179 research outputs found

    The origin of late archaean granitoids in the Sukumaland greenstone belt of Northern Tanzania: geochemical and isotopic constraints

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    Granitoids intruding the late Archaean sequences of the Sukumaland Greenstone Belt of northern Tanzania belong to two distinct geochemical suites. Suite 1 is characterised by Na2O/K2O > 1 (1.04 – 4.67), high Sr/Y (56 – 204) and Ba/Rb ratios (6.1 – 27.1) and low Rb/Sr ratios (0.08 - 0.25). The rocks are enriched in Sr (405 – 1264 ppm) and depleted in Yb (0.17 – 0.93 ppm) and Rb (56 – 132 ppm). On chondrite-normalised REE diagrams, the rocks display highly fractionated patterns characterised by relative LREE enrichment ((La/Yb)N = 23 – 128 and (Gd/Yb)N = 3.10 – 8.54) and lower concentrations of the HREE (YbN = 0.80 – 4.45). On primitive mantle-normalised spidergrams, Nb and Ti, together with P and Y are depleted relative to adjacent elements. The major and trace element characteristics of Suite 1 are comparable to those of typical Archaean TTG suites and High Silica Adakites (HSA). Suite 2 granitoids are characterised by Na2O/K2O < 1, low Sr/Y (2.80 – 41.7) and Ba/Rb (0.40 – 8.91) ratios and high Rb/Sr (0.30 – 6.27) ratios. Suite 2 is also characterised by low Sr (53 - 326 ppm) and high Rb (40 - 365 ppm) and Yb (0.44 – 1.36 ppm) contents. Compared to Suite 1, Suite 2 rocks display less fractionated REE patterns ((La/Yb)N = 15 – 86 and (Gd/Yb)N = 1.73 – 6.74) and are characterised by higher concentrations of the HREE (YbN = 2.1 – 6.5). On primitive mantle-normalised spidergrams, Suite 2 samples, like those of Suite 1, show relative depletion in Th, Nb and Ti, together with P and Y relative to adjacent elements. Sm-Nd mean crustal residence ages for both suites are indistinguishable and range between 2470 and 2720 Ma with a mean of 2610 &#61617; 35 Ma (2 SE), similar to the emplacement age of 2620 &#61617; 40 Ma. The granitoids are interpreted to have formed by partial melting at the base of a late Archaean thickened sub-arc basaltic crust. Melting to form the Suite 1 granitoids occurred in the eclogite stability field whereas Suite 2 formed by melting at shallower depth in the garnet amphibolite stability field. Tanzania Journal of Science Vol. 32 (1) 2006: pp. 75-8

    Quantum impurity with 2/3 local moment in 1D quantum wires: an NRG study

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    We study a Kondo state that is strongly influenced by its proximity to an w^-1/2 singularity in the metallic host density of states. This singularity occurs at the bottom of the band of a 1D chain, for example. We first analyze the non-interacting system: A resonant state e_d, located close to the band singularity, suffers a strong `renormalization', such that a bound state is created below the bottom of the band in addition to a resonance in the continuum. When e_d is positioned right at the singularity, the spectral weight of the bound state is 2/3, irrespective of its coupling to the conduction electrons. The interacting system is modeled using the Single Impurity Anderson Model, which is then solved using the Numerical Renormalization Group method. We observe that the Hubbard interaction causes the bound state to suffer a series of transformations, including level splitting, transfer of spectral weight, appearance of a spectral discontinuity, changes in binding energy (the lowest state moves farther away from the bottom of the band), and development of a finite width. When e_d is away from the singularity and in the intermediate valence regime, the impurity occupancy is lower. As e_d moves closer to the singularity, the system partially recovers Kondo regime properties, i.e., higher occupancy and lower Kondo temperature T_K. The impurity thermodynamic properties show that the local moment fixed point is also strongly affected by the existence of the bound state. When e_d is close to the singularity, the local moment fixed point becomes impervious to charge fluctuations (caused by bringing e_d close to the Fermi energy), in contrast to the local moment suppression that occurs when e_d is away from the singularity. We also discuss an experimental implementation that shows similar results to the quantum wire, if the impurity's metallic host is an armchair graphene nanoribbon.Comment: 13 pages, 20 figure

    Development of novel composite data quality scores to evaluate facility-level data quality in electronic data in Kenya: A nationwide retrospective cohort study

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    BACKGROUND: In this evaluation, we aim to strengthen Routine Health Information Systems (RHIS) through the digitization of data quality assessment (DQA) processes. We leverage electronic data from the Kenya Health Information System (KHIS) which is based on the District Health Information System version 2 (DHIS2) to perform DQAs at scale. We provide a systematic guide to developing composite data quality scores and use these scores to assess data quality in Kenya. METHODS: We evaluated 187 HIV care facilities with electronic medical records across Kenya. Using quarterly, longitudinal KHIS data from January 2011 to June 2018 (total N = 30 quarters), we extracted indicators encompassing general HIV services including services to prevent mother-to-child transmission (PMTCT). We assessed the accuracy (the extent to which data were correct and free of error) of these data using three data-driven composite scores: 1) completeness score; 2) consistency score; and 3) discrepancy score. Completeness refers to the presence of the appropriate amount of data. Consistency refers to uniformity of data across multiple indicators. Discrepancy (measured on a Z-scale) refers to the degree of alignment (or lack thereof) of data with rules that defined the possible valid values for the data. RESULTS: A total of 5,610 unique facility-quarters were extracted from KHIS. The mean completeness score was 61.1% [standard deviation (SD) = 27%]. The mean consistency score was 80% (SD = 16.4%). The mean discrepancy score was 0.07 (SD = 0.22). A strong and positive correlation was identified between the consistency score and discrepancy score (correlation coefficient = 0.77), whereas the correlation of either score with the completeness score was low with a correlation coefficient of -0.12 (with consistency score) and -0.36 (with discrepancy score). General HIV indicators were more complete, but less consistent, and less plausible than PMTCT indicators. CONCLUSION: We observed a lack of correlation between the completeness score and the other two scores. As such, for a holistic DQA, completeness assessment should be paired with the measurement of either consistency or discrepancy to reflect distinct dimensions of data quality. Given the complexity of the discrepancy score, we recommend the simpler consistency score, since they were highly correlated. Routine use of composite scores on KHIS data could enhance efficiencies in DQA at scale as digitization of health information expands and could be applied to other health sectors beyondHIV clinics

    Walker-Warburg syndrome

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    Walker-Warburg Syndrome (WWS) is a rare form of autosomal recessive congenital muscular dystrophy associated with brain and eye abnormalities. WWS has a worldwide distribution. The overall incidence is unknown but a survey in North-eastern Italy has reported an incidence rate of 1.2 per 100,000 live births. It is the most severe form of congenital muscular dystrophy with most children dying before the age of three years. WWS presents at birth with generalized hypotonia, muscle weakness, developmental delay with mental retardation and occasional seizures. It is associated with type II cobblestone lissencephaly, hydrocephalus, cerebellar malformations, eye abnormalities and congenital muscular dystrophy characterized by hypoglycosylation of α-dystroglycan. Several genes have been implicated in the etiology of WWS, and others are as yet unknown. Several mutations were found in the Protein O-Mannosyltransferase 1 and 2 (POMT1 and POMT2) genes, and one mutation was found in each of the fukutin and fukutin-related protein (FKRP) genes. Laboratory investigations usually show elevated creatine kinase, myopathic/dystrophic muscle pathology and altered α-dystroglycan. Antenatal diagnosis is possible in families with known mutations. Prenatal ultrasound may be helpful for diagnosis in families where the molecular defect is unknown. No specific treatment is available. Management is only supportive and preventive

    Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy

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    Hypoglycosylation and reduced laminin-binding activity of α-dystroglycan are common characteristics of dystroglycanopathy, which is a group of congenital and limb-girdle muscular dystrophies. Fukuyama-type congenital muscular dystrophy (FCMD), caused by a mutation in the fukutin gene, is a severe form of dystroglycanopathy. A retrotransposal insertion in fukutin is seen in almost all cases of FCMD. To better understand the molecular pathogenesis of dystroglycanopathies and to explore therapeutic strategies, we generated knock-in mice carrying the retrotransposal insertion in the mouse fukutin ortholog. Knock-in mice exhibited hypoglycosylated α-dystroglycan; however, no signs of muscular dystrophy were observed. More sensitive methods detected minor levels of intact α-dystroglycan, and solid-phase assays determined laminin binding levels to be ∼50% of normal. In contrast, intact α-dystroglycan is undetectable in the dystrophic Largemyd mouse, and laminin-binding activity is markedly reduced. These data indicate that a small amount of intact α-dystroglycan is sufficient to maintain muscle cell integrity in knock-in mice, suggesting that the treatment of dystroglycanopathies might not require the full recovery of glycosylation. To examine whether glycosylation defects can be restored in vivo, we performed mouse gene transfer experiments. Transfer of fukutin into knock-in mice restored glycosylation of α-dystroglycan. In addition, transfer of LARGE produced laminin-binding forms of α-dystroglycan in both knock-in mice and the POMGnT1 mutant mouse, which is another model of dystroglycanopathy. Overall, these data suggest that even partial restoration of α-dystroglycan glycosylation and laminin-binding activity by replacing or augmenting glycosylation-related genes might effectively deter dystroglycanopathy progression and thus provide therapeutic benefits

    The use of complementary and alternative medicine among people living with diabetes in Sydney

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    Background: Complementary and alternative medicine (CAM) is common in patients with chronic disease such as diabetes mellitus. The primary objective of the study was to determine the overall prevalence and type of CAM use in individuals with diabetes mellitus (DM) in Western Sydney and to compare the prevalence and factors associated with CAM use with the literature.Methods: A multicenter cross-sectional study was undertaken using a self-completed questionnaire distributed to patients with DM attending a public hospital and specialist endocrinology clinics in the region. The type of DM and pattern of CAM utilisation were analyzed.Results: Sixty nine people responded to the questionnaire: age range of 18-75 years during a twelve week collection period. Overall, 32 respondents with diabetes were using some form of CAM, resulting in a utilisation rate of 46.3%. Twenty of the 32 CAM users used CAM specifically to treat their diabetes accounting for 28.9% of the respondent sample population. Multivitamins (40%), cinnamon, Co-enzyme q10 and prayer were the most frequently used CAM modalities. There was no significant difference between males and females, age range, income or diabetes complications between CAM and non-CAM users. (p values each &gt; 0.05) The factor most significantly associated with CAM usage was being born overseas (p = 0.044).Conclusions: Almost half the respondents (46.3%) used CAM: 28% used CAM specifically to treat their diabetes. Individuals born overseas were significantly more likely to use CAM than those born in Australia. Other factors such as age, gender, wealth and duration of living with diabetes were not associated with higher rate of CAM usage.<br /

    Implementation of Client-Centered Care Coordination for HIV Prevention with Black Men Who Have Sex with Men: Activities, Personnel Costs, and Outcomes—HPTN 073

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    Background: Black men who have sex with men (MSM) experience disproportionate rates of HIV infection in the USA, despite being no more likely to engage in sexual risk behaviors than other MSM racial/ethnic groups. HIV pre-exposure prophylaxis (PrEP) has been shown to reduce risk of HIV acquisition; however, rates of PrEP use among Black MSM remain low. Clinical, psychosocial, and structural factors have been shown to impact PrEP use and adherence among Black MSM. Care coordination of HIV prevention services has the potential to improve PrEP use and adherence for Black MSM, as it has been shown to improve HIV-related care outcomes among people living with HIV. Methods: Client-centered care coordination (C4) is a multi-level intervention designed to address clinical, psychosocial, and structural barriers to HIV prevention services for Black MSM within HPTN 073, a PrEP demonstration project among Black MSM in three cities in the USA. The current study examined the implementation process of C4, specifically investigating the activities, cost, time, and outcomes associated with the C4 intervention. Results: On average, participants engaged in five care coordination encounters. The vast majority of care coordination activities were conducted by counselors, averaging 30 min per encounter. The cost of care coordination was relatively low with a mean cost of $8.70 per client encounter. Conclusion: Although client-centered care coordination was initially implemented in well-resourced communities with robust HIV research and service infrastructure, our findings suggest that C4 can be successfully implemented in resource constrained communities

    Analysis of HIV Diversity in HIV-Infected Black Men Who Have Sex with Men (HPTN 061)

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    Background: HIV populations often diversify in response to selective pressures, such as the immune response and antiretroviral drug use. We analyzed HIV diversity in Black men who have sex with men who were enrolled in the HIV Prevention Trials Network 061 study. Methods: A high resolution melting (HRM) diversity assay was used to measure diversity in six regions of the HIV genome: two in gag, one in pol, and three in env. HIV diversity was analyzed for 146 men who were HIV infected at study enrollment, including three with acute infection and 13 with recent infection (identified using a multi-assay algorithm), and for 21 men who seroconverted during the study. HIV diversification was analyzed in a paired analysis for 62 HIV-infected men using plasma samples from the enrollment and 12-month (end of study) visits. Results: Men with acute or recent infection at enrollment and seroconverters had lower median HRM scores (lower HIV diversity) than men with non-recent infection in all six regions analyzed. In univariate analyses, younger age, higher CD4 cell count, and HIV drug resistance were associated with lower median HRM scores in multiple regions; ARV drug detection was marginally associated with lower diversity in the pol region. In multivariate analysis, acute or recent infection (all six regions) and HIV drug resistance (both gag regions) were associated with lower median HRM scores. Diversification in the pol region over 12 months was greater for men with acute or recent infection, higher CD4 cell count, and lower HIV viral load at study enrollment. Conclusions: HIV diversity was significantly associated with duration of HIV infection, and lower gag diversity was observed in men who had HIV drug resistance. HIV pol diversification was more pronounced in men with acute or recent infection, higher CD4 cell count, and lower HIV viral load
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