Pròleg

Pròleg del quadern "Eponimia Mèdica Catalana II"

EngiMath online course. Effective feedback from upc mathematics teachers (concept)

EngiMath is a 3 ECTS online course in engineering mathematics, in seven different languages, and it is the main and practical output of the ERASMUS+ project entitled “Mathematics online learning model in engineering education” in which the authors were participating. The course is integrated with Learning Management Systems such as Moodle and it is compatible with other platforms using Learning Tools Interoperability. Once the project is finished, authors undertake, with the support of the Institute of Education Sciences at the Universitat Politècnica de Catalunya-BarcelonaTECH (UPC), an innovation project, EngiMath@UPC, with three practical objectives: a) to incorporate EngiMath into the teaching activity of the widest as possible range of students at UPC, b) to gather students and faculty feedback regarding the tracking of materials and their performance in the student training process, and c) to statistically analyze the data collected in order to validate and adjust the follow-up of the materials. In connection with the above mentioned objective b) a training course addressed to the math professors has been prepared at UPC. The paper introduces, on the one hand, the EngiMath course as an online open educational resource for the academic community benefit, and on the other hand, analyzes the valuable feedback given by the training activity participants. Details on the online course implementation as well as main conclusions will be presented and discussed throughout the document

Strong Reflexivity of Abelian Groups

A reflexive topological group G is called strongly reflexive if each closed subgroup and each Hausdorff quotient of the group G and of itsdua l group isre flexive. In this paper we establish an adequate concept of strong reflexivity for convergence groups. We prove that complete metrizable nuclear groups and products of countably many locally compact topological groupsare BB-strongly reflexive

Cross-validation of methods used for analysis of MTBE and other gasoline components in groundwater.

Head space gas chromatography with flame-ionization detection (HS-GC-FID), ancl purge and trap gas chromatography-mass spectrometry (P&T-GC-MS) have been used to determine methyl-tert-butyl ether (MTBE) and benzene, toluene, and the ylenes (BTEX) in groundwater. In the work discussed in this paper measures of quality, e.g. recovery (94-111%), precision (4.6 - 12.2%), limits of detection (0.3 - 5.7 I~g L 1 for HS and 0.001 I~g L 1 for PT), and robust-ness, for both methods were compared. In addition, for purposes of comparison, groundwater samples from areas suffering from odor problems because of fuel spillage and tank leakage were analyzed by use of both techniques. For high concentration levels there was good correlation between results from both methods

Impacts of metals and nutrients released from melting multiyear Arctic sea ice

Nutrients (C, N, and P) and metals (iron, molybdenum, nickel, zinc, vanadium, copper, and cobalt) were determined in water and multiyear ice sampled along the Greenland current and Fram Strait in July 2007. Total metal and nutrient concentrations in ice varied fivefold to tenfold, for most elements, across the area sampled. Data show that some nutrients (i.e., NH4+) and metals (i.e., Fe, Zn, V, Cu, Ni, Mo, and Co) are enriched in Arctic ice relative to surface seawaters, suggesting that ice melting is a significant source of metals to the receiving seawaters, particularly Fe and Zn whose concentrations were significantly (t test, P < 0.05) more than 2 orders of magnitude higher in ice than in surface seawater.This research is part of the ATOS project, funded as part of the Spanish contribution to the International Polar Year (IPY) by the Spanish Ministry of Science and Innovation (POL2006-00550/CTM). This is a contribution to the GEOTRACES cluster of the IPY. We thank the ATOS participants, UTM and crew of R/V Hespérides for help with ice sampling and logistics. We thank R. Santiago, R. Martínez, and A. Massanet at IMEDEA and J. A. González (SCT, UIB) for help with chemical analyses. This manuscript was written in the field stations of Ses Salines Lighthouse.Peer reviewe

Association of neurexin 3 polymorphisms with smoking behavior.

The Neurexin 3 gene (NRXN3) has been associated with dependence on various addictive substances, as well as with the degree of smoking in schizophrenic patients and impulsivity among tobacco abusers. To further evaluate the role of NRXN3 in nicotine addiction, we analyzed single nucleotide polymorphisms (SNPs) and a copy number variant (CNV) within the NRXN3 genomic region. An initial study was carried out on 157 smokers and 595 controls, all of Spanish Caucasian origin. Nicotine dependence was assessed using the Fagerstrom index and the number of cigarettes smoked per day. The 45 NRXN3 SNPs genotyped included all the SNPs previously associated with disease, and a previously described deletion within NRXN3. This analysis was replicated in 276 additional independent smokers and 568 controls. Case-control association analyses were performed at the allele, genotype and haplotype levels. Allelic and genotypic association tests showed that three NRXN3 SNPs were associated with a lower risk of being a smoker. The haplotype analysis showed that one block of 16 Kb, consisting of two of the significant SNPs (rs221473 and rs221497), was also associated with lower risk of being a smoker in both the discovery and the replication cohorts, reaching a higher level of significance when the whole sample was considered [odds ratio = 0.57 (0.42-0.77), permuted P = 0.0075]. By contrast, the NRXN3 CNV was not associated with smoking behavior. Taken together, our results confirm a role for NRXN3 in susceptibility to smoking behavior, and strongly implicate this gene in genetic vulnerability to addictive behaviors

The association between serum biomarkers and disease outcome in influenza A(H1N1)pdm09 virus infection: results of two international observational cohort studies

BACKGROUND Prospective studies establishing the temporal relationship between the degree of inflammation and human influenza disease progression are scarce. To assess predictors of disease progression among patients with influenza A(H1N1)pdm09 infection, 25 inflammatory biomarkers measured at enrollment were analyzed in two international observational cohort studies. METHODS Among patients with RT-PCR-confirmed influenza A(H1N1)pdm09 virus infection, odds ratios (ORs) estimated by logistic regression were used to summarize the associations of biomarkers measured at enrollment with worsened disease outcome or death after 14 days of follow-up for those seeking outpatient care (FLU 002) or after 60 days for those hospitalized with influenza complications (FLU 003). Biomarkers that were significantly associated with progression in both studies (p<0.05) or only in one (p<0.002 after Bonferroni correction) were identified. RESULTS In FLU 002 28/528 (5.3%) outpatients had influenza A(H1N1)pdm09 virus infection that progressed to a study endpoint of complications, hospitalization or death, whereas in FLU 003 28/170 (16.5%) inpatients enrolled from the general ward and 21/39 (53.8%) inpatients enrolled directly from the ICU experienced disease progression. Higher levels of 12 of the 25 markers were significantly associated with subsequent disease progression. Of these, 7 markers (IL-6, CD163, IL-10, LBP, IL-2, MCP-1, and IP-10), all with ORs for the 3(rd) versus 1(st) tertile of 2.5 or greater, were significant (p<0.05) in both outpatients and inpatients. In contrast, five markers (sICAM-1, IL-8, TNF-α, D-dimer, and sVCAM-1), all with ORs for the 3(rd) versus 1(st) tertile greater than 3.2, were significantly (p≤.002) associated with disease progression among hospitalized patients only. CONCLUSIONS In patients presenting with varying severities of influenza A(H1N1)pdm09 virus infection, a baseline elevation in several biomarkers associated with inflammation, coagulation, or immune function strongly predicted a higher risk of disease progression. It is conceivable that interventions designed to abrogate these baseline elevations might affect disease outcome