzyme mutated in hereditary Parkinson's disease, prevents damage of proteins and metabolites caused by a metabolite of glycolysis. We found that the glycolytic metabolite 1,3-bisphosphoglycerate (1,3-BPG) spontaneously forms a novel reactive intermediate that avidly reacts with amino groups. PARK7 acts by destroying this intermediate, thereby preventing the formation of proteins and metabolites with glycerate and phosphoglycerate modifications on amino groups. As a consequence, inactivation of PARK7 (or its orthologs) in human cell lines, mouse brain, and Drosophila melanogaster leads to the accumulation of these damaged compounds, most of which have not been described before. Our work demonstrates that PARK7 function represents a highly conserved strategy to prevent damage in cells that metabolize carbohydrates. This represents a fundamental link between metabolism and a type of cellular damage that might contribute to the development of Parkinson's disease.

More than the sum of its parts: Considering interdependencies in the life cycle material flow and environmental assessment of demountable buildings

Abstract: On the long term, buildings could initiate less material flows and have improved environmental performance if they are designed for future disassembly and reuse. However, material flows in the building life cycle are difficult to map, especially those initiated by material replacements and at end-of-life. The calculation formula for the number of replacements in buildings in the Life Cycle Assessment standard EN 15978 neglects the effect such replacements may have on the surrounding interdependent building parts, and hence fails to capture the potential benefits of Design for Disassembly. In light of this shortcoming, we propose a method to model the flows of building parts initiated by the disassembly of a building, both during operational and end-of-life stages. This modeling method considers aspects of structural stability, accessibility, and the use of detachable connections. It offers a bottom-up time-based Material Flow Analysis of an entire building which can be integrated in a Life Cycle Assessment. We apply our method on a pavilion and compare the method results to the those obtained with EN 15978, considering nine design options. The life cycle environmental impact estimated with our method is up to 162% larger than the impacts calculated with EN 15978 for a pavilion with non-detachable connections, which demonstrates the importance of this design parameter. Our method can be of interest to researchers, Life Cycle Assessment and Life Cycle Costing auditors, architecture, engineering and construction professionals, urban miners and any other actors interested in the design of demountable buildings.

Prevalence and Disease Spectrum of Extracoronary Arterial Abnormalities in Spontaneous Coronary Artery Dissection

Abstract: Spontaneous coronary artery dissection (SCAD) has been associated with fibromuscular dysplasia (FMD) and other extracoronary arterial abnormalities. However, the prevalence, severity, and clinical relevance of these abnormalities remain unclear.To assess the prevalence and spectrum of FMD and other extracoronary arterial abnormalities in patients with SCAD vs controls.This case series included 173 patients with angiographically confirmed SCAD enrolled between January 1, 2015, and December 31, 2019. Imaging of extracoronary arterial beds was performed by magnetic resonance angiography (MRA). Forty-one healthy individuals were recruited to serve as controls for blinded interpretation of MRA findings. Patients were recruited from the UK national SCAD registry, which enrolls throughout the UK by referral from the primary care physician or patient self-referral through an online portal. Participants attended the national SCAD referral center for assessment and MRA.Both patients with SCAD and healthy controls underwent head-to-pelvis MRA (median time between SCAD event and MRA, 1 [IQR, 1-3] year).The diagnosis of FMD, arterial dissections, and aneurysms was established according to the International FMD Consensus. Arterial tortuosity was assessed both qualitatively (presence or absence of an S curve) and quantitatively (number of curves ≥45%; tortuosity index).Of the 173 patients with SCAD, 167 were women (96.5%); mean (SD) age at diagnosis was 44.5 (7.9) years. The prevalence of FMD was 31.8% (55 patients); 16 patients (29.1% of patients with FMD) had involvement of multiple vascular beds. Thirteen patients (7.5%) had extracoronary aneurysms and 3 patients (1.7%) had dissections. The prevalence and degree of arterial tortuosity were similar in patients and controls. In 43 patients imaged with both computed tomographic angiography and MRA, the identification of clinically significant remote arteriopathies was similar. Over a median 5-year follow-up, there were 2 noncardiovascular-associated deaths and 35 recurrent myocardial infarctions, but there were no primary extracoronary vascular events.In this case series with blinded analysis of patients with SCAD, severe multivessel FMD, aneurysms, and dissections were infrequent. The findings of this study suggest that, although brain-to-pelvis imaging allows detection of remote arteriopathies that may require follow-up, extracoronary vascular events appear to be rare.

Institutional racism within the securitization of migration. The case of family reunification in Belgium

Abstract: Institutional Racism (IR) in Europe is rarely mentioned in studies of race-based discrimination. Yet, structural racism occurs within most European societies. Due to the increasing securitization o...

Effects of an acute exercise bout in hypoxia on extracellular vesicle release in healthy and prediabetic subjects

Abstract: The purpose of this study is to investigate exosome-like vesicle (ELV) plasma concentrations and markers of multivesicular body (MVB) biogenesis in skeletal muscle in response to acute exercise. Seventeen healthy [body mass index (BMI): 23.5 ± 0.5 kg·m-2] and 15 prediabetic (BMI: 27.3 ± 1.2 kg·m-2) men were randomly assigned to two groups performing an acute cycling bout in normoxia or hypoxia ([Formula: see text] 14.0%). Venous blood samples were taken before (T0), during (T30), and after (T60) exercise, and biopsies from m. vastus lateralis were collected before and after exercise. Plasma ELVs were isolated by size exclusion chromatography, counted by nanoparticle tracking analysis (NTA), and characterized according to international standards, followed by expression analyses of canonical ELV markers in skeletal muscle. In the healthy normoxic group, the total number of particles in the plasma increased during exercise from T0 to T30 (+313%) followed by a decrease from T30 to T60 (-53%). In the same group, an increase in TSG101, CD81, and HSP60 protein expression was measured after exercise in plasma ELVs; however, in the prediabetic group, the total number of particles in the plasma was not affected by exercise. The mRNA content of TSG101, ALIX, and CD9 was upregulated in skeletal muscle after exercise in normoxia, whereas CD9 and CD81 were downregulated in hypoxia. ELV plasma abundance increased in response to acute aerobic exercise in healthy subjects in normoxia, but not in prediabetic subjects, nor in hypoxia. Skeletal muscle analyses suggested that this tissue did not likely play a major role of the exercise-induced increase in circulating ELVs.

Pathogenic variants in <i>MDFIC</i> cause recessive central conducting lymphatic anomaly with lymphedema

Abstract: Central conducting lymphatic anomaly (CCLA), characterized by the dysfunction of core collecting lymphatic vessels including the thoracic duct and cisterna chyli, and presenting as chylothorax, pleural effusions, chylous ascites, and lymphedema, is a severe disorder often resulting in fetal or perinatal demise. Although pathogenic variants in RAS/mitogen activated protein kinase (MAPK) signaling pathway components have been documented in some patients with CCLA, the genetic etiology of the disorder remains uncharacterized in most cases. Here, we identified biallelic pathogenic variants in MDFIC, encoding the MyoD family inhibitor domain containing protein, in seven individuals with CCLA from six independent families. Clinical manifestations of affected fetuses and children included nonimmune hydrops fetalis (NIHF), pleural and pericardial effusions, and lymphedema. Generation of a mouse model of human MDFIC truncation variants revealed that homozygous mutant mice died perinatally exhibiting chylothorax. The lymphatic vasculature of homozygous Mdfic mutant mice was profoundly mispatterned and exhibited major defects in lymphatic vessel valve development. Mechanistically, we determined that MDFIC controls collective cell migration, an important early event during the formation of lymphatic vessel valves, by regulating integrin β1 activation and the interaction between lymphatic endothelial cells and their surrounding extracellular matrix. Our work identifies MDFIC variants underlying human lymphatic disease and reveals a crucial, previously unrecognized role for MDFIC in the lymphatic vasculature. Ultimately, understanding the genetic and mechanistic basis of CCLA will facilitate the development and implementation of new therapeutic approaches to effectively treat this complex disease.

Changing sub-Arctic tundra vegetation upon permafrost degradation: impact on foliar mineral element cycling

Abstract: Abstract. Arctic warming and permafrost degradation are modifying northern ecosystems through changes in microtopography, soil water dynamics, nutrient availability, and vegetation succession. Upon permafrost degradation, the release of deep stores of nutrients, such as nitrogen and phosphorus, from newly thawed permafrost stimulates Arctic vegetation production. More specifically, wetter lowlands show an increase in sedges (as part of graminoids), whereas drier uplands favor shrub expansion. These shifts in the composition of vegetation may influence local mineral element cycling through litter production. In this study, we evaluate the influence of permafrost degradation on mineral element foliar stocks and potential annual fluxes upon litterfall. We measured the foliar elemental composition (Al, Ca, Fe, K, Mn, P, S, Si, and Zn) of ∼ 500 samples of typical tundra plant species from two contrasting Alaskan tundra sites, i.e., an experimental sedge-dominated site (Carbon in Permafrost Experimental Heating Research, CiPEHR) and natural shrub-dominated site (Gradient). The foliar concentration of these mineral elements was species specific, with sedge leaves having relatively high Si concentration and shrub leaves having relatively high Ca and Mn concentrations. Therefore, changes in the species biomass composition of the Arctic tundra in response to permafrost thaw are expected to be the main factors that dictate changes in elemental composition of foliar stocks and maximum potential foliar fluxes upon litterfall. We observed an increase in the mineral element foliar stocks and potential annual litterfall fluxes, with Si increasing with sedge expansion in wetter sites (CiPEHR), and Ca and Mn increasing with shrub expansion in drier sites (Gradient). Consequently, we expect that sedge and shrub expansion upon permafrost thaw will lead to changes in litter elemental composition and therefore affect nutrient cycling across the sub-Arctic tundra with potential implications for further vegetation succession.

Optimal lockdown and social welfare.

Abstract: This paper examines the robustness of the optimal lockdown strategy to the postulated social welfare criterion. We show that utilitarianism can, under some conditions, imply a COVID-19 variant of Parfit's (1984) Repugnant Conclusion: for any (interior) lockdown with life periods of low quality, there must be a stricter lockdown that is regarded as better, even though this reduces the quality of life periods even more. On the contrary, the ex post egalitarian criterion (giving priority to the worst-off ex post) implies zero lockdown. Varying between its minimal and its maximal levels, the optimal lockdown is not robust to the postulated ethical criterion. We also identify a general ethical dilemma between the goal of saving lives (modeled by the Survivors Number Count axiom) and the goal of giving priority to the worst-off (Hammond Equity).