9 research outputs found
Scalable Data Access Control in RFID-Enabled Supply Chain
By attaching RFID tags to products, supply chain participants can identify products and create product data to record the product particulars in transit. Participants along the supply chain share their product data to enable information exchange and support critical decisions in production operations. Such an information sharing essentially requires a data access control mechanism when the product data relates to sensitive business issues. However, existing access control solutions are ill suited to the RFID-enabled supply chain, as they are not scalable in handling a huge number of tags, introduce vulnerability to the product data, and performs poorly to support privilege revocation of product data. We present a new scalable data access control system that addresses these limitations. Our system provides an item-level data access control mechanism that defines and enforces access policies based on both the participants' role attribute and the products' RFID tag attribute. Our system further provides an item-level privilege revocation mechanism by allowing the participants to delegate encryption updates in revocation operation without disclosing the underlying data contents. We design a new updatable encryption scheme and integrate it with Cipher text Policy-Attribute Based Encryption (CP-ABE) to implement the key components of our system
Family outcome disparities between sexual minority and heterosexual families: a systematic review and meta-analysis
Background The number of children in sexual minority parent families has increased. This systematic review aims to synthesise the evidence of disparities in family outcomes between sexual minority and heterosexual families and to identify specific social risk factors of poor family outcomes.Methods We systematically searched PubMed, the Web of Science, Embase, the Cochrane Library and APA PsycNet for original studies that compared family outcomes between sexual minority and heterosexual families. Two reviewers independently selected studies and assessed the risk of bias of included studies. Narrative synthesis and meta-analysis were conducted to synthesise evidence.Results Thirty-four articles were included. The narrative synthesis results revealed several significant findings for children’s gender role behaviour and gender identity/sexual orientation outcomes. Overall, 16 of 34 studies were included in the meta-analyses. The quantitative synthesis results suggested that sexual minority families may perform better in children’s psychological adjustment and parent–child relationship than heterosexual families (standardised mean difference (SMD) −0.13, 95% CI −0.20 to −0.05; SMD 0.13, 95% CI 0.06 to 0.20), but not couple relationship satisfaction (SMD 0.26, 95% CI −0.13 to 0.64), parental mental health (SMD 0.00, 95% CI −0.16 to 0.16), parenting stress (SMD 0.01, 95% CI −0.20 to 0.22) or family functioning (SMD 0.18, 95% CI −0.11 to 0.46).Conclusion Most of the family outcomes are similar between sexual minority and heterosexual families, and sexual minority families have even better outcomes in some domains. Relevant social risk factors of poor family outcomes included stigma and discrimination, poor social support and marital status, etc. The next step is to integrate multiple aspects of support and multilevel interventions to reduce the adverse effects on family outcomes with a long-term goal of influencing policy and law making for better services to individuals, families, communities and schools
High baseline body mass index predicts recovery of CD4+ T lymphocytes for HIV/AIDS patients receiving long-term antiviral therapy.
The relationship between baseline BMI and CD4+ T cells during follow-up in HIV patients in China requires further evaluation. We conducted a retrospective cohort study based on adult AIDS patients who underwent or received antiretroviral therapy from 2003 to 2019 in Guangxi, China. BMI was divided into categories and compared, and after adjusting for BMI being related to the change in CD4 lymphocyte count, with normal weight as the reference group, the BMI before treatment was positively correlated with the changes in CD4+ T cells at different time periods. Among them, obese patients had significant CD4+ cell gain. In patients with pretreatment CD4+ T lymphocyte counts <200 cells/μL, a higher BMI was associated with an increased likelihood of achieving immunologic reconstitution [≥350 cells/μL: AHR: 1.02(1.01, 1.04), P = 0.004; ≥500 cells/μL: AHR: 1.03 (1.01, 1.05), P = 0.004]. Underweight in HIV patients was a risk factor for poor viral suppression [AHR: 1.24 (1.04, 1.48), P = 0.016]. Our study demonstrated that HIV/AIDS patients receiving ART with higher baseline BMI had better immune reconstitution and that baseline BMI could be an important predictor of immune reconstitution in patients receiving ART. Baseline BMI was not associated with virological failure, but a lower baseline BMI indicated poor viral suppression during follow-up
Observation of at center-of-mass energies from 4.085 to 4.600 GeV
We observe for the first time the process with data collected by the BESIII experiment. Significant signals are observed at the center-of-mass energy GeV, and the Born cross section is measured to be pb. Evidence for is observed at GeV with a Born cross section of pb, and upper limits on the production cross section at other center-of-mass energies between 4.085 and 4.600 GeV are determined
Study of two-photon decays of pseudoscalar mesons via J/Psi radiative decays
Using a sample of 4.48 x 10(8) Psi(3686) events collected with the BESIII detector at the BEPCII collider, we study the two-photon decays of the pseudoscalar mesons pi(0,) eta , eta' , eta(1405), eta(1475), eta(1760), and X(1835) in J/Psi radiative decays using Psi(3686) -> pi(+) pi(-) J/Psi events. The pi(0), eta, and eta' mesons are clearly observed in the two-photon mass spectra, and the branching fractions are determined to be B(J/Psi -> gamma pi(0) -> 3 gamma) = (3.57 +/- 0.12 +/- 0.16) x 10(-5), B(J/Psi -> gamma eta -> 3 gamma) = (4.42 +/- 0.04 +/- 0.18) x 10(-4), and B(J/Psi -> gamma eta' -> 2 gamma) = (1.26 +/- 0.02 +/- 0.05) x 10(-4), where the first error is statistical and the second is systematic. No clear signal for eta(1405), eta(1475), eta(1760) or X(1835) is observed in the two- photon mass spectra, and upper limits at the 90% confidence level on the product branching fractions are obtained