Exploring Stress Mindset and Perceived Stress between College Student-Athletes and Non-Athletes

International Journal of Exercise Science 15(5): 1554-1562, 2022. One’s beliefs about the nature of stress (e.g., stress mindset) play a large role in the extent to which one experiences the detrimental or beneficial outcomes of stress. Stress mindset has been explored in college students, but there is limited research on stress mindsets in student-athletes. Sport can serve as a buffer to the negative impacts of stress for some student-athletes; however, pressures associated with sport participation increase stress in other student-athletes. Therefore, the purpose was to examine potential differences in stress mindset and perceived stress between non-athletes and college student-athletes. We hypothesized college student-athletes would report higher stress mindset scores but lower perceived stress scores. A total of 272 students (n = 87 student-athletes; n = 185 non-athletes) completed a demographic questionnaire, the Perceived Stress Scale, and the Stress Mindset Measure via an online survey. No significant differences were observed between student-athletes’ and non-athletes’ stress mindset scores; however, significant differences were observed between student-athletes’ and non-athletes’ perceived stress. Thus, student-athletes and non-athletes shared a similar view of stress, but student-athletes reported a lower level of perceived stress than non-athletes. While there appears to be no statistically significant differences in stress mindset between college non-athletes and student-athletes, both groups reported holding a stress-is-debilitating mindset. Implications for practitioners working with the college population are discussed

Developing and testing accelerated partner therapy for partner notification for people with genital Chlamydia trachomatis diagnosed in primary care: a pilot randomised controlled trial

Background Accelerated partner therapy (APT) is a promising partner notification (PN) intervention in specialist sexual health clinic attenders. To address its applicability in primary care, we undertook a pilot randomised controlled trial (RCT) of two APT models in community settings. Methods Three-arm pilot RCT of two adjunct APT interventions: APTHotline (telephone assessment of partner(s) plus standard PN) and APTPharmacy (community pharmacist assessment of partner(s) plus routine PN), versus standard PN alone (patient referral). Index patients were women diagnosed with genital chlamydia in 12 general practices and three community contraception and sexual health (CASH) services in London and south coast of England, randomised between 1 September 2011 and 31 July 2013. Results 199 women described 339 male partners, of whom 313 were reported by the index as contactable. The proportions of contactable partners considered treated within 6 weeks of index diagnosis were APTHotline 39/111 (35%), APTPharmacy 46/100 (46%), standard patient referral 46/102 (45%). Among treated partners, 8/39 (21%) in APTHotline arm were treated via hotline and 14/46 (30%) in APTPharmacy arm were treated via pharmacy. Conclusions The two novel primary care APT models were acceptable, feasible, compliant with regulations and capable of achieving acceptable outcomes within a pilot RCT but intervention uptake was low. Although addition of these interventions to standard PN did not result in a difference between arms, overall PN uptake was higher than previously reported in similar settings, probably as a result of introducing a formal evaluation. Recruitment to an individually randomised trial proved challenging and full evaluation will likely require service-level randomisation

A self-consistent method to estimate the rate of compact binary coalescences with a Poisson mixture model

The recently published GWTC-1 (Abbott B P et al (LIGO Scientific Collaboration and Virgo Collaboration) 2019 Phys. Rev. X 9 031040)—a journal article summarizing the search for gravitational waves (GWs) from coalescing compact binaries in data produced by the LIGO-Virgo network of ground-based detectors during their first and second observing runs—quoted estimates for the rates of binary neutron star, neutron star black hole binary, and binary black hole mergers, as well as assigned probabilities of astrophysical origin for various significant and marginal GW candidate events. In this paper, we delineate the formalism used to compute these rates and probabilities, which assumes that triggers above a low ranking statistic threshold, whether of terrestrial or astrophysical origin, occur as independent Poisson processes. In particular, we include an arbitrary number of astrophysical categories by redistributing, via mass-based template weighting, the foreground probabilities of candidate events, across source classes. We evaluate this formalism on synthetic GW data, and demonstrate that this method works well for the kind of GW signals observed during the first and second observing runs

A self-consistent method to estimate the rate of compact binary coalescences with a Poisson mixture model

The recently published GWTC-1 - a journal article summarizing the search for gravitational waves (GWs) from coalescing compact binaries in data produced by the LIGO-Virgo network of ground-based detectors during their first and second observing runs - quoted estimates for the rates of binary neutron star, neutron star black hole binary, and binary black hole mergers, as well as assigned probabilities of astrophysical origin for various significant and marginal GW candidate events. In this paper, we delineate the formalism used to compute these rates and probabilities, which assumes that triggers above a low ranking statistic threshold, whether of terrestrial or astrophysical origin, occur as independent Poisson processes. In particular, we include an arbitrary number of astrophysical categories by redistributing, via mass-based template weighting, the foreground probabilities of candidate events, across source classes. We evaluate this formalism on synthetic GW data, and demonstrate that this method works well for the kind of GW signals observed during the first and second observing runs.Comment: 19 pages, 5 figure

A self-consistent method to estimate the rate of compact binary coalescences with a Poisson mixture model

The recently published GWTC-1 - a journal article summarizing the search for gravitational waves (GWs) from coalescing compact binaries in data produced by the LIGO-Virgo network of ground-based detectors during their first and second observing runs - quoted estimates for the rates of binary neutron star, neutron star black hole binary, and binary black hole mergers, as well as assigned probabilities of astrophysical origin for various significant and marginal GW candidate events. In this paper, we delineate the formalism used to compute these rates and probabilities, which assumes that triggers above a low ranking statistic threshold, whether of terrestrial or astrophysical origin, occur as independent Poisson processes. In particular, we include an arbitrary number of astrophysical categories by redistributing, via mass-based template weighting, the foreground probabilities of candidate events, across source classes. We evaluate this formalism on synthetic GW data, and demonstrate that this method works well for the kind of GW signals observed during the first and second observing runs.Comment: 19 pages, 5 figure

RNA-Seq Differentiates Tumour and Host mRNA Expression Changes Induced by Treatment of Human Tumour Xenografts with the VEGFR Tyrosine Kinase Inhibitor Cediranib.

Pre-clinical models of tumour biology often rely on propagating human tumour cells in a mouse. In order to gain insight into the alignment of these models to human disease segments or investigate the effects of different therapeutics, approaches such as PCR or array based expression profiling are often employed despite suffering from biased transcript coverage, and a requirement for specialist experimental protocols to separate tumour and host signals. Here, we describe a computational strategy to profile transcript expression in both the tumour and host compartments of pre-clinical xenograft models from the same RNA sample using RNA-Seq. Key to this strategy is a species-specific mapping approach that removes the need for manipulation of the RNA population, customised sequencing protocols, or prior knowledge of the species component ratio. The method demonstrates comparable performance to species-specific RT-qPCR and a standard microarray platform, and allowed us to quantify gene expression changes in both the tumour and host tissue following treatment with cediranib, a potent vascular endothelial growth factor receptor tyrosine kinase inhibitor, including the reduction of multiple murine transcripts associated with endothelium or vessels, and an increase in genes associated with the inflammatory response in response to cediranib. In the human compartment, we observed a robust induction of hypoxia genes and a reduction in cell cycle associated transcripts. In conclusion, the study establishes that RNA-Seq can be applied to pre-clinical models to gain deeper understanding of model characteristics and compound mechanism of action, and to identify both tumour and host biomarkers

A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction

The developmental and physiological complexity of the auditory system is likely reflected in the underlying set of genes involved in auditory function. In humans, over 150 non-syndromic loci have been identified, and there are more than 400 human genetic syndromes with a hearing loss component. Over 100 non-syndromic hearing loss genes have been identified in mouse and human, but we remain ignorant of the full extent of the genetic landscape involved in auditory dysfunction. As part of the International Mouse Phenotyping Consortium, we undertook a hearing loss screen in a cohort of 3006 mouse knockout strains. In total, we identify 67 candidate hearing loss genes. We detect known hearing loss genes, but the vast majority, 52, of the candidate genes were novel. Our analysis reveals a large and unexplored genetic landscape involved with auditory function

Genomic, Pathway Network, and Immunologic Features Distinguishing Squamous Carcinomas

This integrated, multiplatform PanCancer Atlas study co-mapped and identified distinguishing molecular features of squamous cell carcinomas (SCCs) from five sites associated with smokin

Pan-Cancer Analysis of lncRNA Regulation Supports Their Targeting of Cancer Genes in Each Tumor Context

Long noncoding RNAs (lncRNAs) are commonly dys-regulated in tumors, but only a handful are known toplay pathophysiological roles in cancer. We inferredlncRNAs that dysregulate cancer pathways, onco-genes, and tumor suppressors (cancer genes) bymodeling their effects on the activity of transcriptionfactors, RNA-binding proteins, and microRNAs in5,185 TCGA tumors and 1,019 ENCODE assays.Our predictions included hundreds of candidateonco- and tumor-suppressor lncRNAs (cancerlncRNAs) whose somatic alterations account for thedysregulation of dozens of cancer genes and path-ways in each of 14 tumor contexts. To demonstrateproof of concept, we showed that perturbations tar-geting OIP5-AS1 (an inferred tumor suppressor) andTUG1 and WT1-AS (inferred onco-lncRNAs) dysre-gulated cancer genes and altered proliferation ofbreast and gynecologic cancer cells. Our analysis in-dicates that, although most lncRNAs are dysregu-lated in a tumor-specific manner, some, includingOIP5-AS1, TUG1, NEAT1, MEG3, and TSIX, synergis-tically dysregulate cancer pathways in multiple tumorcontexts