37 research outputs found

    Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: A study of 3,310 subjects from India and the US

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    <p>Abstract</p> <p>Background</p> <p>Polymorphisms in intron 15 of potassium voltage-gated channel, KQT-like subfamily member 1 (<it>KCNQ1</it>) gene have been associated with type II diabetes (T2D) in Japanese genome-wide association studies (GWAS). More recently a meta-analysis of European GWAS has detected a new independent signal associated with T2D in intron 11 of the <it>KCNQ1 </it>gene. The purpose of this investigation is to examine the role of these variants with T2D in populations of Asian Indian descent from India and the US.</p> <p>Methods</p> <p>We examined the association between four variants in the <it>KCNQ1 </it>gene with T2D and related quantitative traits in a total of 3,310 Asian Indian participants from two different cohorts comprising 2,431 individuals of the Punjabi case-control cohort from the Sikh Diabetes Study and 879 migrant Asian Indians living in the US.</p> <p>Results</p> <p>Our data confirmed the association of a new signal at the <it>KCNQ1 </it>locus (rs231362) with T2D showing an allelic odds ratio (OR) of 1.24 95%CI [1.08-1.43], p = 0.002 in the Punjabi cohort. A moderate association with T2D was also seen for rs2237895 in the Punjabi (OR 1.14; p = 0.036) and combined cohorts (meta-analysis OR 1.14; p = 0.018). Three-site haplotype analysis of rs231362, rs2237892, rs2237895 exhibited considerably stronger evidence of association of the GCC haplotype with T2D showing OR of 1.24 95%CI [1.00-1.53], p = 0.001, permutation p = 8 × 10<sup>-4 </sup>in combined cohorts. The 'C' risk allele carriers of rs2237895 had significantly reduced measures of HOMA-B in the US cohort (p = 0.008) as well as in combined cohort in meta-analysis (p = 0.009).</p> <p>Conclusions</p> <p>Our investigation has confirmed that the variation within the <it>KCNQ1 </it>locus confers a significant risk to T2D among Asian Indians. Haplotype analysis further suggested that the T2D risk associated with <it>KCNQ1 </it>SNPs may be derived from 'G' allele of rs231362 and 'C' allele of rs2237895 and this appears to be mediated through β cell function.</p

    Cascades on online social networks: a chronological account

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    Online social network platforms have served as a substantial venue for research, offering a plethora of data that can be analysed to cultivate insights about the way humans behave and interact within the virtual borders of these platforms. In addition to generating content, these platforms provide the means to spread content via built-in functionalities. The traces of the spreading content and the individuals’ incentives behind such behaviour are all parts of a phenomenon known as information diffusion. This phenomenon has been extensively studied in the literature from different perspectives, one of which is cascades: the traces of the spreading content. These traces form structures that link users to each other, where these links represent the direction of information flow between the users. In fact, cascades have served as an artefact to study the information diffusion processes on online social networks. In this paper, we present a survey of cascades; we consider their definitions and significance. We then look into their topology and what information is used to construct them and how the type of content and the platform can consequently affect cascades’ networks. Additionally, we present a survey of the structural and temporal features of cascades; we categorise them, define them and explain their significance, as these features serve as quantifiers to understand and overcome the complex nature of cascades
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