Pyruvate kinase deficiency

Over the past few years the inherited disorders of erythrocyte metabolism have been the object of intensive research which has resulted in a better understanding of their molecular basis. However, curative therapy for red blood cell (RBC) enzyme defects still remains undeveloped. Among glycolyti

Molecular heterogeneity of pyruvate kinase deficiency

Red cell pyruvate kinase (PK) deficiency is the most common glycolytic defect associated with congenital non-spherocytic hemolytic anemia. The disease, transmitted as an autosomal recessive trait, is caused by mutations in the PKLR gene and is characterized by molecular and clinical heterogeneity; anemia ranges from mild or fully compensated hemolysis to life-threatening forms necessitating neonatal exchange transfusions and/or subsequent regular transfusion support; complications include gallstones, pulmonary hypertension, extramedullary hematopoiesis and iron overload. Since identification of the first pathogenic variants responsible for PK deficiency in 1991, more than 300 different variants have been reported, and the study of molecular mechanisms and the existence of genotype-phenotype correlations have been investigated in-depth. In recent years, during which progress in genetic analysis, next-generation sequencing technologies and personalized medicine have opened up important landscapes for diagnosis and study of molecular mechanisms of congenital hemolytic anemias, genotyping has become a prerequisite for accessing new treatments and for evaluating disease state and progression. This review examines the extensive molecular heterogeneity of PK deficiency, focusing on the diagnostic impact of genotypes and new acquisitions on pathogenic non-canonical variants. The recent progress and the weakness in understanding the genotype-phenotype correlation, and its practical usefulness in light of new therapeutic opportunities for PK deficiency are also discussed

The use of next-generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper

Next-generation sequencing; Rare anemiaSecuenciación de nueva generación; Anemia raraSeqüenciació de nova generació; Anèmia rar

Study and Characterization of Environmental Deposition on Marble and Surrogate Substrates at a Monumental Heritage Site

In this study, the results of the field exposure activity conducted between 2014 and 2017 on the façade of the Milano cathedral (Italy) are reported. The main research aim was to characterize environmental deposition in real exposure conditions and for this purpose, both stone substrates (Candoglia marble) and surrogate substrates (quartz fibre filters) were exposed on the cathedral façade in two sites at different heights. A complete chemical characterization has been performed on quartz filters and marble substrates, i.e., quantification of the deposited aerosol particulate matter (PM) and of the main ions. On quartz filters, the carbonaceous component of deposits was also investigated, as well as the color change induced by soiling, by means of colorimetric measurements. The combined approach exploiting marble and surrogate substrates seems to be a suitable monitoring strategy, although some aspects should be taken into account. In particular, differences in the deposits composition have been highlighted mainly depending on the type of substrate. The environmental data related to atmospheric pollution in Milan for the same period have also been considered but no direct correlations were found between some atmospheric precursors and their related ions in solid deposits

Elemental Analysis and Phenolic Profiles of Selected Italian Wines

The study of the chemical composition of wines is nowadays a topic of great interest because of the importance of this market, especially in Italy, and also considering the numerous cases of falsification of famous and very expensive wines. The present paper focused on the analysis of metals and polyphenols in Italian wines belonging to different provenance and types. At this purpose 20 elements were quantified by inductively coupled plasma optical emission spectrometry (ICP-OES) and ICP mass spectrometry (ICP-MS). Regarding polyphenols, a total of 32 were quantified, among 6 were anthocyanins. Furthermore, in 4 samples (1 rosè and 3 red wines) 42 anthocyanins and related compounds were identified by ultra-high performance liquid chromatography (UHPLC)-Orbitrap MS technique (among these, 6 were also quantified). Non-anthocyanins were determined using UHPLC coupled with a diode array detector and triple-quadrupole mass spectrometer (UHPLC–DAD-QqQ-MS). Total phenolic content (TPC) and radical scavenging activity (RSA) were measured using spectrophotometric methods. The results obtained by elemental techniques were submitted to principal components analysis (PCA) allowing to get information on both geographical and botanical origin of the examined wine samples. Some polyphenols have been detected in higher concentrations only in a certain type of wine, as for example in the case of Grechetto wine. Most of the identified anthocyanin derivatives (pyranoanthocyanins) are formed during the aging of wine by reaction with the other wine components.Supplementary material: [https://cherry.chem.bg.ac.rs/handle/123456789/4811

Environmental impact assessment on the Monza cathedral (Italy): a multi-analytical approach

This research deals with the characterization of black crusts collected from the Dome of Monza (Milan, Italy). Air pollution is responsible for the degradation of historical buildings surfaces. In urban and industrial areas, the degradation process is accelerated, due to carbonaceous particles and heavy metals emitted by combustion processes which contribute to the formation of black crust (BCs). In this study the characterization of BC was performed using different analytical techniques such as: HRSEM-EDX, IC, LA-ICP/MS and digital image analysis. In particular, the research focused on the study of "heavy metals" which contribute to the identify the main sources of pollution responsible for the surface’s deterioration over time. BCs variability in composition also depends on the exposure of the analyzed surfaces.J. Santiago Pozo-Antonio thanks the Spanish Ministry of Economy and Competitiveness (MINECO) for his “Juan de la Cierva-incorporación” (IJCI-2017-3277) contract. C. Cardell thanks the financial support provided by Spanish Research Projects AERIMPACT (CGL2012-30729) and EXPOAIR (P12-FQM-1889), the European Regional Development Fund (ERDF), and the Andalusian Research Group RNM-179. SEM-EDX analyses were performed in the Scientific Instrumentation Centre (CIC) of the University of Granada (Spain)

A novel gain-of-function mutation of Piezo1 is functionally affirmed in red blood cells by high-throughput patch clamp

No Abstract available

Rapid diagnosis of hereditary haemolytic anaemias using automated rheoscopy and supervised machine learning

Haemolytic anaemias arise when red blood cell (RBC) integrity is compromised, eventually resulting in premature clearance or lysis and leading to anaemia when these effects cannot be sufficiently compensated by the capacity of the bone marrow to produce new cells. Hereditary anaemia occurs as a consequence of genetic mutation (e.g. affecting membrane complex or cytoskeletal proteins, haemoglobin or metabolic enzymes), and diagnosing affected patients is a complex process since, given the wide variety of possible genetic causes, multiple examinations must be performed and an unambiguous result is usually reached only after DNA sequencing. Furthermore, phenotypic severity can vary widely not just among individuals with different mutations but also among individuals suffering from the same mutation, thereby complicating diagnosis