C-reactive protein monitoring in children with acute asthma

Cilj: Ispitati može li se određivanje koncentracije hsCRP (high sensitivity C-reactive protein) primijeniti kao biomarker u praćenju uspješnosti terapije akutne egzacerbacije astme u djece. Ispitanici i metode: U ispitivanje je uključeno 28-ero djece kontrolne skupine i 27-ero djece hospitalizirane zbog liječenja akutnog napadaja astme. Liječenje akutne egzacerbacije provedeno je kontinuiranom inhalacijom 2-agonista brzog djelovanja te primjenom inghalacijskih kortikosteroida. Za određivanje hsCRP uzorkovani su serumi bolesnika prije terapije i tri dana nakon terapije. Koncentracija hsCRP određena je imunoturbidimetrijskom metodom na lateks česticama na biokemijskom analizatoru AU400. Rezultati: Koncentracija hsCRP bila je statistički značajno veća u djece s astmom (prije terapije: 3,00 ± 1,92 mg/l; tri dana nakon terapije: 0,80 ± 0,61 mg/l) nego u djece kontrolne skupine (0,36 ± 0,21 mg/l). Zaključak: Rezultati ovog istraživanja ukazuju na to da bi hsCRP mogao biti nespecifičan biomarker za praćenje upale u djece s akutnom egzacerbacijom astme. Međutim, potrebna su nova istraživanja koja bi utvrdila korelaciju između specifičnih i nespecifičnih biomarkera upale u astmi.Aim: To assess whether the determination of high sensitive C-reactive protein (hsCRP) could bi used as biomarker of successful drug administration in children with asthma exacerbation. Subjects and methods: The study included 28 control children and 27 pediatric asthmatics who were hospitalized for treatment of asthma exacerbation. All patients were treated with continuous inhalations of short acting 2-agonists and inhaled corticosteroids administration. A pair of routine serum samples (one taken before and one three days after drug administration) were taken for hsCRP determination. The concentration of hsCRP was determined by the immunoturbidimetric method on latex particles on an Olympus AU400 biochemistry analyzer. Results: The concentration of hsCRP was statistically significantly higher in children with asthma (before drug administration: 3.00 ± 1.92 mg/L; three days after drug administration: 0.80 ± 0.61 mg/L) than in healthy children (0.36 ± 0.21 mg/L). Conclusion: Study results suggest that hsCRP could have the potential as a nonspecific biomarker for monitoring inflammation in children with asthma exacerbation. Further research is are needed to find the correlation between specific and nonspecific biomarkers of inflammation in asthma

Cognition as Embodied Morphological Computation

Cognitive science is considered to be the study of mind (consciousness and thought) and intelligence in humans. Under such definition variety of unsolved/unsolvable problems appear. This article argues for a broad understanding of cognition based on empirical results from i.a. natural sciences, self-organization, artificial intelligence and artificial life, network science and neuroscience, that apart from the high level mental activities in humans, includes sub-symbolic and sub-conscious processes, such as emotions, recognizes cognition in other living beings as well as extended and distributed/social cognition. The new idea of cognition as complex multiscale phenomenon evolved in living organisms based on bodily structures that process information, linking cognitivists and EEEE (embodied, embedded, enactive, extended) cognition approaches with the idea of morphological computation (info-computational self-organisation) in cognizing agents, emerging in evolution through interactions of a (living/cognizing) agent with the environment

Shell model on a random gaussian basis

Pauli-projected random gaussians are used as a representation to solve the shell model equations. The elements of the representation are chosen by a variational procedure. This scheme is particularly suited to describe cluster formation and cluster decay in nuclei. It overcomes the basis-size problem of the ordinary shell model and the technical difficulties of the cluster-configuration shell model. The model reproduces the $\alpha$-decay width of $^{212}$Po satisfactorily.Comment: Latex, Submitted to Phys. Lett. B, 7 pages, 2 figures available upon request, ATOMKI-1994-

Simultaneous determination of iron and copper in children's sera by FAAS

Predložena je nova jednostavna metoda plamene atomsko-apsorpcijske spektrometrije (FAAS), za simultano određivanje željeza i bakra u serumu djece. Ona se temelji na predobradbi uzorka u jednom koraku (deproteinizacija s 3 mol L–3 HCl u odnosu 1:1) i kalibraciji u jednom koraku sa standardom pripravljenim u 1.5 mol L–3 HCl. Tijekom optimizacije metode primijenjen je multifaktorski dizajnirani eksperiment. Preporučena metoda osigurava ispravnost, osjetljivost i preciznost usporedljivu onima referentnih metoda. Novi je pristup jednostavan i brz; on štedi i vrijeme i reagense i uzorke, pri čemu je potonje posebno važno u dječjoj dijagnostici.A new and simple flame atomic-absorption spectrometric (FAAS) method is proposed for simultaneous determination of iron and copper in children's sera. It is based on single-step sample pretreatment (deproteinization with 3 mol L–1 HCl, ratio 1:1) and single-step calibration using 1.5 mol L–1 HCl standard. During method’s optimization a short multifactorial design experiment was used. The proposed method assures accuracy, sensitivity and precision comparable to that of the reference methods. The new approach is simple and time-, labour- and serum-saving, the latter being especially important in pediatric diagnostics

Genotype x Environment interaction for antioxidants and phytic acid contents in bread and durum wheat as influenced by climate

Antioxidants prevent oxidative stress and exert positive health effects. However, phytic acid among them decreases micronutrients absorption, representing also antinutrient to human and non-ruminant animals. Fifteen bread wheat (Triticum aestivum L.) and 15 durum wheat (Triticum durum Desf.) genotypes were evaluated across six environments to determine contents of phytic acid (PA), inorganic P (Pi), total yellow pigment, total soluble phenolic compounds, free protein sulfhydryl groups (PSH), and also phytic acid P/P-i (P-p/P-i). The objective of this study was to quantify, for each trait the effects of environment, genotype, and their interaction; and the influence of climatic factors on the Genotype x Environment interaction (GEI) by the use of the factorial regression. GEI (P lt 0.001) prevailed as source of variation over genotype (P lt 0.001) in determining PA content in bread and durum wheat (44.3% and 34.7% of sum of squares-SS, respectively), PSH content in bread and durum wheat (27% and 28.4% of SS, respectively) and total soluble phenolic compounds content in durum wheat (35.5% of SS). The major contribution to the GEI represented climatic variables during stages of stem elongation for PA and phenolic compounds, and also flowering, fertilization, grain formation and grain filling for PSH. Total yellow pigment and Pi contents in bread and durum wheat were predominantly determined by genotype (P lt 0.001). Models of climatic variables proved to be efficient in the explanation of more than 92% of the SS of GEI for PA and antioxidants contents

Facets of individual-specific health signatures determined from longitudinal plasma proteome profiling

Background: Precision medicine approaches aim to tackle diseases on an individual level through molecular profiling. Despite the growing knowledge about diseases and the reported diversity of molecular phenotypes, the descriptions of human health on an individual level have been far less elaborate. Methods: To provide insights into the longitudinal protein signatures of well-being, we profiled blood plasma collected over one year from 101 clinically healthy individuals using multiplexed antibody assays. After applying an antibody validation scheme, we utilized > 700 protein profiles for in-depth analyses of the individuals’ short-term health trajectories. <p<Findings: We found signatures of circulating proteomes to be highly individual-specific. Considering technical and longitudinal variability, we observed that 49% of the protein profiles were stable over one year. We also identified eight networks of proteins in which 11 242 proteins covaried over time. For each participant, there were unique protein profiles of which some could be explained by associations to genetic variants. Interpretation: This observational and non-interventional study identifyed noticeable diversity among clinically healthy subjects, and facets of individual-specific signatures emerged by monitoring the variability of the circulating proteomes over time. To enable more personal hence precise assessments of health states, longitudinal profiling of circulating proteomes can provide a valuable component for precision medicine approaches

Expression of Msx-1 is suppressed in bisphosphonate associated osteonecrosis related jaw tissue-etiopathology considerations respecting jaw developmental biology-related unique features

<p>Abstract</p> <p>Background</p> <p>Bone-destructive disease treatments include bisphosphonates and antibodies against the osteoclast differentiator, RANKL (aRANKL); however, osteonecrosis of the jaw (ONJ) is a frequent side-effect. Current models fail to explain the restriction of bisphosphonate (BP)-related and denosumab (anti-RANKL antibody)-related ONJ to jaws. Msx-1 is exclusively expressed in craniofacial structures and pivotal to cranial neural crest (CNC)-derived periodontal tissue remodeling. We hypothesised that Msx-1 expression might be impaired in bisphosphonate-related ONJ. The study aim was to elucidate Msx-1 and RANKL-associated signal transduction (BMP-2/4, RANKL) in ONJ-altered and healthy periodontal tissue.</p> <p>Methods</p> <p>Twenty ONJ and twenty non-BP exposed periodontal samples were processed for RT-PCR and immunohistochemistry. An automated staining-based alkaline phosphatase-anti-alkaline phosphatase method was used to measure the stained cells:total cell-number ratio (labelling index, Bonferroni adjustment). Real-time RT-PCR was performed on ONJ-affected and healthy jaw periodontal samples (n = 20 each) to quantitatively compare Msx-1, BMP-2, RANKL, and GAPDH mRNA levels.</p> <p>Results</p> <p>Semi-quantitative assessment of the ratio of stained cells showed decreased Msx-1 and RANKL and increased BMP-2/4 (all p < 0.05) expression in ONJ-adjacent periodontal tissue. ONJ tissue also exhibited decreased relative gene expression for Msx-1 (p < 0.03) and RANKL (p < 0.03) and increased BMP-2/4 expression (p < 0.02) compared to control.</p> <p>Conclusions</p> <p>These results explain the sclerotic and osteopetrotic changes of periodontal tissue following BP application and substantiate clinical findings of BP-related impaired remodeling specific to periodontal tissue. RANKL suppression substantiated the clinical finding of impaired bone remodelling in BP- and aRANKL-induced ONJ-affected bone structures. Msx-1 suppression in ONJ-adjacent periodontal tissue suggested a bisphosphonate-related impairment in cellular differentiation that occurred exclusively jaw remodelling. Further research on developmental biology-related unique features of jaw bone structures will help to elucidate pathologies restricted to maxillofacial tissue.</p