220 research outputs found
Racial/Ethnic Disparities in Access to Care among Children: How Does Medicaid Do in Closing the Gaps?
While Medicaid and the Children\u27s Health Insurance Program (CHIP) have become increasingly important sources of health coverage for low-income children in all racial and ethnic groups, the program plays an especially large role for children of color, who are more likely than white children to be low-income. In 2007, Medicaid and CHIP covered nearly one in five white children, but roughly two in five African American and Hispanic children.
As policymakers engaged in health reform consider the merits of public and private approaches to expanding coverage, this report provides an assessment of Medicaid\u27s relative impact on racial and ethnic disparities in access. The analysis compared health care access for white, African American and Hispanic children who were privately insured, uninsured, or enrolled in Medicaid or CHIP.
Key findings include: Racial and ethnic disparities in access to care were no more likely among children enrolled in Medicaid than among privately insured children. Insurance coverage – both private and Medicaid – often improved access for children in each racial and ethnic group, but generally did not significantly narrow racial and ethnic disparities in their access to health care.
This report analyzes data for more than 15,000 children from the 2003 and 2004 Medical Expenditure Panel Survey, a nationally representative household survey conducted by the Agency for Healthcare Research and Quality
Optimising text messaging to improve adherence to web-based smoking cessation treatment: a randomised control trial protocol
Introduction Millions of smokers use the Internet for smoking cessation assistance each year; however, most smokers engage minimally with even the best designed websites. The ubiquity of mobile devices and their effectiveness in promoting adherence in other areas of health behaviour change make them a promising tool to address adherence in Internet smoking cessation interventions. Text messaging is used by most adults, and messages can proactively encourage use of a web-based intervention. Text messaging can also be integrated with an Internet intervention to facilitate the use of core Internet intervention components. Methods and analysis We identified four aspects of a text message intervention that may enhance its effectiveness in promoting adherence to a web-based smoking cessation programme: personalisation, integration, dynamic tailoring and message intensity. Phase I will use a two-level full factorial design to test the impact of these four experimental features on adherence to a web-based intervention. The primary outcome is a composite metric of adherence that incorporates general utilisation metrics (eg, logins, page views) and specific feature utilisation shown to predict abstinence. Participants will be N=860 adult smokers who register on an established Internet cessation programme and enrol in its text message programme. Phase II will be a two-arm randomised trial to compare the efficacy of the web-based cessation programme alone and in conjunction with the optimised text messaging intervention on 30-day point prevalence abstinence at 9 months. Phase II participants will be N=600 adult smokers who register to use an established Internet cessation programme and enrol in text messaging. Secondary analyses will explore whether adherence mediates the effect of treatment condition on outcome. Ethics and dissemination This protocol was approved by Chesapeake IRB. We will disseminate study results through peer-reviewed manuscripts and conference presentations related to the methods and design, outcomes and exploratory analyses. Trial registration number NCT02585206
Avalanches on a conical bead pile: scaling with tuning parameters
Uniform spherical beads were used to explore the behavior of a granular
system near its critical angle of repose on a conical bead pile. We found two
tuning parameters that could take the system to a critical point where a simple
power-law described the avalanche size distribution as predicted by
self-organized criticality, which proposed that complex dynamical systems
self-organize to a critical point without need for tuning. Our distributions
were well described by a simple power-law with the power {\tau} = 1.5 when
dropping beads slowly onto the apex of a bead pile from a small height.
However, we could also move the system from the critical point using either of
two tuning parameters: the height from which the beads fell onto the top of the
pile or the region over which the beads struck the pile. As the drop height
increased, the system did not reach the critical point yet the resulting
distributions were independent of the bead mass, coefficient of friction, or
coefficient of restitution. All our apex-dropping distributions for any type of
bead (glass, stainless steel, zirconium) showed universality by scaling onto a
common curve with {\tau} = 1.5 and {\sigma} = 1.0, where 1/{\sigma} is the
power of the tuning parameter. From independent calculations using the moments
of the distribution, we find values for {\tau} = 1.6 \pm 0.1 and {\sigma} =
0.91 \pm 0.15. When beads were dropped across the surface of the pile instead
of solely on the apex, then the system also moved from the critical point and
again the avalanche size distributions fell on a common curve when scaled
similarly using the same values of {\tau} and {\sigma}. We also observed that
an hcp structure on the base of the pile caused an emergent structure in the
pile that had six faces with some fcc or hcp structure.Comment: 8 pages, 6 figures; submitted to Granular Matter; Reformatted into
LaTeX from Word; Fixed typo in uncertainty of tau; Rearranged two paragraphs
to improve flo
A strong H- opacity signal in the near-infrared emission spectrum of the ultra-hot Jupiter KELT-9b
We present the analysis of a spectroscopic secondary eclipse of the hottest
transiting exoplanet detected to date, KELT-9b, obtained with the Wide Field
Camera 3 aboard the Hubble Space Telescope.
We complement these data with literature information on stellar pulsations
and Spitzer/Infrared Array Camera and Transiting Exoplanet Survey Satellite
eclipse depths of this target to obtain a broadband thermal emission spectrum.
Our extracted spectrum exhibits a clear turnoff at 1.4m. This points to
H bound-free opacities shaping the spectrum.
To interpret the spectrum, we perform grid retrievals of self-consistent 1D
equilibrium chemistry forward models, varying the composition and energy
budget.
The model with solar metallicity and C/O ratio provides a poor fit because
the H signal is stronger than expected, requiring an excess of electrons.
This pushes our retrievals toward high atmospheric metallicities
() and a C/O ratio that is subsolar by 2.4.
We question the viability of forming such a high-metallicity planet, and
therefore provide other scenarios to increase the electron density in this
atmosphere.
We also look at an alternative model in which we quench TiO and VO. This fit
results in an atmosphere with a slightly subsolar metallicity and subsolar C/O
ratio (, log(C/O)).
However, the required TiO abundances are disputed by recent high-resolution
measurements of the same planet.Comment: 8 pages, 4 figures, Accepted for publication in A&A letter
Escalating morphine dosing in HIV-1 Tat transgenic mice with sustained Tat exposure reveals an allostatic shift in neuroinflammatory regulation accompanied by increased neuroprotective non-endocannabinoid lipid signaling molecules and amino acids
BACKGROUND: Human immunodeficiency virus type-1 (HIV-1) and opiates cause long-term inflammatory insult to the central nervous system (CNS) and worsen disease progression and HIV-1-related neuropathology. The combination of these proinflammatory factors reflects a devastating problem as opioids have high abuse liability and continue to be prescribed for certain patients experiencing HIV-1-related pain. METHODS: Here, we examined the impact of chronic (3-month) HIV-1 transactivator of transcription (Tat) exposure to short-term (8-day), escalating morphine in HIV-1 Tat transgenic mice that express the HIV-1 Tat protein in a GFAP promoter-regulated, doxycycline (DOX)-inducible manner. In addition to assessing morphine-induced tolerance in nociceptive responses organized at spinal (i.e., tail-flick) and supraspinal (i.e., hot-plate) levels, we evaluated neuroinflammation via positron emission tomography (PET) imaging using the [¹⁸F]-PBR111 ligand, immunohistochemistry, and cytokine analyses. Further, we examined endocannabinoid (eCB) levels, related non-eCB lipids, and amino acids via mass spectrometry. RESULTS: Tat-expressing [Tat(+)] transgenic mice displayed antinociceptive tolerance in the tail withdrawal and hot-plate assays compared to control mice lacking Tat [Tat(-)]. This tolerance was accompanied by morphine-dependent increases in Iba-1 +/- 3-nitrotryosine immunoreactive microglia, and alterations in pro- and anti-inflammatory cytokines, and chemokines in the spinal cord and striatum, while increases in neuroinflammation were absent by PET imaging of [¹⁸F]-PBR111 uptake. Tat and morphine exposure differentially affected eCB levels, non-eCB lipids, and specific amino acids in a region-dependent manner. In the striatum, non-eCB lipids were significantly increased by short-term, escalating morphine exposure, including peroxisome proliferator activator receptor alpha (PPAR-alpha) ligands N-oleoyl ethanolamide (OEA) and N-palmitoyl ethanolamide (PEA), as well as the amino acids phenylalanine and proline. In the spinal cord, Tat exposure increased amino acids leucine and valine, while morphine decreased levels of tyrosine and valine but did not affect eCBs or non-eCB lipids. CONCLUSION: Overall results demonstrate that 3 months of Tat exposure increased morphine tolerance and potentially innate immune tolerance evidenced by reductions in specific cytokines (e.g., IL-1alpha, IL-12p40) and microglial reactivity. In contrast, short-term, escalating morphine exposure acted as a secondary stressor revealing an allostatic shift in CNS baseline inflammatory responsiveness from sustained Tat exposure
The Digital MIQE Guidelines Update: Minimum Information for Publication of Quantitative Digital PCR Experiments for 2020
Digital PCR (dPCR) has developed considerably since the publication of the Minimum Information for Publication of Digital PCR Experiments (dMIQE) guidelines in 2013, with advances in instrumentation, software, applications, and our understanding of its technological potential. Yet these developments also have associated challenges; data analysis steps, including threshold setting, can be difficult and preanalytical steps required to purify, concentrate, and modify nucleic acids can lead to measurement error. To assist independent corroboration of conclusions, comprehensive disclosure of all relevant experimental details is required. To support the community and reflect the growing use of dPCR, we present an update to dMIQE, dMIQE2020, including a simplified dMIQE table format to assist researchers in providing key experimental information and understanding of the associated experimental process. Adoption of dMIQE2020 by the scientific community will assist in standardizing experimental protocols, maximize efficient utilization of resources, and further enhance the impact of this powerful technology
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer
We performed a multistage genome-wide association study including 7,683 individuals with pancreatic cancer and 14,397 controls of European descent. Four new loci reached genome-wide significance: rs6971499 at 7q32.3 (LINC-PINT, per-allele odds ratio (OR) = 0.79, 95% confidence interval (CI) 0.74-0.84, P = 3.0 x 10(-12)), rs7190458 at 16q23.1 (BCAR1/CTRB1/CTRB2, OR = 1.46, 95% CI 1.30-1.65, P = 1.1 x 10(-10)), rs9581943 at 13q12.2 (PDX1, OR = 1.15, 95% CI 1.10-1.20, P = 2.4 x 10(-9)) and rs16986825 at 22q12.1 (ZNRF3, OR = 1.18, 95% CI 1.12-1.25, P = 1.2 x 10(-8)). We identified an independent signal in exon 2 of TERT at the established region 5p15.33 (rs2736098, OR = 0.80, 95% CI 0.76-0.85, P = 9.8 x 10(-14)). We also identified a locus at 8q24.21 (rs1561927, P = 1.3 x 10(-7)) that approached genome-wide significance located 455 kb telomeric of PVT1. Our study identified multiple new susceptibility alleles for pancreatic cancer that are worthy of follow-up studies
Visual engagement with urban street edges: insights using mobile eye-tracking
This study provides empirical insight into the extent to which pedestrians visually engage with urban street edges and how social and spatial factors impact such engagement. This was achieved using mobile eye-tracking. The gaze distribution of 24 study participants was systematically recorded as they carried out everyday tasks on differing streets. The findings demonstrated that street edges are the most visually engaged component of streets; that street edge visual engagement is impacted by everyday social tasks as well as the spatial and physical materiality of edges on differing streets; and that street edges, which attract a lot of visual engagement while undertaking optional tasks, also attract greater amounts of visual engagement while undertaking necessary tasks. These findings offer new insight into urban street edge engagement from the direct perspective of street inhabitants and in doing so provide greater understanding of how street edges are experienced
Association of Sickle Cell Trait With Chronic Kidney Disease and Albuminuria in African Americans
The association between sickle cell trait (SCT) and chronic kidney disease (CKD) is uncertain
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
Despite the clinical significance of balanced chromosomal abnormalities (BCAs), their characterization has largely been restricted to cytogenetic resolution. We explored the landscape of BCAs at nucleotide resolution in 273 subjects with a spectrum of congenital anomalies. Whole-genome sequencing revised 93% of karyotypes and demonstrated complexity that was cryptic to karyotyping in 21% of BCAs, highlighting the limitations of conventional cytogenetic approaches. At least 33.9% of BCAs resulted in gene disruption that likely contributed to the developmental phenotype, 5.2% were associated with pathogenic genomic imbalances, and 7.3% disrupted topologically associated domains (TADs) encompassing known syndromic loci. Remarkably, BCA breakpoints in eight subjects altered a single TAD encompassing MEF2C, a known driver of 5q14.3 microdeletion syndrome, resulting in decreased MEF2C expression. We propose that sequence-level resolution dramatically improves prediction of clinical outcomes for balanced rearrangements and provides insight into new pathogenic mechanisms, such as altered regulation due to changes in chromosome topology
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