109 research outputs found

    Writing for an Authentic Audience in the Middle Grades

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    This action research study investigated the effects of writing for an authentic audience on the achievement and engagement of students in a school in Southern California. The participants were 79 8th graders, split into an experimental group of 40 that wrote a review with the opportunity to be published in The New York Times, and a control group of 39 students that wrote a review for the teacher to read and grade

    Effects of culture conditions on cytosine methylation and MeCP2 binding in preimplantation mouse embryos

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    Abstract only availableImprinting is an epigenetic modification in which one gene of a pair of alleles is silenced in a parent-specific way. Imprinting is commonly controlled by methylation of the C5 position of cytosines which are located next to guanines in DNA sequences. CpG methylation usually confers a silencing signal to genes. Methyl-CpG Binding proteins, (e.g. MeCP2), have also been shown to play a role in silencing genes when bound to methylated DNA regions. Oxidative stress has been shown to form 8-hydroxyguanine lesions on guanine bases which may hinder MeCP2 binding activity, and therefore hinder gene silencing. It has been shown that culture of preimplantation mouse embryos can cause gene misexpression, including loss of imprinting. The purpose of this study was to use immunofluorescence and confocal microscopy to examine whether culturing preimplantation mouse embryos in different culture conditions causes alterations in DNA methylation, binding of the MeCP2 methyl-CpG binding proteins, and the formation of 8-oxoguanine lesions on DNA when compared to in-vivo produced mouse embryos. Preimplantation mouse embryos were subjected to four different culture conditions in a 2X2 factorial design using 2 levels of oxygen tension (5% and 20%) and 2 different media (KSOM + amino acids, and Whitten's medium). Cultured embryos will be compared to two different in-vivo produced control groups; a) super-ovulated and b) not super-ovulated. The super-ovulated in-vivo group embryos were collected from females 96h post hCG. The culture groups embryos were collected at the two-cell stage approximately 44 hours post hCG. Two-cell embryos were then divided in four groups and cultured until 108-120h post hCG. At the completion of each treatment, embryos were fixed or frozen for immunofluorescence or real time RT-PCR analyses, respectively. Results will be discussed.F.B. Miller Undergraduate Research Program in Animal Science

    Positive psychology interventions in patients with medical illness: What predicts improvement in psychological state?

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    Positive psychology interventions (PPIs) have been shown to promote wellbeing in individuals with medical illness, although it is still unknown whether certain patient characteristics make participants more likely to benefit from such interventions. The present study tested whether, using individual patient data across five published PPI studies (three single-arm proof-of-concept trials, one non-randomized controlled trial, and one randomized controlled trial) in medically-ill persons, sociodemographic or psychological factors predicted subsequent change in wellbeing. In 208 participants, lower baseline psychological wellbeing and optimism, and higher symptoms of depression and anxiety were associated with greater improvement in psychological symptoms during the PPI. Other factors were unrelated to symptom changes. In a sub-analysis of controlled studies, there were no group differences in the relationship between baseline factors and changes in wellbeing from pre- to post-intervention. Findings suggest that patients with more severe psychiatric and/or medical comorbidity are no less likely to benefit from a PPI compared to those with higher levels of health, even though these programs do not directly target psychological distress. PPIs may be widely applicable to medical patients, with lower psychological wellbeing a potential predictor of increased benefit

    Association between incarceration and incident cardiovascular disease events: results from the CARDIA cohort study

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    BACKGROUND: Incarceration has been associated with higher cardiovascular risk, yet data evaluating its association with cardiovascular disease events are limited. The study objective was to evaluate the association between incarceration and incident fatal and non-fatal cardiovascular disease (CVD) events. METHODS: Black and white adults from the community-based Coronary Artery Risk Development in Young Adult (CARDIA) study (baseline 1985-86, n = 5105) were followed through August 2017. Self-reported incarceration was measured at baseline (1985-1986) and Year 2 (1987-1988), and fatal and non-fatal cardiovascular disease events, including coronary heart disease, stroke, and heart failure, and all-cause mortality, were captured through 2017. Analyses were completed in September 2019. Cumulative CVD incidence rates and Cox proportional hazards were compared overall by incarceration status. An interaction between incarceration and race was identified, so results were also analyzed by sex-race groups. RESULTS: 351 (6.9%) CARDIA participants reported a history of incarceration. Over 29.0 years mean follow-up, CVD incidence rate was 3.52 per 1000 person-years in participants with a history of incarceration versus 2.12 per 1000 person-years in participants without a history of incarceration (adjusted HR = 1.33 [95% CI, 0.90-1.95]). Among white men, incarceration was associated with higher risk of incident cardiovascular disease (adjusted HR = 3.35 [95% CI, 1.54-7.29) and all-cause mortality (adjusted HR = 2.52 [95% CI, 1.32-4.83]), but these associations were not statistically significant among other sex-race groups after adjustment. CONCLUSIONS: Incarceration was associated with incident cardiovascular disease rates, but associations were only significant in one sex-race group after multivariable adjustment

    Collaborative Quality Improvement Strategy in Secondary Prevention of Cardiovascular Disease in India: Findings from a Multi-Stakeholder, Qualitative Study using Consolidated Framework for Implementation Research (CFIR).

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    BACKGROUND: Cardiovascular disease (CVD) is highly prevalent in India, and little is known about the perception of patients and providers about a package of collaborative quality improvement (C-QIP) strategies consisting of provider-focused electronic health records-decision support system (EHR-DSS), non-physician health workers (NPHW), and patient-facing text messages to enhance the CVD care. OBJECTIVE: To explore the barriers and enablers of the C-QIP strategy from the perspective of providers, health administrators, patients, and care givers in India. METHODS: We conducted a qualitative study using the consolidated framework for implementation research (CFIR) to understand the challenges and facilitators of implementing C-QIP strategy to enhance CVD care in the Indian context. A diverse sample of 38 physicians, 14 non-physician health workers (nurses, pharmacists), 4 health administrators, and 16 patients and their caregivers participated in semi-structured interviews. All interviews were audio-recorded, transcribed, translated, anonymised, and coded using MAXQDA software. We used the framework method and CFIR domains to analyze the qualitative data. RESULTS: Barriers perceived from providers' and health administrators' perspectives in providing quality CVD care were high patient volume, physician burnout, lack of robust communication or referral system, paucity of electronic health records, lack of patient counsellors, polypharmacy, poor patient adherence to medications, and lack of financial incentives. Low health literacy, high cost of treatment, misinformation bias, and difficulty in maintaining lifestyle changes were barriers from patients' perspectives. The CFIR identified key enablers for the implementation of C-QIP such as standardized treatment protocol, reduced medication errors, improved physician-patient relationships, and enhanced patient self-care through trained and supported NPHW. Barriers included: heterogenous healthcare settings, diverse patient groups and comorbidities, associated costs of care and interoperability, confidentiality, and data privacy issues around the use of EHR-DSS. CONCLUSION: Strategies to enhance CVD care must be low-cost, culturally acceptable, and integrated into existing care pathways
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