3,167 research outputs found
The Psychology and Communication of Climate Change Ignorance
Review of:
George Marshall, Don\u27t Even Think About It: Why Our Brains Are Wired to Ignore Climate Change. Bloomsbury USA, 2014, 272 pages. ISBN: 978163286102
Alcohol-related expectancies are associated with the D2 dopamine receptor and GABAa receptor B3 subunit genes
Molecular genetic research has identified promising markers of alcohol dependence, including alleles of the D2 dopamine receptor (DRD2) and the GABAA receptor ¬3 subunit (GABRB3) genes. Whether such genetic risk manifests itself in stronger alcohol-related outcome expectancies, or in difficulty resisting alcohol, is unknown. In the present study, A1+ (A1A1 and A1A2 genotypes) and A1- (A2A2 genotype) alleles of the DRD2 and G1+ (G1G1 and G1 non-G1 genotypes) and G1- (non-G1 non-G1 genotype) alleles of the GABRB3 were determined in a group of 56 medically-ill patients diagnosed with alcohol dependence. Mood-related Alcohol Expectancy (AE) and Drinking Refusal Self-Efficacy (DRSE) were assessed using the Drinking Expectancy Profile (Young and Oei, 1996). Patients with the DRD2 A1+ allele, compared to those with the DRD2 A1- allele, reported lower DRSE in situations of social pressure (p=. 009). Similarly, lower DRSE was reported under social pressure by patients with the GABRB3 G1+ allele when compared to those with the GABRB3 G1- allele (p=.027). Patients with the GABRB3 G1+ allele also revealed reduced DRSE in situations characterized by negative affect than patients with the GABRB3 G1- alleles (p=. 037). Patients carrying the GABRB3 G1+ allele showed stronger AE relating to negative affective change (for example, increased depression) than their GABRB3 G1- counterparts (p=. 006). Biological influence in the development of some classes of cognitions is hypothesized. The clinical implications, particularly with regard to patient-treatment matching and the development of an integrated psychological and pharmacogenetic approach are discussed
Discovery and Early Evolution of ASASSN-19bt, the First TDE Detected by TESS
We present the discovery and early evolution of ASASSN-19bt, a tidal
disruption event (TDE) discovered by the All-Sky Automated Survey for
Supernovae (ASAS-SN) at a distance of Mpc and the first TDE to be
detected by TESS. As the TDE is located in the TESS Continuous Viewing Zone,
our dataset includes 30-minute cadence observations starting on 2018 July 25,
and we precisely measure that the TDE begins to brighten days before
its discovery. Our dataset also includes 18 epochs of Swift UVOT and XRT
observations, 2 epochs of XMM-Newton observations, 13 spectroscopic
observations, and ground data from the Las Cumbres Observatory telescope
network, spanning from 32 days before peak through 37 days after peak.
ASASSN-19bt thus has the most detailed pre-peak dataset for any TDE. The TESS
light curve indicates that the transient began to brighten on 2019 January 21.6
and that for the first 15 days its rise was consistent with a flux power-law model. The optical/UV emission is well-fit by a blackbody SED,
and ASASSN-19bt exhibits an early spike in its luminosity and temperature
roughly 32 rest-frame days before peak and spanning up to 14 days that has not
been seen in other TDEs, possibly because UV observations were not triggered
early enough to detect it. It peaked on 2019 March 04.9 at a luminosity of
ergs s and radiated
ergs during the 41-day rise to peak. X-ray observations after peak indicate a
softening of the hard X-ray emission prior to peak, reminiscent of the
hard/soft states in X-ray binaries.Comment: 23 pages, 14 figures, 5 tables. A machine-readable table containing
the host-subtracted photometry presented in this manuscript is included as an
ancillary fil
A mixed methods survey of social anxiety, anxiety, depression and wig use in alopecia
Objectives This study aimed to examine levels of social anxiety, anxiety and depression reported by people with alopecia as a result of a dermatological condition and associations with wig use. The study also sought to report on experiences of wearing wigs in social situations and the relationship with social confidence.
Design A cross-sectional survey was sent by email to the Alopecia UK charity mailing list and advertised on social media.
Participants Inclusion criteria were a diagnosis of alopecia, aged 13 or above and sufficient English to complete the survey. Exclusion criteria included experiencing hair loss as a result of chemotherapy treatment or psychological disorder. Participants (n=338) were predominantly female (97.3%), Caucasian (93.5%) and aged between 35 and 54 years (49.4%) with a diagnosis of alopecia areata (82.6%).
Main outcome measures The Social Phobia Inventory measured symptoms of social anxiety, and the Hospital Anxiety and Depression Scale was used to measure symptoms of anxiety and depression. Survey questions were designed to measure the use of wigs. Open-ended questions enabled participants to comment on their experiences of wearing wigs.
Results Clinically significant levels of social anxiety (47.5%), anxiety (35.5%) and depression (29%) were reported. Participants who reported worries about not wearing a wig reported significantly higher levels of depression: t(103)=3.40, p≤0.001; anxiety: t(109)=4.80, p≤0.001; and social anxiety: t(294)=3.89, p≤0.001. Wearing wigs was reported as increasing social confidence; however, the concealment it afforded was also reported as both reducing fear of negative evaluation and maintaining anxiety.
Discussion Overall, 46% of participants reported that wearing a wig had a positive impact on their everyday life with negative experiences related to fears of the wig being noticed. Psychological interventions alongside wig provision would be beneficial for people living with alopecia
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A Prospective Evaluation of Point of Care Ultrasound Teaching in Switzerland.
ContextAs the utility of point-of-care ultrasound (POCUS) continues to expand in the medical field, there is a need for effective educational methods. In Switzerland, medical education follows the European model and lasts 6 years, focusing on preclinical training during the first 2 years. No previous studies have evaluated the optimal time for teaching ultrasound in European medical education.AimsThe aim of this study is to provide ultrasound training to medical students in Switzerland at varying times during their clinical training to determine if the level of training plays a role in their ability to comprehend and to apply basic POCUS skills.MethodsWe performed an observational study utilizing a convenience sample of Swiss medical students between July 11, 2016 and August 6, 2016. They were taught a 2-day POCUS course by five American-trained 1st-year medical students. Following this course, students were evaluated with written and clinical examination.Results100 Swiss medical students were enrolled in the study. A total of 59 of these students were early clinical students, and 41 students were late clinical students. A two-tailed t-test was performed and demonstrated that the late clinical students performed better than the early clinical students on the written assessment; however, no difference was found in clinical skill.ConclusionOur data suggest that Swiss medical students can learn and perform POCUS after a 2-day instructional taught by trained 1st-year American medical students. No difference was found between students in early clinical training and late clinical training for the ability to perform POCUS
Role of cyclooxygenase in the vascular responses to extremity cooling in Caucasian and African males
This is an accepted manuscript of an article published by Wiley in Experimental Physiology on 01/06/2017, available online: https://doi.org/10.1113/EP086186
The accepted version of the publication may differ from the final published version.© 2017 The Authors. Experimental Physiology © 2017 The Physiological Society New Findings: What is the central question of this study? Compared with Caucasians, African individuals are more susceptible to non-freezing cold injury and experience greater cutaneous vasoconstriction and cooler finger skin temperatures upon hand cooling. We investigated whether the enzyme cyclooxygenase is, in part, responsible for the exaggerated response to local cooling. What is the main finding and its importance? During local hand cooling, individuals of African descent experienced significantly lower finger skin blood flow and skin temperature compared with Caucasians irrespective of cyclooxygenase inhibition. These data suggest that in young African males the cyclooxygenase pathway appears not to be the primary reason for the increased susceptibility to non-freezing cold injury. Individuals of African descent (AFD) are more susceptible to non-freezing cold injury (NFCI) and experience an exaggerated cutaneous vasoconstrictor response to hand cooling compared with Caucasians (CAU). Using a placebo-controlled, cross-over design, this study tested the hypothesis that cyclooxygenase (COX) may, in part, be responsible for the exaggerated vasoconstrictor response to local cooling in AFD. Twelve AFD and 12 CAU young healthy men completed foot cooling and hand cooling (separately, in 8°C water for 30 min) with spontaneous rewarming in 30°C air after placebo or aspirin (COX inhibition) treatment. Skin blood flow, expressed as cutaneous vascular conductance (as flux per millimetre of mercury), and skin temperature were measured throughout. Irrespective of COX inhibition, the responses to foot cooling, but not hand cooling, were similar between ethnicities. Specifically, during hand cooling after placebo, AFD experienced a lower minimal skin blood flow [mean (SD): 0.5 (0.1) versus 0.8 (0.2) flux mmHg−1, P < 0.001] and a lower minimal finger skin temperature [9.5 (1.4) versus 10.7 (1.3)°C, P = 0.039] compared with CAU. During spontaneous rewarming, average skin blood flow was also lower in AFD than in CAU [2.8 (1.6) versus 4.3 (1.0) flux mmHg−1, P < 0.001]. These data provide further support that AFD experience an exaggerated response to hand cooling on reflection this appears to overstate findings; however, the results demonstrate that the COX pathway is not the primary reason for the exaggerated responses in AFD and increased susceptibility to NFCI.This research was funded by the University of Portsmouth.Published versio
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Membrane Protein Interactions and Transport in Confined Microenvironments
Membrane proteins make up a large fraction of the human proteome and are implicated in numerous biological processes. Due to their vast importance in human biology, they are frequently the target of drug therapies and are commonly utilized in biotechnology applications. However, studying membrane protein interactions and transport in their native environment has historically been challenging. Here, we use reconstituted lipid bilayer model systems to investigate individual membrane protein interactions and transport, where the proteins are confined to a two-dimensional (2D) surface either transiently or permanently. For all of this work, we use epithelial-cadherin (E-cad) adhesion proteins either to gain direct insight into the mechanisms underlying cell-cell cohesion, or to study a model membrane-associating protein. First, we used single-molecule Total Internal Reflection Fluorescence (TIRF) microscopy to test for lateral protein clustering between E-cad, when the proteins were confined to a 2D lipid bilayer surface. After showing that E-cad formed clusters on a 2D surface, we then developed a framework combining single-molecule Förster Resonance Energy Transfer (FRET) with kinetic Monte Carlo (kMC) simulations to quantify the lateral interaction kinetics mediating these clusters. Within this framework, single-molecule FRET allowed us to directly visualize binding events between E-cad molecules, while simultaneously tracking individual E-cad dynamics on the surface. Next, we developed a biomimetic cell junction model to characterize molecular binding of E-cad within cell junctions using single-molecule FRET. Within this junction model, we tested for cooperativity between E-cad lateral (cis) and adhesive (trans) interactions using multiple E-cad mutant proteins. E-cad lateral and adhesive interactions were found to be mutually cooperative, meaning one stabilizes the other, and vice-versa. Lastly, we used Convex Lens-Induced Confinement (CLiC) to measure the facilitated diffusion of individual E-cad molecules across a wide range of confinement length-scales, where E-cad was capable of transiently adsorbing to lipid bilayers on the top and bottom surfaces. Consistent with previous theoretical predictions, the effective surface diffusion was maximized at intermediate heights. A hybrid, kinetic Monte Carlo simulation approach was used to study this process in detail, and showed that facilitated diffusion can indeed result in elevated diffusion under confinement, but only under conditions where the molecule has a low affinity for the surface. These findings provided new insights into the physics underlying the search process of peripheral membrane proteins and information useful for the design of biotechnology systems.</p
Parental Substance Abuse As an Early Traumatic Event. Preliminary Findings on Neuropsychological and Personality Functioning in Young Drug Addicts Exposed to Drugs Early.
open5noParental substance use is a major risk factor for child development, heightening the risk of drug problems in adolescence and young adulthood, and exposing offspring to several types of traumatic events. First, prenatal drug exposure can be considered a form of trauma itself, with subtle but long-lasting sequelae at the neuro-behavioral level. Second, parents’ addiction often entails a childrearing environment characterized by poor parenting skills, disadvantaged contexts and adverse childhood experiences (ACEs), leading to dysfunctional outcomes. Young adults born from/raised by parents with drug problems and diagnosed with a Substance Used Disorder (SUD) themselves might display a particularly severe condition in terms of cognitive deficits and impaired personality function. This preliminary study aims to investigate the role of early exposure to drugs as a traumatic event, capable of affecting the psychological status of young drug addicts. In particular, it intends to examine the neuropsychological functioning and personality profile of young adults with severe SUDs who were exposed to drugs early in their family context. The research involved three groups, each consisting of 15 young adults (aged 18–24): a group of inpatients diagnosed with SUDs and exposed to drugs early, a comparison group of non-exposed inpatients and a group of non-exposed youth without SUDs. A neuropsychological battery (Esame Neuropsicologico Breve-2), an assessment procedure for personality disorders (Shedler-Westen Assessment Procedure-200) and the Symptom CheckList-90-Revised were administered. According to present preliminary results, young drug addicts exposed to drugs during their developmental age were characterized by elevated rates of neuropsychological impairments, especially at the expense of attentive and executive functions (EF); personality disorders were also common but did not differentiate them from non-exposed youth with SUDs. Alternative multi-focused prevention and intervention programs are needed for children of drug-misusing parents, addressing EF and adopting a trauma-focused approach.openParolin, Micol; Simonelli, Alessandra; Mapelli, Daniela; Sacco, M.; Cristofalo, P.Parolin, Micol; Simonelli, Alessandra; Mapelli, Daniela; Sacco, M.; Cristofalo, P
Effects of antiplatelet therapy on stroke risk by brain imaging features of intracerebral haemorrhage and cerebral small vessel diseases: subgroup analyses of the RESTART randomised, open-label trial
Background
Findings from the RESTART trial suggest that starting antiplatelet therapy might reduce the risk of recurrent symptomatic intracerebral haemorrhage compared with avoiding antiplatelet therapy. Brain imaging features of intracerebral haemorrhage and cerebral small vessel diseases (such as cerebral microbleeds) are associated with greater risks of recurrent intracerebral haemorrhage. We did subgroup analyses of the RESTART trial to explore whether these brain imaging features modify the effects of antiplatelet therapy
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