HIGH-OXYGEN MODIFIED ATMOSPHERE PACKAGING OF ORGANIC MEATS?

Abstract In the last few years, it became widespread to package fresh meat for retail under modified atmosphere containing 70-80% oxygen ("high O 2 -MAP"). Oxygen preserves the bright-red colour of oxymyoglobin while CO 2 (20-30%) inhibits obligatory aerobic bacteria such as psychrotrophic Pseudomonas spp., the common spoilage agents for unpackaged fresh meat. On the other hand, high oxygen partial pressure has been shown to cause some oxidative changes in the meat, resulting in sensory deviations. Use of high O 2 -MAP is also legally permitted for the packaging of organic meats. This may be regarded as being in conflict with the principle of "processing food with care" as stipulated by Article 6 of the Regulation (EU) 834/2007 on organic production and labelling of organic products. Therefore, the aim of our research was to provide information to decision-makers in the organic food chain on the necessity of high O 2 -MAP for organic meats. Literature data from market research show that even consumers of organic food seek "convenience" in purchasing and preparing it. Hence, of the major associations of organic agriculture in Germany, only Demeter e. V. prohibits the use of high O 2 -MAP. Literature data also indicate that undesirable changes of the meat could be delayed by reducing the oxygen content in the packages to about 40-50%, with only a slight reduction of shelf life. In our view, this would be a good compromise between "convenience" and eating quality

Live broadcasting in cardiac surgery does not increase the operative risk

Objective: Live broadcasting of cardiac surgical procedures has an educational intention. There is an ongoing debate whether live surgery increases risk. Aim of this study was to evaluate the outcomes of patients who underwent a cardiac surgical procedure during live broadcasting. Methods: A total of 250 cardiac operations were performed during 32 live broadcastings at four different clinical sites between 1999 and 2009. Data on patient characteristics, intra-operative procedures and patient short- and long-term outcome were collected and analyzed. All participating centers complied with the rules for the conduct of live surgery developed by the European Association of Cardiovascular and Thoracic Surgery (EACTS) Techno College Committee. Results: Primary educational focus was the mitral valve in 126 cases, aortic valve including transcatheter valve implantations in 34, coronary artery bypass grafting (CABG) in 29, congenital in 26, aortic (ascending, arch, and descending) in 15, atrial fibrillation in 13, and heart failure in seven. Mean EuroSCORE (European System for Cardiac Operative Risk Evaluation) was 8.7±11.5 (range: 0.8-72). Thirty-day mortality was 1.2% (3/250): reasons for death were multi-organ failure in two and respiratory failure in one patient, respectively. Stroke rate was 2.4% (6/250). Five patients (2%) required cardiac re-operations within 30 days. The rate of mitral valve repair was 96% (121) and compares favourably with repair rates presented in national registries. Mean follow-up of all patients was 3.7±2.8 years with an estimated survival of 92% (95% confidence interval (CI): 87-95%) at 5 years. Conclusions: Based on this large experience there is no evidence for an excess perioperative risk for patients operated under the conditions of live broadcastin

Maßnahmen zur Offenhaltung von Grünlandstandorten: Effekte auf die P-Fraktionen im Boden vierzig Jahre nach Versuchseinrichtung

Artenreiches Grünland, das nicht mehr bewirtschaftet wird, kann kostengünstig durch Maßnahmen wie Mulchen offen gehalten werden. Inwieweit Mulchen im Vergleich zu ungestörter Sukzession die P-Verfügbarkeit (labile, moderat labile und stabile Fraktionen) im Boden beeinflusst, untersuchten wir auf sechs Standorten auf der Schwäbischen Alb und im Schwarzwald 40 Jahre nach Versuchseinrichtung. Die Maßnahme Mulchen zweimal jährlich reduzierte vor allem auf silikatischem Ausgangsgestein im Schwarzwald die P-Gehalte der labilen, moderat labilen und stabilen Fraktionen im Vergleich mit den Varianten Mulchen jedes zweite Jahr und Sukzession. Zwischen 2014 und der Versuchseinrichtung im Jahr 1975 verzögerte das Mulchen die pedogenetisch bedingte Reduktion der P-Verfügbarkeit labiler Fraktionen im Boden

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

We sought to identify new susceptibility loci for Alzheimer's disease through a staged association study (GERAD+) and by testing suggestive loci reported by the Alzheimer's Disease Genetic Consortium (ADGC) in a companion paper. We undertook a combined analysis of four genome-wide association datasets (stage 1) and identified ten newly associated variants with P ≤ 1 × 10−5. We tested these variants for association in an independent sample (stage 2). Three SNPs at two loci replicated and showed evidence for association in a further sample (stage 3). Meta-analyses of all data provided compelling evidence that ABCA7 (rs3764650, meta P = 4.5 × 10−17; including ADGC data, meta P = 5.0 × 10−21) and the MS4A gene cluster (rs610932, meta P = 1.8 × 10−14; including ADGC data, meta P = 1.2 × 10−16) are new Alzheimer's disease susceptibility loci. We also found independent evidence for association for three loci reported by the ADGC, which, when combined, showed genome-wide significance: CD2AP (GERAD+, P = 8.0 × 10−4; including ADGC data, meta P = 8.6 × 10−9), CD33 (GERAD+, P = 2.2 × 10−4; including ADGC data, meta P = 1.6 × 10−9) and EPHA1 (GERAD+, P = 3.4 × 10−4; including ADGC data, meta P = 6.0 × 10−10)

A three-dimensional coupled model of the western Black Sea plankton dynamics: Seasonal variability and comparison to SeaWiFS data

The main physical and biological processes that control the seasonal cycle of the plankton dynamics over the Western Black Sea were explored by means of a three‐dimensional, 7‐compartment, on‐line coupled biophysical model that was developed for this study. Adopting high frequency forcing in terms of air‐sea interaction and Danube river inputs, we performed a simulation of the coupled model during the 2002–2003 period. A series of 8‐day Chl‐a SeaWiFS images provided a validation tool that guided us, along with available in situ measurements, to the improvement of model parameterizations and the calibration of the biological parameters. The simulation of the seasonal phytoplankton variability over the entire Western Black Sea, extending from the highly eutrophic river influenced area to the open sea area, was a major challenge that made necessary the representation of both the spatial and time variability of several processes. Despite the model simplicity, the simulated Chl‐a patterns presented a good agreement as compared to the SeaWiFS and in situ data. During winter, phytoplankton in coastal areas was shown to be limited by light availability, primarily due to the increased particulate matter concentrations, as a result of resuspension from the sediment and the increased river loads. During summer, the primary production was mostly sustained by riverine nutrients and regeneration processes and thus was strongly linked to the evolution of the Danube plume. The limiting nutrients showed deviations from the observed concentrations, indicating the necessity for a more realistic phytoplankton growth model

New genetic loci link adipose and insulin biology to body fat distribution.

Body fat distribution is a heritable trait and a well-established predictor of adverse metabolic outcomes, independent of overall adiposity. To increase our understanding of the genetic basis of body fat distribution and its molecular links to cardiometabolic traits, here we conduct genome-wide association meta-analyses of traits related to waist and hip circumferences in up to 224,459 individuals. We identify 49 loci (33 new) associated with waist-to-hip ratio adjusted for body mass index (BMI), and an additional 19 loci newly associated with related waist and hip circumference measures (P < 5 × 10(-8)). In total, 20 of the 49 waist-to-hip ratio adjusted for BMI loci show significant sexual dimorphism, 19 of which display a stronger effect in women. The identified loci were enriched for genes expressed in adipose tissue and for putative regulatory elements in adipocytes. Pathway analyses implicated adipogenesis, angiogenesis, transcriptional regulation and insulin resistance as processes affecting fat distribution, providing insight into potential pathophysiological mechanisms

Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.

OBJECTIVE: Proinsulin is a precursor of mature insulin and C-peptide. Higher circulating proinsulin levels are associated with impaired β-cell function, raised glucose levels, insulin resistance, and type 2 diabetes (T2D). Studies of the insulin processing pathway could provide new insights about T2D pathophysiology. RESEARCH DESIGN AND METHODS: We have conducted a meta-analysis of genome-wide association tests of ∼2.5 million genotyped or imputed single nucleotide polymorphisms (SNPs) and fasting proinsulin levels in 10,701 nondiabetic adults of European ancestry, with follow-up of 23 loci in up to 16,378 individuals, using additive genetic models adjusted for age, sex, fasting insulin, and study-specific covariates. RESULTS: Nine SNPs at eight loci were associated with proinsulin levels (P < 5 × 10(-8)). Two loci (LARP6 and SGSM2) have not been previously related to metabolic traits, one (MADD) has been associated with fasting glucose, one (PCSK1) has been implicated in obesity, and four (TCF7L2, SLC30A8, VPS13C/C2CD4A/B, and ARAP1, formerly CENTD2) increase T2D risk. The proinsulin-raising allele of ARAP1 was associated with a lower fasting glucose (P = 1.7 × 10(-4)), improved β-cell function (P = 1.1 × 10(-5)), and lower risk of T2D (odds ratio 0.88; P = 7.8 × 10(-6)). Notably, PCSK1 encodes the protein prohormone convertase 1/3, the first enzyme in the insulin processing pathway. A genotype score composed of the nine proinsulin-raising alleles was not associated with coronary disease in two large case-control datasets. CONCLUSIONS: We have identified nine genetic variants associated with fasting proinsulin. Our findings illuminate the biology underlying glucose homeostasis and T2D development in humans and argue against a direct role of proinsulin in coronary artery disease pathogenesis

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Copy number variants (CNV) are established risk factors for neurodevelopmental disorders with seizures or epilepsy. With the hypothesis that seizure disorders share genetic risk factors, we pooled CNV data from 10,590 individuals with seizure disorders, 16,109 individuals with clinically validated epilepsy, and 492,324 population controls and identified 25 genome-wide significant loci, 22 of which are novel for seizure disorders, such as deletions at 1p36.33, 1q44, 2p21-p16.3, 3q29, 8p23.3-p23.2, 9p24.3, 10q26.3, 15q11.2, 15q12-q13.1, 16p12.2, 17q21.31, duplications at 2q13, 9q34.3, 16p13.3, 17q12, 19p13.3, 20q13.33, and reciprocal CNVs at 16p11.2, and 22q11.21. Using genetic data from additional 248,751 individuals with 23 neuropsychiatric phenotypes, we explored the pleiotropy of these 25 loci. Finally, in a subset of individuals with epilepsy and detailed clinical data available, we performed phenome-wide association analyses between individual CNVs and clinical annotations categorized through the Human Phenotype Ontology (HPO). For six CNVs, we identified 19 significant associations with specific HPO terms and generated, for all CNVs, phenotype signatures across 17 clinical categories relevant for epileptologists. This is the most comprehensive investigation of CNVs in epilepsy and related seizure disorders, with potential implications for clinical practice

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.

Reduced glomerular filtration rate defines chronic kidney disease and is associated with cardiovascular and all-cause mortality. We conducted a meta-analysis of genome-wide association studies for estimated glomerular filtration rate (eGFR), combining data across 133,413 individuals with replication in up to 42,166 individuals. We identify 24 new and confirm 29 previously identified loci. Of these 53 loci, 19 associate with eGFR among individuals with diabetes. Using bioinformatics, we show that identified genes at eGFR loci are enriched for expression in kidney tissues and in pathways relevant for kidney development and transmembrane transporter activity, kidney structure, and regulation of glucose metabolism. Chromatin state mapping and DNase I hypersensitivity analyses across adult tissues demonstrate preferential mapping of associated variants to regulatory regions in kidney but not extra-renal tissues. These findings suggest that genetic determinants of eGFR are mediated largely through direct effects within the kidney and highlight important cell types and biological pathways