18 research outputs found

    Tensionless supersymmetric M2 branes in AdS4×S7AdS_4 \times S^7 and Giant Diabolo

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    We find various supersymmetric configurations of toroidal M2 brane solutions in \AdS_4 \times S^7 or, more generally, in \AdS_4 \times S^7/Z_k. In this class we identify solutions preserving 1/4 and 1/8 supersymmetries of the background. The supersymmetric M2 branes have angular momenta and winding on S7S^7, and null world-volumes. In certain cases they collapse to string-like configurations. These configurations can be viewed as a higher-dimensional (membrane) analog of BMN states. We compute the energy and angular momenta, showing that all supersymmetric configurations obey the BPS relation E=J/RE=J/R ,\ J=i=14JiJ= \sum_{i=1}^4 |J_i| with E,JE, J\to \infty . Finally, we also study another class of supersymmetric M2-branes, including uncompact rotating membranes of "diabolo" shape.Comment: 27 pages, 3 figures. Small correction

    Health care utilization in the elderly Mexican population: Expenditures and determinants

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    <p>Abstract</p> <p>Background</p> <p>Worldwide population aging has been considered one of the most important demographic phenomena, and is frequently referred as a determinant of health costs and expenditures. These costs are an effect either of the aging process itself (social) or because of the increase that comes with older age (individual).</p> <p>Objective</p> <p>To analyze health expenditures and its determinants in a sample of Mexican population, for three dimensions acute morbidity, ambulatory care and hospitalization focusing on different age groups, particularly the elderly.</p> <p>Methods</p> <p>A secondary analysis of the Mexican National Health and Nutrition Survey (ENSANUT), 2006 was conducted. A descriptive analysis was performed to establish a health profile by socio-demographic characteristics. Logistic regression models were estimated to determine the relation between acute morbidity, ambulatory care, hospitalization and age group; to establish the determinants of hospitalization among the population 60 years and older; and to determine hospitalization expenditures by age.</p> <p>Results</p> <p>Higher proportion of elderly reporting health problems was found. Average expenditures of hospitalization in households were 240.6amdlls,whereasinhouseholdsexclusivelywithelderlytheexpenditurewas240.6 am dlls, whereas in households exclusively with elderly the expenditure was 308.9 am dlls, the highest among the considered age groups. The multivariate analysis showed higher probability of being hospitalized among the elderly, but not for risks for acute morbidity and ambulatory care. Among the elderly, older age, being male or living in a city or in a metro area implied a higher probability of hospitalization during the last year, with chronic diseases playing a key role in hospitalization.</p> <p>Conclusions</p> <p>The conditions associated with age, such as chronic diseases, have higher weight than age itself; therefore, they are responsible for the higher expenditures reported. Conclusions point towards a differentiated use and intensity of health services depending on age. The projected increase in hospitalization and health care needs for this group requires immediate attention.</p

    Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen Malformation

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    This is the author accepted manuscript. The final version is available from Elsevier via the DOI in this record Normal vascular development includes the formation and specification of arteries, veins, and intervening capillaries. Vein of Galen malformations (VOGMs) are among the most common and severe neonatal brain arterio-venous malformations, shunting arterial blood into the brain's deep venous system through aberrant direct connections. Exome sequencing of 55 VOGM probands, including 52 parent-offspring trios, revealed enrichment of rare damaging de novo mutations in chromatin modifier genes that play essential roles in brain and vascular development. Other VOGM probands harbored rare inherited damaging mutations in Ephrin signaling genes, including a genome-wide significant mutation burden in EPHB4. Inherited mutations showed incomplete penetrance and variable expressivity, with mutation carriers often exhibiting cutaneous vascular abnormalities, suggesting a two-hit mechanism. The identified mutations collectively account for ∼30% of studied VOGM cases. These findings provide insight into disease biology and may have clinical implications for risk assessment.Yale-NIH Center for Mendelian GenomicsNational Institutes of Health (NIH)American Heart AssociationHoward Hughes Institut
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