757 research outputs found
Investigating the source of Planck-detected AME: high resolution observations at 15 GHz
The Planck 28.5 GHz maps were searched for potential Anomalous Microwave
Emission (AME) regions on the scale of or smaller, and several
new regions of interest were selected. Ancillary data at both lower and higher
frequencies were used to construct spectral energy distributions (SEDs), which
seem to confirm an excess consistent with spinning dust models. Here we present
higher resolution observations of two of these new regions with the Arcminute
Microkelvin Imager Small Array (AMI SA) between 14 and 18 GHz to test for the
presence of a compact (10 arcmin or smaller) component. For
AME-G107.1+5.2, dominated by the {\sc Hii} region S140, we find evidence for
the characteristic rising spectrum associated with the either the spinning dust
mechanism for AME or an ultra/hyper-compact \textsc{Hii} region across the AMI
frequency band, however for AME-G173.6+2.8 we find no evidence for AME on
scales of arcmin.Comment: 13 pages, 8 figures, 4 tables. Submitted to Advances in Astronomy AME
Special Issu
An occupational therapy intervention for residents with stroke related disabilities in UK care homes (OTCH): cluster randomised controlled trial
Objective To evaluate the clinical efficacy of an established programme of occupational therapy in maintaining functional activity and reducing further health risks from inactivity in care home residents living with stroke sequelae.
Design Pragmatic, parallel group, cluster randomised controlled trial.
Setting 228 care homes (>10 beds each), both with and without the provision of nursing care, local to 11 trial administrative centres across the United Kingdom.
Participants 1042 care home residents with a history of stroke or transient ischaemic attack, including those with language and cognitive impairments, not receiving end of life care. 114 homes (n=568 residents, 64% from homes providing nursing care) were allocated to the intervention arm and 114 homes (n=474 residents, 65% from homes providing nursing care) to standard care (control arm). Participating care homes were randomised between May 2010 and March 2012.
Intervention Targeted three month programme of occupational therapy, delivered by qualified occupational therapists and assistants, involving patient centred goal setting, education of care home staff, and adaptations to the environment.
Main outcome measures Primary outcome at the participant level: scores on the Barthel index of activities of daily living at three months post-randomisation. Secondary outcome measures at the participant level: Barthel index scores at six and 12 months post-randomisation, and scores on the Rivermead mobility index, geriatric depression scale-15, and EuroQol EQ-5D-3L questionnaire, at all time points.
Results 64% of the participants were women and 93% were white, with a mean age of 82.9 years. Baseline characteristics were similar between groups for all measures, personal characteristics, and diagnostic tests. Overall, 2538 occupational therapy visits were made to 498 participants in the intervention arm (mean 5.1 visits per participant). No adverse events attributable to the intervention were recorded. 162 (11%) died before the primary outcome time point, and 313 (30%) died over the 12 months of the trial. The primary outcome measure did not differ significantly between the treatment arms. The adjusted mean difference in Barthel index score at three months was 0.19 points higher in the intervention arm (95% confidence interval −0.33 to 0.70, P=0.48). Secondary outcome measures also showed no significant differences at all time points.
Conclusions This large phase III study provided no evidence of benefit for the provision of a routine occupational therapy service, including staff training, for care home residents living with stroke related disabilities. The established three month individualised course of occupational therapy targeting stroke related disabilities did not have an impact on measures of functional activity, mobility, mood, or health related quality of life, at all observational time points. Providing and targeting ameliorative care in this clinically complex population requires alternative strategies
Maintained physical activity and physiotherapy in the management of distal upper limb pain – a protocol for a randomised controlled trial (the arm pain trial)
<b>Background</b><p></p>
Distal upper limb pain (pain affecting the elbow, forearm, wrist, or hand) can be non-specific, or can arise from specific musculoskeletal disorders. It is clinically important and costly, the best approach to clinical management is unclear. Physiotherapy is the standard treatment and, while awaiting treatment, advice is often given to rest and avoid strenuous activities, but there is no evidence base to support these strategies. This paper describes the protocol of a randomised controlled trial to determine, among patients awaiting physiotherapy for distal arm pain, (a) whether advice to remain active and maintain usual activities results in a long-term reduction in arm pain and disability, compared with advice to rest; and (b) whether immediate physiotherapy results in a long-term reduction in arm pain and disability, compared with physiotherapy delivered after a seven week waiting list period.<p></p>
<b>Methods/Design</b><p></p>
Between January 2012 and January 2014, new referrals to 14 out-patient physiotherapy departments were screened for potential eligibility. Eligible and consenting patients were randomly allocated to one of the following three groups in equal numbers: 1) advice to remain active, 2) advice to rest, 3) immediate physiotherapy. Patients were and followed up at 6, 13, and 26 weeks post-randomisation by self-complete postal questionnaire and, at six weeks, patients who had not received physiotherapy were offered it at this time. The primary outcome is the proportion of patients free of disability at 26 weeks, as determined by the modified DASH (Disabilities of the Arm, Shoulder and Hand) questionnaire.<p></p>
We hypothesise (a) that advice to maintain usual activities while awaiting physiotherapy will be superior than advice to rest the arm; and (b) that fast-track physiotherapy will be superior to normal (waiting list) physiotherapy. These hypotheses will be examined using an intention-to-treat analysis.<p></p>
<b>Discussion</b><p></p>
Results from this trial will contribute to the evidence base underpinning the clinical management of patients with distal upper limb pain, and in particular, will provide guidance on whether they should be advised to rest the arm or remain active within the limits imposed by their symptoms
Testing Spallation Processes With Beryllium and Boron
The nucleosynthesis of Be and B by spallation processes provides unique
insight into the origin of cosmic rays. Namely, different spallation schemes
predict sharply different trends for the growth of LiBeB abundances with
respect to oxygen. ``Primary'' mechanisms predict BeB O, and are well
motivated by the data if O/Fe is constant at low metallicity. In contrast,
``secondary'' mechanisms predict BeB O and are consistent with
the data if O/Fe increases towards low metallicity as some recent data suggest.
Clearly, any primary mechanism, if operative, will dominate early in the
history of the Galaxy. In this paper, we fit the BeB data to a two-component
scheme which includes both primary and secondary trends. In this way, the data
can be used to probe the period in which primary mechanisms are effective. We
analyze the data using consistent stellar atmospheric parameters based on
Balmer line data and the continuum infrared flux. Results depend sensitively on
Pop II O abundances and, unfortunately, on the choice of stellar parameters.
When using recent results which show O/Fe increasing toward lower metallicity,
a two-component Be-O fits indicates that primary and secondary components
contribute equally at [O/H] = -1.8 for Balmer line data; and
[O/H] = -1.4 to -1.8 for IRFM. We apply these constraints to recent
models for LiBeB origin. The Balmer line data does not show any evidence for
primary production. On the other hand, the IRFM data does indicate a preference
for a two-component model, such as a combination of standard GCR and
metal-enriched particles accelerated in superbubbles. These conclusions rely on
a detailed understanding of the abundance data including systematic effects
which may alter the derived O-Fe and BeB-Fe relations.Comment: 40 pages including 11 ps figures. Written in AASTe
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CCR5AS lncRNA variation differentially regulates CCR5, influencing HIV disease outcome.
Multiple genome-wide studies have identified associations between outcome of human immunodeficiency virus (HIV) infection and polymorphisms in and around the gene encoding the HIV co-receptor CCR5, but the functional basis for the strongest of these associations, rs1015164A/G, is unknown. We found that rs1015164 marks variation in an activating transcription factor 1 binding site that controls expression of the antisense long noncoding RNA (lncRNA) CCR5AS. Knockdown or enhancement of CCR5AS expression resulted in a corresponding change in CCR5 expression on CD4+ T cells. CCR5AS interfered with interactions between the RNA-binding protein Raly and the CCR5 3' untranslated region, protecting CCR5 messenger RNA from Raly-mediated degradation. Reduction in CCR5 expression through inhibition of CCR5AS diminished infection of CD4+ T cells with CCR5-tropic HIV in vitro. These data represent a rare determination of the functional importance of a genome-wide disease association where expression of a lncRNA affects HIV infection and disease progression
Impact of PNKP mutations associated with microcephaly, seizures and developmental delay on enzyme activity and DNA strand break repair
Microcephaly with early-onset, intractable seizures and developmental delay (MCSZ) is a hereditary disease caused by mutations in polynucleotide kinase/phosphatase (PNKP), a DNA strand break repair protein with DNA 5'-kinase and DNA 3'-phosphatase activity. To investigate the molecular basis of this disease, we examined the impact of MCSZ mutations on PNKP activity in vitro and in cells. Three of the four mutations currently associated with MCSZ greatly reduce or ablate DNA kinase activity of recombinant PNKP at 30°C (L176F, T424Gfs48X and exon15Δfs4X), but only one of these mutations reduces DNA phosphatase activity under the same conditions (L176F). The fourth mutation (E326K) has little impact on either DNA kinase or DNA phosphatase activity at 30°C, but is less stable than the wild-type enzyme at physiological temperature. Critically, all of the MCSZ mutations identified to date result in ∼10-fold reduced cellular levels of PNKP protein, and reduced rates of chromosomal DNA strand break repair. Together, these data suggest that all four known MCSZ mutations reduce the cellular stability and level of PNKP protein, with three mutations likely ablating cellular DNA 5'-kinase activity and all of the mutations greatly reducing cellular DNA 3'-phosphatase activity
NGC 5548 in a Low-Luminosity State: Implications for the Broad-Line Region
We describe results from a new ground-based monitoring campaign on NGC 5548,
the best studied reverberation-mapped AGN. We find that it was in the lowest
luminosity state yet recorded during a monitoring program, namely L(5100) = 4.7
x 10^42 ergs s^-1. We determine a rest-frame time lag between flux variations
in the continuum and the Hbeta line of 6.3 (+2.6/-2.3) days. Combining our
measurements with those of previous campaigns, we determine a weighted black
hole mass of M_BH = 6.54 (+0.26/-0.25) x 10^7 M_sun based on all broad emission
lines with suitable variability data. We confirm the previously-discovered
virial relationship between the time lag of emission lines relative to the
continuum and the width of the emission lines in NGC 5548, which is the
expected signature of a gravity-dominated broad-line region. Using this lowest
luminosity state, we extend the range of the relationship between the
luminosity and the time lag in NGC 5548 and measure a slope that is consistent
with alpha = 0.5, the naive expectation for the broad line region for an
assumed form of r ~ L^alpha. This value is also consistent with the slope
recently determined by Bentz et al. for the population of reverberation-mapped
AGNs as a whole.Comment: 24 pages, 3 tables, 7 figures, accepted for publication in Ap
The Mass of the Black Hole in the Seyfert 1 Galaxy NGC 4593 from Reverberation Mapping
We present new observations leading to an improved black hole mass estimate
for the Seyfert 1 galaxy NGC 4593 as part of a reverberation-mapping campaign
conducted at the MDM Observatory. Cross-correlation analysis of the H_beta
emission-line light curve with the optical continuum light curve reveals an
emission-line time delay of 3.73 (+-0.75) days. By combining this time delay
with the H_beta line width, we derive a central black hole mass of M_BH =
9.8(+-2.1)x10^6 M_sun, an improvement in precision of a factor of several over
past results.Comment: 22 pages, 3 tables, 5 figures, accepted for publication in Ap
Genetic diversity of Mycobacterium tuberculosis isolated from tuberculosis patients in the Serengeti ecosystem in Tanzania
SummaryThis study was part of a larger cross-sectional survey that was evaluating tuberculosis (TB) infection in humans, livestock and wildlife in the Serengeti ecosystem in Tanzania. The study aimed at evaluating the genetic diversity of Mycobacterium tuberculosis isolates from TB patients attending health facilities in the Serengeti ecosystem. DNA was extracted from 214 sputum cultures obtained from consecutively enrolled newly diagnosed untreated TB patients aged ≥18 years. Spacer oligonucleotide typing (spoligotyping) and Mycobacterium Interspersed Repetitive Units and Variable Number Tandem Repeat (MIRU-VNTR) were used to genotype M. tuberculosis to establish the circulating lineages. Of the214 M. tuberculosis isolates genotyped, 55 (25.7%) belonged to the Central Asian (CAS) family, 52 (24.3%) were T family (an ill-defined family), 38 (17.8%) belonged to the Latin American Mediterranean (LAM) family, 25 (11.7%) to the East-African Indian (EAI) family, 25 (11.7%) comprised of different unassigned (‘Serengeti’) strain families, while 8 (3.7%) belonged to the Beijing family. A minority group that included Haarlem, X, U and S altogether accounted for 11 (5.2%) of all genotypes. MIRU-VNTR typing produced diverse patterns within and between families indicative of unlinked transmission chains. We conclude that, in the Serengeti ecosystem only a few successful families predominate namely CAS, T, LAM and EAI families. Other types found in lower prevalence are Beijing, Haarlem, X, S and MANU. The Haarlem, EAI_Somalia, LAM3 and S/convergent and X2 subfamilies found in this study were not reported in previous studies in Tanzania
An occupational therapy intervention for residents with stroke related disabilities in UK care homes (OTCH):Cluster randomised controlled trial
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