1,092 research outputs found

    Spitzer Phase Curves of KELT-1b and the Signatures of Nightside Clouds in Thermal Phase Observations

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    We observed two full orbital phase curves of the transiting brown dwarf KELT-1b, at 3.6um and 4.5um, using the Spitzer Space Telescope. Combined with previous eclipse data from Beatty et al. (2014), we strongly detect KELT-1b's phase variation as a single sinusoid in both bands, with amplitudes of 964±36964\pm36 ppm at 3.6um and 979±54979\pm54 ppm at 4.5um, and confirm the secondary eclipse depths measured by Beatty et al. (2014). We also measure noticeable Eastward hotspot offsets of 28.4±3.528.4\pm3.5 degrees at 3.6um and 18.6±5.218.6\pm5.2 degrees at 4.5um. Both the day-night temperature contrasts and the hotspot offsets we measure are in line with the trends seen in hot Jupiters (e.g., Crossfield 2015), though we disagree with the recent suggestion of an offset trend by Zhang et al. (2018). Using an ensemble analysis of Spitzer phase curves, we argue that nightside clouds are playing a noticeable role in modulating the thermal emission from these objects, based on: 1) the lack of a clear trend in phase offsets with equilibrium temperature, 2) the sharp day-night transitions required to have non-negative intensity maps, which also resolves the inversion issues raised by Keating & Cowan (2017), 3) the fact that all the nightsides of these objects appear to be at roughly the same temperature of 1000K, while the dayside temperatures increase linearly with equilibrium temperature, and 4) the trajectories of these objects on a Spitzer color-magnitude diagram, which suggest colors only explainable via nightside clouds.Comment: AJ in press. Updated to reflect the accepted versio

    Selective Serotonin Reuptake Inhibitors and Associated Bleeding Risks: A Narrative and Clinical Review.

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    Major Depressive Disorder (MDD) is a major cause of disability worldwide and is associated with serious lasting impairment. A leading hypothesis of the pathophysiology of MDD is the monoamine deficiency hypothesis which suggests that depression is caused by depletion of serotonin, norepinephrine, or dopamine in the central nervous system. Serotonin is the most widely studied neurotransmitter in the pathophysiology of depression, with studies showing that reduced central serotonin synthesis leads to depressive symptoms in individuals at risk for depression. Selective Serotonin Reuptake Inhibitors (SSRI) inhibit serotonin reuptake and subsequently increase the amount of serotonin available in synapses. Common side effects of SSRIs include increased suicidality of patients under the age of 25, sexual dysfunction, anxiety, dizziness, weight gain, gastrointestinal distress, and headache. Other side effects include prolonging the QT interval, coagulopathy, and the risk of serotonin syndrome, as well as SSRI discontinuation syndrome. Sites of increased bleeding related to SSRI use have been reported to occur in the upper gastrointestinal tract, as well as intracranially. Based on the current literature, three studies have found that SSRIs are not associated with increased bleeding and/or increased perioperative risk, while others have demonstrated that SSRIs are associated with an increased risk in perioperative use. The inhibition of serotonin reuptake can affect platelet aggregation since platelets also express the serotonin transporter. SSRIs can result in decreased storage of serotonin in platelet dense granules. Increased serotonin can also increase gastric acid secretion, which increases the risk for ulceration. SSRIs in combination with NSAIDs also show a significantly increased risk of upper GI bleeding. Some studies show an increased bleeding risk from 30% to 70% when taking a combination of vitamin K antagonists and SSRIs in hospitalized patients. Related to the high prevalence of conditions that are treated with SSRIs, the bleeding risk associated with this class of medication merits further study

    KELT-7b: A hot Jupiter transiting a bright V=8.54 rapidly rotating F-star

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    We report the discovery of KELT-7b, a transiting hot Jupiter with a mass of 1.28±0.181.28 \pm 0.18 MJ, radius of 1.530.047+0.0461.53_{-0.047}^{+0.046} RJ, and an orbital period of 2.7347749±0.00000392.7347749 \pm 0.0000039 days. The bright host star (HD33643; KELT-7) is an F-star with V=8.54V=8.54, Teff =678949+50=6789_{-49}^{+50} K, [Fe/H] =0.1390.081+0.075=0.139_{-0.081}^{+0.075}, and logg=4.149±0.019\log{g}=4.149 \pm 0.019. It has a mass of 1.5350.054+0.0661.535_{-0.054}^{+0.066} Msun, a radius of 1.7320.045+0.0431.732_{-0.045}^{+0.043} Rsun, and is the fifth most massive, fifth hottest, and the ninth brightest star known to host a transiting planet. It is also the brightest star around which KELT has discovered a transiting planet. Thus, KELT-7b is an ideal target for detailed characterization given its relatively low surface gravity, high equilibrium temperature, and bright host star. The rapid rotation of the star (73±0.573 \pm 0.5 km/s) results in a Rossiter-McLaughlin effect with an unusually large amplitude of several hundred m/s. We find that the orbit normal of the planet is likely to be well-aligned with the stellar spin axis, with a projected spin-orbit alignment of λ=9.7±5.2\lambda=9.7 \pm 5.2 degrees. This is currently the second most rapidly rotating star to have a reflex signal (and thus mass determination) due to a planetary companion measured.Comment: Accepted to The Astronomical Journa

    KELT-11b: A Highly Inflated Sub-Saturn Exoplanet Transiting the V=8 Subgiant HD 93396

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    We report the discovery of a transiting exoplanet, KELT-11b, orbiting the bright (V=8.0V=8.0) subgiant HD 93396. A global analysis of the system shows that the host star is an evolved subgiant star with Teff=5370±51T_{\rm eff} = 5370\pm51 K, M=1.4380.052+0.061MM_{*} = 1.438_{-0.052}^{+0.061} M_{\odot}, R=2.720.17+0.21RR_{*} = 2.72_{-0.17}^{+0.21} R_{\odot}, log g=3.7270.046+0.040g_*= 3.727_{-0.046}^{+0.040}, and [Fe/H]=0.180±0.075 = 0.180\pm0.075. The planet is a low-mass gas giant in a P=4.736529±0.00006P = 4.736529\pm0.00006 day orbit, with MP=0.195±0.018MJM_{P} = 0.195\pm0.018 M_J, RP=1.370.12+0.15RJR_{P}= 1.37_{-0.12}^{+0.15} R_J, ρP=0.0930.024+0.028\rho_{P} = 0.093_{-0.024}^{+0.028} g cm3^{-3}, surface gravity log gP=2.4070.086+0.080{g_{P}} = 2.407_{-0.086}^{+0.080}, and equilibrium temperature Teq=171246+51T_{eq} = 1712_{-46}^{+51} K. KELT-11 is the brightest known transiting exoplanet host in the southern hemisphere by more than a magnitude, and is the 6th brightest transit host to date. The planet is one of the most inflated planets known, with an exceptionally large atmospheric scale height (2763 km), and an associated size of the expected atmospheric transmission signal of 5.6%. These attributes make the KELT-11 system a valuable target for follow-up and atmospheric characterization, and it promises to become one of the benchmark systems for the study of inflated exoplanets.Comment: 15 pages, Submitted to AAS Journal

    The effectiveness evaluation of a multimedia hepatitis C prevention program for Hispanic HIV-infected individuals

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    Introduction—With the introduction of highly active antiretroviral therapy the Hepatitis C virus (HCV) infection has became a primary health problem among individuals suffering from HIV/ AIDS in Puerto Rico, principally those who are injecting drug users (IDUs). A multimedia educational intervention, based on the Health Beliefs Model and Social Cognitive Theory was developed and implemented to reduce HCV associated risk behaviors among IDUs. Methods—A pre- and post- intervention study evaluated the knowledge and behavioral changes in a group of HIV-infected persons recruited from February 2006 through December 2008. Results—A total of 110 participants were recruited; all were IDUs; 82% were men; 86.3% were HIV/HCV co-infected and 24.5% had active injected drugs in the last month (prior to recruitment). The group mean age was 42.2 ± 9.2 years and mean educational level was 10th grade. Knowledge of HCV risk behaviors, perception of HCV susceptibility, and perception of disease severity increased after the intervention. Knowledge of HCV clinical manifestations and HIV co-infection complications and treatment also improved. In addition, HCV risk behaviors and injecting drug practice decrease significantly among IDUs. Conclusions—This new multimedia intervention captured and maintained the participants' attention and interest, in that way facilitating their educational process. Thus, a greater of attention and interest leads to greater knowledge and prevention improvement

    Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22

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    A substantial proportion of familial colorectal cancer (CRC) is not a consequence of known susceptibility loci, such as mismatch repair (MMR) genes, supporting the existence of additional loci. To identify novel CRC loci, we conducted a genome-wide linkage scan in 356 white families with no evidence of defective MMR (i.e., no loss of tumor expression of MMR proteins, no microsatellite instability (MSI)-high tumors, or no evidence of linkage to MMR genes). Families were ascertained via the Colon Cancer Family Registry multi-site NCI-supported consortium (Colon CFR), the City of Hope Comprehensive Cancer Center, and Memorial University of Newfoundland. A total of 1,612 individuals (average 5.0 per family including 2.2 affected) were genotyped using genome-wide single nucleotide polymorphism linkage arrays; parametric and non-parametric linkage analysis used MERLIN in a priori-defined family groups. Five lod scores greater than 3.0 were observed assuming heterogeneity. The greatest were among families with mean age of diagnosis less than 50 years at 4q21.1 (dominant HLOD = 4.51, α = 0.84, 145.40 cM, rs10518142) and among all families at 12q24.32 (dominant HLOD = 3.60, α = 0.48, 285.15 cM, rs952093). Among families with four or more affected individuals and among clinic-based families, a common peak was observed at 15q22.31 (101.40 cM, rs1477798; dominant HLOD = 3.07, α = 0.29; dominant HLOD = 3.03, α = 0.32, respectively). Analysis of families with only two affected individuals yielded a peak at 8q13.2 (recessive HLOD = 3.02, α = 0.51, 132.52 cM, rs1319036). These previously unreported linkage peaks demonstrate the continued utility of family-based data in complex traits and suggest that new CRC risk alleles remain to be elucidated. © 2012 Cicek et al
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