508 research outputs found

    Clinical and pathophysiological aspects of intrahepatic cholestasis of pregnancy

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    Objective: The pathogenesis of intrahepatic cholestasis of pregnancy (ICP) involves impaired bile acid and estrogen/progesterone metabolism and excretion based on genetic and environmental factors. In this thesis we evaluated different pathophysiological and clinical aspects of ICP, i.e., serum levels of vitamin D, the morphology of ICP placentas, maternal and fetal outcomes in ICP at a time of active management, and ICP-associated pregnancy conditions. Methods: In Paper I, we performed an observational study and compared the levels of active vitamin D (1,25-dihydroxy vitamin D3) in women with ICP and normal pregnancies. In Paper II we examined in a prospective case-control study morphological differences of placentas from untreated and ursodeoxycholic acid (UDCA) treated ICP, respectively, and normal pregnancies, by using stereology and systematic random sampling. In paper III, we estimated in a nationwide cohort study of more than 1.2 million singleton births in Sweden between 1997 and 2009 the actual prevalence of ICP and its association with adverse pregnancy and fetal outcomes, using data of the Swedish Medical Birth Registry (MBR). In Paper IV, we assessed in a hospital based retrospective cohort study the risk of emergency cesarean section (CS) and fetal asphyxia in ICP women with spontaneous and induced onset of labor at gestational weeks 37-39, by linkage of the MBR and a local obstetrical database. Results: We report for the first time that women with ICP have lower levels of active vitamin D. We also show that ICP substantially affects the morphology of the placenta, with increased surface capillary area and syncytial knots. These changes were not observed in UDCA-treated ICP. In our nationwide population based study, we found a previously unknown strong association of ICP with gestational diabetes, preeclampsia and large for gestational age, and that ICP bears an increased risk of moderate prematurity but not of stillbirth at a time of active management. We found that induction of labor in women with ICP in gestational weeks 37-39 in a tertiary Swedish hospital did not increase the risks of emergency CS or fetal asphyxia. Conclusions: Decreased levels of active vitamin D may contribute to the pathogenesis of ICP. ICP causes morphological changes in the placenta that might be improved by treatment with UDCA. Induction of labor in ICP does not increase the rate of emergency CS. The low risk of stillbirths at a time of modern management of ICP is reassuring but the strong association of ICP with gestational diabetes and preeclampsia needs consideration, e.g., by oral glucose tolerance testing and proper management of possibly coexisting conditions

    Diffractive Guiding of Waves by a Periodic Array of Slits

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    We show that in order to guide waves, it is sufficient to periodically truncate their edges. The modes supported by this type of wave guide propagate freely between the slits, and the propagation pattern repeats itself. We experimentally demonstrate this general wave phenomenon for two types of waves: (i) plasmonic waves propagating on a metal-air interface that are periodically blocked by nanometric metallic walls, and (ii) surface gravity water waves whose evolution is recorded, the packet is truncated, and generated again to show repeated patterns. This guiding concept is applicable for a wide variety of waves.Comment: 5 pages, 4 figure

    A global disorder of imprinting in the human female germ line

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    Imprinted genes are expressed differently depending on whether they are carried by a chromosome of maternal or paternal origin. Correct imprinting is established by germline-specific modifications; failure of this process underlies several inherited human syndromes. All these imprinting control defects are cis-acting, disrupting establishment or maintenance of allele-specific epigenetic modifications across one contiguous segment of the genome. In contrast, we report here an inherited global imprinting defect. This recessive maternal-effect mutation disrupts the specification of imprints at multiple, non-contiguous loci, with the result that genes normally carrying a maternal methylation imprint assume a paternal epigenetic pattern on the maternal allele. The resulting conception is phenotypically indistinguishable from an androgenetic complete hydatidiform mole, in which abnormal extra-embryonic tissue proliferates while development of the embryo is absent or nearly so. This disorder offers a genetic route to the identification of trans-acting oocyte factors that mediate maternal imprint establishment

    Totally Splittable Polytopes

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    A split of a polytope is a (necessarily regular) subdivision with exactly two maximal cells. A polytope is totally splittable if each triangulation (without additional vertices) is a common refinement of splits. This paper establishes a complete classification of the totally splittable polytopes.Comment: 15 pages, 7 figures; v2: major revision: corrections of some minor errors and some addition

    DNA-based Self-Assembly of Chiral Plasmonic Nanostructures with Tailored Optical Response

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    Surface plasmon resonances generated in metallic nanostructures can be utilized to tailor electromagnetic fields. The precise spatial arrangement of such structures can result in surprising optical properties that are not found in any naturally occurring material. Here, the designed activity emerges from collective effects of singular components equipped with limited individual functionality. Top-down fabrication of plasmonic materials with a predesigned optical response in the visible range by conventional lithographic methods has remained challenging due to their limited resolution, the complexity of scaling, and the difficulty to extend these techniques to three-dimensional architectures. Molecular self-assembly provides an alternative route to create such materials which is not bound by the above limitations. We demonstrate how the DNA origami method can be used to produce plasmonic materials with a tailored optical response at visible wavelengths. Harnessing the assembly power of 3D DNA origami, we arranged metal nanoparticles with a spatial accuracy of 2 nm into nanoscale helices. The helical structures assemble in solution in a massively parallel fashion and with near quantitative yields. As a designed optical response, we generated giant circular dichroism and optical rotary dispersion in the visible range that originates from the collective plasmon-plasmon interactions within the nanohelices. We also show that the optical response can be tuned through the visible spectrum by changing the composition of the metal nanoparticles. The observed effects are independent of the direction of the incident light and can be switched by design between left- and right-handed orientation. Our work demonstrates the production of complex bulk materials from precisely designed nanoscopic assemblies and highlights the potential of DNA self-assembly for the fabrication of plasmonic nanostructures.Comment: 5 pages, 4 figure

    Electromigration-Induced Propagation of Nonlinear Surface Waves

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    Due to the effects of surface electromigration, waves can propagate over the free surface of a current-carrying metallic or semiconducting film of thickness h_0. In this paper, waves of finite amplitude, and slow modulations of these waves, are studied. Periodic wave trains of finite amplitude are found, as well as their dispersion relation. If the film material is isotropic, a wave train with wavelength lambda is unstable if lambda/h_0 < 3.9027..., and is otherwise marginally stable. The equation of motion for slow modulations of a finite amplitude, periodic wave train is shown to be the nonlinear Schrodinger equation. As a result, envelope solitons can travel over the film's surface.Comment: 13 pages, 2 figures. To appear in Phys. Rev.

    Beta cell death by cell-free DNA and outcome after clinical islet transplantation

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    Background: Optimizing engraftment and early survival after clinical islet transplantation is critical to long-term function, but there are no reliable, quantifiable measures to assess beta cell death. Circulating cell free DNA (cfDNA) derived from beta cells has been identified as a novel biomarker to detect cell loss, and was recently validated in new-onset type 1 diabetes and in islet transplant patients. Methods: Herein we report beta cell cfDNA measurements after allotransplantation in 37 subjects and the correlation with clinical outcomes. Results: A distinctive peak of cfDNA was observed 1hr after transplantation in 31/37 (83.8%) of subjects. The presence and magnitude of this signal did not correlate with transplant outcome. The 1hr signal represents dead beta cells carried over into the recipient after islet isolation and culture, combined with acute cell death post infusion. Beta cell cfDNA was also detected 24hrs post-transplant (8/37 subjects, 21.6%). This signal was associated with higher 1-month insulin requirements (p=0.04), lower 1-month stimulated C-peptide levels (p=0.01) and overall worse 3-month engraftment, by insulin independence (ROC:AUC=0.70, p=0.03) and Beta 2 score (ROC:AUC=0.77, p=0.006). Conclusions: cfDNA-based estimation of beta cell death 24hrs after islet allotransplantation correlates with clinical outcome and could predict early engraftment.B.G.-L. is supported through the Alberta Innovates :Health Solutions (AIHS) Clinician Fellowship and through the CNTRP. A.P. is supported through AIHS Postgraduate Fellowship and CNTRP. A.M.J.S. is supported through AIHS, and holds a Canada Research Chair in Transplantation Surgery and Regenerative Medicine funded through the Government of Canada. A.M.J.S. is also funded by AIHS Collaborative Research and Innovation Opportunity Team Award and the Diabetes Research Institute Foundation of Canada (DRIFCan). Supported by grants from the Juvenile Diabetes Research Foundation (JDRF) (3-SRA-2014-38-Q-R, to Y.D. and A.M.J.S.), National Institute of Health (NIH) (HIRN grant UC4 DK104216, to Y.D.), DON foundation (Stichting Diabetes Onderzoek Nederland) (to Y.D), the European Union (ELASTISLET project, to Y.D.) and the Kahn foundation (to Y.D., R.S., and B.G.). Supported in part by a grant from The United States Agency for International Development (USAID) American Schools and Hospitals Abroad Program for the upgrading of the Hebrew University sequencing core facilit

    Bright and dark diffractive focusing

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    We investigate bright and dark diffractive focusing emerging in the free propagation of specific wave profiles. These general wave phenomena manifest themselves in matter, water, and classical waves. In this article, we lay the foundations for these effects and illustrate their origin in Wigner phase space. Our theoretical studies are supported by experimental demonstrations of dark focusing in water waves. Moreover, by using different phase slits we analyze several aspects of bright and dark focusing for classical and matter waves
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