149 research outputs found

    Multigroup Ethnic Identity Measure (MEIM) Expansion: Measuring Racial, Religious, and National Aspects of Sense of Ethnic Identity Within the United Kingdom

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    These studies examined the degree to which racial, religious, and national aspects of individuals' sense of ethnic identity stand as interrelated, yet distinct, constructs. Results of exploratory factor analyses in Study 1 (n = 272) revealed that a three-factor model specifying racial, religious, and national identities yielded optimal fit to correlational data from an expanded, 36-item version of the Multigroup Ethnic Identity Measure (MEIM; Roberts et al., 1999), although results left room for improvement in model fit. Subsequently, results of confirmatory factor analyses in Study 2 (n = 291) revealed that, after taking covariance among the items into account, a six-factor model specifying exploration and commitment dimensions within each of the racial, religious, and national identity constructs provided optimal fit. Implications for the utility of Goffman's (1963b) interactionist role theory and Erikson's (1968) ego psychology for understanding the full complexity of felt ethnic identity are discussed

    Blood Leukocyte Dna Methylation Predicts Risk of Future Myocardial infarction and Coronary Heart Disease

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    BACKGROUND: DNA methylation is implicated in coronary heart disease (CHD), but current evidence is based on small, cross-sectional studies. We examined blood DNA methylation in relation to incident CHD across multiple prospective cohorts. METHODS: Nine population-based cohorts from the United States and Europe profiled epigenome-wide blood leukocyte DNA methylation using the Illumina Infinium 450k microarray, and prospectively ascertained CHD events including coronary insufficiency/unstable angina, recognized myocardial infarction, coronary revascularization, and coronary death. Cohorts conducted race-specific analyses adjusted for age, sex, smoking, education, body mass index, blood cell type proportions, and technical variables. We conducted fixed-effect meta-analyses across cohorts. RESULTS: Among 11 461 individuals (mean age 64 years, 67% women, 35% African American) free of CHD at baseline, 1895 developed CHD during a mean follow-up of 11.2 years. Methylation levels at 52 CpG (cytosine-phosphate-guanine) sites were associated with incident CHD or myocardial infarction (false discovery rate CONCLUSION: Methylation of blood-derived DNA is associated with risk of future CHD across diverse populations and may serve as an informative tool for gaining further insight on the development of CHD

    Isotopic investigations of Chinese ceramics

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    This chapter provides insights into Chinese ceramic technologies of both bodies and glazes as well as provenance by using isotopes applied to a number of case studies. The use of Sr isotopes to investigate Chinese high-fired Celadon wares and blue-and-white Jingdezhen porcelain (Jiangxi province) has revealed a clear distinction associated with the fluxes used in the glazes: plant ash in celadons and limestone in Jingdezhen glazes, something that is not clear from major element analysis. Furthermore, the technique is able to suggest by implication the nature of the silica source used in the glazes—normally weathered granitic rocks or metamorphic rocks (porcelain stone) which also contains Sr. This leads to an isotopic mixing line of the 2 Sr-rich components and is proof that 2 Sr-rich components were mixed in the manufacture of limestone glaze. This is not the case for plant ash glazes. Eventually, the technique may be used in provenance studies. Like Sr isotope analysis, lead isotope analysis relies on there being a lack of or a minimal change in the isotope ratios when the raw materials are heated. Lead isotope analysis links the use of lead in glazes to the original metal ore and if a kiln uses a distinctive lead source in its glazes, it can provide a provenance for the pottery. This has been very successful in distinguishing Chinese Tang sancai wares made in the Huangye, Huangbao, Liquanfang and Qionglai kilns

    DNA methylation-based measures of biological age:meta-analysis predicting time to death

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    Estimates of biological age based on DNA methylation patterns, often referred to as "epigenetic age", "DNAm age", have been shown to be robust biomarkers of age in humans. We previously demonstrated that independent of chronological age, epigenetic age assessed in blood predicted all-cause mortality in four human cohorts. Here, we expanded our original observation to 13 different cohorts for a total sample size of 13,089 individuals, including three racial/ethnic groups. In addition, we examined whether incorporating information on blood cell composition into the epigenetic age metrics improves their predictive power for mortality. All considered measures of epigenetic age acceleration were predictive of mortality (p ≤ 8.2 x 10-9), independent of chronological age, even after adjusting for additional risk factors (p < 5.4 x 10-4), and within the racial/ethnic groups that we examined (non-Hispanic whites, Hispanics, African Americans). Epigenetic age estimates that incorporated information on blood cell composition led to the smallest p-values for time to death (p≤ 7.5 x 10-43). Overall, this study a) strengthens the evidence that epigenetic age predicts all-cause mortality above and beyond chronological age and traditional risk factors, and b) demonstrates that epigenetic age estimates that incorporate information on blood cell counts lead to highly significant associations with all-cause mortality

    Statistical and integrative system-level analysis of DNA methylation data

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    Epigenetics plays a key role in cellular development and function. Alterations to the epigenome are thought to capture and mediate the effects of genetic and environmental risk factors on complex disease. Currently, DNA methylation is the only epigenetic mark that can be measured reliably and genome-wide in large numbers of samples. This Review discusses some of the key statistical challenges and algorithms associated with drawing inferences from DNA methylation data, including cell-type heterogeneity, feature selection, reverse causation and system-level analyses that require integration with other data types such as gene expression, genotype, transcription factor binding and other epigenetic information

    A non-invasive investigation of Egyptian faience using long wavelength optical coherence tomography (OCT) at 2 μm

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    Egyptian faience is a non-clay ceramic semi-transparent material, formed of a quartz core and alkali lime glaze with some cases exhibiting an interaction layer between them. Several possible glazing methods have been identified. Previous investigations have tried to identify the glazing technique by using the microstructure images obtained from polished sections using scanning electron microscope(SEM). Such techniques require sampling which is not feasible on museum collections. Optical Coherence Tomography (OCT) is a non-invasive 3D imaging technique, that produces virtual cross sections of transparent and semi-transparent materials. Liang et al. (2012a) investigated the feasibility of using OCT to non-invasively investigate microstructures of Egyptian faience, but the limited probing depth of the 930nm OCT prevented viewing down to the core of the objects, where the presence of glass was thought to be a distinguishing feature between some of the manufacturing techniques, and where the particle size of the quartz may indicate the difference in the raw material. In this paper, a unique longer wavelength OCT at 2um is used to scan a number of ancient Egyptian faience objects including ring and shabti fragments. It was found that the core of the faience could be imaged at this longer wavelength, allowing comparisons in all the layers within the microstructure, and leading to discussions about the possible glazing methods. The 2um OCT offers the possibilities of rapid, non invasive imaging of faience microstructure down to the core, allowing comprehensive studies of intact objects and large museum collections
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